Re: [R] Substituting Greek symbols in some tick labels

2013-07-05 Thread David Winsemius


On Jul 4, 2013, at 8:14 PM, Eric Archer - NOAA Federal wrote:

I have a character vector that I'm using to label ticks in a  
dotchart. Some

of the elements in the vector have an asterisk (*) where a Greek Delta
needs to be placed when the plot is generated. Here's a simple  
example:


x - 1:4
x.lab - c(a*a, bbb, c*c, ddd)
dotchart(x, labels = x.lab)

The first and third labels should be 'aDeltaa' and 'cDeltac'. I've
tried things like,

x.lab - strsplit(x.lab, [*])
x.lab - lapply(x.lab, function(y) expression(paste(y, sep = Delta)))


The plotmath function paste has no sep argument.

Do you want to do this by hand? (Since you have not offered values  
of 'y'.)


x.lab - expression( a*Delta*a, bbb, c*Delta*c, ddd)

#   Note use of * and no quotes in an expression vector.

 x - 1:4
dotchart(x, labels = x.lab)

--
David.



but because 'y' is unevaluated, the resulting list elements won't  
work as
tick labels. I've tried to modify it by using bquote and substitute,  
but

couldn't get anything closer. Any suggestions? Thanks!

Cheers,
eric

--

Eric Archer, Ph.D.
Southwest Fisheries Science Center
NMFS, NOAA
8901 La Jolla Shores Drive
La Jolla, CA 92037 USA
858-546-7121 (work)
858-546-7003 (FAX)

Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp

The universe doesn't care what you believe.
The wonderful thing about science is that it
  doesn't ask for your faith, it just asks
  for your eyes.  - Randall Munroe

Lighthouses are more helpful than churches.
  - Benjamin Franklin

  ...but I'll take a GPS over either one.
  - John C. Craig George

[[alternative HTML version deleted]]

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David Winsemius, MD
Alameda, CA, USA

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Re: [R] Substituting Greek symbols in some tick labels

2013-07-05 Thread Eric Archer - NOAA Federal
David, thanks for the reply.

No, I don't want to do it by hand because the actual data that I need to
label is much larger and variable. The deltas occur in the label character
vector for some labels and not others and are in different positions in the
character strings.

In the example I gave, the 'y' is the argument in the function to the
lapply where I was trying to iterate over the results from 'strsplit' to
insert the 'Delta' - the results showed me it wasn't the way to go, but I
was giving an example of what I'd tried.

Cheers,
eric


On Thu, Jul 4, 2013 at 11:31 PM, David Winsemius dwinsem...@comcast.netwrote:


 On Jul 4, 2013, at 8:14 PM, Eric Archer - NOAA Federal wrote:

  I have a character vector that I'm using to label ticks in a dotchart.
 Some
 of the elements in the vector have an asterisk (*) where a Greek Delta
 needs to be placed when the plot is generated. Here's a simple example:

 x - 1:4
 x.lab - c(a*a, bbb, c*c, ddd)
 dotchart(x, labels = x.lab)

 The first and third labels should be 'aDeltaa' and 'cDeltac'. I've
 tried things like,

 x.lab - strsplit(x.lab, [*])
 x.lab - lapply(x.lab, function(y) expression(paste(y, sep = Delta)))


 The plotmath function paste has no sep argument.

 Do you want to do this by hand? (Since you have not offered values of
 'y'.)

 x.lab - expression( a*Delta*a, bbb, c*Delta*c, ddd)

 #   Note use of * and no quotes in an expression vector.

  x - 1:4
 dotchart(x, labels = x.lab)

 --
 David.


 but because 'y' is unevaluated, the resulting list elements won't work as
 tick labels. I've tried to modify it by using bquote and substitute, but
 couldn't get anything closer. Any suggestions? Thanks!

 Cheers,
 eric

 --

 Eric Archer, Ph.D.
 Southwest Fisheries Science Center
 NMFS, NOAA
 8901 La Jolla Shores Drive
 La Jolla, CA 92037 USA
 858-546-7121 (work)
 858-546-7003 (FAX)

 Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
 ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp

 The universe doesn't care what you believe.
 The wonderful thing about science is that it
   doesn't ask for your faith, it just asks
   for your eyes.  - Randall Munroe

 Lighthouses are more helpful than churches.
   - Benjamin Franklin

   ...but I'll take a GPS over either one.
   - John C. Craig George

 [[alternative HTML version deleted]]

 __**
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/**listinfo/r-helphttps://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/**
 posting-guide.html http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


 David Winsemius, MD
 Alameda, CA, USA




-- 

Eric Archer, Ph.D.
Southwest Fisheries Science Center
NMFS, NOAA
8901 La Jolla Shores Drive
La Jolla, CA 92037 USA
858-546-7121 (work)
858-546-7003 (FAX)

Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp

The universe doesn't care what you believe.
 The wonderful thing about science is that it
   doesn't ask for your faith, it just asks
   for your eyes.  - Randall Munroe

Lighthouses are more helpful than churches.
   - Benjamin Franklin

   ...but I'll take a GPS over either one.
   - John C. Craig George

[[alternative HTML version deleted]]

__
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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] g2 test...

2013-07-05 Thread Ben Bolker
Fernando Marmolejo Ramos fernando.marmolejoramos at adelaide.edu.au writes:

 

 [snip]

 is it appropriate to use a Log likelihood ratio (G-test) test of
independence when dealing with repeated
 categorical responses (e.g. 2 by 2 table) instead of the McNemar test?

 [snip]

  Not an R question.  Try http://stats.stackexchange.com instead?

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Re: [R] g2 test...

2013-07-05 Thread peter dalgaard

On Jul 5, 2013, at 08:49 , Ben Bolker wrote:

 Fernando Marmolejo Ramos fernando.marmolejoramos at adelaide.edu.au 
 writes:
 
 
 
 [snip]
 
 is it appropriate to use a Log likelihood ratio (G-test) test of
 independence when dealing with repeated
 categorical responses (e.g. 2 by 2 table) instead of the McNemar test?
 
 [snip]
 
  Not an R question.  Try http://stats.stackexchange.com instead?

It probably has a no-homework rule too, though

-- 
Peter Dalgaard, Professor,
Center for Statistics, Copenhagen Business School
Solbjerg Plads 3, 2000 Frederiksberg, Denmark
Phone: (+45)38153501
Email: pd@cbs.dk  Priv: pda...@gmail.com

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[R] Error when building a custom package

2013-07-05 Thread cvo
Hi

I'm have trouble building a custom package in R. Building the package on my
colleagues computer (who made the R code content) has been (and is still)
working fine for a long time, but I simply can't duplicate the setup right
somehow (even with his help)

I have installed the same versions of software as my colleague: Windows 7, R
2.13.1 (with the required additional packages), Rtools 2.13, Miktex 2.9. All
of which are included in the Windows PATH variable as instructed by him (and
in various online tutorials)

I only get an error message, when trying to build a binary file (or runnning
/R CMD check package name/), not the standard tar.gz. Here is what the
output looks like in the command prompt:
/  * installing *source* package 'slo' ...
  ** R
  ** inst
  ** preparing package for lazy loading
  Loading required package: car
  Warning: package 'car' was built under R version 2.13.2
  Loading required package: MASS
  Loading required package: nnet
  Loading required package: survival
  Loading required package: splines
  Creating a new generic function for plot in slo
  Error in file(file, r, encoding = encoding) : 
cannot open the connection
  ERROR: lazy loading failed for package 'slo'
  * removing 'C:/Users/CVO/workspace/slo.Rcheck/slo'/

These are the lines which follow, when my colleague run the build
successfully:
/Creating a new generic function for plot in slo in .GlobalEnv
** help
...
/
I have tried following a tutorial to see if the trouble was with building
packages in general, but that does not seem to be the case, as I could get
the same outputs as described in this tutorial:  
http://stevemosher.wordpress.com/ten-steps-to-building-an-r-package-under-windows/
http://stevemosher.wordpress.com/ten-steps-to-building-an-r-package-under-windows/
  
(which builds a simple package using the skeleton package).

I have gotten the impression that generally the error with the  Error in
file... is a problem with a wrong path or problems with permissions, but am
unable to find a solution. I'm running the commands in the Command prompt
with Administrator rights and have Admin right on the computer.

Any suggestions on how I can solve this issue or simply get more detailed
information about the error will be greatly appreciated.

Thanks,
Christer V., DK



--
View this message in context: 
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[R] problem on reading many files

2013-07-05 Thread RODRIGUEZ MORENO VICTOR MANUEL
Hi, I have to run almost 120 stations files of temperatura (mx and min), 
separated, and rain. I am following the instructions on RHtests tutorial as on 
http://www.cmc.org.ve/mediawiki/index.php?title=Preparando_los_datos link. Bit 
I have no success on running on multiple files. I have the .ls file which 
include the names of the file station, which I include on this msg for your 
consideration.
The instruction that I wrote on the console is

listatmn - readLines (“tmaxcopia.ls”, warn=false)
for(ifile in listatmn) 
FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)





Of course the tmaxcopia.ls is the list of stations for tmax data. But once 
running on the console, this is the error msg I got

 listatmn - readLines (‘tmaxcopia.ls’, warn=false)
Error: inesperado entrada in listatmn - readLines (‘
 for(ifile in listatmn) 
 FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)
 Error: objeto 'ifnames' no encontrado

What I'd like to do is to make easier and fast running the RHtest

Thank's a lot in advance for your help.




Dr Victor M Rodríguez M
Doctor en Ciencias, en Ciencias de la Tierra / Geociencias Ambientales
INIFAP. CEPAB. (465) 9580167 y 86 Ext 108 y 220

/
Este msg y su(s) atado(s) tiene carácter de CONFIDENCIAL y solo es para los 
fines descritos en su contenido. Queda expresamente prohibida bajo la ley de 
protección de datos del Gobierno de los Estados Unidos Mexicanos y para su 
difusion o extensión a terceros, se requiere del consentimiento expresso del 
titular de la cuenta de correo electrónico y/o del administrador del sitio en 
extenso de sus responsabilidades .
/

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[R] coding variables which are independent or grouped

2013-07-05 Thread Stratford, Jeffrey
Hi everyone,

I have observations of the habitats of birds that I consider independent. I
also have observations of habitats from several forest fragments with
several observations within each fragment that are non-independent.

I'm curious to know the best strategy to code these observations for
analysis (JAGS or WinBUGS through R)

Using R 3.0.1 in Windows.

Here's what I have so far:

code indicates the individual fragment (four digits) and the bird species
(one digit and nine species), type indicates fragment size (in hectares)
and species (now two digits). species just lets me know what species are
which (taken out later) and leafno is the average number of dead leaves
in a plot.

Let me know if there's anything I can clarify.

Thanks so much,

Jeff

structure(list(code = c(1112L, 1112L, 2107L, 2107L, 2107L, 2107L,
2108L, 2108L, 2108L, 2108L, 3114L, 3114L, 3114L, 3114L, 3114L,
3114L, 4101L, 4101L, 4101L, 4101L, 1212L, 1212L, 1212L, 1212L,
1212L, 1212L, 1212L, 1212L, 2206L, 2206L, 2206L, 2206L, 2206L,
2206L, 2206L, 2206L, 3209L, 3209L, 3209L, 3209L, 3209L, 3209L,
3209L, 3209L, 4201L, 4201L, 4201L, 4201L, 4201L, 4201L, 4201L,
4201L, 1L, 1L, 1L, 1L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L,
2L, 2L, 2L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L,
3L, 3L, 3L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L,
4L, 4L, 4L, 4L, 5L, 5L, 5L, 5L, 6L, 6L, 6L, 7L, 7L, 7L, 7L, 7L,
7L, 7L, 7L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L,
8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 9L, 9L, 9L, 9L, 9L, 9L,
9L, 9L, 9L, 9L, 9L, 9L, 2303L, 2303L, 2303L, 2303L, 2303L, 2303L,
2303L, 2303L, 2303L, 2303L, 2303L, 2303L, 2303L, 2303L, 2303L,
3304L, 3304L, 3304L, 3304L, 3304L, 3304L, 3304L, 3304L, 3304L,
3304L, 3304L, 3304L, 3304L, 3304L, 3304L, 3304L), type = c(1L,
1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L,
1L, 1L, 1L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L,
10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L,
10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 91L, 91L, 91L, 91L,
92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L, 92L,
93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L, 93L,
93L, 93L, 93L, 94L, 94L, 94L, 94L, 94L, 94L, 94L, 94L, 94L, 94L,
94L, 94L, 94L, 94L, 94L, 94L, 94L, 95L, 95L, 95L, 95L, 96L, 96L,
96L, 97L, 97L, 97L, 97L, 97L, 97L, 97L, 97L, 98L, 98L, 98L, 98L,
98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L, 98L,
98L, 98L, 98L, 98L, 98L, 98L, 99L, 99L, 99L, 99L, 99L, 99L, 99L,
99L, 99L, 99L, 99L, 99L, 100L, 100L, 100L, 100L, 100L, 100L,
100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L,
100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L, 100L,
100L, 100L, 100L), species = structure(c(11L, 11L, 11L, 11L,
11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L, 11L,
11L, 11L, 11L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L,
12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L,
12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 12L, 1L, 1L, 1L, 1L,
2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 3L, 3L, 3L,
3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 3L, 4L, 4L, 4L,
4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 4L, 5L, 5L,
5L, 5L, 7L, 7L, 7L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 8L, 9L, 9L, 9L,
9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L, 9L,
9L, 9L, 9L, 9L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L, 10L,
10L, 10L, 10L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L,
6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L, 6L,
6L, 6L, 6L), .Label = c(CA, CT, FA, FC, GV, HFR,
HM, MC, MF, MT, OFR, TFR), class = factor), leafno = c(1.8,
2.65, 1.25, 2.6, 1.55, 2.35, 2.3, 1.7, 2.2, 3.2, 3.1, 1.25, 2.35,
1.9, 1.75, 2.8, 1.95, 2.45, 1.55, 1.65, 0.85, 1, 1.85, 1.45,
2.55, 4.05, 3.4, 2.1, 2.05, 1.95, 2.75, 2.6, 1.95, 2.15, 2.2,
2.1, 1.7, 2.2, 1.65, 2.2, 2.95, 2, 2.05, 1.45, 1.55, 0.7, 1.45,
2.05, 1.6, 1.4, 1.25, 2.25, 2.35, 2.4, 2.15, 1.65, 1.8, 2.25,
1.45, 2.15, 2.05, 1.5, 2, 1.7, 1.15, 1.25, 1, 1.15, 1.95, 1.05,
2.4, 1.1, 1.75, 1.7, 1.7, 1.75, 1.1, 1.05, 1.8, 1.45, 2.05, 1.9,
1.15, 2, 1.15, 2.9, 1.6, 2.65, 2.1, 2.35, 1.25, 1.8, 0.85, 1.6,
2.35, 1.75, 1.5, 1.75, 1.3, 1.8, 1.05, 1.45, 0.85, 0.9, 1.7,
2.05, 1.55, 1.55, 1.4, 1.8, 1.5, 1.2, 1.3, 2, 1.4, 2.6, 2.05,
1.05, 2.55, 2.4, 0.4, 2.1, 1.65, 1.65, 1.5, 1.5, 1.55, 2.4, 1.8,
2.2, 1.7, 1.05, 1.45, 1.5, 1.1, 0.95, 0.6, 1.3, 1.95, 1.3, 1.9,
1.55, 1.75, 1.65, 2.35, 3.2, 1.55, 1.65, 1.05, 2.6, 1.75, 1.6,
2.35, 1.2, 1.35, 2.5, 0.95, 2.15, 2.15, 2.55, 1.6, 2.1, 1.9,
0.95, 2.1, 2.4, 2.4, 1.7, 2.45, 1.85, 1.15, 1.25, 0.65, 1.35,
1.8, 1.4, 1.15, 2.75, 2.25, 2, 1.75, 1.4, 2.25)), .Names = c(code,
type, species, leafno), class = data.frame, row.names = c(NA,
-183L))


-- 

Jeffrey A. Stratford, PhD
Department of Biology and Health Sciences
Wilkes University, PA 18766 USA
570-332-2942
http://web.wilkes.edu/jeffrey.stratford/



Re: [R] Subsetting multiple rows of a data frame at once

2013-07-05 Thread arun
Hi Anika,
?merge() is a better solution.

To get the row.names intact, you could do:
carbon.fit- within(carbon.fit,{x-round(x,10);y- round(y,10)}) #Using Bill's 
solution

dat1- data.frame(x=round(xt,10),y=round(yt,10))
carbon.fit1- 
data.frame(carbon.fit,rNames=row.names(carbon.fit),stringsAsFactors=FALSE) 
#changed here
 res1-merge(dat1,carbon.fit1,by=c(x,y))
 row.names(res1)- res1[,3]
 res1- res1[,-3]
A.K.



- Original Message -
From: William Dunlap wdun...@tibco.com
To: arun smartpink...@yahoo.com; Shaun ♥ Anika pro_pa...@hotmail.com
Cc: R help r-help@r-project.org
Sent: Thursday, July 4, 2013 8:02 PM
Subject: RE: [R] Subsetting multiple rows of a data frame at once

 xt- c(1.05, 2.85, 3.40, 4.25, 0.25, 3.05, 3.70, 0.20, 0.30, 0.70, 1.05, 
 1.20, 1.40, 1.90,
 2.70, 3.25, 3.55, 4.60, 2.05, 2.15, 3.70, 4.85, 4.90, 1.60, 2.45, 3.20, 3.90, 
 4.45)
 
 yt- c(0.25, 0.10, 0.90, 0.25, 1.05, 1.70, 2.05, 2.90, 2.35, 2.60, 2.55, 
 2.15, 2.75, 2.05,
 2.70, 2.25, 2.55, 2.05, 3.65, 3.05, 3.00, 3.50, 3.75, 4.85, 4.50, 4.50, 3.35, 
 4.90)
 carbon.fit = expand.grid(list(x=seq(0, 5, 0.01), y=seq(0, 5, 0.01)))
 trees-do.call(rbind,lapply(seq_along(xt),function(i) 
 subset(carbon.fit,x==xt[i]y==yt[i])))
 
 ## xt is 28 integers long and when i run the above code it only returns the 
 values of 18
 out of the 28 (xt,yt) pairs that i want.

You are running into the problem that two different computational methods that 
give
the same result when applied to real numbers often give different results when 
applied
to 64-bit floating point numbers.  (In your case you expect seq(0,5,.01) to 
contain, e.g.,
the floating point number generate by parsing the string 3.05.)   Hence x==y 
is not true
when you expect it to be.  Here is where your 18 came from:
   R table(xt %in% carbon.fit$x, yt %in% carbon.fit$y)
          
           FALSE TRUE
     FALSE     1    6
     TRUE      3   18
Round your number to the nearest 10^-10 and you get
   table(round(xt,10) %in% round(carbon.fit$x,10), round(yt,10) %in% 
round(carbon.fit$y,10))
        
         TRUE
    TRUE   28

By the way, you may prefer using the merge() function rather than the 
do.call(rbind,lapply(...)))
business.  I think the following call to merge will do about what you want (the 
row names differ -
if they are important it is possible to get them with some minor trickery):
    merge(data.frame(x=xt,y=yt), carbon.fit)
(You still want to round your numbers as before.)

