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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
ROS-scavenging, Oxygen Nitric Oxide-generating Prop, Biomater 286:121597
Biogerontology, R
[PubMed] [Google Scholar] 33.Li M, Cheung BM
