Hi, I have read count of circRNA junctions obtained by analyzing RNA-Seq data. How can I merge these files to calculate fold change using DeSeq2?Some sample may contain junctions that are not detected in other sample or replicate analysis and I need to put zero in that condition. Any help will be appreciated. .
Question: How to merge read count of multiple sample in one fiel to be used for DESeq2 fold change study?
2.0 years ago by
Neu • 10
Neu • 10 wrote:
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