Repeated measures vs factorial analysis

2002-02-06 Thread Kasper Hornbaek

Hi all.

I have a question regarding analysis of data using repeated measures.
I can easily analyse the data using a standard, factorial approach
(entering each observation as a row in SPSS). However, I can not
figure out how to do a repeated measures analysis.

The study I am trying to analyse has two factors, A & B, each with two
levels. Each subject in the study solved 10 tasks in two combinations
of factors, e.g. A1B1 followed by A2B2. Due to the nature of the
study, each subject only experienced each level of the factors once
(i.e. only one time A1 and one time A2, as in A1B1 followed by A2B2).
The ten tasks are specific (i.e. nested within) one of the factors,
say B.

Now, do I analyse this design based on four groups, one for each
combination of A and B, and use contrasts to find the main effects and
interaction of A and B? Or is there some other approach?

Kindest regards,
Kasper Hornbæk


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Re: Sensitivity Analysis

2002-02-06 Thread JJ Diamond

[EMAIL PROTECTED] (Christopher J. Mecklin) wrote in message 
news:<[EMAIL PROTECTED]>...
> Judith, Rich, Art, edstat-l list;
> 
> My thanks to your replies and my apologies for not articulating my question 
> better in my initial post.  To be somewhat less vague about my question 
> (I'll probably be still a little vague because of my lack of knowledge), 
> the colleague of mine who asked about "sensitivity analysis" meant the 
> question in regards to population ecology. To try to be more specific about 
> a topic that I know little about, an ecologist might be modelling the risk 
> of extinction.  The model will involve several parameters.  The use of the 
> term "sensitivity analysis" in this context apparently means determining 
> how "sensitive" the model's predictions are to uncertainty in the estimates 
> of the parameters to help determine what parameters need to be estimated 
> "more carefully".  (These last few sentences were paraphrased from 
> http://www.ramas.com/pva.htm, a hit I got from a hastily conducted Google 
> search of "sensitivity analysis ecological model".)
> 
> I was sent a list of references by another reader of this newsgroup that I 
> passed on to my colleague that he found satisfactory for his purposes.  I 
> suppose I could post that list of references if anyone else is interested.
> 
> The use of this term "sensitivity analysis" is apparently  from the use of 
> the term "sensitivity" in epidemiology (and quite possibly others use of 
> the term).  This seems to be one of those situations where the same word 
> means different things to different people.
> 
> Again, my apologies for the vague request.
> 
> CJM
> 
> At 11:27 AM 02/06/2002 -0500, Conn, Judith wrote:
> >I do know that in epidemiology and medical science the purpose is to find
> >out how "sensitive" the test is .  This ia what I think of when talking
> >sensitivity analysis.  Further info can be obtained from P Armitage & G
> >Berry, "Statistical Methods in Medical Research", Blackwell Scientific
> >Publications.  Judy Conn
> >
> > > -Original Message-
> > > From: Rich Ulrich [SMTP:[EMAIL PROTECTED]]
> > > Sent: Wednesday, February 06, 2002 9:55 AM
> > > To:   [EMAIL PROTECTED]
> > > Subject:  Re: Sensitivity Analysis
> > >
> > > On 31 Jan 2002 10:06:36 -0800, [EMAIL PROTECTED]
> > > (Christopher J. Mecklin) wrote:
> > >
> > > > I had a colleague (a biologist) ask me about sensitivity analysis.  I am
>  
> > > > not familiar with the technique (above and beyond knowing that the
> > > > technique exists). What books/articles/websites/etc. would be good
>  sources
> > > > for my colleague to learn about sensitivity analysis.  Since he's a
> > > > biologist and not a statistician, I'm assuming he would prefer a
>  treatment
> > > > geared towards application rather than theory.
> > >
> > > I have not seen any reply to this.  I suspect that there might be
> > > too many options that refer to 'sensitivity'  and none of us
> > > are sure what you are interested in, precisely.
> > >
> > > What's another keyword?  I pair specificity with sensitivity;  but
> > > I don't refer to  'sensitivity analysis', I say 'discriminability.'
> > > Your question -- and my background thoughts of 1000-generation,
> > > simulation analyses in genetic model ling -- makes me think of
> > > something I saw years ago, called  'perturbation analyses'.
> > >
> > > Try Google, or try us again with additional detail.
> > >
> > > Hope this helps.
> > > --
> > > Rich Ulrich, [EMAIL PROTECTED]
> > > http://www.pitt.edu/~wpilib/index.html
> > >
> > >
> > > =
> > > Instructions for joining and leaving this list, remarks about the
> > > problem of INAPPROPRIATE MESSAGES, and archives are available at
> > >   http://jse.stat.ncsu.edu/
> > > =
> >
> >
> >=
> >Instructions for joining and leaving this list, remarks about the
> >problem of INAPPROPRIATE MESSAGES, and archives are available at
> >   http://jse.stat.ncsu.edu/
> >=
> 
> Christopher J. Mecklin, PhD
> Assistant Professor
> Department of Mathematics and Statistics
> Murray State University
> Murray, KY 42071
> Phone: 270 762-5437
> Fax: 270 762-2314
> http://campus.murraystate.edu/academic/faculty/chris.mecklin/index.htm
> 
> 
> 
> =
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> problem of INAPPROPRIATE MESSAGES, and archives are available at
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sensitivity analysis is not the same as sensitivity and specificity
from epidemiology.  these latter terms are used when describing the
characteristics of 

