Article

Toward fast and accurate SNP genotyping from whole genome sequencing data for bedside diagnostics

2017-12-26

Abstract excerpt

<h4>Motivation</h4> Genotyping a set of variants from a database is an important step for identifying known genetic traits and disease related variants within an individual. The growing size of variant databases as well as the high depth of sequencing data pose an efficiency challenge. In clinical applications, where time is crucial, alignment-based methods are often not fast enough. To fill the gap, Shajii et al...

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Literature Corpus work: df4ff49c-cec3-5bb0-9384-65fa76616e70
DOI: 10.1101/239871

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