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

• Main Authors: Ege Ülgen (Author), Özge Can (Author), Kaya Bilguvar (Author), Cemaliye Akyerli Boylu (Author), Şirin Kılıçturgay Yüksel (Author), Ayça Erşen Danyeli (Author), O. Uğur Sezerman (Author), M. Cengiz Yakıcıer (Author), M. Necmettin Pamir (Author), Koray Özduman (Author)
• Format: Book
• Published: BMC, 2021-02-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...