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[Bioc-devel] A geneSet data class for facilitating GSEA

Dear bioc-developers,

would it be useful to introduce an additional slot for the direction and/or
magnitude of expression change of each gene in the gene set?

It seems that GSEA and GSEA-like methods use sets of genes that are
homogeneously down- or upregulated (correct me if I am wrong, I am far from
being up to date on GSEA methods).

This seems to be reflected in the example presented in the PGSEA vignette
where target genes of Ras and Myc are separated into 'UP' and 'DN' regulated
genes. 

However, (alternative?) methods could actually use the quantitative
information about expression changes to score each gene set. Adding a
corresponding slot in the geneSet class would allow to accommodate such
methods.

Best,
Alexandre


-----Original Message-----
From: bioc-devel-bounces at stat.math.ethz.ch
[mailto:bioc-devel-bounces at stat.math.ethz.ch] On Behalf Of Dykema, Karl
Sent: mercredi, 14. mars 2007 16:15
To: bioc-devel at stat.math.ethz.ch
Subject: Re: [Bioc-devel] A geneSet data class for facilitating GSEA

Sorry I forgot to attach the str()

$ 15-delta prostaglandin J2 10 uM  DOWN : list()
  ..- attr(*, "reference")= chr "15-delta prostaglandin J2 10 uM  DOWN "
  ..- attr(*, "desc")= chr "DOWN "
  ..- attr(*, "source")= chr "PubMed"
  ..- attr(*, "design")= chr "????"
  ..- attr(*, "identifier")= chr "17008526"
  ..- attr(*, "species")= chr "human"
  ..- attr(*, "data")= chr "raw"
  ..- attr(*, "private")= chr "no"
  ..- attr(*, "creator")= chr "Karl Dykema <karl.dykema at vai.org>"
  ..- attr(*, "ids")= chr [1:75] "171392" "5680" "2149" "54557" ...
  ..- attr(*, "class")= atomic [1:1] smc
  .. ..- attr(*, "package")= chr "PGSEA"


This closely mirrors the geneSet proposed and we will be happy to adopt
a consensus structure.

The only significant difference is a "creator" to let folk know who
curated the gene list... This may help if groups are collaborating to
the collect gene sets.


-------------------------------
Karl Dykema
Bioinformatics Programmer/Analyst
Laboratory of Computational Biology
Van Andel Research Institute
333 Bostwick Ave. NE
Grand Rapids, MI 49503
(616) 234-5554



-----Original Message-----
From: Vincent Carey 525-2265 <stvjc at channing.harvard.edu>
Date: Wed, 14 Mar 2007 10:19:36 -0400 (EDT)
To: Sean Davis <sdavis2 at mail.nih.gov>
Cc: <bioc-devel at stat.math.ethz.ch>, Ross Lazarus
<rerla at channing.harvard.edu>
Subject: Re: [Bioc-devel] A geneSet data class for facilitating GSEA

i like this idea in principle.  the RGenetics folks may have done
something in this direction.

you might want to have geneList as an abstract class, and then extend to
EntrezGeneList, RefseqGeneList and so forth so that dispatch could work
without looking into the idType ...

a version or date field might also be important

---
Vince Carey, PhD
Assoc. Prof Med (Biostatistics)
Harvard Medical School
Channing Laboratory - ph 6175252265 fa 6177311541
181 Longwood Ave Boston MA 02115 USA
stvjc at channing.harvard.edu
On Wed, 14 Mar 2007, Sean Davis wrote:

            
useful for general consumption) like:
etc.).
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