Question: (Closed) How do I Creat count table from raw seqdata ( fastq) and run Deseq2?
Hey Guys, I am new to Deseq2. However, I want to generate a count table for my sample to be used in Deseq2. I have four replicates of treated and untreated files. Help.
modified 18 months ago
ATpoint ♦ 36k
18 months ago by
jaqx008 • 70