[R-sig-phylo] Plotting ancestral reconstructions on subtrees

2013-04-05 Thread Petter Zahl Marki






Dear all,
I am attempting to plot ancestral reconstructions (using asr.marginal in 
Diversitree) of a discrete trait on a number of subtrees (subtree=T in ape), 
but I'm having trouble assigning node probabilites and tip states to the 
correct nodes and tips.
I have been using the following code:
#Extract state probabilitiesst - asr.marginal(lik.l, 
coef(fit.l))pie.probs-t(st) pr-apply(t(st), 1, which.max)tree$node.label-pr
#Assign colours to extant statesstatesLabel - statesnames(statesLabel) - 
names(states)statesLabel[states==1] - redstatesLabel[states==2] - 
bluestatesLabel[states==3] - green
#Extract subtreetrd - drop.tip(tree, 65:761, subtree=T)
#Plot subtreeplot(trd, show.tip.label=T, edge.width 
=1)nodelabels(pie=pie.probs,piecol=c(red, blue, green))tiplabels(pch=22, 
bg=statesLabel)
This works fine for my first subtree, i.e. tips 1-64, but when I try running 
the same code on subsequent parts of the tree, visual inspection confirms that 
tip colours and node probabilities are no longer correctly assigned to the 
correct tips and nodes.
#I.e. running the following code plots the correct subtree, but states are 
incorrectly assigned to nodes and tips. trd - drop.tip(tree, c(1:64, 167:761), 
subtree=T)plot(trd, show.tip.label=T, edge.width 
=1)nodelabels(pie=pie.probs,piecol=c(red, blue, green))tiplabels(pch=22, 
bg=statesLabel)
I'm guessing the solution is quite simple, but I haven't been able to work it 
out. Any suggestions would be greatly appreciated.
Kind regards,Petter Zahl Marki








  
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[R-sig-phylo] atomic vector for write.nexus

2013-04-05 Thread Elaine Kuo
Hello,

This is Elaine.
I am using the command write.nexusin package (ape)
to generate a nexus file after pruning a phylogeny tree.

However, an error appeared, saying
Error in obj[[i]]$tip.label : $ operator is invalid for atomic vectors

I searched the archive but found no similar experience in this command.
Please kindly help explain what it means and how to solve it.

code
library(ape)

# read data and tree
  birddata - read.csv(H:/birddata_family_20130405.csv, header = TRUE)
  birdtree - read.nexus(H:/birddata_family_20130405.nexus)
  setwd(H:)

  species.to.keep -read.csv(H:/birddata_family_20130405.csv, header =
TRUE)
  pruned.tree-drop.tip(birdtree,birdtree$tip.label[-
  na.omit(match(species.to.keep[,1],birdtree$tip.label))])


  ## prune the data to include only those taxa in the pruned tree
  data.pruned - birddata[tree.pruned$tip.label, ] (Thanks to Klaus and
others)

  write.nexus(tree.pruned, H:/pruneddata_20130405.nexus, translate  =
 FALSE)

Elaine

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[R-sig-phylo] Fwd: atomic vector for write.nexus

2013-04-05 Thread Elaine Kuo
I changed  pruned.tree to tree.pruned.
The error still existed.

Elaine

-- Forwarded message --
From: Elaine Kuo elaine.kuo...@gmail.com
Date: Fri, Apr 5, 2013 at 6:12 PM
Subject: atomic vector for write.nexus
To: r-sig-phylo@r-project.org


Hello,

This is Elaine.
I am using the command write.nexusin package (ape)
to generate a nexus file after pruning a phylogeny tree.