panel data - fixed effects

2002-02-06 Thread Mark

Re: panel data - fixed effects

I've been playing with some regressions
The sample is 500 listed firms in Malaysia.
I'm using MV/BV as a performance measure and various variables such as
ownership structure, log of sales etc etc.

Someone has suggested I use panel data - fixed effects method

Is this referring to pooled data? Do I pool my data over a number of years
rather than each individual year?

I gather that fixed effects is using dummy variables. What variables might I
use as dummy variables?

Can you point me in the right direction. I've about a half a dozen books on
my desk on stats and econometrics and none give me clear guidance

Many thanks
Mark




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Re: 'Distance' between two normal distributions

2002-02-06 Thread Charles Metz

Francis Dermot Sweeney wrote:
 =

 > If I have two normal distributions N(m1, s1) and N(m2, =

 > s2), what is a good measure of the distance between them? =

 > I was thinking of something like a K-S distance like =

 > max|phi1-phi2|. I know it probably depende on what I
 > want it for, or what exactly I mean by distance, but any =

 > ideas would be helpful.

Francis,

This question arises in receiver operating characteristic (ROC)
analysis, where an effective ("latent") pair of univariate normal data
distributions often may be assumed to underlie an ROC curve.

Given two univariate normal probability densities with generally
different means (m1 and m2) and standard deviations (s1 and s2), the
common indices of separation are

  d=92_e =3D (m1 - m2)/((s1 + s2)/2)

and

  d_a =3D (m1 - m2)/SQRT((s1**2 + s2**2)/2),

whereas a less well-known measure is

  Sakitt's D =3D (m1 - m2)/SQRT(s1 * s2).

In the special case where s1 =3D s2 =3D s, all three of these indices red=
uce
to

  d' =3D (m1 - m2)/s .

All three indices also apply rigorously to *non-normal*
decision-variable densities in ROC analysis if some (usually unknown)
monotonic transformation of the decision variable yields normal
densities.  This generalization is possible because ROC curves are
invariant under any monotonic transformation of the decison axis, so the
requirement for strict interpretability of the indices becomes one of
having an ROC curve that plots as a straight line on "normal deviate
axes" (e.g., see Metz CE.  ROC methodology in radiologic imaging. =

Investigative Radiology 1986; 21: 720).  In non-normal situations of
this kind, the indices are *not* defined in terms of means and standard
deviations, but instead in terms of the straight-line ROC curve on
normal-deviate axes.  If the "y intercept" and "slope" of such an ROC
are given by "a" and "b", respectively, then

  d=92_e =3D 2a/(1 + b)

and

  d_a =3D a*SQRT(2/(1 + b**2)) ,

whereas

 Sakitt's D =3D a/SQRT(b).

