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Genentech Nonclinical Biostatistics
not sure now - does ranef(fm1) give
the (total) slope and
intercept values directly for each group or not?
Thanks a lot for clarifying - because I might well have been wrong.
Dimitri
On Mon, Oct 18, 2010 at 5:57 PM, Bert Gunter gunter.ber...@gene.com wrote:
Dmitri:
Not quite sure what you
Unintelligible -- to me anyway. You will have to explain what you mean
more explicitly and with greater clarity -- at least for my feeble
mind-- to get help.
-- Bert Gunter
On Fri, Oct 22, 2010 at 11:01 AM, Marcelo Lima mlim...@gmail.com wrote:
Dear all,
I generated a covariance matrix and I
://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.
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Genentech Nonclinical Biostatistics
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Genentech Nonclinical Biostatistics
, minimal, self-contained, reproducible code.
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Genentech Nonclinical Biostatistics
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Diversity 1 14 1.53025 0.2364
Management 2 30 6.01972 0.0063
Species 3 163 51.86699 .0001
Height 1 163 30.08090 .0001
Diversity:Height 1 163 12.57603 0.0005
--
Bert Gunter
Genentech Nonclinical Biostatistics
.
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
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]]
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/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.
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Genentech Nonclinical Biostatistics
http://www.R-project.org/posting-guide.html
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PLEASE
... and/or perhaps ?coplot in base R graphics or ?xyplot in trellis.
-- Bert Gunter
On Mon, Nov 15, 2010 at 2:25 PM, Greg Snow greg.s...@imail.org wrote:
Look at Predict.Plot (and TkPredict) from the TeachingDemos package.
--
Gregory (Greg) L. Snow Ph.D.
Statistical Data Center
and provide commented, minimal, self-contained, reproducible code.
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Genentech Nonclinical Biostatistics
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with his
comments is wrong.
Cheers,
Bert
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.
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Genentech Nonclinical Biostatistics
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/mailman/listinfo/r-help
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Bert Gunter
Genentech Nonclinical Biostatistics
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languages like C or Fortran (or Java?).
Cheers,
Bert Gunter
Genentech Nonclinical Statistics
** His approach also has the advantage of explicitly passing the
function you want to masterf rather than forcing R to look for it (in
the environment in which masterf was defined). More typically
)
Greg
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Bert
, reproducible code.
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-contained, reproducible code.
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.
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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self
: there may be no good way to do what you want.
Note to experts: Please view this post as an invitation to correct my errors
and provide authoritative info.
Cheers to all,
Bert
Bert Gunter
Genentech Nonclinical Biostatistics
-Original Message-
From: r-help-boun...@r-project.org [mailto:r
job.
-- You need to consult with your local statistician. This forum is not the
appropriate venue for difficult statistical questions that require intimate
familiarity with the data and an understanding of the scientific questions
of interest.
-- Bert Gunter
Genentech Nonclinical Statistics
Rich:
I suspect it's a cultural relic of the storage is scarce era that begat
C and R in the first place. Cutesiness. Culture is hard to change, but I
think you make a very salient point!
-- Bert
Bert Gunter
Genentech Nonclinical Statistics
-Original Message-
From: r-help-boun...@r
-Original Message-
From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org] On
Behalf Of Hadley Wickham
Sent: Thursday, July 15, 2010 12:15 AM
To: Yves Rosseel
Cc: r-help@r-project.org; richard_rauber...@merck.com
Subject: Re: [R] [R-pkgs] New package list for analyzing
complain, try writing some
documentation yourself. It's damn hard! ;)
Cheers,
Bert
Bert Gunter
Genentech Nonclinical Biostatistics
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--
it is for R, not TINN-R. Perhaps someone will be able to tell you where to
post TINN-R questions. I just had to struggle to figure it out and get it
set up; but I use it all the time as a pseudo- IDE.
Bert Gunter
Genentech Nonclinical Statistics
-Original Message-
From: r-help-boun
Have you read AN INTRODUCTION TO R?
?%in%
Bert Gunter
Genentech Nonclinical Statistics
-Original Message-
From: r-help-boun...@r-project.org [mailto:r-help-boun...@r-project.org]
On Behalf Of chipmaney
Sent: Friday, July 23, 2010 3:39 PM
To: r-help@r-project.org
Subject: [R
before -- what is the scientific
context? What is the scientific question?
I suspect you need to seek the help of a local statistician before you
sweep possibly important data under the outlier rug.
Bert Gunter
Genentech Nonclinical Biostatistics
On Mon, Jul 26, 2010 at 5:40 AM, Tim Smith tim_smith_
a parametric form.
My guess is that your distribution is right-skew but not Poisson --
probably more like a truncated Poisson. But of course I have no idea
what sorts of documents you've got, so how would I know?