However, an error appeared, saying
Error in obj[[i]]$tip.label : $ operator is invalid for atomic vectors

I searched the archive but found no similar experience in this command.
Please kindly help explain what it means and how to solve it.

code
library(ape)

# read data and tree
  birddata - read.csv(H:/birddata_family_20130405.csv, header = TRUE)
  birdtree - read.nexus(H:/birddata_family_20130405.nexus)
  setwd(H:)

  species.to.keep -read.csv(H:/birddata_family_20130405.csv, header =
TRUE)
  tree.pruned-drop.tip(birdtree,birdtree$tip.label[-
  na.omit(match(species.to.keep[,1],birdtree$tip.label))])


  ## prune the data to include only those taxa in the pruned tree
  data.pruned - birddata[tree.pruned$tip.label, ] (Thanks to Klaus and
others)

  write.nexus(tree.pruned, H:/pruneddata_20130405.nexus, translate  =
 FALSE)

Elaine

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[R-sig-phylo] pruning a tree

2013-04-05 Thread Elaine Kuo
Hello



This Elaine.



I tried to prune a phylogeny tree using two methods based on the code
attached.



Method 1 returned the tip.label sharing between birddata and birdtree.

Method 2 returned nothing.



Please kindly indicate why Method 2 failed to prune the tree.

Also, please kindly explain the command “birdtree$tip.label[-na.omit”



Thank you again.



Code

Method 1

Library(ape)

birddata - read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree - read.nexus(H:/ birddata_family_20130405.nexus)

setwd(H:)



## prune the phylogeny to include only species which are in the data set

species.to.keep-read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree.pruned-drop.tip(birdtree,birdtree$tip.label[-na.omit(match(species.to.keep[,1],birdtree$tip.label))])





Method 2

Library(ape)

birddata - read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree - read.nexus(H:/ birddata_family_20130405.nexus)

setwd(H:)



## prune the phylogeny to include only species which are in the data set

temp - name.check(birdtree, birddata)

birdtree.pruned - drop.tip(birdtree, tip=temp$Tree.not.data)

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Re: [R-sig-phylo] ML ancestral state reconstruction using different softwares

2013-04-05 Thread Emmanuel Paradis
Jingchun,

Thanks to Daniel for giving a detailed answer to your first question.

You can use ace() to fit a model with irreversible change. You need to build a 
custom model like this:

 Q - matrix(0, 2, 2)
 Q[2, 1] - 1
 Q
 [,1] [,2]
[1,]00
[2,]10

In this case there's one rate to be estimated and the other is fixed to zero 
(the 0's on the diagonal are ignored). This can be generalized to more 
complicated models (there's an example in my book). Then call ace with:

ace(traits_data, tree, type = d, model = Q)

This time you cannot compare this model with the ER one with an LRT: compare 
directly the log-liks since they have the same number of parameters or use 
AIC(). BTW, there is an anova methods to compare nested models fitted with ace: 
this avoids the pain to compute correctly df's.

Cheers,

Emmanuel
-Original Message-
From: Jingchun Li jingc...@umich.edu
Date: Thu, 4 Apr 2013 22:25:09 
To: emmanuel.para...@ird.fr; r-sig-phylo@r-project.org
Subject: Re: [R-sig-phylo] ML ancestral state reconstruction using different 
softwares

Sorry, I forgot to include the list. there we go.

 --
 *From: * Jingchun Li jingc...@umich.edu
 *Date: *Thu, 4 Apr 2013 21:58:56 -0400
 *To: *emmanuel.para...@ird.fr
 *Subject: *Re: [R-sig-phylo] ML ancestral state reconstruction using
 different softwares

 Thank you very much, Dr.Paradis. You are right that the two parameter
 model does not fit the data significantly better. I guess I'm more puzzled
 about why the three softwares gave me different likelihoods.

 I did fit the symmetrical model using BayesTraits later and it gave me
 about the same transition rates as the asymmetrical model and a
 similar likelihood value (-14.08 for symmetrical and -14.00 for
 asymmetrical). However I do have biological evidence that transition from 0
 to 1 might be extremely hard. So maybe I can also try set q01 to 0 (which
 is actually what ace gave me under the asymmetrical model)?