All of these indices approach =


  d' =3D a

in the special case where b =3D 1.  =


When an ROC curve plots as a straight line on normal-deviate axes, its
value of d_a happens to equals the normal deviate which corresponds to
the area under the ROC when that curve is plotted on *conventional*
(i.e., probability, rather than normal-deviate) axes.  The latter
interpretation of d_a is sometimes used for other ROC curve forms as
well, which isn't strictly "legal" but, from a practical standpoint, is
rarely misleading.

If you=92d like to do some additional reading, I would recommend that you=

begin with

   Simpson AJ, Fitter MJ.  What is the best index of detectability? =

Psych Bull 1973; 80:481-488.

And finally, I feel obliged to emphasize the importance of a point that
you raised yourself:  The validity of any summary index *does* depend --
sometimes strongly -- upon what it=92s used for.

Hoping this helps,

   Charles Metz


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Re: 'Distance' between two normal distributions

2002-02-06 Thread Dennis Roberts

seems, as you have said, depends what you want to do with it

if there is considerable overlap, then whatever distance you use will have 
some of both distributions included ... if there is essentially no overlap 
... then any pair of values ... one from each ...will reflect a real difference

of course, if there is a small difference in means but very large sds ... 
that is one thing wheres ... if there were the same small differences in 
means but, minuscule sds ... that would be another thing

the simple thing would be to use the mean difference but, that really does 
not reflect if there is any overlap between the two and, that seems to be 
part of the issue

At 07:28 PM 2/6/02 +, Francis Dermot Sweeney wrote:
>If I have two normal distributions N(m1, s1) and N(m2, s2), what is a
>good measure of the distance between them? I was thinking of something
>like a K-S distance like max|phi1-phi2|. I know it probably depende on
>what I want it for, or what exactly I mean by distance, but any ideas
>would be helpful.
>
>Thanks,
>Francis.
>
>--
>
>Francis Sweeney
>Dept. of Aero/Astro
>Stanford U.
>
>
>=
>Instructions for joining and leaving this list, remarks about the
>problem of INAPPROPRIATE MESSAGES, and archives are available at
>   http://jse.stat.ncsu.edu/
>=

Dennis Roberts, 208 Cedar Bldg., University Park PA 16802

WWW: http://roberts.ed.psu.edu/users/droberts/drober~1.htm
AC 8148632401



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RE: Sensitivity Analysis

2002-02-06 Thread Christopher J. Mecklin

Judith, Rich, Art, edstat-l list;

My thanks to your replies and my apologies for not articulating my question 
better in my initial post.  To be somewhat less vague about my question 
(I'll probably be still a little vague because of my lack of knowledge), 
the colleague of mine who asked about "sensitivity analysis" meant the 
question in regards to population ecology. To try to be more specific about 
a topic that I know little about, an ecologist might be modelling the risk 
of extinction.  The model will involve several parameters.  The use of the 
term "sensitivity analysis" in this context apparently means determining 
how "sensitive" the model's predictions are to uncertainty in the estimates 
of the parameters to help determine what parameters need to be estimated 
"more carefully".  (These last few sentences were paraphrased from 
http://www.ramas.com/pva.htm, a hit I got from a hastily conducted Google 
search of "sensitivity analysis ecological model".)

I was sent a list of references by another reader of this newsgroup that I 
passed on to my colleague that he found satisfactory for his purposes.  I 
suppose I could post that list of references if anyone else is interested.

The use of this term "sensitivity analysis" is apparently  from the use of 
the term "sensitivity" in epidemiology (and quite possibly others use of 
the term).  This seems to be one of those situations where the same word 
means different things to different people.

Again, my apologies for the vague request.

