Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

Abstract 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) analys...

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Bibliographic Details
Main Authors: Ege Ülgen, Özge Can, Kaya Bilguvar, Cemaliye Akyerli Boylu, Şirin Kılıçturgay Yüksel, Ayça Erşen Danyeli, O. Uğur Sezerman, M. Cengiz Yakıcıer, M. Necmettin Pamir, Koray Özduman
Format: Article
Language:English
Published: BMC 2021-02-01
Series:BMC Medical Genomics
Subjects:
Whole exome sequencing
NGS
Glioma
Brain tumor
Clinical analysis
Online Access:https://doi.org/10.1186/s12920-021-00904-3

Internet

https://doi.org/10.1186/s12920-021-00904-3

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