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Comparative Annotation Toolkit (CAT)-simultaneous clade and personal genome annotation.
Fiddes, Ian T; Armstrong, Joel; Diekhans, Mark; Nachtweide, Stefanie; Kronenberg, Zev N; Underwood, Jason G; Gordon, David; Earl, Dent; Keane, Thomas; Eichler, Evan E; Haussler, David; Stanke, Mario; Paten, Benedict.
Afiliação
  • Fiddes IT; Genomics Institute, University of California Santa Cruz and Howard Hughes Medical Institute, Santa Cruz, California 95064, USA.
  • Armstrong J; 10x Genomics, Pleasanton, California 94566, USA.
  • Diekhans M; Genomics Institute, University of California Santa Cruz and Howard Hughes Medical Institute, Santa Cruz, California 95064, USA.
  • Nachtweide S; Genomics Institute, University of California Santa Cruz and Howard Hughes Medical Institute, Santa Cruz, California 95064, USA.
  • Kronenberg ZN; Institute of Mathematics and Computer Science, University of Greifswald, 17489 Greifswald, Germany.
  • Underwood JG; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
  • Gordon D; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
  • Earl D; Pacific Biosciences of California, Incorporated, Menlo Park, California 94025, USA.
  • Keane T; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
  • Eichler EE; Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195, USA.
  • Haussler D; Genomics Institute, University of California Santa Cruz and Howard Hughes Medical Institute, Santa Cruz, California 95064, USA.
  • Stanke M; European Bioinformatics Institute, Wellcome Genome Campus, Hinxton CB10 1SD, United Kingdom.
  • Paten B; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Genome Res ; 28(7): 1029-1038, 2018 07.
Article em En | MEDLINE | ID: mdl-29884752
ABSTRACT
The recent introductions of low-cost, long-read, and read-cloud sequencing technologies coupled with intense efforts to develop efficient algorithms have made affordable, high-quality de novo sequence assembly a realistic proposition. The result is an explosion of new, ultracontiguous genome assemblies. To compare these genomes, we need robust methods for genome annotation. We describe the fully open source Comparative Annotation Toolkit (CAT), which provides a flexible way to simultaneously annotate entire clades and identify orthology relationships. We show that CAT can be used to improve annotations on the rat genome, annotate the great apes, annotate a diverse set of mammals, and annotate personal, diploid human genomes. We demonstrate the resulting discovery of novel genes, isoforms, and structural variants-even in genomes as well studied as rat and the great apes-and how these annotations improve cross-species RNA expression experiments.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article