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Simultaneous Analysis of Common and Rare Variants in Complex Traits: Application to SNPs (SCARVAsnp)

Advances in technology and reduced costs are facilitating large-scale sequencing of genes and exomes as well as entire genomes. Recently, we described an approach based on haplotypes called SCARVA1 that enables the simultaneous analysis of the association between rare and common variants in disease...

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Detaylı Bibliyografya
Asıl Yazarlar: Chen, Guanjie, Yuan, Ao, Zhou, Yanxun, Bentley, Amy R., Zhou, Jie, Chen, Weiping, Shriner, Daniel, Adeyemo, Adebowale, Rotimi, Charles N.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Libertas Academica 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3418150/
https://ncbi.nlm.nih.gov/pubmed/22904618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/BBI.S9966
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