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Weighted pedigree-based statistics for testing the association of rare variants
BACKGROUND: With the advent of next-generation sequencing (NGS) technologies, researchers are now generating a deluge of data on high dimensional genomic variations, whose analysis is likely to reveal rare variants involved in the complex etiology of disease. Standing in the way of such discoveries,...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3827928/ https://ncbi.nlm.nih.gov/pubmed/23176082 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-667 |
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