User: Novice

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(Closed) How to use Deseq2 to merge the biological triplicates (for two seperate conditions) for analysing differential expression of genes
... I am very new to R, I have used Deseq2 package after my feature counts. I have 2 stages of control and treated with triplicates of each. I am forwarding the code that I have used step 1 : dds <- DESeqDataSetFromMatrix(countData = Feature_counts$counts, colData = col ...
replicates biological rna-seq deseq2 written 10 weeks ago by Novice0

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