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Finishing the euchromatic sequence of the human genome

  • International Human Genome Sequencing Consortium
  • Wellcome Trust Genome Campus
  • BGI-Shenzhen
  • United States Department of Energy
  • Computational Earth Science, Earth and Environmental Sciences Division, Los Alamos National Laboratory
  • Whitehead Institute
  • Broad Institute
  • Washington University St. Louis
  • LBL
  • Chem./Materials Science Directorate
  • Stanford University
  • Case Western Reserve University
  • University of Washington
  • Baylor College of Medicine
  • RIKEN
  • Genoscope and CNRS UMR-8030
  • Keio University
  • Setsunan University
  • Kyorin University
  • University of Geneva
  • Oscient Pharmaceuticals Corporation
  • Danaher Corporation
  • Institute for Systems Biology
  • Leibniz Institute on Aging - Fritz Lipmann Institute
  • Chinese Academy of Sciences
  • Wenzhou Medical University
  • Aarhus University
  • Chinese National Human Genome Center
  • Southern National Genome Center
  • High School Affiliated to Renmin University of China
  • Southeast University, Nanjing
  • Xi'an Jiaotong University
  • University of Communication
  • Hebei Medical University
  • Peking University
  • Provincial Health Services Authority
  • CAS - Institute of Microbiology
  • Max Planck Institute for Molecular Genetics
  • Helmholtz Centre for Infection Research
  • PerkinElmer, Inc.
  • Vita Genomics Inc.
  • University of California at Santa Cruz
  • National Institutes of Health
  • University of Oxford
  • Wistar Institute

Research output: Contribution to journal › Article › peer-review

4052 Scopus citations

Abstract

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead.

Original languageEnglish
Pages (from-to)931-945
Number of pages15
JournalNature
Volume431
Issue number7011
DOIs
StatePublished - 21 Oct 2004

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