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Improving somatic variant identification through integration of genome and exome data
BACKGROUND: Cost-effective high-throughput sequencing technologies, together with efficient mapping and variant calling tools, have made it possible to identify somatic variants for cancer study. However, integrating somatic variants from whole exome and whole genome studies poses a challenge to res...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657037/ https://www.ncbi.nlm.nih.gov/pubmed/29513195 http://dx.doi.org/10.1186/s12864-017-4134-3 |