 Cheers,

 Jingchun


 On Thu, Apr 4, 2013 at 9:21 PM, Emmanuel Paradis 
 emmanuel.para...@ird.frwrote:

 Hi,

 You cannot really say that in both ace and Mesquite, it slightly favors
 the asymmetrical model: the increase in log-likelihood is less than 1
 which is far from being significant with one additional parameter. So it
 seems that all three pieces of software agree well on the estimate of rate
 for the symmetrical model. You should fit also this model with BayeTraits
 to do the full comparison.

 Cheers,

 Emmanuel
 -Original Message-
 From: Jingchun Li jingc...@umich.edu
 Sender: r-sig-phylo-boun...@r-project.org
 Date: Thu, 4 Apr 2013 10:15:05
 To: r-sig-phylo@r-project.org
 Subject: [R-sig-phylo] ML ancestral state reconstruction using different
 softwares

 Hi all,

 I am exploring different methods for ancestral state reconstruction for a
 small phylogeny I have (26 OTUs). I have one binary trait coded as 0s and
 1s for all the taxa. And I am more interested in the transition rates
 between the two states.

 If I understand correctly, a maximum likelihood ancestral state
 reconstruction using a MK1 model or an asymmetrical rates model should
 give
 me the optimized estimated transition rates between the two states. The
 formal will assume the two rates are the same, the later will
 assume independent rates.

 So I firstly did this using the ape function in ace.

 ERreconstruction - ace(traits_data, tree, type=discrete, model=ER)
 ERreconstruction$rates
 ERreconstruction$loglik

 ARDreconstruction - ace(traits_data, tree, type=discrete, model=ARD)
 ARDreconstruction$rates
 ARDreconstruction$loglik

 Then I tried using Mesquite, using MK1 model and the Asymmetrical
 2-param.
 Markov-k Model 

 Then I tried using BayesTraits, with the MultiState - Maximum Likelihood
 option, with no restrictions on q10 and q01.

 What puzzled me is that I'm getting different results from the three
 softwares.
 --
 aceER:
 transition rate: 0.0059, likelihood: -7.00
 aceARD:
 transition rate: 0.019 and 0.00, likelihood: -6.11

 Mesquite MK1:
 transition rate: 0.0059, likelihood: -7.70
 Mesquite Asymmetrical:
 transition rate: 0.015 and 0.005, likelihood: -7.30

 BayesTraits no restriction:
 transition rate: 0.0057 and 0.0057, likelihood: -14.09
 

 I can see that in both ace and Mesquite,
 it slightly favors the asymmetrical model with two different rates, and
 the
 rates and likelihoods are more of less comparable. But BayesTraits seems
 to
 think the two rates should be equal, and it has a different likelihood.

 Does this has something to do with different searching algorithms? Or am I
 missing something here? I am aware that the scaled likelihoods in ace are
 the scaled conditional likelihoods, not the joint or marginal
 reconstructions. But this should not affect the estimated transition
 rates?


 Thank you very much!

 [[alternative HTML version deleted]]

 

Re: [R-sig-phylo] ML ancestral state reconstruction using different softwares

2013-04-05 Thread Jingchun Li
Thank you very much Daniel and Emmanuel! Now things start to make sense.

I guess my last question is, if there is biological evidence that the
transition rates between the two traits are different, is it even
meaningful to compare the two models? Should I simply avoid using the equal
rates model?

Cheers,

Jingchun


On Fri, Apr 5, 2013 at 9:12 AM, Emmanuel Paradis emmanuel.para...@ird.frwrote:

 **
 Jingchun,

 Thanks to Daniel for giving a detailed answer to your first question.

 You can use ace() to fit a model with irreversible change. You need to
 build a custom model like this:

  Q - matrix(0, 2, 2)
  Q[2, 1] - 1
  Q
 [,1] [,2]
 [1,] 0 0
 [2,] 1 0

 In this case there's one rate to be estimated and the other is fixed to
 zero (the 0's on the diagonal are ignored). This can be generalized to more
 complicated models (there's an example in my book). Then call ace with:

 ace(traits_data, tree, type = d, model = Q)

 This time you cannot compare this model with the ER one with an LRT:
 compare directly the log-liks since they have the same number of parameters
 or use AIC(). BTW, there is an anova methods to compare nested models
 fitted with ace: this avoids the pain to compute correctly df's.

