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Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools
BACKGROUND: Imputation has become a standard approach in genome-wide association studies (GWAS) to infer in silico untyped markers. Although feasibility for common variants imputation is well established, we aimed to assess rare and ultra-rare variants’ imputation in an admixed Caribbean Hispanic po...
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| Vydáno v: | Front Genet |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6456789/ https://ncbi.nlm.nih.gov/pubmed/31001313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00239 |
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