Joint genotype inference with germline and somatic mutations

The joint sequencing of related genomes has become an important means to discover rare variants. Normal-tumor genome pairs are routinely sequenced together to find somatic mutations and their associations with different cancers. Parental and sibling genomes reveal de novo germline mutations and inhe...

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Detalles Bibliográficos
Autores principales: Bareke, Eric, Saillour, Virginie, Spinella, Jean-François, Vidal, Ramon, Healy, Jasmine, Sinnett, Daniel, Csűrös, Miklós
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622648/
https://www.ncbi.nlm.nih.gov/pubmed/23734724
http://dx.doi.org/10.1186/1471-2105-14-S5-S3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622648/
https://www.ncbi.nlm.nih.gov/pubmed/23734724
http://dx.doi.org/10.1186/1471-2105-14-S5-S3

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