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Identification of Genetic Association of Multiple Rare Variants Using Collapsing Methods
Next-generation sequencing technology allows investigation of both common and rare variants in humans. Exomes are sequenced on the population level or in families to further study the genetics of human diseases. Genetic Analysis Workshop 17 (GAW17) provided exomic data from the 1000 Genomes Project...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3289287/ https://ncbi.nlm.nih.gov/pubmed/22128049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20658 |
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