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MapCaller – An integrated and efficient tool for short-read mapping and variant calling using high-throughput sequenced data

2019-09-26

Abstract excerpt

With the advance of next-generation sequencing (NGS) technologies, more and more medical and biological researches adopt NGS technologies to characterize the genetic variations between individuals. The identification of personal genome variants using NGS technology is a critical factor for the success of clinical genomics studies. It requires an accurate and consistent analysis procedure to distinguish functional...

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Literature Corpus work
16e83c34-84aa-5187-a147-a80a65457d2c
DOI
10.1101/783605
Open publication

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MapCaller – An integrated and efficient tool for short-read mapping and variant calling using high-throughput sequenced dataDOI 10.1101/783605
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