Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform

Despite the ever-increasing throughput and steadily decreasing cost of next generation sequencing (NGS), whole genome sequencing of humans is still not a viable option for the majority of genetics laboratories. This is particularly true in the case of complex disease studies, where large sample sets...

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Detalles Bibliográficos
Autores principales: Hedges, Dale J., Guettouche, Toumy, Yang, Shan, Bademci, Guney, Diaz, Ashley, Andersen, Ashley, Hulme, William F., Linker, Sara, Mehta, Arpit, Edwards, Yvonne J. K., Beecham, Gary W., Martin, Eden R., Pericak-Vance, Margaret A., Zuchner, Stephan, Vance, Jeffery M., Gilbert, John R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084696/
https://www.ncbi.nlm.nih.gov/pubmed/21559511
http://dx.doi.org/10.1371/journal.pone.0018595

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