Article

MUMdex: MUM-based structural variation detection

2016-09-30

Abstract excerpt

<h4>Motivation</h4> Standard genome sequence alignment tools primarily designed to find one alignment per read have difficulty detecting inversion, translocation and large insertion and deletion (indel) events. Moreover, dedicated split read alignment methods that depend only upon the reference genome may misidentify or find too many potential split read alignments because of reference genome anomalies. <h4>Metho...

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Literature Corpus work: d72a29b5-4a3f-5145-9c3e-9097b078905e
DOI: 10.1101/078261

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