Genome wide copy number analysis of single cells

Copy number variation (CNV) is increasingly recognized as an important contributor to phenotypic variation in health and disease. Most methods for determining CNV rely on admixtures of cells, where information regarding genetic heterogeneity is lost. Here, we present a protocol that allows for the g...

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Detaylı Bibliyografya
Yayımlandı:Nat Protoc
Asıl Yazarlar: Baslan, Timour, Kendall, Jude, Rodgers, Linda, Cox, Hilary, Riggs, Mike, Stepansky, Asya, Troge, Jennifer, Ravi, Kandasamy, Esposito, Diane, Lakshmi, B., Wigler, Michael, Navin, Nicholas, Hicks, James
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2012
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5069701/
https://ncbi.nlm.nih.gov/pubmed/22555242
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nprot.2012.039
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