Bill Dunlap
Spotfire, TIBCO Software
wdunlap tibco.com

 -Original Message-
 From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org] On 
 Behalf
 Of arun
 Sent: Wednesday, July 03, 2013 10:15 PM
 To: Shaun ♥ Anika
 Cc: R help
 Subject: Re: [R] Subsetting multiple rows of a data frame at once
 
 Hi,
 
 carbon.fit = expand.grid(list(x=seq(0, 5, 0.01), y=seq(0, 5, 0.01)))
  dim(carbon.fit)
 #[1] 251001  2
 
 
  xtNew-sprintf(%.2f,xt)
  ytNew- sprintf(%.2f,yt)
  carbon.fit[]- lapply(carbon.fit,function(x) sprintf(%.2f,x))
 res-do.call(rbind,lapply(seq_along(xtNew),function(i)
 subset(carbon.fit,x==xtNew[i]y==ytNew[i])))
  nrow(res)
 #[1] 28
 res
 #  x    y
 #12631  1.05 0.25
 #5296   2.85 0.10
 #45431  3.40 0.90
 #12951  4.25 0.25
 #52631  0.25 1.05
 #85476  3.05 1.70
 #103076 3.70 2.05
 #145311 0.20 2.90
 #117766 0.30 2.35
 #130331 0.70 2.60
 #127861 1.05 2.55
 #107836 1.20 2.15
 #137916 1.40 2.75
 #102896 1.90 2.05
 #135541 2.70 2.70
 #113051 3.25 2.25
 #128111 3.55 2.55
 #103166 4.60 2.05
 #183071 2.05 3.65
 #153021 2.15 3.05
 #150671 3.70 3.00
 #175836 4.85 3.50
 #188366 4.90 3.75
 #243146 1.60 4.85
 #225696 2.45 4.50
 #225771 3.20 4.50
 #168226 3.90 3.35
 #245936 4.45 4.90
 A.K.
 
 
 
 From: Shaun ♥ Anika pro_pa...@hotmail.com
 To: smartpink...@yahoo.com smartpink...@yahoo.com
 Sent: Thursday, July 4, 2013 12:08 AM
 Subject: RE: Subsetting multiple rows of a data frame at once
 
 
 
 
 Hi There,
 i can give you the data needed to perform this task...
 
 library(akima)
 library(fields)
 
 xt- c(1.05, 2.85, 3.40, 4.25, 0.25, 3.05, 3.70, 0.20, 0.30, 0.70, 1.05, 
 1.20, 1.40, 1.90,
 2.70, 3.25, 3.55, 4.60, 2.05, 2.15, 3.70, 4.85, 4.90, 1.60, 2.45, 3.20, 3.90, 
 4.45)
 
 yt- c(0.25, 0.10, 0.90, 0.25, 1.05, 1.70, 2.05, 2.90, 2.35, 2.60, 2.55, 
 2.15, 2.75, 2.05,
 2.70, 2.25, 2.55, 2.05, 3.65, 3.05, 3.00, 3.50, 3.75, 4.85, 4.50, 4.50, 3.35, 
 4.90)
 
 xs- c(0.45, 1.05, 2.75, 3.30, 4.95, 0.40, 1.05, 2.30, 3.45, 4.60, 0.05, 
 1.95, 2.95, 3.70,
 4.55, 0.75, 1.60, 2.10, 3.60, 4.90, 0.05, 1.35, 2.60, 3.40, 4.25)
 
 ys- c(0.45, 0.95, 0.75, 0.95, 0.10, 1.90, 1.45, 1.25, 1.45, 1.05, 2.85, 
 2.60, 2.05, 2.60,
 2.55, 3.75, 3.30, 3.95, 3.45, 3.70, 4.95, 4.35, 4.55, 4.40, 4.95)
 
 carbon- c(1.43, 1.82, 1.40, 1.43, 1.96, 1.61, 1.91, 1.53, 1.17, 1.83, 2.43, 
 2.02, 1.66,
 2.45, 2.46, 1.39, 1.10, 1.38, 1.91, 2.13, 1.88, 1.26, 2.15, 1.89, 1.69)
 
 carbon.df=data.frame(x=xs,y=ys,z=carbon)
 carbon.loess= loess(z~x*y, data= carbon.df, degree= 2)
 

[R] Subscript out of bound error

2013-07-05 Thread Chirag Gupta
Hi All

I have a huge matrix m (10276 X 10276) dimension with same column name and
row names. (its a gene correlation matrix). I have another text file which
has 2700 names, basically locus ID of genes, which are also
rownames/colnames in m. Now I want to select all those columns from m whose
names match with the names in the text file and return ONLY those columns
and ALL the rows in a matrix format.
That is, the output should a matrix of dimension 10276 X 2700.

I have played around with subset and also tried all different methods like
reading the text file, converting to matrix and character and DF and tried
all possible ways I found on the web. The problem is that some of them work
on a smaller simulated dataset but says Subscript out of bounds  when I
try on the bigger matrix(m).

Please help.. :(

Thanks!



-- 
*Chirag Gupta*
Department of Crop, Soil, and Environmental Sciences,
115 Plant Sciences Building, Fayetteville, Arkansas 72701

[[alternative HTML version deleted]]

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Re: [R] problem on reading many files

2013-07-05 Thread Pascal Oettli
Hello,

I'm not sure whether it is dur to the HTML version or not, but there is a
problem with quotation marks in your first line.

Regards,
Pascal


2013/7/5 RODRIGUEZ MORENO VICTOR MANUEL rodriguez.vic...@inifap.gob.mx

 Hi, I have to run almost 120 stations files of temperatura (mx and min),
 separated, and rain. I am following the instructions on RHtests tutorial as
 on http://www.cmc.org.ve/mediawiki/index.php?title=Preparando_los_datoslink. 
 Bit I have no success on running on multiple files. I have the .ls
 file which include the names of the file station, which I include on this
 msg for your consideration.
 The instruction that I wrote on the console is

 listatmn - readLines (“tmaxcopia.ls”, warn=false)
 for(ifile in listatmn)
 FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)





 Of course the tmaxcopia.ls is the list of stations for tmax data. But
 once running on the console, this is the error msg I got

  listatmn - readLines (‘tmaxcopia.ls’, warn=false)
 Error: inesperado entrada in listatmn - readLines (‘
  for(ifile in listatmn)
 FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)
  Error: objeto 'ifnames' no encontrado

 What I'd like to do is to make easier and fast running the RHtest

 Thank's a lot in advance for your help.




 Dr Victor M Rodríguez M
 Doctor en Ciencias, en Ciencias de la Tierra / Geociencias Ambientales
 INIFAP. CEPAB. (465) 9580167 y 86 Ext 108 y 220


 /
 Este msg y su(s) atado(s) tiene carácter de CONFIDENCIAL y solo es para
 los fines descritos en su contenido. Queda expresamente prohibida bajo la
 ley de protección de datos del Gobierno de los Estados Unidos Mexicanos y
 para su difusion o extensión a terceros, se requiere del consentimiento
 expresso del titular de la cuenta de correo electrónico y/o del
 administrador del sitio en extenso de sus responsabilidades .

 /

 [[alternative HTML version deleted]]


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Re: [R] R and MatLab implementations of the same model differs

2013-07-05 Thread Berend Hasselman

On 05-07-2013, at 09:53, Jannetta Steyn janne...@henning.org wrote:

 
 
 
  I don't quite know how to explain the doesn't work in more detail without
  any visual aid.
 
 You said that R got into an indefinite loop, whatever that maybe.
 
 
  When I change the solver to ode45 the script never stops running. I have 
  even left it over night at one stage but the next day it was still busy. Is 
  there a way to see what it is doing and to determine why it seems to be in 
  an 
  infinite loop?
 
 The script just ran using ode45!! For the first time ever.
 

Please keep the conversation on R-help.
Don't reply to me personally.

Which script?
With the corrections suggested by me and Peter? (gK_axon_AB=52.5-3 == 
gK_axon_AB=52.5e-3)

For what it's worth: lsdoda seems quicker.
Variable v_acon_AB now converges to -60 (the equilibrium state?)

Berend

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[R] Unique in discerning missing values NA

2013-07-05 Thread Pancho Mulongeni
Hi,
I am trying to remove duplicate Patient numbers in a clinical record, I used 
unique
menPatients[1:40,1]
 [1] abr1160(C)/001 ABR1363(A)/001 ABR1363(A)/001 ABR1363(A)/001 abr1772(B)/001
 [6] AFR0003/001AFR0003/001afr0290(C)/001 afr1861(B)/001 Aga0007/001   
[11] AGA1548(A)/001 AGA1548(A)/001 AGA1548(A)/001 AGU1680(A)/001 AGU1680(A)/001
[16] AIS0492/001AIS0492/001AKO4268(C)/001 AKO4268(C)/001 AKT0042(B)/001
[21] AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001
[26] AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 alf1722(B)/001 ALF1735(A)/001
[31] ALF1735(A)/001 ALP4321(C)/001 NA   NA   ALU4262(B)/001
[36] ALV4286(C)/001 ALW2579(C)/001 NA   ALW4330(B)/001 AMA0011/001   
3886 Levels: 0750/002 0751/001 0984/002 ABE2560(C)/001 ... zul1737(B)/001

testData-menPatients[1:40,1]

I then used unique, please note the NA at position 32 in testData
testUnique-unique(testData)
testUnique
 [1] abr1160(C)/001 ABR1363(A)/001 abr1772(B)/001 AFR0003/001afr0290(C)/001
 [6] afr1861(B)/001 Aga0007/001AGA1548(A)/001 AGU1680(A)/001 AIS0492/001   
[11] AKO4268(C)/001 AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 alf1722(B)/001
[16] ALF1735(A)/001 ALP4321(C)/001 NA   ALU4262(B)/001 ALV4286(C)/001
[21] ALW2579(C)/001 ALW4330(B)/001 AMA0011/001   

The missing value NA originally at position 32 in testdata is still there, it 
is in position 18. Why is this? How can I prevent this?
I tried using incomprables=c(NA), but this did not work.

Thanks


Pancho Mulongeni
Research Assistant
PharmAccess Foundation
1 Fouché Street
Windhoek West
Windhoek
Namibia
 
Tel:   +264 61 419 000
Fax:  +264 61 419 001/2
Mob: +264 81 4456 286

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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Subscript out of bound error

2013-07-05 Thread Jim Holtman
use 'match' to convert the names to column indices and then use that for 
indexing

indx - match(subCols, names(yourMatrix)
mySubset - yourMatrix[, indx]

Sent from my iPad

On Jul 5, 2013, at 2:22, Chirag Gupta cxg...@email.uark.edu wrote:

 Hi All
 
 I have a huge matrix m (10276 X 10276) dimension with same column name and
 row names. (its a gene correlation matrix). I have another text file which
 has 2700 names, basically locus ID of genes, which are also
 rownames/colnames in m. Now I want to select all those columns from m whose
 names match with the names in the text file and return ONLY those columns
 and ALL the rows in a matrix format.
 That is, the output should a matrix of dimension 10276 X 2700.
 
 I have played around with subset and also tried all different methods like
 reading the text file, converting to matrix and character and DF and tried
 all possible ways I found on the web. The problem is that some of them work
 on a smaller simulated dataset but says Subscript out of bounds  when I
 try on the bigger matrix(m).
 
 Please help.. :(
 
 Thanks!
 
 
 
 -- 
 *Chirag Gupta*
 Department of Crop, Soil, and Environmental Sciences,
 115 Plant Sciences Building, Fayetteville, Arkansas 72701
 
[[alternative HTML version deleted]]
 
 __
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 https://stat.ethz.ch/mailman/listinfo/r-help
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 and provide commented, minimal, self-contained, reproducible code.

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[R] Revolutions blog: June roundup

2013-07-05 Thread David Smith
Revolution Analytics staff write about R every weekday at the Revolutions blog:
 http://blog.revolutionanalytics.com
and every month I post a summary of articles from the previous month
of particular interest to readers of r-help.

In case you missed them, here are some articles related to R from the
month of June:

You can create a Word document from a template and an R script with
the R2DOCX package: http://bit.ly/17XigAJ

Joe Rickert reviews books and other resources for learning about time
series analysis in R: http://bit.ly/17Xiisn

Timely Portfolio covers 15 years of history of time series plotting
with R: http://bit.ly/17Xiisp

An online beer recommendation application serves as an in-depth
example of building a recommendation system with R:
http://bit.ly/17XigAK

Software company SAP says that skills around the open source R
programming language and advanced analytics are rapidly shifting from
'niche' to 'standard' requirements: http://bit.ly/17Xiiso

A primer on maximum likelihood estimation in R with the bbmle package:
http://bit.ly/17XigAI

American Century Investments describe how they created their own R
package to optimize investments and model supplier relationships in a
video presentation: http://bit.ly/17Xiisq

How to draw attractive decision trees using the rpart.plot package:
http://bit.ly/17Xiisr

What is a data scientist, what skills should they have, and how is the
practice evolving? My take: http://bit.ly/17XigAL

Computerworld's 6-part beginner's guide to R: http://bit.ly/17XigAM

RStudio has made CRAN download statistics available, enabling a
ranking of the top R packages by downloads: http://bit.ly/17XigAN

Big Data and statistical modeling is changing video games: helping to
identify bottlenecks for new players, detect fraud, and maximize
in-app purchases. Details in this webinar replay:
http://bit.ly/17Xiiss

A mini-tutorial on using the Quandl package to import public financial
data sets into R: http://bit.ly/17Xiist

Dirk Eddelbuettel's book, Seamless R and C++ Integration with Rcpp, is
now available: http://bit.ly/17XigAO

An interactive application based on R and Shiny maps dialect
differences across the USA: http://bit.ly/17XigAP

Generating parallel random number streams with the RevoScaleR package:
http://bit.ly/17Xiisu

R again shows strong growth in the annual KDNuggets software poll:
http://bit.ly/17XigAQ

Some very useful guidelines for setting up a reproducible R project:
http://bit.ly/17Xiisv

Some non-R stories in the past month included: A new Hadoop appliance
from Teradata (http://bit.ly/17XigAT), a new Big Data Innovation
Center in Singapore (http://bit.ly/17XigAU), a drum/keyboard Billie
Jean cover (http://bit.ly/17XigAW), women in movies
(http://bit.ly/17XigAV), a Daft Punk / Soul Train mashup
(http://bit.ly/17Xiisw), and It Gets Better at NASA
(http://bit.ly/17Xiisx).

Meeting times for local R user groups
(http://blog.revolutionanalytics.com/local-r-groups.html) can be found
on the updated R Community Calendar at:
http://blog.revolutionanalytics.com/calendar.html

If you're looking for more articles about R, you can find summaries
from previous months at http://blog.revolutionanalytics.com/roundups/.
Join the Revolution mailing list at
http://revolutionanalytics.com/newsletter to be alerted to new
articles on a monthly basis.

As always, thanks for the comments and please keep sending suggestions
to me at da...@revolutionanalytics.com . Don't forget you can also
follow the blog using an RSS reader, or by following me on Twitter
(I'm @revodavid).

Cheers,
# David

--
David M Smith da...@revolutionanalytics.com
VP of Marketing, Revolution Analytics  http://blog.revolutionanalytics.com
Tel: +1 (650) 646-9523 (Seattle WA, USA)
Twitter: @revodavid
We're hiring! www.revolutionanalytics.com/careers

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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] Meta-analysis on a repeated measures design with multiple trials per subject using metafor

2013-07-05 Thread Marc Heerdink

Dear Wolfgang and other readers of the r-help list,

Thank you very much for your suggestion. Unfortunately, the data that I 
have can not be described with a table such as the one you have made, 
because there's no identical trial under both treatment 1 and treatment 
2. To explain, let me explain a bit more about the experiments:


* All subjects were presented with the same number of trials
* Half of these trials were preceded by a prime from category 1 
(treatment 1) and half of these trials with a prime from category 2 
(treatment 2)
* Subjects were asked to respond to these trials (a unique stimulus for 
each trial) by pressing one of two keys on the keyboard.


Because everything was randomized, I can only calculate the total number 
of times a certain response was used under each type of trial. There is 
no pairing of trials under two treatments, so I am forced to use the 
marginal totals from your table.


I have uploaded a simplified version of the data for one experiment to 
illustrate this (the actual experiments have five treatments and some 
have moderators):

https://www.dropbox.com/s/rhgo12cm1asl6x8/exampledata.csv

This is the script that I used to generate the data:
https://www.dropbox.com/s/7uyeaexhnqiiy55/exampledata.R

The problem thus appears to lie mainly in estimating the variance of the 
proportion difference from only the marginal totals, is that correct? Is 
there a way to calculate it from only the marginal totals?


One alternative that I have tried over the last few days, is to use the 
b parameter of interest and it's corresponding standard error from the 
lme4 regression output that I use to analyse the individual experiments. 
Then, I use rma(yi, sei) to do a meta-analysis on these parameters. I am 
not sure this is correct though, since it takes into account 
between-subjects variance (through a random effect for subject), and it 
is sensitive to the covariates/moderators I include in the models that I 
get the b parameters from.


Thanks again for your help, and for any suggestions for solving this 
problem!


Regards,
Marc


On 07/04/2013 11:21 PM, Viechtbauer Wolfgang (STAT) wrote:

Dear Marc,

Let me see if I understand the type of data you have. You say that you have 5 
experiments. And within each experiment, you have n subjects and for each 
subject, you have data in the form described in your post. Now for each 
subject, you want to calculate some kind of measure that quantifies how much 
more likely it was that subjects gave/chose response 2 under treatment 2 versus 
treatment 1. So, you would have n such values. And then you want to pool those 
values over the n subjects within a particular experiment and then ultimately 
over the 5 experiments. Is that correct so far?

Assuming I got this right, let me ask you about those data that you have for 
each subject. In particular, are these paired data? In other words, is there 
are 1:1 relationship between the 30 trials under treatment 1 versus treatment 
2? Or phrased yet another way, can you construct a table like this for every 
subject:

 trt 2
  
  resp1 resp2
trt 1 resp1  a b  10
   resp2  c d  20
  2010 30

Note that I added the marginal counts based on your example data, but this is not 
sufficient to reconstruct how often response 1 was chosen for the same trial under both 
treatment 1 and treatment 2 (cell a). And so on for the other 3 cells.

If all of this applies, then essentially you are dealing with dependent 
proportions and you can calculate the difference y = (20/30)-(10/30) as you 
have done. The corresponding sampling variance can be estimated with v = var(y) 
= (a+b)*(c+d)/t^3 + (a+c)*(b+d)/t^3 - 2*(a*d/t^3 - b*c/t^3) (where t is the 
number of trials, i.e., 30 in the example above). See, for example, section 
10.1.1. in Agresti (2002) (Categorical data analysis, 2nd ed.).

So, ultimately, you will have n values of y and v for a particular experiment 
and then the same thing for all 5 experiments. You can then pool those values 
with rma(yi, vi) in metafor (yi and vi being the vectors of the y and v 
values). You probably want to add a factor to the model that indicates which 
experiment those values came from. So, something like: rma(yi, vi, mods = ~ 
factor(experiment)).

Well, I hope that I understood your data correctly.

Best,
Wolfgang

--
Wolfgang Viechtbauer, Ph.D., Statistician
Department of Psychiatry and Psychology
School for Mental Health and Neuroscience
Faculty of Health, Medicine, and Life Sciences
Maastricht University, P.O. Box 616 (VIJV1)
6200 MD Maastricht, The Netherlands
+31 (43) 388-4170 | http://www.wvbauer.com

From: r-help-boun...@r-project.org [r-help-boun...@r-project.org] On Behalf Of 
Marc Heerdink [m.w.heerd...@uva.nl]
Sent: Wednesday, July 03, 2013 2:15 PM
To: r-help@r-project.org
Subject: [R] Meta-analysis on a repeated measures design 

[R] To approach time series using a data set

2013-07-05 Thread fsantos
Dear R community,

I have to approach a time serie as a linear combination of many time
series in a dataset. Of course, I would like that this linear combination
is optimal (I would like to use the minimal number of times series)
although I can loose some information.  Moreover, each variable of the
dataset has associated a cost which range from 0 to 9. I also would like
to find this optimal combination and to make minimal de sum of this
cost. Could you give to me some suggestions? Do your know some
interesting reference for starting?

