call peaks of single-end mapping bam files

0

Hi, for certain reasons, I need to map double-end sequencing result seperately, for example, I mapped A_R1.fastq to A_R1.bam, and A_R2.fastq to A_R2.bam, now I want to call peaks of this file, how can I call peaks of these two files? Do I need to merge them and call peaks?


ChIP-Seq


alignment


error


software


genome

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