CJM

At 11:27 AM 02/06/2002 -0500, Conn, Judith wrote:
>I do know that in epidemiology and medical science the purpose is to find
>out how "sensitive" the test is .  This ia what I think of when talking
>sensitivity analysis.  Further info can be obtained from P Armitage & G
>Berry, "Statistical Methods in Medical Research", Blackwell Scientific
>Publications.  Judy Conn
>
> > -Original Message-
> > From: Rich Ulrich [SMTP:[EMAIL PROTECTED]]
> > Sent: Wednesday, February 06, 2002 9:55 AM
> > To:   [EMAIL PROTECTED]
> > Subject:  Re: Sensitivity Analysis
> >
> > On 31 Jan 2002 10:06:36 -0800, [EMAIL PROTECTED]
> > (Christopher J. Mecklin) wrote:
> >
> > > I had a colleague (a biologist) ask me about sensitivity analysis.  I am
> >
> > > not familiar with the technique (above and beyond knowing that the
> > > technique exists). What books/articles/websites/etc. would be good
> > sources
> > > for my colleague to learn about sensitivity analysis.  Since he's a
> > > biologist and not a statistician, I'm assuming he would prefer a
> > treatment
> > > geared towards application rather than theory.
> >
> > I have not seen any reply to this.  I suspect that there might be
> > too many options that refer to 'sensitivity'  and none of us
> > are sure what you are interested in, precisely.
> >
> > What's another keyword?  I pair specificity with sensitivity;  but
> > I don't refer to  'sensitivity analysis', I say 'discriminability.'
> > Your question -- and my background thoughts of 1000-generation,
> > simulation analyses in genetic model ling -- makes me think of
> > something I saw years ago, called  'perturbation analyses'.
> >
> > Try Google, or try us again with additional detail.
> >
> > Hope this helps.
> > --
> > Rich Ulrich, [EMAIL PROTECTED]
> > http://www.pitt.edu/~wpilib/index.html
> >
> >
> > =
> > Instructions for joining and leaving this list, remarks about the
> > problem of INAPPROPRIATE MESSAGES, and archives are available at
> >   http://jse.stat.ncsu.edu/
> > =
>
>
>=
>Instructions for joining and leaving this list, remarks about the
>problem of INAPPROPRIATE MESSAGES, and archives are available at
>   http://jse.stat.ncsu.edu/
>=

Christopher J. Mecklin, PhD
Assistant Professor
Department of Mathematics and Statistics
Murray State University
Murray, KY 42071
Phone: 270 762-5437
Fax: 270 762-2314
http://campus.murraystate.edu/academic/faculty/chris.mecklin/index.htm



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EViews 3.1 error message

2002-02-06 Thread James McQueen

Hi,

I tried to run a workfile on EViews 3.1 that I had created in EViews
4.0. It is a three equation system estimated via full information
maximum likelihood. It worked fine in 4.0. Now, I'm using 3.1 and it
opens the 4.0 workfile no problem but when I hit the estimate button
(via FIML) it returns: error, near singular matrix. As far as I know
the workfile was unchanged from the one that worked fine in 4.0. Do I
need to create a new workfile in 3.1 and re-enter the equations and
re-import the excel file to make it work in 3.1?

thanks,

james


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'Distance' between two normal distributions

2002-02-06 Thread Francis Dermot Sweeney

If I have two normal distributions N(m1, s1) and N(m2, s2), what is a 
good measure of the distance between them? I was thinking of something
like a K-S distance like max|phi1-phi2|. I know it probably depende on 
what I want it for, or what exactly I mean by distance, but any ideas 
would be helpful.

Thanks,
Francis.

-- 

Francis Sweeney  
Dept. of Aero/Astro  
Stanford U. 


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Re: can multicollinearity force a correlation?

2002-02-06 Thread Jay Warner

I can't help it.  the last paragraph in this post absolutely _demands_ a
response.

Wuzzy wrote:

> > You made a model with the "exact same exposure in different units",
> > which is something that no one would do,
>
> Hehe, translation is don't post messages until you've thought them
> through.
>
> Anyway, turns out that the answer to my question is "No"..
> Multicollinearity cannot force a correlation.  It turns out that ONE
> of the variables *was* correlated With R^2=0.45 and so
> multicollinearity had no effect on overall R^2.
>
> I'm sure no-one is interested in my data as it has nothing to do with
> statistics, my subject of interest is not statistics.. but i need to
> learn it as a tool..

