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Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers
BACKGROUND: Next-generation sequencing of matched tumor and normal biopsy pairs has become a technology of paramount importance for precision cancer treatment. Sequencing costs have dropped tremendously, allowing the sequencing of the whole exome of tumors for just a fraction of the total treatment...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5209852/ https://ncbi.nlm.nih.gov/pubmed/28049408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-1417-7 |
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