SCNVSim: somatic copy number variation and structure variation simulator

BACKGROUND: Somatically acquired structure variations (SVs) and copy number variations (CNVs) can induce genetic changes that are directly related to tumor genesis. Somatic SV/CNV detection using next-generation sequencing (NGS) data still faces major challenges introduced by tumor sample characteri...

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Pubblicato in:BMC Bioinformatics
Autori principali: Qin, Maochun, Liu, Biao, Conroy, Jeffrey M, Morrison, Carl D, Hu, Qiang, Cheng, Yubo, Murakami, Mitsuko, Odunsi, Adekunle O, Johnson, Candace S, Wei, Lei, Liu, Song, Wang, Jianmin
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
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Software
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4349766/
https://ncbi.nlm.nih.gov/pubmed/25886838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0502-7
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