Bert Gunter
Genentech Nonclinical Biostatistics
On Mon, Jul 26, 2010 at 1:28 PM, Majonu
effects models, so just walking
you through a lme model specification is not likely to help.
Bert Gunter
On Tue, Jul 27, 2010 at 8:24 PM, Murat Tasan mmu...@gmail.com wrote:
hi all - i'm having trouble using lme to specify a mixed effects
model.
i'm pretty sure this is quite easy
... just a note: you don't have to first sort the vector to do this:
x - sample(1:7)
x
[1] 3 5 7 6 2 4 1
which(x==min(x[x4]))
[1] 2
Bert Gunter
Genentech Nonclinical Biostatistics
On Wed, Jul 28, 2010 at 3:12 AM, Raghu r.raghura...@gmail.com wrote:
Hi
I have a sorted array
not work if the data frame contain calculated numeric
values which theoretically (infinite precision) are equal but are not
exactly due to finite precision. For example, try:
0 %in% pi/2
If this is what you have, then you have to do something fancier working
directly with the numeric values.
Bert
can, have a look at Jack Youden's classic paper Enduring
Values, which comments to some extent on these issues, here:
http://www.jstor.org/pss/1266913
Cheers,
Bert
Bert Gunter
Genentech Nonclinical Biostatistics
On Mon, Aug 2, 2010 at 10:32 AM, David Winsemius dwinsem...@comcast.netwrote
My sympathies, but I don't think it's the business of list
contributors to facilitate stupidity.
Confidence interval for the p-value is nonsense. You could try
sensitivity analyses via simulation, though.
Cheers,
Bert Gunter
Genentech Nonclinical Biostatistics
On Mon, Aug 2, 2010 at 11:31 AM
of the
frame. Whence one concludes that the f argument must be vectorized for
the Reduce to work on the columns of the data frame as you expect.
e.g.
Reduce(min,data.frame(a=1:3,b=4:6))
[1] 1
but
Reduce(pmin,data.frame(a=1:3,b=4:6))
[1] 1 2 3
Cheers,
Bert Gunter
Genentech Nonclinical Biostatistics
Just for fun, here are another couple of versions that work for data frames.
For Reduce with |
do.call(pmax,c(mydata,na.rm=TRUE)) 0
and for
do.call(pmin,c(mydata,na.rm=TRUE)) 0
Cheers,
Bert Gunter
Genentech Nonclinical Biostatistics
On Mon, Aug 2, 2010 at 2:28 PM, Joshua Wiley jwiley.ps
-- and
this ignorance gets them into a world of trouble.
-- Bert
Bert Gunter
Genentech Nonclinical Biostatistics
On Tue, Aug 3, 2010 at 12:57 PM, Dennis Murphy djmu...@gmail.com wrote:
Hi:
On Tue, Aug 3, 2010 at 6:51 AM, haenl...@gmail.com wrote:
I'm sorry -- I think I chose a bad example
about the basic concepts.
Bert Gunter
Genentech Nonclinical Biostatistics
On Tue, Aug 3, 2010 at 1:42 PM, Michael Haenlein haenl...@escpeurope.eu wrote:
Thanks for all your comments!
@Dennis: Are there any thresholds that I can use to evaluate the Variance
Inflation Factor? I think I learned
Actually, you probably want to remove the remaining level -- that is,
remove the variable altogether, since if it has only a single value
its effect is indistinguishable from the overall mean.
Again, complying with the posting guide would be advisable.
Bert Gunter
Genentech Nonclinical
Is there a way to set constraints on the fixed effects parameters?
Yes.
(I suggest you read and follow the posting guide to get a better answer).
Bert Gunter
Genentech Nonclinical Statistics
On Tue, Aug 3, 2010 at 11:11 AM, Marston, Sarah
sarah.mars...@otsuka.com wrote:
Dear R Help
, albeit with different syntax.
Alternatively, his reshape package (?melt,?cast therein) may also
suffice, depending on what you are trying to do.
Cheers,
Bert Gunter
Genentech Nonclinical Biostatistics
On Tue, Aug 3, 2010 at 9:06 PM, David Winsemius dwinsem...@comcast.net wrote:
On Aug 3, 2010
I am thinking about using 'predict' command to generate the prediction of z
with the new data.frame but there should be a better way.
I'm puzzled. Why would you think that? This is the canonical way to do
predictions in R.
Bert Gunter
Genentech Nonclinical Statistics
be useful for this.
-- Bert Gunter
Genentech Nonclinical Biostatistics
On Wed, Aug 11, 2010 at 10:53 AM, Mendolia, Franco fmendo...@mcw.edu wrote:
I could do that. However, the function f that I mentioned below is part of a
bigger program and is nested inside another function, say function
?RsiteSearch
or consult package sos.
