Article

SCCNV: a software tool for identifying copy number variation from single-cell whole-genome sequencing

2019-01-31

Abstract excerpt

<h4>Background</h4> Identification of de novo mutations from cell populations requires single-cell whole-genome sequencing (SCWGS). Although many experimental protocols of SCWGS have been developed, few computational tools are available for downstream analysis of different types of somatic mutations, including copy number variation (CNV). <h4>Results</h4> We developed SCCNV, a software tool for detecting CNVs fr...

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Literature Corpus work: 70c852bc-d78b-5a1e-ba94-41b2a9ec5565
DOI: 10.1101/535807

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