A clinically feasible algorithm for the parallel detection of glioma‐associated copy number variation markers based on shallow whole genome sequencing

• 主要な著者: Shuai Wu (著者), Chenyu Ma (著者), Jiawei Cai (著者), Chenkang Yang (著者), Xiaojia Liu (著者), Chen Luo (著者), Jingyi Yang (著者), Zhang Xiong (著者), Dandan Cao (著者), Hong Chen (著者)
• フォーマット: 図書
• 出版事項: Wiley, 2024-11-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Abstract Molecular features are incorporated into the integrated diagnostic system for adult diffuse gliomas. Of these, copy number variation (CNV) markers, including both arm‐level (1p/19q codeletion, +7/−10 signature) and gene‐level (EGFR gene amplification, CDKN2A/B homozygous deletion) changes,...