SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes

SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes

Copy number variants are duplications and deletions of the genome that play an important role in phenotypic changes and human disease. Many software applications have been developed to detect copy number variants using either whole-genome sequencing or whole-exome sequencing data. However, there is...

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Bibliographic Details
Main Authors:	Yue Xing, Alan R. Dabney, Xiao Li, Guosong Wang, Clare A. Gill, Claudio Casola
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2020-02-01
Series:	Frontiers in Genetics
Subjects:	copy number variation simulation software whole-exome sequencing read depth
Online Access:	https://www.frontiersin.org/article/10.3389/fgene.2020.00082/full

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