Thanks in advance

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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
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Re: [R] Unique in discerning missing values NA

2013-07-05 Thread Pascal Oettli
Hi,

testUnique - unique(testData[!is.na(testData)])

or

testUnique - unique(na.omit(testData))

And probably some other solutions.

Regards,
Pascal


2013/7/5 Pancho Mulongeni p.mulong...@namibia.pharmaccess.org

 Hi,
 I am trying to remove duplicate Patient numbers in a clinical record, I
 used unique
 menPatients[1:40,1]
  [1] abr1160(C)/001 ABR1363(A)/001 ABR1363(A)/001 ABR1363(A)/001
 abr1772(B)/001
  [6] AFR0003/001AFR0003/001afr0290(C)/001 afr1861(B)/001
 Aga0007/001
 [11] AGA1548(A)/001 AGA1548(A)/001 AGA1548(A)/001 AGU1680(A)/001
 AGU1680(A)/001
 [16] AIS0492/001AIS0492/001AKO4268(C)/001 AKO4268(C)/001
 AKT0042(B)/001
 [21] AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001
 AKT0042(B)/001
 [26] AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 alf1722(B)/001
 ALF1735(A)/001
 [31] ALF1735(A)/001 ALP4321(C)/001 NA   NA
 ALU4262(B)/001
 [36] ALV4286(C)/001 ALW2579(C)/001 NA   ALW4330(B)/001
 AMA0011/001
 3886 Levels: 0750/002 0751/001 0984/002 ABE2560(C)/001 ... zul1737(B)/001

 testData-menPatients[1:40,1]

 I then used unique, please note the NA at position 32 in testData
 testUnique-unique(testData)
 testUnique
  [1] abr1160(C)/001 ABR1363(A)/001 abr1772(B)/001 AFR0003/001
  afr0290(C)/001
  [6] afr1861(B)/001 Aga0007/001AGA1548(A)/001 AGU1680(A)/001
 AIS0492/001
 [11] AKO4268(C)/001 AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001
 alf1722(B)/001
 [16] ALF1735(A)/001 ALP4321(C)/001 NA   ALU4262(B)/001
 ALV4286(C)/001
 [21] ALW2579(C)/001 ALW4330(B)/001 AMA0011/001

 The missing value NA originally at position 32 in testdata is still there,
 it is in position 18. Why is this? How can I prevent this?
 I tried using incomprables=c(NA), but this did not work.

 Thanks


 Pancho Mulongeni
 Research Assistant
 PharmAccess Foundation
 1 Fouché Street
 Windhoek West
 Windhoek
 Namibia

 Tel:   +264 61 419 000
 Fax:  +264 61 419 001/2
 Mob: +264 81 4456 286

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


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and provide commented, minimal, self-contained, reproducible code.


[R] kruskal.test followed by kruskalmc

2013-07-05 Thread Humber Andrade
Hi all,

After running kruskal.test I have got results (p0,005) pointing to reject
the hypothesis that the samples were draw from the same population.
Howerver when I run the kruskalmc there are no significant differences in
any of the multiple comparisons. Is that possible? Some clarification?

Thanks, Humber


https://sites.google.com/site/humberandrade

[[alternative HTML version deleted]]

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Re: [R] Unique in discerning missing values NA

2013-07-05 Thread Rui Barradas

Hello,

Your data example is difficult to read into an R session. Next time, 
post the output of ?dput. Like this:


dput(menPatients[1:40, 1])  # post the output of this


The help page for unique says that Missing values are regarded as 
equal  so you should expect one NA to still be present in the final result.

If you want to remove NAs, use ?is.na. With fake data,

x1 - c(1:3, NA, 4, NA, 2:9)
x2 - unique(x1)
x3 - x2[!is.na(x2)]
x3


Hope this helps,

Rui Barradas


Em 05-07-2013 10:28, Pancho Mulongeni escreveu:

Hi,
I am trying to remove duplicate Patient numbers in a clinical record, I used 
unique
menPatients[1:40,1]
  [1] abr1160(C)/001 ABR1363(A)/001 ABR1363(A)/001 ABR1363(A)/001 abr1772(B)/001
  [6] AFR0003/001AFR0003/001afr0290(C)/001 afr1861(B)/001 Aga0007/001
[11] AGA1548(A)/001 AGA1548(A)/001 AGA1548(A)/001 AGU1680(A)/001 AGU1680(A)/001
[16] AIS0492/001AIS0492/001AKO4268(C)/001 AKO4268(C)/001 AKT0042(B)/001
[21] AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001
[26] AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 alf1722(B)/001 ALF1735(A)/001
[31] ALF1735(A)/001 ALP4321(C)/001 NA   NA   ALU4262(B)/001
[36] ALV4286(C)/001 ALW2579(C)/001 NA   ALW4330(B)/001 AMA0011/001
3886 Levels: 0750/002 0751/001 0984/002 ABE2560(C)/001 ... zul1737(B)/001

testData-menPatients[1:40,1]

I then used unique, please note the NA at position 32 in testData
testUnique-unique(testData)
testUnique
  [1] abr1160(C)/001 ABR1363(A)/001 abr1772(B)/001 AFR0003/001afr0290(C)/001
  [6] afr1861(B)/001 Aga0007/001AGA1548(A)/001 AGU1680(A)/001 AIS0492/001
[11] AKO4268(C)/001 AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 alf1722(B)/001
[16] ALF1735(A)/001 ALP4321(C)/001 NA   ALU4262(B)/001 ALV4286(C)/001
[21] ALW2579(C)/001 ALW4330(B)/001 AMA0011/001

The missing value NA originally at position 32 in testdata is still there, it 
is in position 18. Why is this? How can I prevent this?
I tried using incomprables=c(NA), but this did not work.

Thanks


Pancho Mulongeni
Research Assistant
PharmAccess Foundation
1 Fouché Street
Windhoek West
Windhoek
Namibia

Tel:   +264 61 419 000
Fax:  +264 61 419 001/2
Mob: +264 81 4456 286

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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.



__
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Re: [R] Unique in discerning missing values NA

2013-07-05 Thread Pancho Mulongeni
Yes thanks, this is what I ended up doing, but I though there would be a 
'internal' way to disregard NAs in unique.
Thanks for the tip on dput

-Original Message-
From: Rui Barradas [mailto:ruipbarra...@sapo.pt] 
Sent: 05 July 2013 11:39
To: Pancho Mulongeni
Cc: r-help@r-project.org
Subject: Re: [R] Unique in discerning missing values NA

Hello,

Your data example is difficult to read into an R session. Next time, post the 
output of ?dput. Like this:

dput(menPatients[1:40, 1])  # post the output of this


The help page for unique says that Missing values are regarded as equal  so 
you should expect one NA to still be present in the final result.
If you want to remove NAs, use ?is.na. With fake data,

x1 - c(1:3, NA, 4, NA, 2:9)
x2 - unique(x1)
x3 - x2[!is.na(x2)]
x3


Hope this helps,

Rui Barradas


Em 05-07-2013 10:28, Pancho Mulongeni escreveu:
 Hi,
 I am trying to remove duplicate Patient numbers in a clinical record, 
 I used unique menPatients[1:40,1]
   [1] abr1160(C)/001 ABR1363(A)/001 ABR1363(A)/001 ABR1363(A)/001 
 abr1772(B)/001
   [6] AFR0003/001AFR0003/001afr0290(C)/001 afr1861(B)/001 Aga0007/001
 [11] AGA1548(A)/001 AGA1548(A)/001 AGA1548(A)/001 AGU1680(A)/001 
 AGU1680(A)/001
 [16] AIS0492/001AIS0492/001AKO4268(C)/001 AKO4268(C)/001 
 AKT0042(B)/001
 [21] AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 AKT0042(B)/001 
 AKT0042(B)/001 [26] AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 
 alf1722(B)/001 ALF1735(A)/001
 [31] ALF1735(A)/001 ALP4321(C)/001 NA   NA   
 ALU4262(B)/001
 [36] ALV4286(C)/001 ALW2579(C)/001 NA   ALW4330(B)/001 AMA0011/001
 3886 Levels: 0750/002 0751/001 0984/002 ABE2560(C)/001 ... 
 zul1737(B)/001

 testData-menPatients[1:40,1]

 I then used unique, please note the NA at position 32 in testData
 testUnique-unique(testData)
 testUnique
   [1] abr1160(C)/001 ABR1363(A)/001 abr1772(B)/001 AFR0003/001
 afr0290(C)/001
   [6] afr1861(B)/001 Aga0007/001AGA1548(A)/001 AGU1680(A)/001 AIS0492/001
 [11] AKO4268(C)/001 AKT0042(B)/001 alb4423(C)/001 ALF1651(A)/001 
 alf1722(B)/001
 [16] ALF1735(A)/001 ALP4321(C)/001 NA   ALU4262(B)/001 
 ALV4286(C)/001
 [21] ALW2579(C)/001 ALW4330(B)/001 AMA0011/001

 The missing value NA originally at position 32 in testdata is still there, it 
 is in position 18. Why is this? How can I prevent this?
 I tried using incomprables=c(NA), but this did not work.

 Thanks


 Pancho Mulongeni
 Research Assistant
 PharmAccess Foundation
 1 Fouché Street
 Windhoek West
 Windhoek
 Namibia

 Tel:   +264 61 419 000
 Fax:  +264 61 419 001/2
 Mob: +264 81 4456 286

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide 
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


__
R-help@r-project.org mailing list
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Re: [R] kruskal.test followed by kruskalmc

2013-07-05 Thread Jose Iparraguirre
Humber,
Have a look at this: 
http://r.789695.n4.nabble.com/Multiple-Comparisons-Kruskal-Wallis-Test-kruskal-agricolae-and-kruskalmc-pgirmess-don-t-yield-the-sa-td4639004.html
Hope it helps.
Kind regards,

José

Prof. José Iparraguirre
Chief Economist
Age UK



-Original Message-
From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org] On 
Behalf Of Humber Andrade
Sent: 05 July 2013 11:38
To: r-help@r-project.org
Subject: [R] kruskal.test followed by kruskalmc

Hi all,

After running kruskal.test I have got results (p0,005) pointing to reject the 
hypothesis that the samples were draw from the same population.
Howerver when I run the kruskalmc there are no significant differences in any 
of the multiple comparisons. Is that possible? Some clarification?

Thanks, Humber


https://sites.google.com/site/humberandrade

[[alternative HTML version deleted]]

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and provide commented, minimal, self-contained, reproducible code.

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If you’re looking for a radio station that offers real variety, tune in to The 
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---
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For the purposes of promoting Age UK Insurance, Age UK is an Appointed 
Representative of Age UK Enterprises Limited, Age UK is an Introducer 
Appointed Representative of JLT Benefit Solutions Limited and Simplyhealth 
Access for the purposes of introducing potential annuity and health 
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Solutions Limited and Simplyhealth Access are all authorised and 
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Re: [R] R and MatLab implementations of the same model differs

2013-07-05 Thread Jannetta Steyn
On 5 July 2013 09:44, Berend Hasselman b...@xs4all.nl wrote:


 On 05-07-2013, at 09:53, Jannetta Steyn janne...@henning.org wrote:

 
 
  
   I don't quite know how to explain the doesn't work in more detail
 without
   any visual aid.
 
  You said that R got into an indefinite loop, whatever that maybe.
 
 
   When I change the solver to ode45 the script never stops running. I
 have even left it over night at one stage but the next day it was still
 busy. Is there a way to see what it is doing and to determine why it seems
 to be in an
   infinite loop?
 
  The script just ran using ode45!! For the first time ever.
 

 Please keep the conversation on R-help.
 Don't reply to me personally.



Apologies for that. It was meant to go to the list.



 Which script?
 With the corrections suggested by me and Peter? (gK_axon_AB=52.5-3 ==
 gK_axon_AB=52.5e-3)


The R script. With the correction of AB=52.5e-3



 For what it's worth: lsdoda seems quicker.


Yes, lsoda is quicker but I want to use ode45 because that is what they
used in the paper I am referencing and I am trying to get the same results
as they did.


 Variable v_acon_AB now converges to -60 (the equilibrium state?)


I'm trying to determine now whether this is correct.

Regards
Jannetta


-- 

===
Web site: http://www.jannetta.com
Email: janne...@henning.org
===

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Re: [R] iterative methods

2013-07-05 Thread S Ellison
  Dear R users,
 Please help me with some documentation for newbie about R 
 programming, algorithms, create iterative C++ function (like 
 for, while, if , etc).
Start at  
http://www.R-project.org/posting-guide.html

and especiallly the resources cited towards the end of that page, just after 
the bit titled  Do your homework before posting. It lists useful links. 
Introduction to R and the R language definition (sec 3.2 especially) seem 
relevant.

For books, browse Google for 'R programming books'; there are lots. Some are 
aimed at particular types of problem, but you know your problem best.

S Ellison

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This email and any attachments are confidential. Any use...{{dropped:8}}

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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Error when building a custom package

2013-07-05 Thread S Ellison
 
 I only get an error message, when trying to build a binary 
 file (or runnning /R CMD check package name/), not the 
 standard tar.gz. Here is what the output looks like in the 
 command prompt:
 ...
 I have gotten the impression that generally the error with 
 the  Error in file... is a problem with a wrong path or 
 problems with permissions, 

Not sure whether it will solve your problem, but specifying a writeable 
location for R CMD INSTALL --build (as described in 1.3.3 Building binary 
packages in Writing R extensions) should dodge a permission problem if that 
is the issue. Personally I prefer to do that anyway to avoid overwriting an 
existing (working) package installation.

As an aside - probably unrelated and apparently not a warning anyway - I don't 
see why you would need to be be creating a new plot generic. Isn't the existing 
plot generic sufficient? 

S Ellison


***
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Re: [R] kruskal.test followed by kruskalmc

2013-07-05 Thread Humber Andrade
Thank you Prof. José Iparraguirre. Maybe I am wrong but I think the issues
are not the same. His data doesn't showed significant differences after
kruskal.test(), that was not my case. Anyway follow below my the results
I've got and the database.

Thank you,

#
 kruskal.test(data$resp,data$group)

Kruskal-Wallis rank sum test

data:  data$resp and data$group
Kruskal-Wallis chi-squared = 32.3546, df = 14, p-value = 0.003566

 kruskalmc(data$resp,data$group)
Multiple comparison test after Kruskal-Wallis
p.value: 0.05
Comparisons
   obs.dif critical.dif difference
A-B  4.8303571 62.37688  FALSE
A-C  3.8928571 62.37688  FALSE
A-D  0.4821429 62.37688  FALSE
.
.
.
M-P 14.250 60.26179  FALSE
N-O  1.375 60.26179  FALSE
N-P  6.125 60.26179  FALSE
O-P  4.750 60.26179  FALSE

# database
   group resp  A 0.1  A 581.8  A 90.5  A 70.1  A 820.1  A 1159.2  A 2478.1
A 2475.3  B 351.8  B 370.1  B 326.1  B 751.9  B 931  B 588.2  B 70.1  B
1754.9  C 289.8  C 254.1  C 370.3  C 459.8  C 412.5  C 591.5  C 986.9  C 890
D 425.6  D 397.4  D 464  D 370.9  D 417.3  D 455  D 568.2  D 599.4  E 405.1
E 626.2  E 299  E 493.8  E 362.6  E 309.8  E 522.7  E 433.3  F 698.6  F 42.5
F 7.4  F 10.6  F 95.8  F 497.5  F 987.9  F 925.1  G 492.9  G 376  G 413  G
278.3  G 344.2  G 292.2  G 429.4  G 368  H 241.6  H 230.5  H 310.4  H 372.5
H 366.1  H 307.9  H 480  H 529.8  I 296  I 288.8  I 302.1  I 300.8  I 150.1
I 381.9  I 583.1  I 489.4  J 1.2  J 18.6  J 7.7  J 11.6  J 48.1  J 121.8  J
1284.1  J 944.7  L 0.5  L 44.4  L 80.9  L 15.3  L 80  L 379.9  L 940.6  L
829.3  M 323.6  M 401.5  M 162.1  M 136.5  M 139.4  M 363.3  M 280.7  M
356.5  N 197.6  N 245.9  N 221.5  N 224.3  N 185.4  N 265.3  N 304.8  N
351.9  O 189.9  O 237.3  O 247.1  O 230.4  O 272.2  O 155.1  O 270.7  O
315.2  P 48.4  P 15.5  P 53.1  P 72.8  P 74.8  P 132.3  P 550  P 478.7


On Fri, Jul 5, 2013 at 8:06 AM, Jose Iparraguirre 
jose.iparragui...@ageuk.org.uk wrote:

 Humber,
 Have a look at this:
 http://r.789695.n4.nabble.com/Multiple-Comparisons-Kruskal-Wallis-Test-kruskal-agricolae-and-kruskalmc-pgirmess-don-t-yield-the-sa-td4639004.html
 Hope it helps.
 Kind regards,

 José

 Prof. José Iparraguirre
 Chief Economist
 Age UK



 -Original Message-
 From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org]
 On Behalf Of Humber Andrade
 Sent: 05 July 2013 11:38
 To: r-help@r-project.org
 Subject: [R] kruskal.test followed by kruskalmc

 Hi all,

 After running kruskal.test I have got results (p0,005) pointing to reject
 the hypothesis that the samples were draw from the same population.
 Howerver when I run the kruskalmc there are no significant differences in
 any of the multiple comparisons. Is that possible? Some clarification?

 Thanks, Humber


 https://sites.google.com/site/humberandrade

 [[alternative HTML version deleted]]

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.

 The Wireless from Age UK | Radio for grown-ups.

 www.ageuk.org.uk/thewireless


 If you’re looking for a radio station that offers real variety, tune in to
 The Wireless from Age UK.
 Whether you choose to listen through the website at
 www.ageuk.org.uk/thewireless, on digital radio (currently available in
 London and Yorkshire) or through our TuneIn Radio app, you can look forward
 to an inspiring mix of music, conversation and useful information 24 hours
 a day.




 ---
 Age UK is a registered charity and company limited by guarantee,
 (registered charity number 1128267, registered company number 6825798).
 Registered office: Tavis House, 1-6 Tavistock Square, London WC1H 9NA.

 For the purposes of promoting Age UK Insurance, Age UK is an Appointed
 Representative of Age UK Enterprises Limited, Age UK is an Introducer
 Appointed Representative of JLT Benefit Solutions Limited and Simplyhealth
 Access for the purposes of introducing potential annuity and health
 cash plans customers respectively.  Age UK Enterprises Limited, JLT
 Benefit Solutions Limited and Simplyhealth Access are all authorised and
 regulated by the Financial Services Authority.
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 opinions expressed in this email 

Re: [R] ggplot2

2013-07-05 Thread AlexPiche
Thank you Mr. Kane for your time, I finally achieve my objective with the
package reshape2

n5dt-last(dezdiff,5)
n5dt - as.data.frame(t(n5dt))
n5dt$id - c(1:35)


subm5dt-melt(n5dt, id=id, c(2013-06-28, 2013-07-01, 2013-07-02,
2013-07-03, 2013-07-04) )
 names(subm5dt) - c(Observations, variable,BasisPoints)
ggplot(subm5dt, aes(Observations, BasisPoints, col=variable, group=2)) +
geom_line() + facet_grid(variable~., scale=fixed) + geom_point()

Have a nice day!



