An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasis
Motivation: Despite the prevalence of copy number variation (CNV) in the human genome, only a handful of confirmed associations have been reported between common CNVs and complex disease. This may be partially attributed to the difficulty in accurately genotyping CNVs in large cohorts using array-ba...
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Bibliographic Details
| Main Authors: |
Coin, Lachlan J.M.,
Cao, Dandan,
Ren, Jingjing,
Zuo, Xianbo,
Sun, Liangdan,
Yang, Sen,
Zhang, Xuejun,
Cui, Yong,
Li, Yingrui,
Jin, Xin,
Wang, Jun |
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| Format: | Online
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| Language: | English |
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| Published: |
Oxford University Press
2012
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436806/
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