Improving somatic variant identification through integration of genome and exome data

BACKGROUND: Cost-effective high-throughput sequencing technologies, together with efficient mapping and variant calling tools, have made it possible to identify somatic variants for cancer study. However, integrating somatic variants from whole exome and whole genome studies poses a challenge to res...

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Detalles Bibliográficos
Autores principales: Vijayan, Vinaya, Yiu, Siu-Ming, Zhang, Liqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657037/
https://www.ncbi.nlm.nih.gov/pubmed/29513195
http://dx.doi.org/10.1186/s12864-017-4134-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657037/
https://www.ncbi.nlm.nih.gov/pubmed/29513195
http://dx.doi.org/10.1186/s12864-017-4134-3

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