A framework for the detection of de novo mutations in family-based sequencing data

Germline mutation detection from human DNA sequence data is challenging due to the rarity of such events relative to the intrinsic error rates of sequencing technologies and the uneven coverage across the genome. We developed PhaseByTransmission (PBT) to identify de novo single nucleotide variants a...

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Detalles Bibliográficos
Autores principales: Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, Daly, Mark J, Banks, Eric, DePristo, Mark A, de Bakker, Paul IW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255947/
https://www.ncbi.nlm.nih.gov/pubmed/27876817
http://dx.doi.org/10.1038/ejhg.2016.147

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255947/
https://www.ncbi.nlm.nih.gov/pubmed/27876817
http://dx.doi.org/10.1038/ejhg.2016.147

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