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8.4 years ago
bxia
▴
180
Just curious about how to compare RNA-seq data from clinical patient.
I saw an old tutorial post, which transform all data to Z-score,
Just curious, based on that conversion, we are looking at def expression genes with normal tissue, not the gene with high expression or low expression within the tumor sample.
Is it a standard that all the data should be normalized with their control sample?
Thanks
It's very rare to compare RNA-seq data using Z-scores for the purposes of differential expression. Typically you'd use DESeq2, edgeR or voom (or one of a number of other similar tools), for which the input is raw read counts