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

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,...

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Autors principals:	Shuai Wu, Chenyu Ma, Jiawei Cai, Chenkang Yang, Xiaojia Liu, Chen Luo, Jingyi Yang, Zhang Xiong, Dandan Cao, Hong Chen
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2024-11-01
Col·lecció:	The Journal of Pathology: Clinical Research
Matèries:	CNV detection algorithm shallow whole genome sequencing (sWGS) glioma diagnoses clinical practice
Accés en línia:	https://doi.org/10.1002/2056-4538.70005
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