RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing

With rapid advances in DNA sequencing technologies, whole exome sequencing (WES) has become a popular approach for detecting somatic mutations in oncology studies. The initial intent of WES was to characterize single nucleotide variants, but it was observed that the number of sequencing reads that m...

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Bibliografiska uppgifter
I publikationen:Cancer Inform
Huvudupphovsmän: Chang, Lun-Ching, Das, Biswajit, Lih, Chih-Jian, Si, Han, Camalier, Corinne E., McGregor, Paul M., Polley, Eric
Materialtyp: Artigo
Språk:Inglês
Publicerad: Libertas Academica 2016
Ämnen:
Methodology
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4849420/
https://ncbi.nlm.nih.gov/pubmed/27147817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/CIN.S36612
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