Thank you. Do we need to specify anything for the paired end reads? The bam file is after mapping the paired end reads.
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Hi,
I want to subsample the reads of different depth from a bam file. For eg. 10X, 20X, 30X and so on. I tried with ShortRead R package but I can input only certain number of reads. I couldn't know how depth I am subsampling. Does any one have suggestion on how to subsample paired end reads of desired depth from fastq file or bam file?
Thanks
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