Article

Detection and characterization of copy number variants based on whole-genome sequencing by DNBSEQ platforms

2019-09-30

Abstract excerpt

<h4>Background</h4> Next-generation sequence (NGS) has rapidly developed in past years which makes whole-genome sequencing (WGS) becoming a more cost- and time-efficient choice in wide range of biological researches. We usually focus on some variant detection via WGS data, such as detection of single nucleotide polymorphism (SNP), insertion and deletion (Indel) and copy number variant (CNV), which playing an impo...

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Literature Corpus work: b82c3357-e00f-55f9-a491-40d6a02a3352
DOI: 10.1101/786962

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