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[R] repolr: multivariate repeated analysis possible?

2013-07-05 Thread Torvon
Dear all,

I'm trying to perform a non-parametric multivariate repeated measures
analysis of 9 ordered variables (scale 0-3) at two time points. So
basically a multivariate repeated measure GLM for ordered variables.

While the package repolr can model one ordered variable over time, I have
not found a way to do this with several DVs at the same time (I am
interested in the time * DVs interaction term, so I need a multivariate
model).

Is this possible? Is there example syntax for this problem?

Thank you for your help
 Torvon

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Re: [R] Error when building a custom package

2013-07-05 Thread cvo
Hi Ellison

Thanks for the reply. The test package build I did using the skeleton package 
was in the same folder as the one I'm using now for the custom 'slo' package, 
so that is not the problem.

I just investigated whether it was an issue with program rights regarding 
downloading and installing new packages from RCMD, but even after double 
checking that all packages were installed (and finding some that wasn't,. which 
are now manually installed), it still doesn't work.

Regarding the new plot implementation, I don't have a clue whether that is 
needed, but I fully trust the capabilities of the guy to made the source files 
- and as written previously - he is able to build the package on his machine.

Venlig hilsen / Best regards
Christer P. Volk
Specialist
SenseLab

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[cid:image002.jpg@01CE7995.A881CD10]http://www.madebydelta.com/delta/campaign/newsletter-signup.page?
From: S Ellison-2 [via R] [mailto:ml-node+s789695n4670933...@n4.nabble.com]
Sent: 5. juli 2013 15:07
To: Christer P. Volk
Subject: Re: Error when building a custom package


 I only get an error message, when trying to build a binary
 file (or runnning /R CMD check package name/), not the
 standard tar.gz. Here is what the output looks like in the
 command prompt:
 ...
 I have gotten the impression that generally the error with
 the  Error in file... is a problem with a wrong path or
 problems with permissions,

Not sure whether it will solve your problem, but specifying a writeable 
location for R CMD INSTALL --build (as described in 1.3.3 Building binary 
packages in Writing R extensions) should dodge a permission problem if that 
is the issue. Personally I prefer to do that anyway to avoid overwriting an 
existing (working) package installation.

As an aside - probably unrelated and apparently not a warning anyway - I don't 
see why you would need to be be creating a new plot generic. Isn't the existing 
plot generic sufficient?

S Ellison


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Re: [R] kruskal.test followed by kruskalmc

2013-07-05 Thread peter dalgaard

On Jul 5, 2013, at 15:00 , Humber Andrade wrote:

 Thank you Prof. José Iparraguirre. Maybe I am wrong but I think the issues
 are not the same. His data doesn't showed significant differences after
 kruskal.test(), that was not my case. Anyway follow below my the results
 I've got and the database.
 

This can happen. It is a matter of probability theory, not of R. The following 
is a simplified paraphrase of what is going on:

# 15 random normals, compare range test to variance test
# Simulate everything for simplicity


# Null distribution
M0 - replicate(1, rnorm(15))
vv - apply(M0,2,var)
rg - apply(M0,2,range)
rr - apply(rg,2,diff)
r.95  - quantile(rr, .95)
v.95  - quantile(vv, .95)
v.995 - quantile(vv, .995)

# Distribution at quadrupled variance
M - replicate(1, rnorm(15,sd=2))
vv - apply(M,2,var)
rg - apply(M,2,range)
rr - apply(rg,2,diff)
plot(rr,vv)
abline(h=c(v.95,v.995),v=r.95, col=red)

Notice that the two statistics are correlated, but not equivalent. There are 
cases where one value is beyond the .95 level and the other is not. Since it is 
theoretically optimal to use the variance as the test statistic in this model, 
there are quite a few more cases where  rr is below the cutoff and vv is above 
than the other way around. There are even a sizable number of cases where vv is 
beyond v.995 and rr does not reach r.95.

(The theoretical optimality applies only because I use an increased variance 
alternative. For specific alternatives, the picture can change. Try it, for 
instance with a single mean substantially different from the others:

M - replicate(1, rnorm(15,mean=rep(c(4,0),c(1,14

)


 Thank you,
 
 #
 kruskal.test(data$resp,data$group)
 
Kruskal-Wallis rank sum test
 
 data:  data$resp and data$group
 Kruskal-Wallis chi-squared = 32.3546, df = 14, p-value = 0.003566
 
 kruskalmc(data$resp,data$group)
 Multiple comparison test after Kruskal-Wallis
 p.value: 0.05
 Comparisons
   obs.dif critical.dif difference
 A-B  4.8303571 62.37688  FALSE
 A-C  3.8928571 62.37688  FALSE
 A-D  0.4821429 62.37688  FALSE
 .
 .
 .
 M-P 14.250 60.26179  FALSE
 N-O  1.375 60.26179  FALSE
 N-P  6.125 60.26179  FALSE
 O-P  4.750 60.26179  FALSE
 
 # database
   group resp  A 0.1  A 581.8  A 90.5  A 70.1  A 820.1  A 1159.2  A 2478.1
 A 2475.3  B 351.8  B 370.1  B 326.1  B 751.9  B 931  B 588.2  B 70.1  B
 1754.9  C 289.8  C 254.1  C 370.3  C 459.8  C 412.5  C 591.5  C 986.9  C 890
 D 425.6  D 397.4  D 464  D 370.9  D 417.3  D 455  D 568.2  D 599.4  E 405.1
 E 626.2  E 299  E 493.8  E 362.6  E 309.8  E 522.7  E 433.3  F 698.6  F 42.5
 F 7.4  F 10.6  F 95.8  F 497.5  F 987.9  F 925.1  G 492.9  G 376  G 413  G
 278.3  G 344.2  G 292.2  G 429.4  G 368  H 241.6  H 230.5  H 310.4  H 372.5
 H 366.1  H 307.9  H 480  H 529.8  I 296  I 288.8  I 302.1  I 300.8  I 150.1
 I 381.9  I 583.1  I 489.4  J 1.2  J 18.6  J 7.7  J 11.6  J 48.1  J 121.8  J
 1284.1  J 944.7  L 0.5  L 44.4  L 80.9  L 15.3  L 80  L 379.9  L 940.6  L
 829.3  M 323.6  M 401.5  M 162.1  M 136.5  M 139.4  M 363.3  M 280.7  M
 356.5  N 197.6  N 245.9  N 221.5  N 224.3  N 185.4  N 265.3  N 304.8  N
 351.9  O 189.9  O 237.3  O 247.1  O 230.4  O 272.2  O 155.1  O 270.7  O
 315.2  P 48.4  P 15.5  P 53.1  P 72.8  P 74.8  P 132.3  P 550  P 478.7
 
 
 On Fri, Jul 5, 2013 at 8:06 AM, Jose Iparraguirre 
 jose.iparragui...@ageuk.org.uk wrote:
 
 Humber,
 Have a look at this:
 http://r.789695.n4.nabble.com/Multiple-Comparisons-Kruskal-Wallis-Test-kruskal-agricolae-and-kruskalmc-pgirmess-don-t-yield-the-sa-td4639004.html
 Hope it helps.
 Kind regards,
 
 José
 
 Prof. José Iparraguirre
 Chief Economist
 Age UK
 
 
 
 -Original Message-
 From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org]
 On Behalf Of Humber Andrade
 Sent: 05 July 2013 11:38
 To: r-help@r-project.org
 Subject: [R] kruskal.test followed by kruskalmc
 
 Hi all,
 
 After running kruskal.test I have got results (p0,005) pointing to reject
 the hypothesis that the samples were draw from the same population.
 Howerver when I run the kruskalmc there are no significant differences in
 any of the multiple comparisons. Is that possible? Some clarification?
 
 Thanks, Humber
 
 
 https://sites.google.com/site/humberandrade
 
[[alternative HTML version deleted]]
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.
 
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 If you‚re looking for a radio station 

Re: [R] kruskal.test followed by kruskalmc

2013-07-05 Thread Humber Andrade
Thank you Dr. Dalgaard. I understood. I know that this list is not to
discuss statistics but I would be very glad if you or someone else can give
me some opinion on how to proceed. The kruskal.test says there are
differences but the multiple comparisons do not point out what are the
differences. Can you suggest a suitable way (maybe paired wilcoxon) to
infer what are the differences? I am asking for the hint because I am sure
the journal editor/reviewer will ask me to point out which groups differ
from each other.

Regards, Humber


On Fri, Jul 5, 2013 at 11:04 AM, peter dalgaard pda...@gmail.com wrote:


 On Jul 5, 2013, at 15:00 , Humber Andrade wrote:

  Thank you Prof. José Iparraguirre. Maybe I am wrong but I think the
 issues
  are not the same. His data doesn't showed significant differences after
  kruskal.test(), that was not my case. Anyway follow below my the results
  I've got and the database.
 

 This can happen. It is a matter of probability theory, not of R. The
 following is a simplified paraphrase of what is going on:

 # 15 random normals, compare range test to variance test
 # Simulate everything for simplicity


 # Null distribution
 M0 - replicate(1, rnorm(15))
 vv - apply(M0,2,var)
 rg - apply(M0,2,range)
 rr - apply(rg,2,diff)
 r.95  - quantile(rr, .95)
 v.95  - quantile(vv, .95)
 v.995 - quantile(vv, .995)

 # Distribution at quadrupled variance
 M - replicate(1, rnorm(15,sd=2))
 vv - apply(M,2,var)
 rg - apply(M,2,range)
 rr - apply(rg,2,diff)
 plot(rr,vv)
 abline(h=c(v.95,v.995),v=r.95, col=red)

 Notice that the two statistics are correlated, but not equivalent. There
 are cases where one value is beyond the .95 level and the other is not.
 Since it is theoretically optimal to use the variance as the test statistic
 in this model, there are quite a few more cases where  rr is below the
 cutoff and vv is above than the other way around. There are even a sizable
 number of cases where vv is beyond v.995 and rr does not reach r.95.

 (The theoretical optimality applies only because I use an increased
 variance alternative. For specific alternatives, the picture can change.
 Try it, for instance with a single mean substantially different from the
 others:

 M - replicate(1, rnorm(15,mean=rep(c(4,0),c(1,14

 )


  Thank you,
 
  #
  kruskal.test(data$resp,data$group)
 
 Kruskal-Wallis rank sum test
 
  data:  data$resp and data$group
  Kruskal-Wallis chi-squared = 32.3546, df = 14, p-value = 0.003566
  
  kruskalmc(data$resp,data$group)
  Multiple comparison test after Kruskal-Wallis
  p.value: 0.05
  Comparisons
obs.dif critical.dif difference
  A-B  4.8303571 62.37688  FALSE
  A-C  3.8928571 62.37688  FALSE
  A-D  0.4821429 62.37688  FALSE
  .
  .
  .
  M-P 14.250 60.26179  FALSE
  N-O  1.375 60.26179  FALSE
  N-P  6.125 60.26179  FALSE
  O-P  4.750 60.26179  FALSE
 
  # database
group resp  A 0.1  A 581.8  A 90.5  A 70.1  A 820.1  A 1159.2  A 2478.1
  A 2475.3  B 351.8  B 370.1  B 326.1  B 751.9  B 931  B 588.2  B 70.1  B
  1754.9  C 289.8  C 254.1  C 370.3  C 459.8  C 412.5  C 591.5  C 986.9  C
 890
  D 425.6  D 397.4  D 464  D 370.9  D 417.3  D 455  D 568.2  D 599.4  E
 405.1
  E 626.2  E 299  E 493.8  E 362.6  E 309.8  E 522.7  E 433.3  F 698.6  F
 42.5
  F 7.4  F 10.6  F 95.8  F 497.5  F 987.9  F 925.1  G 492.9  G 376  G 413
  G
  278.3  G 344.2  G 292.2  G 429.4  G 368  H 241.6  H 230.5  H 310.4  H
 372.5
  H 366.1  H 307.9  H 480  H 529.8  I 296  I 288.8  I 302.1  I 300.8  I
 150.1
  I 381.9  I 583.1  I 489.4  J 1.2  J 18.6  J 7.7  J 11.6  J 48.1  J 121.8
  J
  1284.1  J 944.7  L 0.5  L 44.4  L 80.9  L 15.3  L 80  L 379.9  L 940.6  L
  829.3  M 323.6  M 401.5  M 162.1  M 136.5  M 139.4  M 363.3  M 280.7  M
  356.5  N 197.6  N 245.9  N 221.5  N 224.3  N 185.4  N 265.3  N 304.8  N
  351.9  O 189.9  O 237.3  O 247.1  O 230.4  O 272.2  O 155.1  O 270.7  O
  315.2  P 48.4  P 15.5  P 53.1  P 72.8  P 74.8  P 132.3  P 550  P 478.7
 
 
  On Fri, Jul 5, 2013 at 8:06 AM, Jose Iparraguirre 
  jose.iparragui...@ageuk.org.uk wrote:
 
  Humber,
  Have a look at this:
 
 http://r.789695.n4.nabble.com/Multiple-Comparisons-Kruskal-Wallis-Test-kruskal-agricolae-and-kruskalmc-pgirmess-don-t-yield-the-sa-td4639004.html
  Hope it helps.
  Kind regards,
 
  José
 
  Prof. José Iparraguirre
  Chief Economist
  Age UK
 
 
 
  -Original Message-
  From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org
 ]
  On Behalf Of Humber Andrade
  Sent: 05 July 2013 11:38
  To: r-help@r-project.org
  Subject: [R] kruskal.test followed by kruskalmc
 
  Hi all,
 
  After running kruskal.test I have got results (p0,005) pointing to
 reject
  the hypothesis that the 

Re: [R] Error when building a custom package

2013-07-05 Thread S Ellison
 
 Thanks for the reply. The test package build I did using the 
 skeleton package was in the same folder as the one I'm using 
 now for the custom 'slo' package, so that is not the problem.
 
Have you checked the detailed logs to see exactly which file is causing the 
trouble?


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[R] Obtaining predicted values from a zero-inflated poisson regression model

2013-07-05 Thread Gavin Rudge
I've got a data set of about 5,000 observations with a zero-inflated count 
response variable, two predictor variables and a variable which is effectively 
an area of opportunity, which I want to use as an offset term (all continuous). 
 I want to explore the association between these variables, in particular I'm 
interested in the association of one particular variable net of the others and 
it would be useful when presenting the results of the analysis to hold my other 
variables constant at say their means or medians, and show what my model 
predicts would happen to my RV as it varied.

In reality there are a bunch of methods issues with this that I don't want to 
explore in this post, (like would a hurdle model be better, and as it is a 
model with spatial variables, should I use something optimised for this, 
bootstrapping the CIs etc) as I want to get to an adequate level of 
understanding of how this particular model behaves before I go any further with 
this.

I have incorporated the code to synthesise some data that look a bit like mine, 
I've then gone about making some predictions the best way I can given my 
current level of understanding of the package I've used (pscl), with some brief 
annotation.

#packages required
require(pscl)
require(emdbook)
#get some data
set.seed(33)
dsdata.frame(a=rzinbinom(500,mu=2,zprob=0.6,size=0.8),b=runif(500,3,70),c=runif(500,0.3,10),d=runif(500,0.03,0.8))
#run the model
mymodel-zeroinfl(a~b+c,offset=d,data=ds,dist=negbin,EM=TRUE)
summary(mymodel)
#make a prediction data set, holding c and d at their means and varying b over 
the range of original values
mypred-data.frame(b=3:70,c=5.18,d=0.39)
#generate predicted values of response variable, add to the data frame
pred_rv-predict.zeroinfl(mymodel,newdata=mypred,type=response,model=count,se=TRUE)
#assemble  the prediction data.frame
predfinal-data.frame(mypred,pred_rv)
colnames(predfinal)-c(b,c,d,predicted,lower,upper,se)
predfinal

My questions are:  What exactly does this give me? I am trying to get counts in 
their original scale that my model predicts.  Is what I have here the modelled 
counts from just the count component of the model? If I change the model term 
to zero from count I get the same result, why is this?  Or indeed have i 
simply completely gone the wrong way about getting these estimates?

Also, I can't seem to manually replicate any of these predicted values using 
the model results.

I've tried looking at the help page of the predict.zeroinfl and predict 
commands, but still cannot get much further with this.

Any help is much appreciated.

Regards

GavinR


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Re: [R] Substituting Greek symbols in some tick labels

2013-07-05 Thread David Winsemius

On Jul 4, 2013, at 8:14 PM, Eric Archer - NOAA Federal wrote:

 I have a character vector that I'm using to label ticks in a dotchart. Some
 of the elements in the vector have an asterisk (*) where a Greek Delta
 needs to be placed when the plot is generated. Here's a simple example:
 
 x - 1:4
 x.lab - c(a*a, bbb, c*c, ddd)
 dotchart(x, labels = x.lab)
 
 The first and third labels should be 'aDeltaa' and 'cDeltac'. I've
 tried things like,
 
 x.lab - strsplit(x.lab, [*])
 x.lab - lapply(x.lab, function(y) expression(paste(y, sep = Delta)))
 
 but because 'y' is unevaluated, the resulting list elements won't work as
 tick labels. I've tried to modify it by using bquote and substitute, but
 couldn't get anything closer. Any suggestions? Thanks!

Right. I would not throw away the * but rather change it to an inline Delta:

x.lab - gsub(\\*, *Delta*, x.lab)

# parse(text=x.lab)
# returns: expression(a*Delta*a, bbb, c*Delta*c, ddd)# 

Then parse it:

dotchart(x, labels = parse(text=x.lab) )


 
 Cheers,
 eric
 
 -- 
 
 Eric Archer, Ph.D.
 Southwest Fisheries Science Center
 NMFS, NOAA
 8901 La Jolla Shores Drive
 La Jolla, CA 92037 USA
 858-546-7121 (work)
 858-546-7003 (FAX)
 
 Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
 ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp
 
 The universe doesn't care what you believe.
 The wonderful thing about science is that it
   doesn't ask for your faith, it just asks
   for your eyes.  - Randall Munroe
 
 Lighthouses are more helpful than churches.
   - Benjamin Franklin
 
   ...but I'll take a GPS over either one.
   - John C. Craig George
 
   [[alternative HTML version deleted]]
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.

David Winsemius
Alameda, CA, USA

__
R-help@r-project.org mailing list
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Re: [R] Substituting Greek symbols in some tick labels

2013-07-05 Thread Eric Archer - NOAA Federal
David,

That's perfect! I just didn't think to use 'parse'. Thanks!

Cheers,
eric


On Fri, Jul 5, 2013 at 8:20 AM, David Winsemius dwinsem...@comcast.netwrote:


 On Jul 4, 2013, at 8:14 PM, Eric Archer - NOAA Federal wrote:

  I have a character vector that I'm using to label ticks in a dotchart.
 Some
  of the elements in the vector have an asterisk (*) where a Greek Delta
  needs to be placed when the plot is generated. Here's a simple example:
 
  x - 1:4
  x.lab - c(a*a, bbb, c*c, ddd)
  dotchart(x, labels = x.lab)
 
  The first and third labels should be 'aDeltaa' and 'cDeltac'. I've
  tried things like,
 
  x.lab - strsplit(x.lab, [*])
  x.lab - lapply(x.lab, function(y) expression(paste(y, sep = Delta)))
 
  but because 'y' is unevaluated, the resulting list elements won't work as
  tick labels. I've tried to modify it by using bquote and substitute, but
  couldn't get anything closer. Any suggestions? Thanks!

