User: bananaal1

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bananaal110
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Creating a count matrix from 8 bam files in R (RNAseq experiment)
... I have 8 BAM files from an RNAseq experiment (4 different individuals, 2 different tissue types per). The Illumina run was singled-end 50s and we have about 3.2million reads per sample. I need to know how many counts align to the different parts of the reference genome from each sample identified b ...
rnaseq deseq2 granges count matrix galignments written 5 months ago by bananaal110 • updated 5 months ago by Michael Love14k

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