 Cheers,

 Emmanuel
 --
 *From: * Jingchun Li jingc...@umich.edu
 *Date: *Thu, 4 Apr 2013 22:25:09 -0400
 *To: *emmanuel.para...@ird.fr; r-sig-phylo@r-project.org
 *Subject: *Re: [R-sig-phylo] ML ancestral state reconstruction using
 different softwares

 Sorry, I forgot to include the list. there we go.

 --
 *From: * Jingchun Li jingc...@umich.edu
 *Date: *Thu, 4 Apr 2013 21:58:56 -0400
 *To: *emmanuel.para...@ird.fr
 *Subject: *Re: [R-sig-phylo] ML ancestral state reconstruction using
 different softwares

 Thank you very much, Dr.Paradis. You are right that the two parameter
 model does not fit the data significantly better. I guess I'm more puzzled
 about why the three softwares gave me different likelihoods.

 I did fit the symmetrical model using BayesTraits later and it gave me
 about the same transition rates as the asymmetrical model and a
 similar likelihood value (-14.08 for symmetrical and -14.00 for
 asymmetrical). However I do have biological evidence that transition from 0
 to 1 might be extremely hard. So maybe I can also try set q01 to 0 (which
 is actually what ace gave me under the asymmetrical model)?

 Cheers,

 Jingchun


 On Thu, Apr 4, 2013 at 9:21 PM, Emmanuel Paradis emmanuel.para...@ird.fr
  wrote:

 Hi,

 You cannot really say that in both ace and Mesquite, it slightly favors
 the asymmetrical model: the increase in log-likelihood is less than 1
 which is far from being significant with one additional parameter. So it
 seems that all three pieces of software agree well on the estimate of rate
 for the symmetrical model. You should fit also this model with BayeTraits
 to do the full comparison.

 Cheers,

 Emmanuel
 -Original Message-
 From: Jingchun Li jingc...@umich.edu
 Sender: r-sig-phylo-boun...@r-project.org
 Date: Thu, 4 Apr 2013 10:15:05
 To: r-sig-phylo@r-project.org
 Subject: [R-sig-phylo] ML ancestral state reconstruction using different
 softwares

 Hi all,

 I am exploring different methods for ancestral state reconstruction for a
 small phylogeny I have (26 OTUs). I have one binary trait coded as 0s and
 1s for all the taxa. And I am more interested in the transition rates
 between the two states.

 If I understand correctly, a maximum likelihood ancestral state
 reconstruction using a MK1 model or an asymmetrical rates model should
 give
 me the optimized estimated transition rates between the two states. The
 formal will assume the two rates are the same, the later will
 assume independent rates.

 So I firstly did this using the ape function in ace.

 ERreconstruction - ace(traits_data, tree, type=discrete, model=ER)
 ERreconstruction$rates
 ERreconstruction$loglik

 ARDreconstruction - ace(traits_data, tree, type=discrete, model=ARD)
 ARDreconstruction$rates
 ARDreconstruction$loglik

 Then I tried using Mesquite, using MK1 model and the Asymmetrical
 2-param.
 Markov-k Model 

 Then I tried using BayesTraits, with the MultiState - Maximum Likelihood
 option, with no restrictions on q10 and q01.

 What puzzled me is that I'm getting different results from the three
 softwares.
 --
 aceER:
 transition rate: 0.0059, likelihood: -7.00
 aceARD:
 transition rate: 0.019 and 0.00, likelihood: -6.11

 Mesquite MK1:
 transition rate: 0.0059, likelihood: -7.70
 Mesquite Asymmetrical:
 transition rate: 0.015 and 0.005, likelihood: -7.30

 BayesTraits no restriction:
 transition rate: 0.0057 and 0.0057, likelihood: -14.09
 

 I can see that in both ace and Mesquite,
 it slightly favors the asymmetrical model with two different rates, and
 the
 rates and likelihoods are more of less comparable. But BayesTraits seems
 to
 think the two rates should be 

Re: [R-sig-phylo] pruning a tree

2013-04-05 Thread Liam J. Revell

Hi Elaine.