Dear Wuzzy,

In two short sentences, you have expressed the fundamental issues of
those who claim their "subject is not statistics."  So long as you try
to separate 'statistics' from your specific technology, you will not
develop much of either.

House builders do not spend much time concerned with their hammers or
their nails.  Yet they are sufficiently concerned that (in the USA) they
buy expensive nail guns and special nail packages so they can build
those houses faster and better.  They use roofing nails to hold the roof
shingles in place, finishing nails to hold the interior trim in place,
and they carefully know the differences between them.

In resolving a technical product performance problem, which is what I
largely do with my statistics, I have to carefully decide what I am
going to measure, how it will be measured, and how I will analyze it
(crunch the numbers).  Many people believe that this last step equals
statistics.  They neglect that the analysis methods depend on those
first two items.  They often neglect that each of those numbers I crunch
_means_ something.  They have units.  They relate back to what was
measured.

The statistical analysis in my view is mostly concerned with detecting
and quantifying the relationships between the different things and
conditions which were measured. Thus, without the statistics, you have
no technology; without the technology you have no statistics.  You
cannot relegate one of them down to the level of 'tool.'  Down that path
lies the perennial question, 'which equation should I use,' which begs
its own questions.

In your specific case, it appears that you tried to do a multiple
regression using one response (dependent variable) and three factors
(independent variables).  But the three factors were actually
transformations of the same variable.  Since you said they were in
different units, the transformations were probably linear.  If you tried
to do a full multiple regression on this data in this manner (3
factors), I'm surprised that the software did not warn you it had found
a singular matrix, or at least that it had tried to divide by zero.
Perhaps you made the conversions on a hand calculator, so small rounding
errors kept the matrix that is inside the analysis from blowing up
(inward!?:) on you.

In any case, discovering that a linear transformation of data produces
radically different r^2 values should be a warning that something is
amiss, and it is time to think more carefully about exactly what digits
are being pushed around the screen.  Those numbers _mean_ something,
remember :)  And so does the math of the equations we select.  A
correlation and/or linear or polynomial regression analysis with one
response and one factor would probably be more technically valuable, for
your data, as best I can see from here.

As for interest in your data, I can say that I would like to see it, as
an example I can use for students.  I need to collect real data from
many different technologies - industrial, business, medical, social
sciences, etc. - in order to relate the topic of 'statistics' to the
areas of interest to them.  I will be happy to share the write up with
you, especially if you are willing to correct any errors in the
technology which I am likely to make.  I am also careful not to slam
even the fictitious people who appear in them.

After all, it takes an expert to make a good hammer, and an expert to
make a good house.  They need each other, just as 'statisticians' need
'technology experts.'

Cheers,
Jay
--
Jay Warner
Principal Scientist
Warner Consulting, Inc.
 North Green Bay Road
Racine, WI 53404-1216
USA

Ph: (262) 634-9100
FAX: (262) 681-1133
email: [EMAIL PROTECTED]
web: http://www.a2q.com

The A2Q Method (tm) -- What do you want to improve today?






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RE: Sensitivity Analysis

2002-02-06 Thread Conn, Judith

I do know that in epidemiology and medical science the purpose is to find
out how "sensitive" the test is .  This ia what I think of when talking
sensitivity analysis.  Further info can be obtained from P Armitage & G
Berry, "Statistical Methods in Medical Research", Blackwell Scientific
Publications.  Judy Conn

