[R-sig-phylo] Phylogenetic ANOVA or PGLS for categorical data?

2015-05-28 Thread Carlos H. Biagolini Junior
Hello everyone,


I am comparing a categorical data vs. a continues data, but the continues
data is a frequency of an observed parameter. I'm considering using
phylogenetic ANOVA (Garland 1993) or PGLS for categorical data. But, I am
not sure with one is more appropriate to my data.


I would like to ask if someone have any advice about the subject, or can
recommend me a paper that compare these analyses.


All the best


- Carlos Bagolini-Jr

-- 
Carlos Biagolini-Jr.
Bacharel em Ci�ncias Biol�gicas - Universidade Federal de Lavras
Mestrando em  Diversidade Biol�gica e Conserva��o - Universidade Federal de
S�o Carlos
http://lattes.cnpq.br/4086237188108947

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[R-sig-phylo] Phylogenetic ANOVA with multiple levels

2013-05-01 Thread Oscar Valverde
Hi all

I am trying to analyze the integration between organs in root systems of
angisoperms. My idea is testing if three different angiosperm groups
integrate vascular tissue across root orders in the same way. So far I have
been working with linear mixed effect models to test the idea, like in this
example, nesting the species within the clades I am studying in a nested
model:

model-lmer(log(Stele)~log(RootDiameter)+Root.Order*Clade+Site+(1|Clade/Species),data=dataRoot)

I am wondering if it is possible to integrate the phylogeny in a more
straight-forward way. I check options in phytools and gieger, but in both
cases the phylogenetic anova seem to test only one categorical variable at
the time and require same number of tips in the tree and the dataset. In my
case, even if I use species means I will have three times the number of
tips, since I have three orders of roots to integrate. I'll appreciate any
hints about how to solve this. Thanks in advance.

-- 
Oscar Valverde
PhD candidate
Department of Biological Sciences
Kent State University

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[R-sig-phylo] Phylogenetic ANOVA

2010-07-26 Thread Alejandro Gonzalez V
Hello,

Some colleagues and I are running some phylogenetic ANOVAS using the geiger 
package. In some of the analyses we get the same phylogentic p-value (very 
small p-value) even though the F-statistic differs between the two analyses, 
albeit it being relatively high in both instances. We were wondering why this 
arises, to get better grip on how the analysis works. We thought it may have to 
do with the randomizations to calculate the phylogenetic p-value. Or that the 
F-statistics are quite high...
Below are two examples :

m11-phy.anova(tree1,tmax,biozone,data.names=X,nsim=1000)
Standard ANOVA:
Analysis of Variance Table

Response: td$data
  Df Sum Sq Mean Sq F valuePr(F)
group  1 967.96  967.96  155.88 3.057e-12 ***
Residuals 25 155.246.21  
---
Signif. codes:  0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1 


Phylogenetic p-value:   0.000999001


m12-phy.anova(tree1,wt,biozone,data.names=X,nsim=1000)
Standard ANOVA:
Analysis of Variance Table

Response: td$data
  Df Sum Sq Mean Sq F valuePr(F)
group  1 602.88  602.88  109.01 1.333e-10 ***
Residuals 25 138.265.53  
---
Signif. codes:  0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1 


Phylogenetic p-value:   0.000999001


Cheers,

Alejandro
__

Alejandro Gonzalez Voyer
Post-doc

NEW ADDRESS  NEW E-MAIL

Estación Biológica de Doñana (CSIC)
Avenida Américo Vespucio s/n
41092 Sevilla 
Spain

E-mail: alejandro.gonza...@ebd.csic.es

Tel: +34- 954 466700, ext 1749

Website (From my previous position): 
http://www.iee.uu.se/zooekol/default.php?type=personalpagelang=enid=146









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Re: [R-sig-phylo] Phylogenetic ANOVA

2010-07-26 Thread Liam J. Revell
Just to clarify the point - the null distribution for the test-statistic 
(F) in this method is generated by Brownian motion simulation on the 
phylogeny.  The P-value of the ANOVA is thus obtained by comparing the 
observed test-statistic to simulated test-statistics (for an arbitrarily 
large number of simulations).  The reference to this is:


Garland, T. Jr., A. W. Dickerman, C. M. Janis,  J. A. Jones. 1993. 
Phylogenetic analysis of covariance by computer simulation. Syst. Biol. 
42: 265-292. (http://www.jstor.org/stable/2992464)


Thus, if you have a test-statistic (F) more extreme then that obtained 
for every last one of your simulated datasets, then the P-value will be 
entirely determined by the number of simulations that are used (as Luke 
says).  This seems to be case for your data (not surprising given the 
very large values for F that were obtained).


- Liam

Liam J. Revell
NESCent, Duke University
web: http://anolis.oeb.harvard.edu/~liam/
NEW email: lrev...@nescent.org



Luke Harmon wrote:

Yes that's a direct result of the number of simulations - if all of the 
simulated F statistics are smaller than the test statistics, then you will get:

p = 1/(n+1) where n is the number of simulated data sets.

lh
On Jul 26, 2010, at 8:44 AM, Alejandro Gonzalez V wrote:

  

Hello,

Some colleagues and I are running some phylogenetic ANOVAS using the geiger 
package. In some of the analyses we get the same phylogentic p-value (very 
small p-value) even though the F-statistic differs between the two analyses, 
albeit it being relatively high in both instances. We were wondering why this 
arises, to get better grip on how the analysis works. We thought it may have to 
do with the randomizations to calculate the phylogenetic p-value. Or that the 
F-statistics are quite high...
Below are two examples :

m11-phy.anova(tree1,tmax,biozone,data.names=X,nsim=1000)
Standard ANOVA:
Analysis of Variance Table

Response: td$data
 Df Sum Sq Mean Sq F valuePr(F)
group  1 967.96  967.96  155.88 3.057e-12 ***
Residuals 25 155.246.21  
---
Signif. codes:  0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1 



Phylogenetic p-value:   0.000999001


m12-phy.anova(tree1,wt,biozone,data.names=X,nsim=1000)
Standard ANOVA:
Analysis of Variance Table

Response: td$data
 Df Sum Sq Mean Sq F valuePr(F)
group  1 602.88  602.88  109.01 1.333e-10 ***
Residuals 25 138.265.53  
---
Signif. codes:  0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1 



Phylogenetic p-value:   0.000999001


Cheers,

Alejandro
__

Alejandro Gonzalez Voyer
Post-doc

NEW ADDRESS  NEW E-MAIL

Estación Biológica de Doñana (CSIC)
Avenida Américo Vespucio s/n
41092 Sevilla 
Spain


E-mail: alejandro.gonza...@ebd.csic.es

Tel: +34- 954 466700, ext 1749

Website (From my previous position): 
http://www.iee.uu.se/zooekol/default.php?type=personalpagelang=enid=146









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Luke Harmon
Assistant Professor
Biological Sciences
University of Idaho
208-885-0346
lu...@uidaho.edu

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