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Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms
BACKGROUND: Indels are an important cause of human variation and central to the study of human disease. The 1000 Genomes Project Low-Coverage Pilot identified over 1.3 million indels shorter than 50 bp, of which over 890 were identified as potentially disruptive variants. Yet, despite their ubiquity...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3334570/ https://ncbi.nlm.nih.gov/pubmed/22377349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2012-13-2-r15 |
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