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A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data
BACKGROUND: Since publication of the human genome in 2003, geneticists have been interested in risk variant associations to resolve the etiology of traits and complex diseases. The International HapMap Consortium undertook an effort to catalog all common variation across the genome (variants with a...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3277631/ https://ncbi.nlm.nih.gov/pubmed/22319179 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/amiajnl-2011-000652 |
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