Learn how to use R's search resources!
--
Bert Gunter
Genentech Nonclinical Statistics
On Wed, Aug 11, 2010 at 8:21 PM, Geoffrey Smith g...@asu.edu wrote:
Hello, does anyone know how to compute the following two normality tests
using R:
(1) the Kiefer
sense in such a world -- and
then studies need to be carefully designed -- happenstance data are
rarely sufficient -- to quantify them.
.. Not what scientists like to hear, I think, but this is the reality.
Further comments and criticisms welcome, of course.
Cheers,
Bert Gunter
Genentech
statistician to help you gain some clarity.
Thanks again,
David Biau.
De : Bert Gunter gunter.ber...@gene.com
À : Biau David djmb...@yahoo.fr
Cc : Frank Harrell f.harr...@vanderbilt.edu; r help list
r-help@r-project.org
Envoyé le : Ven 13 août 2010, 18h
.
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
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] survival_2.35-8 svSocket_0.9-48 lattice_0.18-3 MASS_7.3-5
What does
getOption(digits)
give you just before you run each bootstrap?
Bert Gunter
Genentech nonclinical Statistics
On Thu, Aug 19, 2010 at 12:50 AM, Reiko Akiyama reiko.akiy...@ebc.uu.se wrote:
Dear all,
Could anyone help me figure
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PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
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--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
http://devo.gene.com
more informative imho).
--
Bert Gunter
Genentech Nonclinical Statistics
On Fri, Aug 20, 2010 at 8:23 AM, mau...@alice.it mau...@alice.it wrote:
I have the following data table:
[,1] [,2] [,3] [,4] [,5]
[1,] 2575 1927 1754 581 354
[2,] 1156 810 730 541 237
[3,] 417 297 199 125
elegant solution from a true regex expert.
(Special note to Thomas Lumley: This seems one of the few instances
where eval(parse..)) may actually be appropriate.)
Cheers to all,
Bert
--
Bert Gunter
Genentech Nonclinical Biostatistics
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... I forgot to add: Base R regex functionality only. No special
string packages or functions (like gsubfn). I'm sure those would help,
but that's not what I'm after.
-- Bert
--
Bert Gunter
Genentech Nonclinical Biostatistics
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5 3 4 5 6 4 8 5 6 7 10
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
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PLEASE do read
This is easy to do in xyplot (latice package) via the index.cond and
skip arguments. Don't know about ggplot though.
-- Bert
On Mon, Aug 23, 2010 at 11:02 AM, Alison Macalady a...@kmhome.org wrote:
Hi,
I have a 5-paneled figure that i made using the facet function in qplot
(ggplot). I've
. Using lists and list operations usually allows both to
be done more efficiently and conveniently in one step.
--
Bert Gunter
Genentech Nonclinical Statistics
On Tue, Aug 24, 2010 at 8:19 AM, r.ookie r.oo...@live.com wrote:
Do you mean something like this?
n - 5
(vec1 - matrix(rep(1, n
, Room 1.04
University of East Anglia
Norwich, UK
NR4 7TJ
+44 (0) 1603 591412
-Original Message-
From: Bert Gunter [mailto:gunter.ber...@gene.com]
Sent: Tuesday, August 24, 2010 4:39 PM
To: r.ookie
Cc: Maas James Dr (MED); r-help@r-project.org
Subject: Re: [R] multiple assignments
???
You were provided exactly what you requested. I think you either need
to read up on what random effects models mean or more clearly
communicate what YOU mean. (It's unclear to me, anyway).
--
Bert Gunter
Genentech Nonclinical Statistics
On Thu, Aug 26, 2010 at 8:57 AM, Samantha Patrick
modeled, fitted, and compared as functions of temperature -- provided
that the design permits this (i.e. provides sufficient precision for
the characterizations/comparisons).
If you don't know how to do this, seek further statistical help.
--
Bert Gunter
Genentech Nonclinical Statistics
are nonlinear. A detailed understanding and explanation of exactly
what this means exceeds my understanding. Doug Bates's PhD thesis and
subsequent papers (+ others, no doubt) go into this.
Cheers,
Bert Gunter
Genentech Nonclinical Statistics
On Fri, Aug 27, 2010 at 7:45 AM, John Ludlam ludlam.j
Your question is unclear. If the calculation of B[3] now depends on the
newly calculated value of B[2], then the answer is no: you must loop. If
B[3] is based on the original B[2] value, then the answer is yes, and the
solution is just a matter of simple indexing, which I leave as an exercise.
--
way ANOVA on *zij*:
In particular, it is NOT a substitute for the normal ANOVA F statistic for
when there are unequal variances, and when there is evidence of
non-normality.
