Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection

Despite declining sequencing costs, few methods are available for cost-effective single-nucleotide polymorphism (SNP), insertion/deletion (INDEL) and copy number variation (CNV) discovery in a single assay. Commercially available methods require a high investment to a specific region and are only co...

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Detalles Bibliográficos
Autores principales: Alvarado, David M., Yang, Ping, Druley, Todd E., Lovett, Michael, Gurnett, Christina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041413/
https://www.ncbi.nlm.nih.gov/pubmed/24682816
http://dx.doi.org/10.1093/nar/gku218

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041413/
https://www.ncbi.nlm.nih.gov/pubmed/24682816
http://dx.doi.org/10.1093/nar/gku218

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