Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases

Although emerging sequencing technologies can characterize all genetic variants, the cost is still high. Illumina released the HumanOmni5M-4v1 (Omni5) genotype array with ~4.3M assayed SNPs, a much denser array compared with other available arrays. The Omni5 balances both cost and array density. In...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Eur J Hum Genet
Prif Awduron: Xing, Chuanhua, Huang, Jie, Hsu, Yi-Hsiang, DeStefano, Anita L, Heard-Costa, Nancy L, Wolf, Philip A, Seshadri, Sudha, Kiel, Douglas P, Cupples, L Adrienne, Dupuis, Josée
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2016
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5070895/
https://ncbi.nlm.nih.gov/pubmed/26577045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.244
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