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Instructions: you would have to download and format the Marks et al. data from | |
their supplement first. Then, save this file as an .Rnw, Stangle and | |
source the resulting .R file. | |
Import data from Marks et al. Cell 2012. | |
<<>>= | |
dat <- read.table('./marks2i.serum.example.txt') | |
# > head(dat) | |
# GeneSymbol log2Fold pval | |
# 1 0610007C21Rik -1.0501235 0.02 | |
# 2 0610007L01Rik 0.3659197 0.11 | |
# 3 0610007P08Rik 0.4903256 0.23 | |
# 4 0610007P14Rik -0.2574317 0.20 | |
# 5 0610007P22Rik -0.3934814 0.19 | |
# 6 0610009B22Rik 0.2751580 0.07 | |
all.genes.universe <- as.character(dat$GeneSymbol) | |
@ | |
Get GO list from bioConductor-curated database: | |
<<>>= | |
require(goseq) | |
# replace line below with the org database for your genome of interest | |
require(org.Mm.eg.db) | |
goannotlist <- goseq::getgo( all.genes.universe, 'mm9', 'geneSymbol', | |
fetch.cats = 'GO:BP' ) | |
@ | |
Turn list into a two column data frame (actually data table): | |
<<>>= | |
require(plyr) | |
require(data.table) | |
f.golist.to.godf <- function(goannot){ | |
gonames <- unlist(goannot,use.names=FALSE) | |
genenames <- ldply(goannot, length) | |
genenames <- rep( genenames[['.id']], genenames[['V1']]) | |
goannotlong <- data.frame( GeneSymbol = genenames, Category = gonames) | |
return( data.table(goannotlong) ) | |
} | |
goannotlong <- f.golist.to.godf( goannotlist ) | |
@ | |
Apply criteria used by Marks et al. for differential expression. | |
<<>>= | |
genes.high2i <- subset(dat, log2Fold < -1 & pval <0.2, | |
select = 'GeneSymbol', drop = TRUE) | |
genes.highserum <- subset(dat, log2Fold > 1 & pval <0.2, | |
select = 'GeneSymbol', drop = TRUE) | |
@ | |
<<>>= | |
go.highserum <- f.makegreedyGOtable( genehits = genes.highserum, | |
gotable = goannotlong, gosizecutoff = 300, abbrlength = 50) | |
go.high2i <- f.makegreedyGOtable( genehits = genes.high2i, | |
gotable = goannotlong, gosizecutoff = 300, abbrlength = 50) | |
@ | |
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