A simpler way to do method 1 that doesn't require na.omit or match is:

# if there are species in the tree that are missing from the data:
ss-species.to.keep[,1] # species in the data
tree-birdtree
tree.pruned-drop.tip(tree,setdiff(tree$tip.label,ss))

I would guess that method 2 isn't working because your species names are 
not row names in your data matrix. To have that, you could do:


birddata-read.csv(H:/birddata_family_20130405.csv,header=T,row.names=1)

All the best, Liam

Liam J. Revell, Assistant Professor of Biology
University of Massachusetts Boston
web: http://faculty.umb.edu/liam.revell/
email: liam.rev...@umb.edu
blog: http://blog.phytools.org

On 4/5/2013 8:54 AM, Elaine Kuo wrote:

Hello



This Elaine.



I tried to prune a phylogeny tree using two methods based on the code
attached.



Method 1 returned the tip.label sharing between birddata and birdtree.

Method 2 returned nothing.



Please kindly indicate why Method 2 failed to prune the tree.

Also, please kindly explain the command “birdtree$tip.label[-na.omit”



Thank you again.



Code

Method 1

Library(ape)

birddata - read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree - read.nexus(H:/ birddata_family_20130405.nexus)

setwd(H:)



## prune the phylogeny to include only species which are in the data set

species.to.keep-read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree.pruned-drop.tip(birdtree,birdtree$tip.label[-na.omit(match(species.to.keep[,1],birdtree$tip.label))])





Method 2

Library(ape)

birddata - read.csv(H:/ birddata_family_20130405.csv, header = TRUE)

birdtree - read.nexus(H:/ birddata_family_20130405.nexus)

setwd(H:)



## prune the phylogeny to include only species which are in the data set

temp - name.check(birdtree, birddata)

birdtree.pruned - drop.tip(birdtree, tip=temp$Tree.not.data)

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[R-sig-phylo] Seeking list of nucleotide substitution models

2013-04-05 Thread Daniel Barker
Hello,

Is there a review or list of ~every specific nucleotide substitution model
that has been proposed or used in the literature (with references)?

I'm interested in reversible models.

The most exhaustive list I have is from the jModeltest documentation,
https://code.google.com/p/jmodeltest2/wiki/TheoreticalBackground#Models_of_
nucleotide_substitution

I realise an enormous number of models is possible (and may have been used
in model averaging). I'm keen to know which have some precedent in the
literature, along the lines of those listed above. I'm finding it
difficult to get beyond the standard sources.

Thank you in advance,

Daniel

-- 
Daniel Barker
http://bio.st-andrews.ac.uk/staff/db60.htm
The University of St Andrews is a charity registered in Scotland : No
SC013532

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[R-sig-phylo] read.nexus.data parser

2013-04-05 Thread Jessica Sabo
Hi All,

I am wondering if there is anyway to increase the speed of the
read.nexus.data parser. Or if there is an alternative that is a faster
nexus file data parser.

THanks,
Jess

-- 

Jessica L. Sabo
js...@ufl.edu
sabo.j...@gmail.com

PhD Student, The Edward Braun Lab
Department of Biology, Zoology Program
University of Florida
P.O. Box 118525
Gainesville, FL 32611

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[R-sig-phylo] Exporting Ancestor Reconstruction from Mesquite to R for ouch

2013-04-05 Thread Martin Turcotte
Dear forum, 
I am trying to conduct an ouch analysis and for it I must determine the 
ancestral selective regime at each node in my tree. To do so I need to conduct 
ancestral reconstruction on discrete unordered data. To my knowledge no package 
can do this in R (I hope I am wrong) and thus I used Mesquite's function to 
'Trace Character History'. The problem is exporting this information to R. 
In Mesquite the only export option I see is  'Export Ancestral State 
Trace' but the only option is SIMMAP 1.5 format. I tried opening this file 
using  phytools'read.simmap  but it just hangs. I can open the file with 
FigTree and I can see the Nodel labels but when I export the tree as a nexus 
file it does not save the model labels. 
Any advice would be appreciated.

