| Literature DB >> 35088059 |
Edith Heard1, Alexander D Johnson2, Jan O Korbel3, Charles Lee4, Michael P Snyder5, David Sturgill6.
Abstract
While the human genome represents the most accurate vertebrate reference assembly to date, it still contains numerous gaps, including centromeric and other large repeat-containing regions - often termed the "dark side" of the genome - many of which are of fundamental biological importance. Miga et al.1,2 present the first gapless assembly of the human X chromosome, with the help of ultra-long-read nanopore reads generated for the haploid complete hydatidiform mole (CHM13) genome. They reconstruct the ~3.1 megabase centromeric satellite DNA array and map DNA methylation patterns across complex tandem repeats and satellite arrays. This Telomere-to-Telomere assembly provides a superior human X chromosome reference enabling future sex-determination and X-linked disease research, and provides a path towards finishing the entire human genome sequence. Copyright:Entities:
Keywords: CpG islands; DNA methylation; High-coverage sequencing; Human X chromosome; Telomere
Year: 2021 PMID: 35088059 PMCID: PMC8753988 DOI: 10.12703/r-01-000001
Source DB: PubMed Journal: Fac Rev ISSN: 2732-432X