A Clinically Feasible Algorithm for the Parallel Detection of Glioma-Associated Copy Number Variation Markers Based on Shallow Whole Genome Sequencing

Shuai Wu, Chenyu Ma,Jiawei Cai, Chenkang Yang,Xiaojia Liu,Chen Luo, Jingyi Yang, Zhang Xiong,Dandan Cao, Hong Chen

JOURNAL OF PATHOLOGY CLINICAL RESEARCH（2024）

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Key words

CNV detection algorithm,shallow whole genome sequencing (sWGS),glioma diagnoses,clinical practice

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