Dear all,
I am kind of new at RNAseq analysis. I hope someone can help me? I got like 880 genes with a p-value <0.01, using edgeR. I got the table with those 880 genes, and I separate the genes by up (+) and down (-) regulated by the LogFC option. But then I found that some of the 880 genes had a p value > 0.01 like 2,01E+05
Is there any explanation for this? What is the best way to get the DE genes, by p-value or logFC?
Thanks,
I am kind of new at RNAseq analysis. I hope someone can help me? I got like 880 genes with a p-value <0.01, using edgeR. I got the table with those 880 genes, and I separate the genes by up (+) and down (-) regulated by the LogFC option. But then I found that some of the 880 genes had a p value > 0.01 like 2,01E+05
Is there any explanation for this? What is the best way to get the DE genes, by p-value or logFC?
Thanks,
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