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Genotype Imputation Reference Panel Selection Using Maximal Phylogenetic Diversity
The recent dramatic cost reduction of next-generation sequencing technology enables investigators to assess most variants in the human genome to identify risk variants for complex diseases. However, sequencing large samples remains very expensive. For a study sample with existing genotype data, such...
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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: |
Genetics Society of America
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3781962/ https://ncbi.nlm.nih.gov/pubmed/23934887 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.113.154591 |
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