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

    A clinically feasible algorithm for the parallel detection of glioma‐associated copy number variation markers based on shallow whole genome sequencing by Shuai Wu, Chenyu Ma, Jiawei Cai, Chenkang Yang, Xiaojia Liu, Chen Luo, Jingyi Yang, Zhang Xiong, Dandan Cao, Hong Chen

    Published 2024-11-01
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