Article

Indel variant analysis of short-read sequencing data with Scalpel

2015-10-01

Abstract excerpt

<h4>ABSTRACT</h4> As the second most common type of variations in the human genome, insertions and deletions (indels) have been linked to many diseases, but indels of more than a few bases are still challenging to discover from short-read sequencing data. Scalpel ( http://scalpel.sourceforge.net ) is open-source software for reliable indel detection based on the micro-assembly technique. To date, it has been suc...

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Literature Corpus work: bb57a061-3a57-54fa-a422-6396a4816e3d
DOI: 10.1101/028050

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