Cargando…
A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysis
Existing cancer benchmark data sets for human sequencing data use germline variants, synthetic methods, or expensive validations, none of which are satisfactory for providing a large collection of true somatic variation across a whole genome. Here we propose a data set, Lineage derived Somatic Truth...
Autores principales: | Shand, Megan, Soto, Jose, Lichtenstein, Lee, Benjamin, David, Farjoun, Yossi, Brody, Yehuda, Maruvka, Yosef, Blainey, Paul C., Banks, Eric |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722876/ https://www.ncbi.nlm.nih.gov/pubmed/33293579 http://dx.doi.org/10.1038/s42003-020-01460-9 |
Ejemplares similares
-
Quantification of somatic mutation flow across individual cell division events by lineage sequencing
por: Brody, Yehuda, et al.
Publicado: (2018) -
A synthetic-diploid benchmark for accurate variant calling evaluation
por: Li, Heng, et al.
Publicado: (2018) -
Somatic Markers, Rhetoric, and Post-truth
por: Muñoz, José M.
Publicado: (2017) -
Case report on trial: Do you, Doctor, swear to tell the truth, the whole truth and nothing but the truth?
por: Yitschaky, Oded, et al.
Publicado: (2011) -
Recommendations for open data science
por: Gymrek, Melissa, et al.
Publicado: (2016)