Rare variant association test in family-based sequencing studies

The objective of this article is to introduce valid and robust methods for the analysis of rare variants for family-based exome chips, whole-exome sequencing or whole-genome sequencing data. Family-based designs provide unique opportunities to detect genetic variants that complement studies of unrel...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Brief Bioinform
Asıl Yazarlar: Wang, Xuefeng, Zhang, Zhenyu, Morris, Nathan, Cai, Tianxi, Lee, Seunggeun, Wang, Chaolong, Yu, Timothy W, Walsh, Christopher A, Lin, Xihong
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2017
Konular:
Papers
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5862290/
https://ncbi.nlm.nih.gov/pubmed/27677958
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbw083
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