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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...
| Autores principales: | , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793408/ https://www.ncbi.nlm.nih.gov/pubmed/29385983 http://dx.doi.org/10.1186/s12859-018-2046-0 |