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  • I have a sorted BAM file, now what?

    So basically I have some RNAseq data (mouse) aligned to the mouse genome (outputed as a SAM file). From this, I made a sorted BAM file using SAMtools. I was curious how I go about looking at the top hits, or even just analyzing it at all.

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    Pick a tool (common examples are DESeq2, edgeR, and limma) and go through the vignettes/user guides.

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