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recover unmapped reads

We want to get more information on a variant of interest. We believe we can get more information from recovering unmapped reads . The current whole genome we are looking at is mapped to hg19 reference genome . how can we recover the unmapped reads?

whole genome sequencing next-gen

how can we recover the unmapped reads?

By using methods @ATPoint linked above. Assuming your BAM file contains unmapped reads in first place.

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