I want to call variants using whole genome RNA-seq datasets of wheat. I have generated BAM files using STAR, I want to ask should I apply any post processing steps to these BAM files like Removing duplicates, removing reads based on quality scores etc before performing further downstream analysis?
Question: Pre_processing BAM file for variant calling using RNA-seq data
20 months ago by
ammarsabir15 • 60
ammarsabir15 • 60 wrote:
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