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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...
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| 發表在: | BMC Genomics |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5657037/ https://ncbi.nlm.nih.gov/pubmed/29513195 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-4134-3 |
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