Comprehensive variation discovery in single human genomes

Complete knowledge of the genetic variation in individual human genomes is a crucial foundation for understanding the etiology of disease. Genetic variation is typically characterized by sequencing individual genomes and comparing reads to a reference. Existing methods do an excellent job of detecti...

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Detalles Bibliográficos
Autores principales: Weisenfeld, Neil I., Yin, Shuangye, Sharpe, Ted, Lau, Bayo, Hegarty, Ryan, Holmes, Laurie, Sogoloff, Brian, Tabbaa, Diana, Williams, Louise, Russ, Carsten, Nusbaum, Chad, Lander, Eric S., MacCallum, Iain, Jaffe, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244235/
https://www.ncbi.nlm.nih.gov/pubmed/25326702
http://dx.doi.org/10.1038/ng.3121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244235/
https://www.ncbi.nlm.nih.gov/pubmed/25326702
http://dx.doi.org/10.1038/ng.3121

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