Impact of DNA source on genetic variant detection from human whole-genome sequencing data

BACKGROUND: Whole blood is currently the most common DNA source for whole-genome sequencing (WGS), but for studies requiring non-invasive collection, self-collection, greater sample stability or additional tissue references, saliva or buccal samples may be preferred. However, the relative quality of...

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Detalles Bibliográficos
Autores principales: Trost, Brett, Walker, Susan, Haider, Syed A, Sung, Wilson W L, Pereira, Sergio, Phillips, Charly L, Higginbotham, Edward J, Strug, Lisa J, Nguyen, Charlotte, Raajkumar, Akshaya, Szego, Michael J, Marshall, Christian R, Scherer, Stephen W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929712/
https://www.ncbi.nlm.nih.gov/pubmed/31515274
http://dx.doi.org/10.1136/jmedgenet-2019-106281

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929712/
https://www.ncbi.nlm.nih.gov/pubmed/31515274
http://dx.doi.org/10.1136/jmedgenet-2019-106281

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