> -Original Message-
> From: Rich Ulrich [SMTP:[EMAIL PROTECTED]]
> Sent: Wednesday, February 06, 2002 9:55 AM
> To:   [EMAIL PROTECTED]
> Subject:  Re: Sensitivity Analysis
> 
> On 31 Jan 2002 10:06:36 -0800, [EMAIL PROTECTED]
> (Christopher J. Mecklin) wrote:
> 
> > I had a colleague (a biologist) ask me about sensitivity analysis.  I am
> 
> > not familiar with the technique (above and beyond knowing that the 
> > technique exists). What books/articles/websites/etc. would be good
> sources 
> > for my colleague to learn about sensitivity analysis.  Since he's a 
> > biologist and not a statistician, I'm assuming he would prefer a
> treatment 
> > geared towards application rather than theory.
> 
> I have not seen any reply to this.  I suspect that there might be
> too many options that refer to 'sensitivity'  and none of us
> are sure what you are interested in, precisely.
> 
> What's another keyword?  I pair specificity with sensitivity;  but
> I don't refer to  'sensitivity analysis', I say 'discriminability.'
> Your question -- and my background thoughts of 1000-generation, 
> simulation analyses in genetic model ling -- makes me think of
> something I saw years ago, called  'perturbation analyses'.
> 
> Try Google, or try us again with additional detail.
> 
> Hope this helps.
> -- 
> Rich Ulrich, [EMAIL PROTECTED]
> http://www.pitt.edu/~wpilib/index.html
> 
> 
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> problem of INAPPROPRIATE MESSAGES, and archives are available at
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Re: Sensitivity Analysis

2002-02-06 Thread Rich Ulrich

On 31 Jan 2002 10:06:36 -0800, [EMAIL PROTECTED]
(Christopher J. Mecklin) wrote:

> I had a colleague (a biologist) ask me about sensitivity analysis.  I am 
> not familiar with the technique (above and beyond knowing that the 
> technique exists). What books/articles/websites/etc. would be good sources 
> for my colleague to learn about sensitivity analysis.  Since he's a 
> biologist and not a statistician, I'm assuming he would prefer a treatment 
> geared towards application rather than theory.

I have not seen any reply to this.  I suspect that there might be
too many options that refer to 'sensitivity'  and none of us
are sure what you are interested in, precisely.

What's another keyword?  I pair specificity with sensitivity;  but
I don't refer to  'sensitivity analysis', I say 'discriminability.'
Your question -- and my background thoughts of 1000-generation, 
simulation analyses in genetic model ling -- makes me think of
something I saw years ago, called  'perturbation analyses'.

Try Google, or try us again with additional detail.

Hope this helps.
-- 
Rich Ulrich, [EMAIL PROTECTED]
http://www.pitt.edu/~wpilib/index.html


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WSCH : A Revolutionary Acne Treatment and More RHOKEN

