Your browser doesn't support javascript.
loading
Genome assembly in the telomere-to-telomere era.
Li, Heng; Durbin, Richard.
  • Li H; Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA. hli@ds.dfci.harvard.edu.
  • Durbin R; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. hli@ds.dfci.harvard.edu.
Nat Rev Genet ; 25(9): 658-670, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38649458
ABSTRACT
Genome sequences largely determine the biology and encode the history of an organism, and de novo assembly - the process of reconstructing the genome sequence of an organism from sequencing reads - has been a central problem in bioinformatics for four decades. Until recently, genomes were typically assembled into fragments of a few megabases at best, but now technological advances in long-read sequencing enable the near-complete assembly of each chromosome - also known as telomere-to-telomere assembly - for many organisms. Here, we review recent progress on assembly algorithms and protocols, with a focus on how to derive near-telomere-to-telomere assemblies. We also discuss the additional developments that will be required to resolve remaining assembly gaps and to assemble non-diploid genomes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Telómero Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Telómero Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article