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Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing
BACKGROUND: Rare genetic variation in the human population is a major source of pathophysiological variability and has been implicated in a host of complex phenotypes and diseases. Finding disease-related genes harboring disparate functional rare variants requires sequencing of many individuals acro...
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| Autori principali: | , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3534616/ https://ncbi.nlm.nih.gov/pubmed/23216810 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-683 |
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