How to call small SVs (<50bp) from single end reads?
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3.5 years ago
jseg • 0

Hi all,

I'm looking for a way to efficiently call small structural variants (<50bp) using single-end reads (inputs from ChIP-seq). The methods I found require paired-end reads, so do you know any efficient approach that uses single-end reads?

Regards.

SNPs single-end-reads SVs • 585 views
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I might be wrong here, but SV is hard (impossible) to detect with SE reads, mainly because aligning the reads with such mismatch/gap will be nearly impossible.

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