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Pysim-sv: a package for simulating structural variation data with GC-biases

BACKGROUND: Structural variations (SVs) are wide-spread in human genomes and may have important implications in disease-related and evolutionary studies. High-throughput sequencing (HTS) has become a major platform for SV detection and simulation serves as a powerful and cost-effective approach for...

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Bibliografiske detaljer
Udgivet i:BMC Bioinformatics
Main Authors: Xia, Yuchao, Liu, Yun, Deng, Minghua, Xi, Ruibin
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5374556/
https://ncbi.nlm.nih.gov/pubmed/28361688
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1464-8
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