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Validation of Customized Cancer Panel for Detecting Somatic Mutations and Copy Number Alterations
Accurate detection of genomic alterations, especially druggable hotspot mutations in tumors, has become an essential part of precision medicine. With targeted sequencing, we can obtain deeper coverage of reads and handle data more easily with a relatively lower cost and less time than whole-exome or...
Tallennettuna:
| Julkaisussa: | Genomics Inform |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Society of Gastrointestinal Intervention
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5769856/ https://ncbi.nlm.nih.gov/pubmed/29307139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2017.15.4.136 |
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