2002-02-06 Thread WSCH1739
Title: SPECIAL ALERT

  Special Alert :  WASATCH  PHARMACEUTICALS  (OTCBB: WSCH)TOP 4 REASONS TO BUY WSCH1.The products and medical therapies developed by WSCH represent possibly the most important breakthrough in the field of Dermatology in the last fifty years.2.WSCH anticipates FDA approval on seven over-the-counter products within the next year, which will provide significant revenue in the retail drug market.3.WSCH has experienced a success rate of 90% during clinical studies, completely eliminating skin disease from 90% of all patients treated.4.By year five, WSCH plans to have annualized revenue over $525 million and over $125 million in EBIT.  This does not take into account income from OTC products which will be substantial.   PROJECTIONS, OBJECTIVES AND STATISTICS    Over a five year period, AISC (WSCH's subsidiary) plans to establish 350 clinics in over 100 major population areas. The company plans to hire over 150 medical doctors for these clinics, train over 1,000 medical assistants and treat over 2,000,000 patients. Also by year five, WSCH plans to have annualized over $525 million in revenue and over $125 million in EBIT. This does not take into account income from OTC products which will be substantial.As of 1991, there were approximately 14 million chronic acne and eczema patients annually in the United States, with the highest percentage between 18 to 44 years of age. The actual number of patients with any type of acne Is significantly higher. Seven billion dollars is spent annually on dermatological pharmaceutical products for these disorders.In 1994, the teen population reached 25 million. During the next decade, it will grow at nearly twice the rate of the overall population (according to U.S. Census Bureau projections). Acne patients are primarily teenagers, whereas eczema patients range from infants to the elderly.      SYMBOL:    WSCH   CURRENT PRICE:   $0.059   52 WEEK HIGH:   $27.50   52 WEEK LOW:   $0.056COMPANY BACKGROUNDWasatch Pharmaceutical, Inc. is a fourteen year old company with a record of outstanding achievements in the field of Dermatology. Dermatology. Under the name of its subsidiary, American Institute of Skin Care (AISC), Wasatch has operated two prototype clinics for the last five years where the products and medical therapies have been tested and proven on hundreds of patients. The Company's activities have been centered on research in the area of serious skin diseases. A concurrent discovery and benefit is WSCH's dramatic success in the area of skin rejuvenation.Seeing the high growth potential from major funding, WSCH elected to become a public company less than two years ago.Wasatch's major successes in the area of skin diseases include:Cystic Acne, Eczema, Seborrhea, Contact Dermatitis, Molluscum, Folliculitis, Acne Rosacea and less prevalent skin diseases.Interestingly, these skin disorders account for more than 70% of all business in the field of dermatology for which there are very few (if any) safe, effective therapies like those developed by Wasatch.Because the therapies developed by Wasatch dominate this area of medicine, WSCH has elected to market its products via company-owned clinics throughout the United States. This decision has resulted in the establishment of two research clinics in Utah for the purpose of implementing procedures within the clinics pursuant to testing and confirming the results that were achieved in past clinical trials. Due to its success rate of 90% on hundreds of patients over a five year period, WSCH's clinics are now on line with insurance providers independent of HMOs. Efforts to establish Preferred Providership status with HMOs are presently being pursued.THIS JUST IN : WSCH BREAKING NEWS Wasatch Pharmaceutical Inc. Announces a New Physician Marketing Campaign and Listing On German Stock Exchanges MURRAY, Utah--(BUSINESS WIRE)--Nov. 27, 2001--Wasatch Pharmaceutical Inc. (OTCBB:WSCH - news) CEO Gary Heesch announced today a marketing campaign directed to physicians. A direct link has been established on a physician recruiting Web site making available therapies for the treatment of cystic acne, acne, folliculitis and skin rejuvenation. Physicians will find the benefits of these treatment therapies by logging on to the "X Acne" link at the Physician Search website. This physician search Web site typically receives over 200,000 hits per month. Mr. Heesch reminded, "Our treatment therapy products are also available via the AISC Online Store."These skin treatment products come in kit form providing a 90-day supply to patients for the full treatment program. Included in the kit is an instructional video on the treatment therapy allowing the patient to use these products in their home. The therapies, when used as instructed, achieve a success rate of eradication in excess of 90% with no side effects of any consequence. Previousl

Hello!

2002-02-06 Thread Alex Seregin

 I'm russian student/
 Alex Seregin/


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Re: can multicollinearity force a correlation?

2002-02-06 Thread J.Russell

Dear Wuzzy

The answer is yes they can.

Consider the case where x1 is highly correlated to x2 and Y is 
correlated with X1-X2.

I on a simulation of this for 100 cases got a R-squared for the 
regression model of  .998 but the individual correlations

x1 vs y = -.072 p=.476
x2 vs y=-.105 p=.301
x1 vs x2=.999 p<.001

This was a simulation and this situation is a minority case in my 
experience but the answer is yes they can. 

However this case is of course a nonsense if you have perfectly 
correlated cases as you would have if only the units had been 
changed.

Jean M. Russell


To: [EMAIL PROTECTED]
Date sent:  5 Feb 2002 18:15:00 -0800
From:   [EMAIL PROTECTED] (Wuzzy)
Organization:   http://groups.google.com/
Subject:Re: can multicollinearity force a correlation?

> In my own defense:
> 
> I was asking a simple question:
> 
> will highly correlated cause an irregularly high R^2.
> 
> My answer to my own question is  "no" it can't.. 
> No-one here was able to give me this answer and I believe it is
> correct: if your sample is large enough,(as mine is) then "no",
> multicollinearity cannot affect your R^2, it will only affect the
> coefficients and their signs and errors.
> 
> 
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--
Jean M. Russell M.A. M.Sc.   [EMAIL PROTECTED]
Corporate Information & Computing Services, 
University of Sheffield 
285 Glossop Road
Sheffield
S10 2HB
United Kingdom
Phone:  0114-222-3098
Fax  :  0114-222-3040


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toner cartridges

2002-02-06 Thread webmaster





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