| Literature DB >> 35212372 |
Yiwei Niu1,2, Xueyi Teng1,3, Honghong Zhou1, Yirong Shi1,3, Yanyan Li1,2, Yiheng Tang1,3, Peng Zhang1, Huaxia Luo1, Quan Kang1, Tao Xu2,4, Shunmin He1,2.
Abstract
Mobile element insertions (MEIs) are a major class of structural variants (SVs) and have been linked to many human genetic disorders, including hemophilia, neurofibromatosis, and various cancers. However, human MEI resources from large-scale genome sequencing are still lacking compared to those for SNPs and SVs. Here, we report a comprehensive map of 36 699 non-reference MEIs constructed from 5675 genomes, comprising 2998 Chinese samples (∼26.2×, NyuWa) and 2677 samples from the 1000 Genomes Project (∼7.4×, 1KGP). We discovered that LINE-1 insertions were highly enriched in centromere regions, implying the role of chromosome context in retroelement insertion. After functional annotation, we estimated that MEIs are responsible for about 9.3% of all protein-truncating events per genome. Finally, we built a companion database named HMEID for public use. This resource represents the latest and largest genomewide study on MEIs and will have broad utility for exploration of human MEI findings.Entities:
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Year: 2022 PMID: 35212372 PMCID: PMC8934628 DOI: 10.1093/nar/gkac128
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971