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Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches
BACKGROUND: When interpreting sequencing data from multiple spatial or longitudinal biopsies, detecting sample mix-ups is essential, yet more difficult than in studies of germline variation. In most genomic studies of tumors, genetic variation is detected through pairwise comparisons of the tumor an...
Autores principales: | Pedersen, Brent S., Bhetariya, Preetida J., Brown, Joe, Kravitz, Stephanie N., Marth, Gabor, Jensen, Randy L., Bronner, Mary P., Underhill, Hunter R., Quinlan, Aaron R. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362544/ https://www.ncbi.nlm.nih.gov/pubmed/32664994 http://dx.doi.org/10.1186/s13073-020-00761-2 |
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