thanks, 
Mart
 
Martin Turcotte, Ph. D.
Dept. of Biology
University of Toronto at Mississauga
3359 Mississauga Road North, Mississauga, 
Ontario, Canada, L5L 1C6
http://individual.utoronto.ca/martinturcotte



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Re: [R-sig-phylo] Exporting Ancestor Reconstruction from Mesquite to R for ouch

2013-04-05 Thread Liam J. Revell

Hi Martin.

Without more information or your input file, it's hard for me to 
evaluate why read.simmap is hanging. Did you run:


tree-read.simmap(filename,format=nexus,version=1.5)

If you have your discrete character data in R, you can also use the 
phytools function make.simmap to generate stochastic maps. Make sure 
that you are using a recent version of phytools (=0.2-26; =0.2-33 for 
uncertain/unknown tip states; =0.2-37 for non-symmetric transition 
matrices) as earlier versions are buggy.


My advice would be to use make.simmap to generate stochastic maps (or 
read them from file), and then use OUwie (in the package OUwie) to fit a 
multiple optima OU model to each mapped tree.


For discrete character x and continuous trait y (each vectors in the 
same order with names(x)=names(y)=species names); and a phylogeny, tree, do:


library(phytools)
library(OUwie)

mtrees-make.simmap(tree,x,nsim=100)
XX-data.frame(names(x),x,y)
result-lapply(mtrees,OUwie,data=XX,model=OUM,simmap.tree=TRUE)

This just gives you a giant list of the results returned by OUwie for 
each tree. It would probably be a good idea to organize your results of 
interest more sensibly than this so that they can be easily aggregated 
across mappings.


Good luck. All the best, Liam

Liam J. Revell, Assistant Professor of Biology
University of Massachusetts Boston
web: http://faculty.umb.edu/liam.revell/
email: liam.rev...@umb.edu
blog: http://blog.phytools.org

On 4/5/2013 6:13 PM, Martin Turcotte wrote:

Dear forum,
I am trying to conduct an ouch analysis and for it I must determine the 
ancestral selective regime at each node in my tree. To do so I need to conduct 
ancestral reconstruction on discrete unordered data. To my knowledge no package 
can do this in R (I hope I am wrong) and thus I used Mesquite's function to 
'Trace Character History'. The problem is exporting this information to R.
In Mesquite the only export option I see is  'Export Ancestral State 
Trace' but the only option is SIMMAP 1.5 format. I tried opening this file 
using  phytools'read.simmap  but it just hangs. I can open the file with 
FigTree and I can see the Nodel labels but when I export the tree as a nexus 
file it does not save the model labels.
Any advice would be appreciated.

thanks,
Mart

Martin Turcotte, Ph. D.
Dept. of Biology
University of Toronto at Mississauga
3359 Mississauga Road North, Mississauga,
Ontario, Canada, L5L 1C6
http://individual.utoronto.ca/martinturcotte



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[R-sig-phylo] R-Heatmap--- node stack overflow

2013-04-05 Thread Yan Wang
Dear All R-sig-phylo users,

I was using R ploting a heatmap recently. The datatable consisting 2400 rows 
and 6 columns, which I do not think is too big for R to handle, however I keep 
receiving the error message node stack overflow. Does anyone have similar 
problem? Any help will be appreciated. Thanks.

With regards,
Yan Wang, Ph.D student
Dr. Moncalvo's Group
Dept. Ecology  Evolutionary Biology,
University of Toronto 
Dept. Natural History,
Royal Ontario Museum,
100 Queens Park
Toronto, ON M5S 2C6
Office: (416)586-8025
Skype: yan.wang.fungi

“Nothing in biology makes sense except in the light of evolution”
—Theodosius Dobzhansky, 1977

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