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A Robust GWSS Method to Simultaneously Detect Rare and Common Variants for Complex Disease
The rapid advances in sequencing technologies and the resulting next-generation sequencing data provide the opportunity to detect disease-associated variants with a better solution, in particular for low-frequency variants. Although both common and rare variants might exert their independent effects...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399906/ https://www.ncbi.nlm.nih.gov/pubmed/25880329 http://dx.doi.org/10.1371/journal.pone.0120873 |