 Right. I would not throw away the * but rather change it to an inline
 Delta:

 x.lab - gsub(\\*, *Delta*, x.lab)

 # parse(text=x.lab)
 # returns: expression(a*Delta*a, bbb, c*Delta*c, ddd)#

 Then parse it:

 dotchart(x, labels = parse(text=x.lab) )


 
  Cheers,
  eric
 
  --
 
  Eric Archer, Ph.D.
  Southwest Fisheries Science Center
  NMFS, NOAA
  8901 La Jolla Shores Drive
  La Jolla, CA 92037 USA
  858-546-7121 (work)
  858-546-7003 (FAX)
 
  Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
  ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp
 
  The universe doesn't care what you believe.
  The wonderful thing about science is that it
doesn't ask for your faith, it just asks
for your eyes.  - Randall Munroe
 
  Lighthouses are more helpful than churches.
- Benjamin Franklin
 
...but I'll take a GPS over either one.
- John C. Craig George
 
[[alternative HTML version deleted]]
 
  __
  R-help@r-project.org mailing list
  https://stat.ethz.ch/mailman/listinfo/r-help
  PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
  and provide commented, minimal, self-contained, reproducible code.

 David Winsemius
 Alameda, CA, USA




-- 

Eric Archer, Ph.D.
Southwest Fisheries Science Center
NMFS, NOAA
8901 La Jolla Shores Drive
La Jolla, CA 92037 USA
858-546-7121 (work)
858-546-7003 (FAX)

Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp

The universe doesn't care what you believe.
 The wonderful thing about science is that it
   doesn't ask for your faith, it just asks
   for your eyes.  - Randall Munroe

Lighthouses are more helpful than churches.
   - Benjamin Franklin

   ...but I'll take a GPS over either one.
   - John C. Craig George

[[alternative HTML version deleted]]

__
R-help@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/r-help
PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] problem on reading many files

2013-07-05 Thread David Winsemius

On Jul 5, 2013, at 1:04 AM, Pascal Oettli wrote:

 Hello,
 
 I'm not sure whether it is dur to the HTML version or not, but there is a
 problem with quotation marks in your first line.

I'm guessing the OP was using Word as an editor, a practice that is doomed to 
frustration.

-- 
David.
 
 Regards,
 Pascal
 
 
 2013/7/5 RODRIGUEZ MORENO VICTOR MANUEL rodriguez.vic...@inifap.gob.mx
 
 Hi, I have to run almost 120 stations files of temperatura (mx and min),
 separated, and rain. I am following the instructions on RHtests tutorial as
 on http://www.cmc.org.ve/mediawiki/index.php?title=Preparando_los_datoslink. 
 Bit I have no success on running on multiple files. I have the .ls
 file which include the names of the file station, which I include on this
 msg for your consideration.
 The instruction that I wrote on the console is
 
 listatmn - readLines („tmaxcopia.ls‰, warn=false)
 for(ifile in listatmn)
 FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)
 
 
 
 
 
 Of course the tmaxcopia.ls is the list of stations for tmax data. But
 once running on the console, this is the error msg I got
 
 listatmn - readLines (Œtmaxcopia.ls‚, warn=false)
 Error: inesperado entrada in listatmn - readLines (Œ
 for(ifile in listatmn)
 FindU(paste(./,ifile,sep=),paste(salidas/,ifile,sep=),-999.9)
 Error: objeto 'ifnames' no encontrado
 
 What I'd like to do is to make easier and fast running the RHtest
 
 Thank's a lot in advance for your help.
 
 
 
 
 Dr Victor M Rodríguez M
 Doctor en Ciencias, en Ciencias de la Tierra / Geociencias Ambientales
 INIFAP. CEPAB. (465) 9580167 y 86 Ext 108 y 220
 
 
 /
 Este msg y su(s) atado(s) tiene carácter de CONFIDENCIAL y solo es para
 los fines descritos en su contenido. Queda expresamente prohibida bajo la
 ley de protección de datos del Gobierno de los Estados Unidos Mexicanos y
 para su difusion o extensión a terceros, se requiere del consentimiento
 expresso del titular de la cuenta de correo electrónico y/o del
 administrador del sitio en extenso de sus responsabilidades .
 
 /
 
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 __
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 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
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Re: [R] R and MatLab implementations of the same model differs

2013-07-05 Thread Jannetta Steyn
Thank you very much to all of you for your help. This model now works as it
should (I believe). This is the final code:

rm(list=ls())

library(deSolve)

ST -  function(time, init, parms) {
  with(as.list(c(init, parms)),{

#functions to calculate activation m and inactivation h of the currents
#Axon
mNax - function(v) 1/(1+exp(-(v+24.7)/5.29))
taumNa - function(v) 1.32-(1.26/(1+exp(-(v+120)/25)))
hNax - function(v) 1/(1+exp((v+48.9)/5.18))
tauhNa - function(v)
0.67/(1+exp(-(v+62.9)/10))*(1.5+(1/(1+exp((v+34.9)/3.6
mKx - function(v) 1/(1+exp(-(v+14.2)/11.8))
taumK - function(v) 7.2-(6.4/(1+exp(-(v+28.3)/19.2)))


# Currents as product of maximal conducatance(g), activation(m) and
inactivation(h)
# Driving force (v-E) where E is the reversal potential of the
particular ion

# AB axon
iNa_axon_AB -
gNa_axon_AB*mNa_axon_AB^3*hNa_axon_AB*(v_axon_AB-ENa_axon_AB)
iK_axon_AB - gK_axon_AB*mK_axon_AB^4*(v_axon_AB-EK_axon_AB)
iLeak_axon_AB - gLeak_axon_AB*(v_axon_AB-ELeak_axon_AB)

# AB Axon equations
dv_axon_AB - (0 -iNa_axon_AB -iK_axon_AB -iLeak_axon_AB)/C_axon_AB
dmNa_axon_AB - (mNax(v_axon_AB)-mNa_axon_AB)/taumNa(v_axon_AB)
dhNa_axon_AB - (hNax(v_axon_AB)-hNa_axon_AB)/tauhNa(v_axon_AB)
dmK_axon_AB - (mKx(v_axon_AB)-mK_axon_AB)/taumK(v_axon_AB)

list(c(dv_axon_AB,dmNa_axon_AB, dhNa_axon_AB, dmK_axon_AB
))

  })}
## Set initial state
init = c(v_axon_AB=-55,mNa_axon_AB=0,hNa_axon_AB=1,mK_axon_AB=0)
## Set parameters
# AB

gNa_axon_AB=300e-3
gK_axon_AB=52.5e-3
gLeak_axon_AB=0.0018e-3

# AB Axon Reversal potentials
ENa_axon_AB=50
EK_axon_AB=-80
ELeak_axon_AB=-60

C_axon_AB=1.5e-3


I=0

parms =
c(ENa_axon_AB,EK_axon_AB,ELeak_axon_AB,gNa_axon_AB,gK_axon_AB,gLeak_axon_AB,C_axon_AB)
## Set integrations times
times = seq(from=0, to=5000, by = 0.05);

out-ode(y=init, times=times, func=ST, parms=parms, method=ode45)

o-data.frame(out)

plot(o$v_axon_AB~o$time,type='l')


My MatLab expert came to my rescue and both model now produce similar
results :-)

Regards
Jannetta


On 5 July 2013 12:11, Jannetta Steyn janne...@henning.org wrote:




 On 5 July 2013 09:44, Berend Hasselman b...@xs4all.nl wrote:


 On 05-07-2013, at 09:53, Jannetta Steyn janne...@henning.org wrote:

 
 
  
   I don't quite know how to explain the doesn't work in more detail
 without
   any visual aid.
 
  You said that R got into an indefinite loop, whatever that maybe.
 
 
   When I change the solver to ode45 the script never stops running. I
 have even left it over night at one stage but the next day it was still
 busy. Is there a way to see what it is doing and to determine why it seems
 to be in an
   infinite loop?
 
  The script just ran using ode45!! For the first time ever.
 

 Please keep the conversation on R-help.
 Don't reply to me personally.



 Apologies for that. It was meant to go to the list.



 Which script?
 With the corrections suggested by me and Peter? (gK_axon_AB=52.5-3 ==
 gK_axon_AB=52.5e-3)


 The R script. With the correction of AB=52.5e-3



 For what it's worth: lsdoda seems quicker.


 Yes, lsoda is quicker but I want to use ode45 because that is what they
 used in the paper I am referencing and I am trying to get the same results
 as they did.


 Variable v_acon_AB now converges to -60 (the equilibrium state?)


 I'm trying to determine now whether this is correct.

 Regards
 Jannetta


 --

 ===
 Web site: http://www.jannetta.com
 Email: janne...@henning.org
 ===




-- 

===
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Email: janne...@henning.org
===

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Re: [R] R and MatLab implementations of the same model differs

2013-07-05 Thread Berend Hasselman

On 05-07-2013, at 17:37, Jannetta Steyn janne...@henning.org wrote:

 Thank you very much to all of you for your help. This model now works as it
 should (I believe). This is the final code:
 
 rm(list=ls())
 
 library(deSolve)
 
 ST -  function(time, init, parms) {
  with(as.list(c(init, parms)),{
 
#functions to calculate activation m and inactivation h of the currents
#Axon
mNax - function(v) 1/(1+exp(-(v+24.7)/5.29))
taumNa - function(v) 1.32-(1.26/(1+exp(-(v+120)/25)))
hNax - function(v) 1/(1+exp((v+48.9)/5.18))
tauhNa - function(v)
 0.67/(1+exp(-(v+62.9)/10))*(1.5+(1/(1+exp((v+34.9)/3.6
mKx - function(v) 1/(1+exp(-(v+14.2)/11.8))
taumK - function(v) 7.2-(6.4/(1+exp(-(v+28.3)/19.2)))
 
 
# Currents as product of maximal conducatance(g), activation(m) and
 inactivation(h)
# Driving force (v-E) where E is the reversal potential of the
 particular ion
 
# AB axon
iNa_axon_AB -
 gNa_axon_AB*mNa_axon_AB^3*hNa_axon_AB*(v_axon_AB-ENa_axon_AB)
iK_axon_AB - gK_axon_AB*mK_axon_AB^4*(v_axon_AB-EK_axon_AB)
iLeak_axon_AB - gLeak_axon_AB*(v_axon_AB-ELeak_axon_AB)
 
# AB Axon equations
dv_axon_AB - (0 -iNa_axon_AB -iK_axon_AB -iLeak_axon_AB)/C_axon_AB
dmNa_axon_AB - (mNax(v_axon_AB)-mNa_axon_AB)/taumNa(v_axon_AB)
dhNa_axon_AB - (hNax(v_axon_AB)-hNa_axon_AB)/tauhNa(v_axon_AB)
dmK_axon_AB - (mKx(v_axon_AB)-mK_axon_AB)/taumK(v_axon_AB)
 
list(c(dv_axon_AB,dmNa_axon_AB, dhNa_axon_AB, dmK_axon_AB
))
 
  })}
 ## Set initial state
 init = c(v_axon_AB=-55,mNa_axon_AB=0,hNa_axon_AB=1,mK_axon_AB=0)
 ## Set parameters
 # AB
 
 gNa_axon_AB=300e-3
 gK_axon_AB=52.5e-3
 gLeak_axon_AB=0.0018e-3
 
 # AB Axon Reversal potentials
 ENa_axon_AB=50
 EK_axon_AB=-80
 ELeak_axon_AB=-60
 
 C_axon_AB=1.5e-3
 
 
 I=0
 
 parms =
 c(ENa_axon_AB,EK_axon_AB,ELeak_axon_AB,gNa_axon_AB,gK_axon_AB,gLeak_axon_AB,C_axon_AB)
 ## Set integrations times
 times = seq(from=0, to=5000, by = 0.05);
 
 out-ode(y=init, times=times, func=ST, parms=parms, method=ode45)
 
 o-data.frame(out)
 
 plot(o$v_axon_AB~o$time,type='l')
 

You must make the parms vector a named vector because the with(.. in your 
function ST is not using the global values for those entities available in the 
global environment.

You can check this by inserting this line after the line with times =  and 
before the line out - ode(…

rm(list=c(ENa_axon_AB,EK_axon_AB,ELeak_axon_AB,gNa_axon_AB,gK_axon_AB,gLeak_axon_AB,C_axon_AB))

You will get an error.

So create the parms vector like this

parms =
c(ENa_axon_AB=ENa_axon_AB,EK_axon_AB=EK_axon_AB,ELeak_axon_AB=ELeak_axon_AB,gNa_axon_AB=gNa_axon_AB,
gK_axon_AB=gK_axon_AB,gLeak_axon_AB=gLeak_axon_AB,C_axon_AB=C_axon_AB)

or better

parms - c(ENa_axon_AB=50,EK_axon_AB=-80,ELeak_axon_AB=-60,gNa_axon_AB=300e-3,
  gK_axon_AB=52.5e-3,gLeak_axon_AB=0.0018e-3,C_axon_AB=1.5e-3)

and remove the expressions with the separate assignments to the variables.


And use - !!

Berend

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Re: [R] R and MatLab implementations of the same model differs

2013-07-05 Thread Jannetta Steyn
Aah. Thanks. I remember someone mentioned a named vector and I meant to ask
what that was, but I forgot. I have now fixed  it.


On 5 July 2013 17:18, Berend Hasselman b...@xs4all.nl wrote:


 On 05-07-2013, at 17:37, Jannetta Steyn janne...@henning.org wrote:

  Thank you very much to all of you for your help. This model now works as
 it
  should (I believe). This is the final code:
 
  rm(list=ls())
 
  library(deSolve)
 
  ST -  function(time, init, parms) {
   with(as.list(c(init, parms)),{
 
 #functions to calculate activation m and inactivation h of the
 currents
 #Axon
 mNax - function(v) 1/(1+exp(-(v+24.7)/5.29))
 taumNa - function(v) 1.32-(1.26/(1+exp(-(v+120)/25)))
 hNax - function(v) 1/(1+exp((v+48.9)/5.18))
 tauhNa - function(v)
  0.67/(1+exp(-(v+62.9)/10))*(1.5+(1/(1+exp((v+34.9)/3.6
 mKx - function(v) 1/(1+exp(-(v+14.2)/11.8))
 taumK - function(v) 7.2-(6.4/(1+exp(-(v+28.3)/19.2)))
 
 
 # Currents as product of maximal conducatance(g), activation(m) and
  inactivation(h)
 # Driving force (v-E) where E is the reversal potential of the
  particular ion
 
 # AB axon
 iNa_axon_AB -
  gNa_axon_AB*mNa_axon_AB^3*hNa_axon_AB*(v_axon_AB-ENa_axon_AB)
 iK_axon_AB - gK_axon_AB*mK_axon_AB^4*(v_axon_AB-EK_axon_AB)
 iLeak_axon_AB - gLeak_axon_AB*(v_axon_AB-ELeak_axon_AB)
 
 # AB Axon equations
 dv_axon_AB - (0 -iNa_axon_AB -iK_axon_AB -iLeak_axon_AB)/C_axon_AB
 dmNa_axon_AB - (mNax(v_axon_AB)-mNa_axon_AB)/taumNa(v_axon_AB)
 dhNa_axon_AB - (hNax(v_axon_AB)-hNa_axon_AB)/tauhNa(v_axon_AB)
 dmK_axon_AB - (mKx(v_axon_AB)-mK_axon_AB)/taumK(v_axon_AB)
 
 list(c(dv_axon_AB,dmNa_axon_AB, dhNa_axon_AB, dmK_axon_AB
 ))
 
   })}
  ## Set initial state
  init = c(v_axon_AB=-55,mNa_axon_AB=0,hNa_axon_AB=1,mK_axon_AB=0)
  ## Set parameters
  # AB
 
  gNa_axon_AB=300e-3
  gK_axon_AB=52.5e-3
  gLeak_axon_AB=0.0018e-3
 
  # AB Axon Reversal potentials
  ENa_axon_AB=50
  EK_axon_AB=-80
  ELeak_axon_AB=-60
 
  C_axon_AB=1.5e-3
 
 
  I=0
 
  parms =
 
 c(ENa_axon_AB,EK_axon_AB,ELeak_axon_AB,gNa_axon_AB,gK_axon_AB,gLeak_axon_AB,C_axon_AB)
  ## Set integrations times
  times = seq(from=0, to=5000, by = 0.05);
 
  out-ode(y=init, times=times, func=ST, parms=parms, method=ode45)
 
  o-data.frame(out)
 
  plot(o$v_axon_AB~o$time,type='l')
 

 You must make the parms vector a named vector because the with(.. in your
 function ST is not using the global values for those entities available in
 the global environment.

 You can check this by inserting this line after the line with times =  and
 before the line out - ode(…


 rm(list=c(ENa_axon_AB,EK_axon_AB,ELeak_axon_AB,gNa_axon_AB,gK_axon_AB,gLeak_axon_AB,C_axon_AB))

 You will get an error.

 So create the parms vector like this

 parms =

 c(ENa_axon_AB=ENa_axon_AB,EK_axon_AB=EK_axon_AB,ELeak_axon_AB=ELeak_axon_AB,gNa_axon_AB=gNa_axon_AB,
 gK_axon_AB=gK_axon_AB,gLeak_axon_AB=gLeak_axon_AB,C_axon_AB=C_axon_AB)

 or better

 parms -
 c(ENa_axon_AB=50,EK_axon_AB=-80,ELeak_axon_AB=-60,gNa_axon_AB=300e-3,

 gK_axon_AB=52.5e-3,gLeak_axon_AB=0.0018e-3,C_axon_AB=1.5e-3)

 and remove the expressions with the separate assignments to the variables.


 And use - !!

 Berend









-- 

===
Web site: http://www.jannetta.com
Email: janne...@henning.org
===

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[R] multcomp on significant interaction in coxme model

2013-07-05 Thread Simon Tragust
Dear R community
I currently try to get post hoc multiple comparisons with the package 
multcomp from a cox mixed-effects model, where the survival is explained 
by two variables (cover with levels: nocover and cover; treatment with 
levels: tx, uv, meta), whose interaction is significant.
I read Hothorn, T. 2011: Additional multcomp Examples and there is an 
example involving a two-way ANOVA with significant interaction. Using 
this guideline I wanted to compare the levels of treatment in my data 
within the levels of cover.

