Deseq2 and gene clustering
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aristotele_m ▴ 40
@aristotele_m-6821
Last seen 7.3 years ago
Italy

Hi!

I use this tutorial  on this site http://www.bioconductor.org/help/workflows/rnaseqGene/:

library("genefilter")
topVarGenes <- head(order(-rowVars(assay(rld))),35)

Why  -rowVars?

 

 

 

deseq2 clustering • 1.4k views
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@mikelove
Last seen 1 day ago
United States
See the man page for the function if you have questions about its behavior: ?order. The default for order() is small to large so adding a minus sign sorts large to small.
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