in
the ratio are thus different.
Best,
Julien
From: sclaramunt...@gmail.com
Date: Thu, 18 Jun 2015 12:52:11 -0500
To: r-sig-phylo@r-project.org
Subject: Re: [R-sig-phylo] Non Parametric PGLS
Hi Sergio,
If what you want to do is to partition your morphometric data into size
whether or not
the shape is independent of the measure of size (the geometric mean of all
others measurements).
I attach a picture to illustrate the bias introduced but it should be easy to
simulate this issue with R...
Hope it makes sense,
Julien
Subject: Re: [R-sig-phylo] Non Parametric PGLS
From
: sclaramunt...@gmail.com
Date: Fri, 19 Jun 2015 08:57:11 -0500
To: r-sig-phylo@r-project.org
Subject: Re: [R-sig-phylo] Non Parametric PGLS
Hi Julien,
Mosimann’s method was proposed for the study of allometry, so it would be
strange if it only applies to isometric cases. Can you provide
Hi Sérgio.
What Simon ( I, in my blog post) suggested is that to test the
'normality assumption' you need to first transform the residuals with
the inverse Cholesky decomposite matrix. This will give you a vector in
which the values should be normal independent (assuming that the
Hi Liam,
Again, thank you for the answer. Yes, I'm aware that they are
phylogenetically correlated and that they need to be subsequently analysed
with methods such as PGLS. In fact, when I apply a normality test to (
chol(solve(vcv(tree)))%*%residuals(fit))the transformed residuals are
normally
Hi Sergio,
If what you want to do is to partition your morphometric data into size and
shape components, then you can use Mosimann’s methods which do not require
regressions or phylogenetic corrections.
Mosimann, J. E. 1970. Size allometry: size and shape variables with charac-
terization of
bias in the ratio are thus different.
Best,
Julien
From: sclaramunt...@gmail.com
Date: Thu, 18 Jun 2015 12:52:11 -0500
To: r-sig-phylo@r-project.org
Subject: Re: [R-sig-phylo] Non Parametric PGLS
Hi Sergio,
If what you want to do is to partition your morphometric data into size and
shape
Hello again,
Thanks for your help. This kind of solved my problem. I normally use some
kind of test (shapiro or komolgorov) to test for normality. I know
histograms or qqnorm plots a more helpful, but they are more vulnerable
to each others interpretation.
So, just to make clear one thing: these
Hi Sérgio.
Liam is right. But we do expect the normalised residuals to be
approximately Normal. You can calculate the normalised residuals by
pre-multiplying the raw residuals by the inverse of the Cholesky
decomposition of the phylogenetic variance-covariance matrix, and then
dividing by
Sergio,
You can fit a non-Gaussian phylo regression with MCMCglmm.
HTH,
Dan.
On Jun 17, 2015, at 9:40 AM, Sergio Ferreira Cardoso
sff.card...@campus.fct.unl.pt wrote:
Hello all,
I'm having a problem with a Multiple Regression PGLS analysis that I'm
performing. The residuals are
Hi Sérgio.
It might be worth pointing out that we do not expect that the residuals
from a phylogenetic regression to be normal. I described this with
respect to the phylogenetic ANOVA on my blog
(http://blog.phytools.org/2013/02/a-comment-on-distribution-of-residuals.html),
but this applies
Hello all,
I'm having a problem with a Multiple Regression PGLS analysis that I'm
performing. The residuals are not normal and it's difficult to bring them
to normality. In these cases, are there any alternatives to the linear
model? I know that for non-phylogenetic analyses other models exist,
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