My model is as follows:

m.lapf-coxme(Surv(day,status)~cover*treatment+(1|r.brood)+(1|r.worker)+(1|species/brood),data=removal.lapf)

First I constructed a contrast matrix based on Tukey-contrasts as follows:

Tukey-contrMat(table(removal.lapf$treatment), Tukey)
Tukey
K1-cbind(Tukey,matrix(0,nrow=nrow(Tukey),ncol=ncol(Tukey)))
K1
rownames(K1)-paste(levels(removal.lapf$cover)[1],rownames(K1),sep=:)
K1
K2-cbind(matrix(0,nrow=nrow(Tukey),ncol=ncol(Tukey)),Tukey)
K2
rownames(K2)-paste(levels(removal.lapf$cover)[2],rownames(K1),sep=:)
K2
K-rbind(K1,K2)
colnames(K)-c(colnames(Tukey),colnames(Tukey))
K

This gives the following matrix
meta tx uv meta tx uv
cocooned:tx - meta  -1   1  0   0 0  0
cocooned:uv - meta -10  1  0 0  0
cocooned:uv - tx0   -1  1  0 0 0
naked:cocooned:tx - meta00  0 -11  0
naked:cocooned:uv - meta0   0  0 -1 0  1
naked:cocooned:uv - tx 00  0  0-1  1

then I constructed a secon matrix

tmp-expand.grid(treatment=unique(removal.lapf$treatment),cover=unique(removal.lapf$cover))
X-model.matrix(~cover*treatment,data=tmp)
X

which gives the following

   (Intercept) covernaked treatmenttx treatmentuv covernaked:treatmenttx 
covernaked:treatmentuv
1   1  1   1 0  
1  0
2   1  1   0 1  
0  1
3   1  1   0 0  
0  0
4   1  0   1 0  
0  0
5   1  0   0 1  
0  0
6   1  0   0 0  
0  0
attr(,assign)
[1] 0 1 2 2 3 3
attr(,contrasts)
attr(,contrasts)$cover
[1] contr.treatment

attr(,contrasts)$treatment
[1] contr.treatment


however when performing the tests via

summary(glht(m.lapf,linfct=K%*%X))

I get the following error message

Error in summary(glht(m.lapf, linfct = K %*% X)) :
   error in evaluating the argument 'object' in selecting a method for 
function 'summary': Error in glht.matrix(m.lapf, linfct = K %*% X) :
   'ncol(linfct)' is not equal to 'length(coef(model))'

Performing exactly the same routine with the same data on a logistic 
model with family=binomial does not give this error message.
So my question is, what am I missing here?

Thanks, for any possible input

-- 
Simon Tragust
Animal Ecology I
University Bayreuth
D-95440 Bayreuth

+49 921 552464


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Re: [R] kruskal.test followed by kruskalmc

2013-07-05 Thread peter dalgaard

On Jul 5, 2013, at 16:34 , Humber Andrade wrote:

 Thank you Dr. Dalgaard. I understood. I know that this list is not to discuss 
 statistics but I would be very glad if you or someone else can give me some 
 opinion on how to proceed. The kruskal.test says there are differences but 
 the multiple comparisons do not point out what are the differences. Can you 
 suggest a suitable way (maybe paired wilcoxon) to infer what are the 
 differences? I am asking for the hint because I am sure the journal 
 editor/reviewer will ask me to point out which groups differ from each other.
 

I'm afraid it can't be done. You really can be in a situation where you reject 
the global null hypothesis that all groups are the same, yet cannot point out 
any two groups that differ from eachother. 

-pd

 Regards, Humber
 
 
 On Fri, Jul 5, 2013 at 11:04 AM, peter dalgaard pda...@gmail.com wrote:
 
 On Jul 5, 2013, at 15:00 , Humber Andrade wrote:
 
  Thank you Prof. José Iparraguirre. Maybe I am wrong but I think the issues
  are not the same. His data doesn't showed significant differences after
  kruskal.test(), that was not my case. Anyway follow below my the results
  I've got and the database.
 
 
 This can happen. It is a matter of probability theory, not of R. The 
 following is a simplified paraphrase of what is going on:
 
 # 15 random normals, compare range test to variance test
 # Simulate everything for simplicity
 
 
 # Null distribution
 M0 - replicate(1, rnorm(15))
 vv - apply(M0,2,var)
 rg - apply(M0,2,range)
 rr - apply(rg,2,diff)
 r.95  - quantile(rr, .95)
 v.95  - quantile(vv, .95)
 v.995 - quantile(vv, .995)
 
 # Distribution at quadrupled variance
 M - replicate(1, rnorm(15,sd=2))
 vv - apply(M,2,var)
 rg - apply(M,2,range)
 rr - apply(rg,2,diff)
 plot(rr,vv)
 abline(h=c(v.95,v.995),v=r.95, col=red)
 
 Notice that the two statistics are correlated, but not equivalent. There are 
 cases where one value is beyond the .95 level and the other is not. Since it 
 is theoretically optimal to use the variance as the test statistic in this 
 model, there are quite a few more cases where  rr is below the cutoff and vv 
 is above than the other way around. There are even a sizable number of cases 
 where vv is beyond v.995 and rr does not reach r.95.
 
 (The theoretical optimality applies only because I use an increased variance 
 alternative. For specific alternatives, the picture can change. Try it, for 
 instance with a single mean substantially different from the others:
 
 M - replicate(1, rnorm(15,mean=rep(c(4,0),c(1,14
 
 )
 
 
  Thank you,
 
  #
  kruskal.test(data$resp,data$group)
 
 Kruskal-Wallis rank sum test
 
  data:  data$resp and data$group
  Kruskal-Wallis chi-squared = 32.3546, df = 14, p-value = 0.003566
  
  kruskalmc(data$resp,data$group)
  Multiple comparison test after Kruskal-Wallis
  p.value: 0.05
  Comparisons
obs.dif critical.dif difference
  A-B  4.8303571 62.37688  FALSE
  A-C  3.8928571 62.37688  FALSE
  A-D  0.4821429 62.37688  FALSE
  .
  .
  .
  M-P 14.250 60.26179  FALSE
  N-O  1.375 60.26179  FALSE
  N-P  6.125 60.26179  FALSE
  O-P  4.750 60.26179  FALSE
 
  # database
group resp  A 0.1  A 581.8  A 90.5  A 70.1  A 820.1  A 1159.2  A 2478.1
  A 2475.3  B 351.8  B 370.1  B 326.1  B 751.9  B 931  B 588.2  B 70.1  B
  1754.9  C 289.8  C 254.1  C 370.3  C 459.8  C 412.5  C 591.5  C 986.9  C 890
  D 425.6  D 397.4  D 464  D 370.9  D 417.3  D 455  D 568.2  D 599.4  E 405.1
  E 626.2  E 299  E 493.8  E 362.6  E 309.8  E 522.7  E 433.3  F 698.6  F 42.5
  F 7.4  F 10.6  F 95.8  F 497.5  F 987.9  F 925.1  G 492.9  G 376  G 413  G
  278.3  G 344.2  G 292.2  G 429.4  G 368  H 241.6  H 230.5  H 310.4  H 372.5
  H 366.1  H 307.9  H 480  H 529.8  I 296  I 288.8  I 302.1  I 300.8  I 150.1
  I 381.9  I 583.1  I 489.4  J 1.2  J 18.6  J 7.7  J 11.6  J 48.1  J 121.8  J
  1284.1  J 944.7  L 0.5  L 44.4  L 80.9  L 15.3  L 80  L 379.9  L 940.6  L
  829.3  M 323.6  M 401.5  M 162.1  M 136.5  M 139.4  M 363.3  M 280.7  M
  356.5  N 197.6  N 245.9  N 221.5  N 224.3  N 185.4  N 265.3  N 304.8  N
  351.9  O 189.9  O 237.3  O 247.1  O 230.4  O 272.2  O 155.1  O 270.7  O
  315.2  P 48.4  P 15.5  P 53.1  P 72.8  P 74.8  P 132.3  P 550  P 478.7
 
 
  On Fri, Jul 5, 2013 at 8:06 AM, Jose Iparraguirre 
  jose.iparragui...@ageuk.org.uk wrote:
 
  Humber,
  Have a look at this:
  http://r.789695.n4.nabble.com/Multiple-Comparisons-Kruskal-Wallis-Test-kruskal-agricolae-and-kruskalmc-pgirmess-don-t-yield-the-sa-td4639004.html
  Hope it helps.
  Kind regards,
 
  José
 
  Prof. José Iparraguirre
  Chief Economist
  Age UK
 
 
 
  -Original Message-
  From: r-help-boun...@r-project.org 

Re: [R] Lattice barchart with error bars

2013-07-05 Thread Shaun Jackman
Hi Bert, Dennis,

I'll agree that using a barchart was a poor choice. I was in fact using a
notched bwplot to show the median and confidence interval of the median. In
this case it's the median and confidence interval that I want to highlight,
and I find that the visual noise of the box and whiskers is detracting from
the focus, and those wee notches are not much to focus on. So, I'd like to
draw a stripplot with error bars, preferably in Lattice. Let's call this a
TIE fighter plot. Any suggestions?

Cheers,
Shaun

On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:

 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)

 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.

 Dennis

 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
  Hi,
 
  I'd like to draw a lattice barchart of means with error bars to show
  the standard deviation. I have the barchart, how do I add the error
  bars?
 
  require(datasets)
  require(lattice)
  x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
  sd=sd(x)))
  barchart(weight[,'mean'] ~ Diet, x)
 
  Thanks,
  Shaun
 
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  PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
  and provide commented, minimal, self-contained, reproducible code.


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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Lattice barchart with error bars

2013-07-05 Thread David Winsemius

On Jul 5, 2013, at 11:15 AM, Shaun Jackman wrote:

 Hi Bert, Dennis,
 
 I'll agree that using a barchart was a poor choice. I was in fact using a
 notched bwplot to show the median and confidence interval of the median. In
 this case it's the median and confidence interval that I want to highlight,
 and I find that the visual noise of the box and whiskers is detracting from
 the focus, and those wee notches are not much to focus on. So, I'd like to
 draw a stripplot with error bars, preferably in Lattice. Let's call this a
 TIE fighter plot. Any suggestions?
 

I like the TIE fighter label. Try this:

library(latticeExtra)
data(USCancerRates)
segplot(reorder(factor(county), rate.male) ~ LCL95.male + UCL95.male,
data = subset(USCancerRates, state == Washington),
draw.bands = FALSE, centers = rate.male, 
segments.fun = panel.arrows, ends = both, 
angle = 90, length = 1, unit = mm)

It's what Sarkar has recommended in the past when this request has been posted.

-- 
David


 Cheers,
 Shaun
 
 On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:
 
 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)
 
 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.
 
 Dennis
 
 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
 Hi,
 
 I'd like to draw a lattice barchart of means with error bars to show
 the standard deviation. I have the barchart, how do I add the error
 bars?
 
 require(datasets)
 require(lattice)
 x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
 sd=sd(x)))
 barchart(weight[,'mean'] ~ Diet, x)
 
 Thanks,
 Shaun
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.
 
 
   [[alternative HTML version deleted]]
 
 __
 R-help@r-project.org mailing list
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 and provide commented, minimal, self-contained, reproducible code.

David Winsemius
Alameda, CA, USA

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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Lattice barchart with error bars

2013-07-05 Thread Bert Gunter
Be careful!

You are talking about 2 different varieties of apples here. As I read
it, the CI's in the  cancer data, which I know is just for example
purposes, are CI's for the **individual means**; the notches in
boxplots are nonparametric and for 2 groups with roughly equal sample
sizes, The idea appears to be to give roughly a 95% confidence
interval for the **difference** in two medians. (from
?boxplot.stats). So I'm not sure which you want, but they are
certainly different (by a factor of around sqrt(2),right?), even if
both are for the mean or both are for the median.

Cheers,
Bert

On Fri, Jul 5, 2013 at 11:28 AM, David Winsemius dwinsem...@comcast.net wrote:

 On Jul 5, 2013, at 11:15 AM, Shaun Jackman wrote:

 Hi Bert, Dennis,

 I'll agree that using a barchart was a poor choice. I was in fact using a
 notched bwplot to show the median and confidence interval of the median. In
 this case it's the median and confidence interval that I want to highlight,
 and I find that the visual noise of the box and whiskers is detracting from
 the focus, and those wee notches are not much to focus on. So, I'd like to
 draw a stripplot with error bars, preferably in Lattice. Let's call this a
 TIE fighter plot. Any suggestions?


 I like the TIE fighter label. Try this:

 library(latticeExtra)
 data(USCancerRates)
 segplot(reorder(factor(county), rate.male) ~ LCL95.male + UCL95.male,
 data = subset(USCancerRates, state == Washington),
 draw.bands = FALSE, centers = rate.male,
 segments.fun = panel.arrows, ends = both,
 angle = 90, length = 1, unit = mm)

 It's what Sarkar has recommended in the past when this request has been 
 posted.

 --
 David


 Cheers,
 Shaun

 On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:

 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)

 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.

 Dennis

 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
 Hi,

 I'd like to draw a lattice barchart of means with error bars to show
 the standard deviation. I have the barchart, how do I add the error
 bars?

 require(datasets)
 require(lattice)
 x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
 sd=sd(x)))
 barchart(weight[,'mean'] ~ Diet, x)

 Thanks,
 Shaun

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


   [[alternative HTML version deleted]]

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.

 David Winsemius
 Alameda, CA, USA




-- 

Bert Gunter
Genentech Nonclinical Biostatistics

Internal Contact Info:
Phone: 467-7374
Website:
http://pharmadevelopment.roche.com/index/pdb/pdb-functional-groups/pdb-biostatistics/pdb-ncb-home.htm

__
R-help@r-project.org mailing list
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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] Lattice barchart with error bars

2013-07-05 Thread Shaun Jackman
Yes! Thank you, David. That's exactly what I'm I'm looking for. For
the record, here's a couple pages leading to this answer:

http://www.hep.by/gnu/r-patched/r-faq/R-FAQ_89.html
http://latticeextra.r-forge.r-project.org/man/segplot.html
http://rgm3.lab.nig.ac.jp/RGM/r_function?p=latticeExtraf=segplot

For a related question, what's the tidiest way to calculate the
medians and confidence intervals? Currently I'm using `boxplot`:

require(datasets)
ci - with(boxplot(weight ~ Diet, ChickWeight), data.frame(
  Diet = names,
  median = stats[3,],
  lower = conf[1,],
  upper = conf[2,]))

Cheers,
Shaun

On 5 July 2013 11:28, David Winsemius dwinsem...@comcast.net wrote:

 On Jul 5, 2013, at 11:15 AM, Shaun Jackman wrote:

 Hi Bert, Dennis,

 I'll agree that using a barchart was a poor choice. I was in fact using a
 notched bwplot to show the median and confidence interval of the median. In
 this case it's the median and confidence interval that I want to highlight,
 and I find that the visual noise of the box and whiskers is detracting from
 the focus, and those wee notches are not much to focus on. So, I'd like to
 draw a stripplot with error bars, preferably in Lattice. Let's call this a
 TIE fighter plot. Any suggestions?


 I like the TIE fighter label. Try this:

 library(latticeExtra)
 data(USCancerRates)
 segplot(reorder(factor(county), rate.male) ~ LCL95.male + UCL95.male,
 data = subset(USCancerRates, state == Washington),
 draw.bands = FALSE, centers = rate.male,
 segments.fun = panel.arrows, ends = both,
 angle = 90, length = 1, unit = mm)

 It's what Sarkar has recommended in the past when this request has been 
 posted.

 --
 David


 Cheers,
 Shaun

 On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:

 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)

 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.

 Dennis

 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
 Hi,

 I'd like to draw a lattice barchart of means with error bars to show
 the standard deviation. I have the barchart, how do I add the error
 bars?

 require(datasets)
 require(lattice)
 x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
 sd=sd(x)))
 barchart(weight[,'mean'] ~ Diet, x)

 Thanks,
 Shaun

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


   [[alternative HTML version deleted]]

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.

 David Winsemius
 Alameda, CA, USA


__
R-help@r-project.org mailing list
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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] Lattice barchart with error bars

2013-07-05 Thread Shaun Jackman
Hmm. Interesting point, Bert. I don't know whether the notches show
the 95% confidence interval or the median, or the 95% confidence
interval that two non-overlapping notches have different medians.
You're saying it's the latter? Anyone know what the 95% confidence
interval of the median would be?

Cheers,
Shaun

 The notches (if requested) extend to +/-1.58 IQR/sqrt(n). This seems to be 
 based on the same calculations as the formula with 1.57 in Chambers et al. 
 (1983, p. 62), given in McGill et al. (1978, p. 16). They are based on 
 asymptotic normality of the median and roughly equal sample sizes for the two 
 medians being compared, and are said to be rather insensitive to the 
 underlying distributions of the samples. The idea appears to be to give 
 roughly a 95% confidence interval for the difference in two medians.


On 5 July 2013 11:48, Bert Gunter gunter.ber...@gene.com wrote:
 Be careful!

 You are talking about 2 different varieties of apples here. As I read
 it, the CI's in the  cancer data, which I know is just for example
 purposes, are CI's for the **individual means**; the notches in
 boxplots are nonparametric and for 2 groups with roughly equal sample
 sizes, The idea appears to be to give roughly a 95% confidence
 interval for the **difference** in two medians. (from
 ?boxplot.stats). So I'm not sure which you want, but they are
 certainly different (by a factor of around sqrt(2),right?), even if
 both are for the mean or both are for the median.

 Cheers,
 Bert

 On Fri, Jul 5, 2013 at 11:28 AM, David Winsemius dwinsem...@comcast.net 
 wrote:

 On Jul 5, 2013, at 11:15 AM, Shaun Jackman wrote:

 Hi Bert, Dennis,

 I'll agree that using a barchart was a poor choice. I was in fact using a
 notched bwplot to show the median and confidence interval of the median. In
 this case it's the median and confidence interval that I want to highlight,
 and I find that the visual noise of the box and whiskers is detracting from
 the focus, and those wee notches are not much to focus on. So, I'd like to
 draw a stripplot with error bars, preferably in Lattice. Let's call this a
 TIE fighter plot. Any suggestions?


 I like the TIE fighter label. Try this:

 library(latticeExtra)
 data(USCancerRates)
 segplot(reorder(factor(county), rate.male) ~ LCL95.male + UCL95.male,
 data = subset(USCancerRates, state == Washington),
 draw.bands = FALSE, centers = rate.male,
 segments.fun = panel.arrows, ends = both,
 angle = 90, length = 1, unit = mm)

 It's what Sarkar has recommended in the past when this request has been 
 posted.

 --
 David


 Cheers,
 Shaun

 On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:

 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)

 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.

 Dennis

 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
 Hi,

 I'd like to draw a lattice barchart of means with error bars to show
 the standard deviation. I have the barchart, how do I add the error
 bars?

 require(datasets)
 require(lattice)
 x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
 sd=sd(x)))
 barchart(weight[,'mean'] ~ Diet, x)

 Thanks,
 Shaun

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.


   [[alternative HTML version deleted]]

 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.

 David Winsemius
 Alameda, CA, USA




 --

 Bert Gunter
 Genentech Nonclinical Biostatistics

 Internal Contact Info:
 Phone: 467-7374
 Website:
 http://pharmadevelopment.roche.com/index/pdb/pdb-functional-groups/pdb-biostatistics/pdb-ncb-home.htm

__
R-help@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/r-help
PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, 

Re: [R] Filter Dataframe for Alarm for particular column(s).

2013-07-05 Thread arun
Hi,
May be this helps:
If you had showed your solution, it would be easier to compare.

res-data.frame(lapply(sapply(MyDF[,c(2,4)],function(x) 
{x1-which(c(0,diff(x))0);x1[length(x1)==0]-0;x1}),`[`,1))
 res
#  TNH BIX
#1   3   9


#Speed

 set.seed(24)
 MyDFNew- 
data.frame(TNH=sample(0:1,1e6,replace=TRUE),BIX=sample(0:1,1e6,replace=TRUE))
system.time(res1-data.frame(lapply(sapply(MyDFNew,function(x) 
{x1-which(c(0,diff(x))0);x1[length(x1)==0]-0;x1}),`[`,1)))
#   user  system elapsed 
#  0.364   0.000   0.363 

 res1
#  TNH BIX
#1   7   2
 MyDFNew[1:10,]
#   TNH BIX
#1    0   1
#2    0   0
#3    1   1
#4    1   1
#5    1   0
#6    1   0
#7    0   1
#8    1   1
#9    1   1
#10   0   0


A.K.


