Germline contamination and leakage in whole genome somatic single nucleotide variant detection

BACKGROUND: The clinical sequencing of cancer genomes to personalize therapy is becoming routine across the world. However, concerns over patient re-identification from these data lead to questions about how tightly access should be controlled. It is not thought to be possible to re-identify patient...

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Vydáno v:BMC Bioinformatics
Hlavní autoři: Sendorek, Dorota H., Caloian, Cristian, Ellrott, Kyle, Bare, J. Christopher, Yamaguchi, Takafumi N., Ewing, Adam D., Houlahan, Kathleen E., Norman, Thea C., Margolin, Adam A., Stuart, Joshua M., Boutros, Paul C.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2018
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5793408/
https://ncbi.nlm.nih.gov/pubmed/29385983
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2046-0
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