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...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Med Genomics
Egile Nagusiak: Ülgen, Ege, Can, Özge, Bilguvar, Kaya, Akyerli Boylu, Cemaliye, Kılıçturgay Yüksel, Şirin, Erşen Danyeli, Ayça, Sezerman, O. Uğur, Yakıcıer, M. Cengiz, Pamir, M. Necmettin, Özduman, Koray
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2021
Gaiak:
Research Article
Sarrera elektronikoa: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
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