Hi,


Hi here i have a dataframe called MyDF. 

a-c(1,1,1,1,1,0,0,0,1,1) 
b-c(1,1,0,1,1,0,0,0,1,1) 
c-c(1,1,1,1,1,1,1,0,1,1) 
d-c(1,1,1,1,1,1,1,1,0,1) 
MyDF-data.frame(DWATT=a,TNH=b,CSGV=c,BIX=d) 

My requirement is, here i need a function - to get for a 
particular row number(s), when particular column(s) value change from 
one-to-zero  (for the first change). Suppose there is no change is 
happening then it should return Zero 

For example,  Using MyDF, 

DWATT TNH CSGV BIX 
1   1    1   1 
1   1    1   1 
1   0    1   1 
1   1    1   1 
1   1    1   1 
0   0    1   1 
0   0    1   1 
0   0    0   1 
1   1    1   0 
1   1    1   1 

Here i want to know, the row number where TNH-column and BIX-column values 
change happening from one-to-zero for the first time. 

Note:- Suppose there is no change is happening then it should return Zero 

Answer should be  a dataframe with single row. 
So here answer should return a dataframe like this. 

TNH  BIX 
    -- 
3      9 


i used some ways to get a solution using loops. But there is a bulk files with 
bulk rows to process. 
So performace is most important. Could someone please suggest better ideas ? 

Thanks, 
Antony.

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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.


Re: [R] converting a list of loglin terms to a model formula

2013-07-05 Thread Michael Friendly

On 7/3/2013 6:38 PM, Henrique Dallazuanna wrote:
 Try this:

  as.formula(sprintf( ~ %s, do.call(paste, c(lapply(mutual(3), paste, 
 collapse = :), sep = +

Thanks for this.  I encapsulated this as a function, loglin2formula() 
and a related function,
loglin2string() to give a character string representation.
They seem to work when used from the command line, but don't give
what I need when I use it in another function.  I think it has something 
to do with the environment
for the formula or how I pass it to MASS::loglm in my function 
test_loglm (below).

I'll demonstrate the problem first, then give the functions  test cases 
I'm using as
runnable code.

  joint(3, table=HairEyeColor)
$term1
[1] Hair Eye

$term2
[1] Sex

  loglin2formula(joint(3, table=HairEyeColor))
~Hair:Eye + Sex
environment: 0x0884a640
  loglin2string(joint(3, table=HairEyeColor))
[1] [Hair,Eye] [Sex]

These look like what I want, more or less; but, when I use these in the 
function test_loglm
(also below) , the formula doesn't get resolved when I call loglm (it 
appears as
formula = form), and the result of loglin2string gets garbled. The 
numerical results are
correct; I'm concerned about the labeling in the computed loglm object.

  test_loglm(HairEyeColor, type='joint')
formula:
~Hair:Eye + Sex
environment: 0x08842de0
model.string:
[1] [~] [+,Hair:Eye,Sex]   ### I want [Hair,Eye] 
[Sex] here
model:
Call:
loglm(formula = form, data = x)   ### I want formula = ~Hair:Eye + 
Sex here

Statistics:
   X^2 df  P( X^2)
Likelihood Ratio 19.85656 15 0.1775045
Pearson  19.56712 15 0.1891745
 

## --- functions and test cases, should be runnable (mod line folding) 
--- ###

#' convert a loglin model to a model formula for loglm

#' @param  x a list of terms in a loglinear model, such as returned by 
\code{joint}, \code{conditional}, \dots
#' @source Code from Henrique Dallazuanna, www...@gmail.com, R-help 
7-4-2013

loglin2formula - function(x) {
 terms - lapply(x, paste, collapse = :)
 as.formula(sprintf( ~ %s, do.call(paste, c(terms, sep = +
}

#' convert a loglin model to a string, using bracket notation for the 
high-order terms

#' @param x a list of terms in a loglinear model, such as returned by 
\code{joint}, \code{conditional}, \dots
#' @param brackets characters to use to surround model terms.
#' @param sep characters used to separate factor names within a term
#' @param collapse  characters used to separate terms
#' @param abbrev

loglin2string - function(x, brackets = c('[', ']'), sep=',', collapse=' 
', abbrev) {
 if (length(brackets)==1  (nchar(brackets)1)) brackets - 
unlist(strsplit(brackets, ))
 terms - lapply(x, paste, collapse=sep)
 terms - paste(brackets[1], terms, brackets[2], sep='')
 paste(terms, collapse= ' ')
}

#' models of joint independence, of some factors wrt one or more other 
factors

#' @param nf number of factors for which to generate model
#' @param table a contingency table used for factor names, typically the 
output from \code{\link[base]{table}}
#' @param factors names of factors used in the model when \code{table} 
is not specified
#' @param withindices of the factors against which others are 
considered jointly independent
#' @export

joint - function(nf, table=NULL, factors=1:nf, with=nf) {
 if (!is.null(table)) factors - names(dimnames(table))
 if (nf == 1) return (list(term1=factors[1]))
 if (nf == 2) return (list(term1=factors[1], term2=factors[2]))
 others - setdiff(1:nf, with)
 result - list(term1=factors[others], term2=factors[with])
 result
   }

### Test using these in another function

test_loglm - function(
 x, type = c(joint, conditional),
 ...)
{
 nf - length(dim(x))
 factors - names(dimnames(x))
 type - match.arg(type)
 margins - switch(type,
   joint = joint(nf, factors=factors),
   conditional = conditional(nf, factors=factors)
   )

   form - loglin2formula(margins);
   cat(formula:\n); print(form)
   model.string - loglin2string(form)
   cat(model.string:\n); print(model.string)
   mod - loglm(formula=form, data=x)
   cat(model:\n); print(mod)
   invisible(list(form=form, model.string=model.string, mod=mod))
}

## tests

loglin2formula(joint(3, table=HairEyeColor))
loglin2string(joint(3, table=HairEyeColor))
test_loglm(HairEyeColor, type='joint')




 On Wed, Jul 3, 2013 at 6:55 PM, Michael Friendly frien...@yorku.ca 
 mailto:frien...@yorku.ca wrote:

 I'm developing some functions to create symbolic specifications
 for loglinear models of different types.
 I don't really know how to 'compute' with model formulas, so I've
 done this in the notation
 for stats::loglin(), which is a list of high-order terms in the model.

 What I'd like is a function to turn the results of these into a
 model formula, suitable for
 MASS::loglm.  That's the reverse of what loglm does.

 For example, the simplest versions of 

[R] Subset and order

2013-07-05 Thread Noah Silverman
Hello,

I have a data frame with several columns.

I'd like to select some subset *and* order by another field at the same time.  

Example:

a   b   c
1   2   3
3   3   4
2   4   5
1   3   4
etc…


I want to select all rows where b=3 and then order by a.

To subset is easy:  x[x$b==3,]
To order is easy: x[order(x$a),]

Is there a way to do both in a single efficient statement?

Thanks,



--
Noah Silverman, M.S., C.Phil
UCLA Department of Statistics
8117 Math Sciences Building
Los Angeles, CA 90095




[[alternative HTML version deleted]]

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Re: [R] Subset and order

2013-07-05 Thread Rui Barradas

Hello,

Maybe like this?

subset(x[order(x$a), ], b == 3)


Hope this helps,

Rui Barradas

Em 05-07-2013 20:33, Noah Silverman escreveu:

Hello,

I have a data frame with several columns.

I'd like to select some subset *and* order by another field at the same time.

Example:

a   b   c
1   2   3
3   3   4
2   4   5
1   3   4
etc…


I want to select all rows where b=3 and then order by a.

To subset is easy:  x[x$b==3,]
To order is easy: x[order(x$a),]

Is there a way to do both in a single efficient statement?

Thanks,



--
Noah Silverman, M.S., C.Phil
UCLA Department of Statistics
8117 Math Sciences Building
Los Angeles, CA 90095




[[alternative HTML version deleted]]



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and provide commented, minimal, self-contained, reproducible code.



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Re: [R] Subset and order

2013-07-05 Thread Noah Silverman
That would work, but is painfully slow.  It forces a new sort of the data with 
every query.  I have 200,000 rows and need almost a hundred queries.

Thanks,

-N


On Jul 5, 2013, at 12:43 PM, Rui Barradas ruipbarra...@sapo.pt wrote:

 Hello,
 
 Maybe like this?
 
 subset(x[order(x$a), ], b == 3)
 
 
 Hope this helps,
 
 Rui Barradas
 
 Em 05-07-2013 20:33, Noah Silverman escreveu:
 Hello,
 
 I have a data frame with several columns.
 
 I'd like to select some subset *and* order by another field at the same time.
 
 Example:
 
 ab   c
 12   3
 33   4
 24   5
 13   4
 etc…
 
 
 I want to select all rows where b=3 and then order by a.
 
 To subset is easy:  x[x$b==3,]
 To order is easy: x[order(x$a),]
 
 Is there a way to do both in a single efficient statement?
 
 Thanks,
 
 
 
 --
 Noah Silverman, M.S., C.Phil
 UCLA Department of Statistics
 8117 Math Sciences Building
 Los Angeles, CA 90095
 
 
 
 
  [[alternative HTML version deleted]]
 
 
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.
 

__
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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Subset and order

2013-07-05 Thread Rui Barradas

Hello,

If time is one of the problems, precompute an ordered index, and use it 
every time you want the df sorted. But that would mean you can't do it 
in a single operation.


iord - order(x$a)
subset(x[iord, ], b == 3)


Rui Barradas

Em 05-07-2013 20:47, Noah Silverman escreveu:

That would work, but is painfully slow.  It forces a new sort of the data with 
every query.  I have 200,000 rows and need almost a hundred queries.

Thanks,

-N


On Jul 5, 2013, at 12:43 PM, Rui Barradas ruipbarra...@sapo.pt wrote:


Hello,

Maybe like this?

subset(x[order(x$a), ], b == 3)


Hope this helps,

Rui Barradas

Em 05-07-2013 20:33, Noah Silverman escreveu:

Hello,

I have a data frame with several columns.

I'd like to select some subset *and* order by another field at the same time.

Example:

a   b   c
1   2   3
3   3   4
2   4   5
1   3   4
etc…


I want to select all rows where b=3 and then order by a.

To subset is easy:  x[x$b==3,]
To order is easy: x[order(x$a),]

Is there a way to do both in a single efficient statement?

Thanks,



--
Noah Silverman, M.S., C.Phil
UCLA Department of Statistics
8117 Math Sciences Building
Los Angeles, CA 90095




[[alternative HTML version deleted]]



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and provide commented, minimal, self-contained, reproducible code.





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Re: [R] Subset and order

2013-07-05 Thread David Carlson
It may be that single and efficient are opposing goals. Two steps
lets you create the subset and then just order each query.
Alternatively, if the data do not change often, create an ordered
version and query that.


David Carlson

Original Message-
From: r-help-boun...@r-project.org
[mailto:r-help-boun...@r-project.org] On Behalf Of Noah Silverman
Sent: Friday, July 5, 2013 2:47 PM
To: Rui Barradas
Cc: R-help@r-project.org
Subject: Re: [R] Subset and order

That would work, but is painfully slow.  It forces a new sort of the
data with every query.  I have 200,000 rows and need almost a
hundred queries.

Thanks,

-N


On Jul 5, 2013, at 12:43 PM, Rui Barradas ruipbarra...@sapo.pt
wrote:

 Hello,
 
 Maybe like this?
 
 subset(x[order(x$a), ], b == 3)
 
 
 Hope this helps,
 
 Rui Barradas
 
 Em 05-07-2013 20:33, Noah Silverman escreveu:
 Hello,
 
 I have a data frame with several columns.
 
 I'd like to select some subset *and* order by another field at
the same time.
 
 Example:
 
 ab   c
 12   3
 33   4
 24   5
 13   4
 etc.
 
 
 I want to select all rows where b=3 and then order by a.
 
 To subset is easy:  x[x$b==3,]
 To order is easy: x[order(x$a),]
 
 Is there a way to do both in a single efficient statement?
 
 Thanks,
 
 
 
 --
 Noah Silverman, M.S., C.Phil
 UCLA Department of Statistics
 8117 Math Sciences Building
 Los Angeles, CA 90095
 
 
 
 
  [[alternative HTML version deleted]]
 
 
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible
code.
 

__
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Re: [R] converting a list of loglin terms to a model formula

2013-07-05 Thread William Dunlap
 Call:
 loglm(formula = form, data = x)   ### I want formula = ~Hair:Eye + Sex 
 here

Since your function made the call
   loglm(form, data=x)
the 'call' component of output is going to show 'form', not '~ Hair:Eye + Sex'.
You can use bquote to pre-evaluate the formula=form argument to get the call
to look nicer, as in:
  form - mpg ~ wt + hp
  eval(bquote(lm(.(form), data=mtcars)))
instead of
   lm(form, data=mtcars)

In your loglin2formula, I would make by environment of the generated formula
the environment of the caller of loglin2formula (or somewhere else if the user 
wishes)
by adding the argument
   env = parent.frame()
and replacing
   as.formula( sprintf(...) )
with
   formula( sprintf(...), env=env)
(I don't think you've run into any problems related to having an irrelevant
environment attached to the formula, but they will happen if the formula
involves any variable names that happen to be in loglin2formula.)

I would also change the loglin2formula so it worked with non-syntactic names.
Wrapping them with backquotes would probably do it, but I may have missed
something in the back and forth between character strings and formula.

As for loglin2string, you complain that it works when given a list of character
vectors but not when is given a formula.  That is not surprising.  Did you mean
for test_loglm to pass it 'margins' instead of 'form'?

Bill Dunlap
Spotfire, TIBCO Software
wdunlap tibco.com


 -Original Message-
 From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org] On 
 Behalf
 Of Michael Friendly
 Sent: Friday, July 05, 2013 12:21 PM
 To: Henrique Dallazuanna
 Cc: R-help
 Subject: Re: [R] converting a list of loglin terms to a model formula
 
 
 On 7/3/2013 6:38 PM, Henrique Dallazuanna wrote:
  Try this:
 
   as.formula(sprintf( ~ %s, do.call(paste, c(lapply(mutual(3), paste,
  collapse = :), sep = +
 
 Thanks for this.  I encapsulated this as a function, loglin2formula()
 and a related function,
 loglin2string() to give a character string representation.
 They seem to work when used from the command line, but don't give
 what I need when I use it in another function.  I think it has something
 to do with the environment
 for the formula or how I pass it to MASS::loglm in my function
 test_loglm (below).
 
 I'll demonstrate the problem first, then give the functions  test cases
 I'm using as
 runnable code.
 
   joint(3, table=HairEyeColor)
 $term1
 [1] Hair Eye
 
 $term2
 [1] Sex
 
   loglin2formula(joint(3, table=HairEyeColor))
 ~Hair:Eye + Sex
 environment: 0x0884a640
   loglin2string(joint(3, table=HairEyeColor))
 [1] [Hair,Eye] [Sex]
 
 These look like what I want, more or less; but, when I use these in the
 function test_loglm
 (also below) , the formula doesn't get resolved when I call loglm (it
 appears as
 formula = form), and the result of loglin2string gets garbled. The
 numerical results are
 correct; I'm concerned about the labeling in the computed loglm object.
 
   test_loglm(HairEyeColor, type='joint')
 formula:
 ~Hair:Eye + Sex
 environment: 0x08842de0
 model.string:
 [1] [~] [+,Hair:Eye,Sex]   ### I want [Hair,Eye]
 [Sex] here
 model:
 Call:
 loglm(formula = form, data = x)   ### I want formula = ~Hair:Eye +
 Sex here
 
 Statistics:
X^2 df  P( X^2)
 Likelihood Ratio 19.85656 15 0.1775045
 Pearson  19.56712 15 0.1891745
  
 
 ## --- functions and test cases, should be runnable (mod line folding)
 --- ###
 
 #' convert a loglin model to a model formula for loglm
 
 #' @param  x a list of terms in a loglinear model, such as returned by
 \code{joint}, \code{conditional}, \dots
 #' @source Code from Henrique Dallazuanna, www...@gmail.com, R-help
 7-4-2013
 
 loglin2formula - function(x) {
  terms - lapply(x, paste, collapse = :)
  as.formula(sprintf( ~ %s, do.call(paste, c(terms, sep = +
 }
 
 #' convert a loglin model to a string, using bracket notation for the
 high-order terms
 
 #' @param x a list of terms in a loglinear model, such as returned by
 \code{joint}, \code{conditional}, \dots
 #' @param brackets characters to use to surround model terms.
 #' @param sep characters used to separate factor names within a term
 #' @param collapse  characters used to separate terms
 #' @param abbrev
 
 loglin2string - function(x, brackets = c('[', ']'), sep=',', collapse='
 ', abbrev) {
  if (length(brackets)==1  (nchar(brackets)1)) brackets -
 unlist(strsplit(brackets, ))
  terms - lapply(x, paste, collapse=sep)
  terms - paste(brackets[1], terms, brackets[2], sep='')
  paste(terms, collapse= ' ')
 }
 
 #' models of joint independence, of some factors wrt one or more other
 factors
 
 #' @param nf number of factors for which to generate model
 #' @param table a contingency table used for factor names, typically the
 output from \code{\link[base]{table}}
 #' @param factors names of factors used in the model when \code{table}
 is not specified
 #' @param with

Re: [R] Lattice barchart with error bars

2013-07-05 Thread Bert Gunter
This is not an R question.  Read the references.

Bert

Sent from my iPhone -- please excuse typos.

On Jul 5, 2013, at 12:15 PM, Shaun Jackman sjack...@gmail.com wrote:

 Hmm. Interesting point, Bert. I don't know whether the notches show
 the 95% confidence interval or the median, or the 95% confidence
 interval that two non-overlapping notches have different medians.
 You're saying it's the latter? Anyone know what the 95% confidence
 interval of the median would be?
 
 Cheers,
 Shaun
 
 The notches (if requested) extend to +/-1.58 IQR/sqrt(n). This seems to be 
 based on the same calculations as the formula with 1.57 in Chambers et al. 
 (1983, p. 62), given in McGill et al. (1978, p. 16). They are based on 
 asymptotic normality of the median and roughly equal sample sizes for the 
 two medians being compared, and are said to be rather insensitive to the 
 underlying distributions of the samples. The idea appears to be to give 
 roughly a 95% confidence interval for the difference in two medians.
 
 
 On 5 July 2013 11:48, Bert Gunter gunter.ber...@gene.com wrote:
 Be careful!
 
 You are talking about 2 different varieties of apples here. As I read
 it, the CI's in the  cancer data, which I know is just for example
 purposes, are CI's for the **individual means**; the notches in
 boxplots are nonparametric and for 2 groups with roughly equal sample
 sizes, The idea appears to be to give roughly a 95% confidence
 interval for the **difference** in two medians. (from
 ?boxplot.stats). So I'm not sure which you want, but they are
 certainly different (by a factor of around sqrt(2),right?), even if
 both are for the mean or both are for the median.
 
 Cheers,
 Bert
 
 On Fri, Jul 5, 2013 at 11:28 AM, David Winsemius dwinsem...@comcast.net 
 wrote:
 
 On Jul 5, 2013, at 11:15 AM, Shaun Jackman wrote:
 
 Hi Bert, Dennis,
 
 I'll agree that using a barchart was a poor choice. I was in fact using a
 notched bwplot to show the median and confidence interval of the median. In
 this case it's the median and confidence interval that I want to highlight,
 and I find that the visual noise of the box and whiskers is detracting from
 the focus, and those wee notches are not much to focus on. So, I'd like to
 draw a stripplot with error bars, preferably in Lattice. Let's call this a
 TIE fighter plot. Any suggestions?
 
