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> One way is to extract the differentially expressed genes with p.val = 0.05 and logFC = +/-1.0
I strongly recommend using FDR < 0.05 and…
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Is there a way to combine the fcs files back into a single file as individual data segments?
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I appreciate your time and response.
Answer: Function Request for Rsubread or tximport: parsing command-line featureCounts ou
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You can read command-line output from `featureCounts` by
```
library(edgeR)
y <- readDGE( fcoutputfiles, columns=c(1,7) )
y$genes <- read.d…
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We have progressed past the point where I show you how to do things using Bioconductor packages, and into the realm where I start telling y…
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