User: tszn1984

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tszn19840
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read counts of paired end reads for DESeq2 analysis
... I got a  list of paired end bam files, and want to do DESeq2 analysis. The first thing is to count the reads at gene level. I tried feature counts. However, it requires reorder of the bam files if I specified paired end is True, which takes infinite time for my huge dataset. I also tried summarizeOv ...
deseq featurecounts paired written 3.2 years ago by tszn19840 • updated 3.2 years ago by Steve Lianoglou12k

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