--
Bert Gunter
Genentech Noclinical Statistics
[[alternative HTML version deleted
Thanks. I stand corrected, then.
-- Bert
On Mon, Aug 30, 2010 at 1:45 PM, JRG loesl...@verizon.net wrote:
On 30 Aug 2010 at 13:25, Bert Gunter wrote:
Inline below.
-- Bert
Wrong. There *is* a Brown-Forsythe test of equality of means given
heterogeneity of variance.
[Kirk's
I would hazard the guess that this would be better estimated as a
multivariate time series (e.g. AR1) in which the covariance between the two
innovation components was NOT assumed to be 0 (nor were their variances
assumed to be the same). The R time series task view lists packages to do
this, but
Learned Folks:
Well, I've already advertised my ignorance about these matters, so I have
nothing to lose by plunging ahead with further Questionable advice.
From the references cited, Brown-Forsythe originated in the statistical
medieval age -- that is, prior to large scale, cheap computing (to
Error of the 3rd kind, (right answer to wrong question), I think. So what if
the test rejects --- then what?
I think the poster is looking for some kind of smoother.
?loess, ?smooth.spline and about 400 others may be useful.
--
Bert Gunter
Genentech Nonclinical Statistics
On Tue, Aug 31, 2010
will not create a copy if it can avoid it
(usually?). Search the list archives for call by value, copy
arguments, etc. for authoritative answers.
--
Bert Gunter
Genentech Nonclinical Statistics
Which is actually doing this:
x- `[-`(x, list=10, values=NA) # The actual call
Assuming this can
a long time ago (in a galaxy far
away), Often, even the data aren't sufficient. (This a cryptic
statistical in joke; example for the in-crowd: is it an outlier or
an indication of curvature?).
Cheers,
Bert
Bert Gunter
Genentech Nonclinical Statistics
On Wed, Sep 1, 2010 at 12:22 PM, Frank Harrell
Why should height be a random effect?
I suspect you may need a tutorial on what a random effect in a mixed
model is. I see no obvious reason why one would cluster on height.
Perhaps if you clarify, it may become obvious either what your
concerns are (and that your model is correct) or that you
]]
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Genentech Nonclinical Biostatistics
467-7374
http
://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
http://devo.gene.com/groups/devo/depts/ncb/home.shtml
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... For those who are interested, enjoy.
Cheers,
Bert
Bert Gunter
Genentech Nonclinical Statistics
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Another task for the ESP package?
Bert Gunter
Genentech Nonclinical Statistics
On Tue, Sep 7, 2010 at 4:29 AM, netrunner giovanna.va...@gmail.com wrote:
Dear all,
I would like to know if there is a R package performing model
identification?
thank you!
--
View this message in context
in a profile file.
Cheers,
Bert Gunter
Genentech Nonclinical Statistics
On Wed, Sep 8, 2010 at 8:20 AM, Joshua Wiley jwiley.ps...@gmail.com wrote:
Hi,
Just create a file called .Rprofile that is located in your working
directory (this means you could actually have different ones in each
code.
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
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with() would seem to be useful here:
m$z - with(m,ifelse(is.na(z), x, z))
(I believe the timing is similar, but haven't checked)
-- Bert
On Wed, Sep 8, 2010 at 11:22 AM, Dimitris Rizopoulos
d.rizopou...@erasmusmc.nl wrote:
one way is the following:
m - data.frame(x = rnorm(100), y =
Well, let's see if the following helps or just adds to the confusion.
First lists are vectors of mode list . But they are general
recursive structures (in fact, completely general).
Second, data frames are lists: each column of a data frame is a
component (member) of the list with the additional
targeted
therapies appear to be more effective. While the context may be new,
the debate, itself, is not: Tukey wrote (or maybe it was talked -- I
can't remember for sure) about this about 30 years ago. I'm sure many
other also have done so.
Cheers,
Bert
--
Bert Gunter
Genentech Nonclinical
, self-contained, reproducible code.
--
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Genentech Nonclinical Biostatistics
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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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
R-help@r-project.org mailing list
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PLEASE do read the posting
-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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
-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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
467-7374
http://devo.gene.com
@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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
OOPs. I Only read Spencer's reply. Sorry for repeating the poster's
original comment.
-- Bert
On Mon, Oct 4, 2010 at 10:10 AM, Bert Gunter bgun...@gene.com wrote:
Well, not really ...
Google on R package Debye . The 5th hit lists the gsl package with
the debye() function.
Moral: DO make
and provide commented, minimal, self-contained, reproducible code.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
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
-contained, reproducible code.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
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
.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
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
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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
R-help@r
://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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
R-help@r
://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.
--
Bert Gunter
Genentech Nonclinical Biostatistics
__
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