PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data

Motivation: Exome sequencing (exome-seq) data, which are typically used for calling exonic mutations, have also been utilized in detecting DNA copy number variations (CNVs). Despite the existence of several CNV detection tools, there is still a great need for a sensitive and an accurate CNV-calling...

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Detaylı Bibliyografya
Asıl Yazarlar: Wang, Chen, Evans, Jared M., Bhagwate, Aditya V., Prodduturi, Naresh, Sarangi, Vivekananda, Middha, Mridu, Sicotte, Hugues, Vedell, Peter T., Hart, Steven N., Oliver, Gavin R., Kocher, Jean-Pierre A., Maurer, Matthew J., Novak, Anne J., Slager, Susan L., Cerhan, James R., Asmann, Yan W.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2014
Konular:
Applications Notes
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4155258/
https://ncbi.nlm.nih.gov/pubmed/24876377
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu363
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