Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing

Single-molecule sequencing (SMS) such as Pacific Biosciences and Oxford Nanopore generate long reads with high error rate. Here, the authors develop Longshot, a computational method that detects and phases single nucleotide variants (SNV) in diploid genomes using SMS data.

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Auteurs principaux: Peter Edge, Vikas Bansal
Format: article
Langue:EN
Publié: Nature Portfolio 2019
Sujets:
Q
Accès en ligne:https://doaj.org/article/a914015fa7154b73858b882af20bfb66
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