 I like the TIE fighter label. Try this:
 
 library(latticeExtra)
 data(USCancerRates)
 segplot(reorder(factor(county), rate.male) ~ LCL95.male + UCL95.male,
data = subset(USCancerRates, state == Washington),
draw.bands = FALSE, centers = rate.male,
segments.fun = panel.arrows, ends = both,
angle = 90, length = 1, unit = mm)
 
 It's what Sarkar has recommended in the past when this request has been 
 posted.
 
 --
 David
 
 
 Cheers,
 Shaun
 
 On 4 July 2013 18:00, Dennis Murphy djmu...@gmail.com wrote:
 
 If you consult the lattice package help, you'll discover there is no
 panel_errorbar() function, which would imply the package developers
 have a distaste for that type of graphic. If you fish around the
 R-help archives, though, you might be able to find someone who wrote a
 function to do error bars in lattice. (Use a searchable archive such
 as Nabble to hunt for it.)
 
 Error bar plots are easier to do in the ggplot2 package, since there
 is a specific function to generate the error bar 'geometry'
 (geom_errorbar). See http://docs.ggplot2.org/current/ for an expanded
 version of the package help pages, which include the graphs generated
 by the code. I believe there's also a base graphics version that you
 can get from the gplots package, but I don't know a lot about it.
 
 Dennis
 
 On Thu, Jul 4, 2013 at 2:53 PM, Shaun Jackman sjack...@gmail.com wrote:
 Hi,
 
 I'd like to draw a lattice barchart of means with error bars to show
 the standard deviation. I have the barchart, how do I add the error
 bars?
 
 require(datasets)
 require(lattice)
 x - aggregate(weight ~ Diet, ChickWeight, function(x) c(mean=mean(x),
 sd=sd(x)))
 barchart(weight[,'mean'] ~ Diet, x)
 
 Thanks,
 Shaun
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.
 
  [[alternative HTML version deleted]]
 
 __
 R-help@r-project.org mailing list
 https://stat.ethz.ch/mailman/listinfo/r-help
 PLEASE do read the posting guide 
 http://www.R-project.org/posting-guide.html
 and provide commented, minimal, self-contained, reproducible code.
 
 David Winsemius
 Alameda, CA, USA
 
 
 
 --
 
 Bert Gunter
 Genentech Nonclinical Biostatistics
 
 Internal Contact Info:
 Phone: 467-7374
 Website:
 http://pharmadevelopment.roche.com/index/pdb/pdb-functional-groups/pdb-biostatistics/pdb-ncb-home.htm


Re: [R] Data Package Query

2013-07-05 Thread Yasmine Refai
Hello,
 
When I run the below syntax:
Trial-read.table(Trial.txt,header=TRUE)
Trial
save.image(file=Trial.RData)
load(Trial.RData)
fit-logistf(data=Trial, y~x1+x2)
summary(fit)
AIC(fit)

I am getting the below error:
 AIC(fit)
Error in UseMethod(logLik) : 
  no applicable method for 'logLik' applied to an object of class logistf

Can you please help with that?
 
Regards,
Yasmine

 
 Date: Sat, 29 Jun 2013 05:05:28 -0800
 From: jrkrid...@inbox.com
 Subject: Re: [R] Data Package Query
 To: y_re...@hotmail.com; rolf.tur...@xtra.co.nz; jdnew...@dcn.davis.ca.us
 CC: r-help@r-project.org
 
 
 I don't know what you think data(Trial) is doing but what it in fact is doing 
 is trying to load a stored data set called Trial and it does not exist.  Have 
 a look at ?data to see what I mean.
 
 In your program data(Trial) is redundant, well actually closer to 
 meaningless. 
 
 Trial is already loaded since you created it in the read statement
 
 John Kane
 Kingston ON Canada
 
 
  -Original Message-
  From: y_re...@hotmail.com
  Sent: Fri, 28 Jun 2013 12:31:11 +
  To: rolf.tur...@xtra.co.nz, jdnew...@dcn.davis.ca.us
  Subject: Re: [R] Data Package Query
  
  hello,
  
  please advice what is wrong at the below syntax:
  Trial-read.table(Trial.txt,header=TRUE)
  Trial
  save.image(file=Trial.RData)
  data(Trial)
  fit-logistf(data=Trial, y~x1+x2)
  
  
  and here is the error I get:
  Warning message:
  In data(Trial) : data set ?Trial? not found
  
  
  regards,
  yasmine
  
  
  Date: Fri, 28 Jun 2013 10:29:21 +1200
  From: rolf.tur...@xtra.co.nz
  To: jdnew...@dcn.davis.ca.us
  CC: y_re...@hotmail.com; r-help@r-project.org
  Subject: Re: [R] Data Package Query
  
  On 28/06/13 04:47, Jeff Newmiller wrote:
  
   SNIP
  A common error by beginners (which may or may not be your problem in
  this case) is to create a variable called data. Unfortunately this
  hides the function named data and from that time forward that R
  session doesn't work when you type example code that uses the data
  function.
  
   SNIP
  
  This is simply not true.  I believe it *used* to be true, sometime
  wa back,
  but hasn't been true for years.  The R language is much cleverer now.
  If there
  is a function melvin() somewhere on the search path and also a data
  object
  melvin (earlier on the search path) then doing
  
   melvin(whatever)
  
  will correctly call the function melvin() with no complaints.  The R
  language
  can tell by the parentheses that you mean the *function* melvin and
  not the
  data object melvin.
  
  E.g.
  
   data - 42
   require(akima)
   akima
   Error: object 'akima' not found
   data(akima)  # No error message, nor nothin'!
   akima
   # The data set akima is displayed.
  
  All that being said it is ***BAD PRACTICE***, just in terms of
  comprehensibility
  and avoiding confusion, to give a data set set the same name as a
  function
  (either built in, or one of your own).
  
   fortune(dog)
  
  is relevant.
  
   cheers,
  
   Rolf Turner
  
  
  [[alternative HTML version deleted]]
  
  __
  R-help@r-project.org mailing list
  https://stat.ethz.ch/mailman/listinfo/r-help
  PLEASE do read the posting guide
  http://www.R-project.org/posting-guide.html
  and provide commented, minimal, self-contained, reproducible code.
 
 
 FREE 3D MARINE AQUARIUM SCREENSAVER - Watch dolphins, sharks  orcas on your 
 desktop!
 Check it out at http://www.inbox.com/marineaquarium
 
 
  
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[R] save rds as text

2013-07-05 Thread alR
I created a table like this:

Analysis of Variance Table
 
 Response: dati
 Df Sum Sq Mean Sq F value Pr(F)
 groups 2114   57.00  76 4.134e-11 ***
   Residuals 24 180.75  
---
   Signif. codes:  0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1 

and saved it to a variable called k.

When I tried to save the variable to txt file using

 dput(k, file = ..\\Readouts\\anova_spike_number.txt)

or

 lapply(k, write, ..\\Readouts\\anova_spike_number.txt, append=TRUE)  

 it destroys the formatting.

Then I saved to rds using

 saveRDS(k, ..\\Readouts\\anova_spike_number.rds)


and the format was preserved.

I would like to convert the rds to txt preserving the table format. Or save
it as excel file or pdf would also be fine.
(If there is a way to avoid passing through rds file better, but  still OK
using rds).

Thank you very much.

Best regards,


Alberto
 
 



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and provide commented, minimal, self-contained, reproducible code.


Re: [R] Non-linear modelling with several variables including a categorical variable

2013-07-05 Thread Prof J C Nash (U30A)

Off list I sent the OP a note that wrapnls() from nlmrt calls nls after
nlxb finishes. This is not, of course, super-efficient, but returns the
nls-structured answer.

JN

On 13-07-05 06:00 AM, r-help-requ...@r-project.org wrote:

Message: 49
Date: Fri, 5 Jul 2013 08:30:39 +0700
From: Robbie Weteringsrobbie.weteri...@gmail.com
To: Prof J C Nash (U30A)nas...@uottawa.ca,r-help@r-project.org
Subject: Re: [R] Non-linear modelling with several variables including
a categorical variable
Message-ID:
CAFe5dHZdXFbFtwKmTE1_QPi1rqNGsd+=82tproyfs6mg6zm...@mail.gmail.com
Content-Type: text/plain

Dear Prof. Nash,

I tried to run nls with the nlxb function and as you mention it is fairly
slower in terms of running the code. However, if I would have used this
function earlier I would have saved a lot of time trying to find the start
values. The output looks a little bit sloppy but I think it is very usefull
to use in combination with nls.

Thanks
Robbie


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[R] geeglm

2013-07-05 Thread nt1006
How to extract the Std.err and the alpha estimated value from the geeglm
function in R.



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[R] Filter Dataframe for Alarm for each column.

2013-07-05 Thread R_Antony
Hi here i have a dataframe called MyDF.

a-c(1,1,1,1,1,0,0,0,1,1)
b-c(1,1,0,1,1,0,0,0,1,1)
c-c(1,1,1,1,1,1,1,0,1,1)
d-c(1,1,1,1,1,1,1,1,0,1)
MyDF-data.frame(DWATT=a,TNH=b,CSGV=c,BIX=d)

My requirement is, here i need a function - to get for a particular row
number(s), when particular column(s) value change from zero to one  (for the
first change).

For example,  Using MyDF,

DWATT TNH CSGV BIX
1   11   1
1   11   1
1   01   1
1   11   1
1   11   1
0   01   1
0   01   1
0   00   1
1   11   0
1   11   1

Here i want to know, the row number where TNH-column and BIX-column values
change happening from one-to-zero for the first time.

Answer should be  a dataframe with single row.
So here answer should return a dataframe like this.

TNH  BIX
--
3  9


i used some ways to get a solution using loops. But there is a bulk files
with bulk rows to process.
So performace is most important. Could someone please suggest better ideas ?

Thanks,
Antony.





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Re: [R] list construction with automatic names

2013-07-05 Thread Greg Snow
I would suggest seeing if you can use the `lapply` or `sapply` function,
that way most of the details of creating the object are taken care of for
you.  If you want the list named then you can use the `names` or `setNames`
function, or the USE.NAMES argument to `sapply`.


On Thu, Jul 4, 2013 at 6:43 AM, Alex van der Spek do...@xs4all.nl wrote:

  I often find myself (wanting t)o constructing lists or
  data.frames
 
  Apologies; previous post should have said Read R inforno on 'Growing
  Objects' and should have added the URL:
 
  http://www.burns-stat.com/pages/Tutor/R_inferno.pdf
 
  S Ellison
 
 
 
  ***
  This email and any attachments are confidential. Any use...{{dropped:8}}
 
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 Thank you! That was very helpful. The R-Inferno pdf makes nice reading too!

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-- 
Gregory (Greg) L. Snow Ph.D.
538...@gmail.com

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[R] Transferring commas in character vector to expression

2013-07-05 Thread Eric Archer - NOAA Federal
I'm trying to format a given character vector as an expression with Greek
symbols to be used in labeling axis ticks. Thanks to some help from David
Winsemius, I've learned how to make the substitution and place the Greek
symbols in, however I've run into another problem: Some of my labels have
commas in them, so when the parse command is executed, there is an
unexpected symbol error. For example:

 x - c(aa, aaa,aa, bb*Delta*b, *Delta*cc,c)
 parse(text = x)
Error in parse(text = x) : text:2:4: unexpected ','
1: aa
2: aaa,
 ^

I've tried various iterations of wrapping the commas in interior quotes
(aaa\,\aa), but then the error shifts to the quote. I see in plotmath
that 'list(a,b,c)' gives me comma separated values, but I haven't been able
to work out how to get this construction for elements that have a comma.

Is this possible?

-- 

Eric Archer, Ph.D.
Southwest Fisheries Science Center
NMFS, NOAA
8901 La Jolla Shores Drive
La Jolla, CA 92037 USA
858-546-7121 (work)
858-546-7003 (FAX)

Marine Mammal Genetics Group: swfsc.noaa.gov/prd-mmgenetics
ETP Cetacean Assessment Program: swfsc.noaa.gov/prd-etp

The universe doesn't care what you believe.
 The wonderful thing about science is that it
   doesn't ask for your faith, it just asks
   for your eyes.  - Randall Munroe

Lighthouses are more helpful than churches.
   - Benjamin Franklin

   ...but I'll take a GPS over either one.
   - John C. Craig George

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Re: [R] Subset and order

2013-07-05 Thread Ben Bolker
David Carlson dcarlson at tamu.edu writes:

 
 It may be that single and efficient are opposing goals. Two steps
 lets you create the subset and then just order each query.
 Alternatively, if the data do not change often, create an ordered
 version and query that.
 

   I don't know the data.table package well, but it seems as though 
this might be an appropriate job for it.

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Re: [R] Operations on a big data frame

2013-07-05 Thread arun
Hi,
May be this helps:
dat1- read.table(text=
   P1_prom Nom
1 -6.17 Pt_00187
2 -6.17 Pt_00187
3 -6.17 Pt_00187
4 -6.17 Pt_00187
5 -6.17 Pt_00187
6 -6.17 Pt_01418
7 -5.77 Pt_01418
8 -5.37 Pt_01418
9 -4.97 Pt_01418
10 -4.57 Pt_01418
,sep=,header=TRUE,stringsAsFactors=FALSE) 

library(zoo)
 dat1$PT_promMean-rollmean(dat1$P1_prom,5,fill=NA,align=left)
 dat1
#   P1_prom  Nom PT_promMean
#1    -6.17 Pt_00187   -6.17
#2    -6.17 Pt_00187   -6.17
#3    -6.17 Pt_00187   -6.09
#4    -6.17 Pt_00187   -5.93
#5    -6.17 Pt_00187   -5.69
#6    -6.17 Pt_01418   -5.37
#7    -5.77 Pt_01418  NA
#8    -5.37 Pt_01418  NA
#9    -4.97 Pt_01418  NA
#10   -4.57 Pt_01418  NA
A.K.


Hello all, 

I have a big data frame that looks like this: 
        P1_prom Nom 
1   -6.17   Pt_00187 
2   -6.17   Pt_00187 
3   -6.17   Pt_00187 
4   -6.17   Pt_00187 
5   -6.17   Pt_00187 
6   -6.17   Pt_01418 
7   -5.77   Pt_01418 
8   -5.37   Pt_01418 
9   -4.97   Pt_01418 
10  -4.57   Pt_01418 
- 
- 
- 
25000 

where Nom represents a point in a map, and P1_prom represents 
the value of an operation we perfomed on each point (note that we 
performed 5 repetitions for each point, hence, each point has 5 values). 
What I am trying to do, with no success, is to create a new column, 
in which each row corresponds to the mean value of P1_prom for each 
point. So basically what I need the program to do is to write in the 
first row of the new column the average of the first five values of 
P1_prom, in the second row the average of the next five values, and so 
on. 
Could anybody guide me on how to do this. 
Thank you very much, 
Veronica

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Re: [R] IF function

2013-07-05 Thread arun
Hi,
May be this helps.  

dat1- read.table(text=
Col1,Col2
High value,9
Low value,0
High value,7
Low value,0
Low value,0
No data,0
High value,8
No data,0
,sep=,,header=TRUE,stringsAsFactors=FALSE)
dat1$Col2[dat1$Col1==No data]- NA
 dat1
#    Col1 Col2
#1 High value    9
#2  Low value    0
#3 High value    7
#4  Low value    0
#5  Low value    0
#6    No data   NA
#7 High value    8
#8    No data   NA

A.K.


Hello, 

I am an R novice so excuse me if this is woefully straight forward, but I have 
tried the help files to no avail. 

I am trying to identify cells in 1 column with the value of 'No data', so I can 
change the values in the next column to 'Null'. 

Currently I am struggling with the data set, as it assigns both 'No data' and 
'Low values' as zero which skews my analysis. 

I've tried a number of different attempts but just get the error unexpected 
symbol ? 


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[R] problem with BootCV for coxph in pec after feature selection with glmnet (lasso)

2013-07-05 Thread E Joffe
Hi,

I am attempting to evaluate the prediction error of a coxph model that was
built after feature selection with glmnet.

In the preprocessing stage I used na.omit (dataset) to remove NAs.
I reconstructed all my factor variables into binary variables with dummies
(using model.matrix)
I then used glmnet lasso to fit a cox model and select the best performing
features.
Then I fit a coxph model using only these feature.

When I try to evaluate the model using pec and a bootstrap I get an error
that the prediction matrix has wrong dimensions.
Suddenly the cox object has 318 variables instead of 356 variables in the
dataset.
I don't know why this is happening.
The cox object I assign to pec and the dataframe are both of the same size.
However, once pec refits the model its size changes (356 - 318 variables).
Apparently something is happening during the bootstrap sampling that removes
some variables.
As mentioned, I used na.omit in the preprocessing so there should not be any
NAs.

Here are some details from my workspace:
Reformat_dataSet: 368 obs. Of 356 variables
print (glmnet.cox)  354 df, p=1  n= 368, number of events= 288 (354 df
= 354 variables + time and status = 356 variables)

Here is the pec function and the error:
pec.f - as.formula(Hist(time,status) ~ 1)
brierGlmnet - pec(list(glmnet.cox), data = reformat_Dataset,
splitMethod=BootCV, B=50, formula = pec.f)

  Error in predictSurvProb.coxph(object = structure(list(coefficients =
structure(c(-4.27787223119601,  : 
Prediction matrix has wrong dimensions:
   368 rows and 318 columns.
But requested are predicted probabilities for
   118 subjects (rows) in newdata and 356 time points (columns)
   This may happen when some covariate values are missing in newdata!?
 
Here are the relevant sections of the code:

trainSet - na.omit (dataset)
  
#creat Y (survival matrix) for glmnet
  surv_obj - Surv(trainSet$time,trainSet$status) 
  

  ## tranform categorical variables into binary variables with dummy for
trainSet
  predict_matrix - model.matrix(~ ., data=trainSet, 
 contrasts.arg = lapply
(trainSet[,sapply(trainSet, is.factor)], contrasts, contrasts=FALSE))
  
 
 ## remove the statu/time variables from the predictor matrix (x) for glmnet
  predict_matrix - subset (predict_matrix, select=c(-time,-status))
  
  
## create a glmnet cox object using lasso regularization
  glmnet.obj - glmnet (predict_matrix, surv_obj, family=cox)
  
  
# find lambda for which dev.ratio is max 
  max.dev.index - which.max(glmnet.obj$dev.ratio) 
  optimal.lambda - glmnet.obj$lambda[max.dev.index] 
  
 
 # take beta for optimal lambda 
  optimal.beta  - glmnet.obj$beta[,max.dev.index] 
  
  
# find non zero beta coef 
  nonzero.coef - abs(optimal.beta)0 
  selectedBeta - optimal.beta[nonzero.coef] 
  
  # take only covariates for which beta is not zero 
  selectedVar   - predict_matrix[,nonzero.coef] 
  
  # create a dataframe for trainSet with time, status and selected variables
in binary representation for evaluation in pec
  reformat_dataSet - as.data.frame(cbind(surv_obj,selectedVar))
  
  # create coxph object with pre-defined coefficients 
  glmnet.cox - coxph(surv_obj ~ selectedVar, init=selectedBeta,iter=0)

## Brier score for the cox-glmnet model
  brierGlmnet - pec(list(glmnet.cox), data = reformat_Dataset,
splitMethod=BootCV, B=50,
 formula = pec.f)

Thank you !!!

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