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2.2.4 High-throughput sequencing High-throughput sequencing technology, also known as Next generation sequencing (NGS), it is often used to detect a large number of submicroscopic copy number variations (CNVs) in the human genome, including deletion, insertion, amplification, and inversion of single DNA fragments, and the most common is genomic microdeletion or microduplication

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Third, tumor heterogeneity means that different cancer types or even cells within the same tumor may vary in their dependence on GSH, making a single-target strategy insufficient

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