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Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma
BACKGROUND: In the clinical setting, workflows for analyzing individual genomics data should be both comprehensive and convenient for clinical interpretation. In an effort for comprehensiveness and practicality, we attempted to create a clinical individual whole exome sequencing (WES) analysis workf...
में बचाया:
| में प्रकाशित: | BMC Med Genomics |
|---|---|
| मुख्य लेखकों: | , , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2021
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7903763/ https://ncbi.nlm.nih.gov/pubmed/33622343 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-021-00904-3 |
| टैग : |
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