Cited by 4,971Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations

Finishing the euchromatic sequence of the human genome

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International Human Genome Sequencing Consortium·2004·Nature

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 approximately 99% of the euchromatic genome and is accurate to an error rate of approximately 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 genome 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.

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References 71 · Cited by 4,971

Authors
International Human Genome Sequencing Consortium
Corresponding author
International Human Genome Sequencing Consortium
Venue
Nature
Published
2004-10
Volume
431
Issue
7011
Pages
931-945
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2612812586
Cited by
4,971
References
71
Citations by year
2026: 82 · 2025: 128 · 2024: 148 · 2023: 177 · 2022: 180 · 2021: 206 · 2020: 252 · 2019: 209 · 2018: 222 · 2017: 233 · 2016: 215 · 2015: 249 · 2014: 231 · 2013: 278 · 2012: 274
FWCI
102.44
Type
journal article
Language
en
Open access
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
  • Civil War Book Review (submittedVersion)
  • HAL (submittedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
  • ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
  • Research Portal (King's College London) (submittedVersion)
  • ANU Open Research (Australian National University) (submittedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
  • UEA Digital Repository (University of East Anglia) (submittedVersion)
Funders
  • U.S. Department of Energy
  • Wellcome Trust
  • European Commission
  • Deutsche Forschungsgemeinschaft
  • Ministry of Education, Culture, Sports, Science and Technology
  • National Natural Science Foundation of China
  • Bundesministerium für Bildung und Forschung
  • Chinese Academy of Sciences
  • National Institutes of Health
  • Medical Research Council
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
Keywords
human genome sequence, genome finishing, genome assembly, sequence gaps, segmental duplication, gene number, gene birth and death
MeSH terms
Amino Acid Sequence, Base Sequence, Centromere, Chromosomes, Human, Genes, Multigene Family, Heterochromatin, Humans, Molecular Sequence Data, Plasmids, Pseudogenes, Research Design, Sensitivity and Specificity, Genome, Human, Human Genome Project, Telomere, Sequence Analysis, DNA, DNA, Complementary, Physical Chromosome Mapping, Gene Duplication, Euchromatin, Chromosomes, Artificial, Bacterial

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