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Identification of rare alleles and their carriers using compressed se(que)nsing
Identification of rare variants by resequencing is important both for detecting novel variations and for screening individuals for known disease alleles. New technologies enable low-cost resequencing of target regions, although it is still prohibitive to test more than a few individuals. We propose...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965256/ https://www.ncbi.nlm.nih.gov/pubmed/20699269 http://dx.doi.org/10.1093/nar/gkq675 |