Closed nmshahir closed 7 years ago
The reason we use DPCoA instead of wuf is because it provides biplots with species loadings that PCoA on wuf doesn't.
On Tue, Aug 16, 2016 at 11:22 AM, nmshahir notifications@github.com wrote:
Hello,
I am a doctoral student working on a microbiomes project and did an principal coordinates analysis in Phyloseq. While I recognize that PCA and PCoA are not exactly the same, I was wondering if there was a way to get the loadings of the PCoA (i.e. determine how much taxa A, taxa B, etc contribute to PC1, and so forth)?
Code Example: ord.wuni <- ordinate(data,"PCoA","wunifrac") PCoA.wuni = plot_ordination(data, ord.wuni, type = "samples", color = "Phenotype") PCoA.wuni
Thanks in advance for any comments, Nur
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Susan Holmes Professor, Statistics and BioX John Henry Samter Fellow in Undergraduate Education Sequoia Hall, 390 Serra Mall Stanford, CA 94305 http://www-stat.stanford.edu/~susan/
I'm going through the documentation (https://github.com/joey711/phyloseq/wiki/ordinate) but it's still a little unclear as to how DPCoA differs from PCoA?
You need to read this paper that lays it out very nicely:
http://www.ncbi.nlm.nih.gov/pubmed/22174277
On Wed, Aug 17, 2016 at 9:38 AM, nmshahir notifications@github.com wrote:
I'm going through the documentation (https://github.com/joey711/ phyloseq/wiki/ordinate) but it's still a little unclear as to how DPCoA differs from PCoA?
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Susan Holmes Professor, Statistics and BioX John Henry Samter Fellow in Undergraduate Education Sequoia Hall, 390 Serra Mall Stanford, CA 94305 http://www-stat.stanford.edu/~susan/
Thank you @spholmes. I've gone through the paper and I have a few questions
Thank you! -N
If you consider the OTUs as independent categories it is fine to use Correspondence analyses (CCA without formula).
Canonical correspondence analyses and RDA are quite different as they involve extra explanaotry variables/environmental factors/ etc..in a formula.
best Susan
On Mon, Aug 22, 2016 at 7:53 PM, nmshahir notifications@github.com wrote:
Thank you @spholmes https://github.com/spholmes. I've gone through the paper and I have a few questions
- It seems that instead of using UniFrac/weighted UniFrac as the distance metric, DPCoA utilizes a patristic distance as the metric?
- The loadings corresponding to species loadings are name_of_dpcoa$dw , correct?
- It was stated here ( #305 https://github.com/joey711/phyloseq/issues/305 ), that you can also use CCA and RDA to obtain OTU loadings? Is there a particular benefit to using DPCoA over CCA and RDA? Or is it more of a case by case situation depending on the question you wish to ask?
Thank you! -N
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Susan Holmes Professor, Statistics and BioX John Henry Samter Fellow in Undergraduate Education Sequoia Hall, 390 Serra Mall Stanford, CA 94305 http://www-stat.stanford.edu/~susan/
Hello,
I am a doctoral student working on a microbiomes project and did an principal coordinates analysis in Phyloseq. While I recognize that PCA and PCoA are not exactly the same, I was wondering if there was a way to get the loadings of the PCoA (i.e. determine how much taxa A, taxa B, etc contribute to PC1, and so forth)?
Code Example: ord.wuni <- ordinate(data,"PCoA","wunifrac") PCoA.wuni = plot_ordination(data, ord.wuni, type = "samples", color = "Phenotype") PCoA.wuni
Thanks in advance for any comments, Nur