Thirty years on from the launch of the Human Genome Project, Richard Gibbs reflects on the promises that this voyage of discovery bore. Its success should be measured by how this project transformed the rules of research, the way of practising biological discovery and the ubiquitous digitization of biological science.
The author
Richard Gibbs, AC, PhD is a human geneticist and the Founding Director of the Baylor College of Medicine Human Genome Sequencing Center (HGSC). He graduated from the University of Melbourne in Genetics and Radiation Biology and moved to Houston, TX, to study the molecular basis of genetic disease. He developed basic methods for DNA and mutation analysis and was an early contributor to the Human Genome Project (HGP), leading one of five sites that generated the majority of the sequence. Since the completion of the HGP, he has led multiple genome projects including the generation of the first personalized whole-genome diploid human sequences. His group pioneered the oligonucleotide exon-capture methods that are widely used today for whole-exome sequencing, and he is currently leading programmes for translation of genomic data into the clinic.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Establishing genome sequencing and assembly for non-model and emerging model organisms: a brief guide
Frontiers in Zoology Open Access 17 April 2025
-
A roadmap to precision medicine through post-genomic electronic medical records
Nature Communications Open Access 17 February 2025
-
The conjugation-associated linear-BAC iterative assembling (CALBIA) method for cloning 2.1-Mb human chromosomal DNAs in bacteria
Cell Research Open Access 06 January 2025
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
27,99 € / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
209,00 € per year
only 17,42 € per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Lander, E. S. et al. Initial sequencing and analysis of the human genome. Nature 409, 860–921 (2001).
Venter, J. C. et al. The sequence of the human genome. Science 291, 1304–1351 (2001).
Cook-Deegan, R. M. The Gene Wars: Science, Politics, and the Human Genome (W.W. Norton & Company, 1994).
Friedland, S. I. The criminal law implications of the Human Genome Project: reimagining a genetically oriented criminal justice system. KY Law J. 86, 303–366 (1997).
Marshall, E. Bermuda rules: community spirit, with teeth. Science 291, 1192 (2001).
Rommens, J. M. et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 245, 1059–1065 (1989).
Dash, D. & Mestre, T. A. Therapeutic update on Huntington’s disease: symptomatic treatments and emerging disease-modifying therapies. Neurotherapeutics https://doi.org/10.1007/s13311-020-00891-w (2020).
King, M.-C. “The race” to clone BRCA1. Science 343, 1462–1465 (2014).
Gibbs, R. A. et al. The International HapMap Project. Nature 426, 789–796 (2003).
Durbin, R. et al. A map of human genome variation from population-scale sequencing. Nature 467, 1061–1073 (2010).
Acknowledgements
R.A.G. is partially supported by grants from the National Human Genome Research Institute.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The author declares no competing interests.
Rights and permissions
About this article
Cite this article
Gibbs, R.A. The Human Genome Project changed everything. Nat Rev Genet 21, 575–576 (2020). https://doi.org/10.1038/s41576-020-0275-3
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41576-020-0275-3
This article is cited by
-
Establishing genome sequencing and assembly for non-model and emerging model organisms: a brief guide
Frontiers in Zoology (2025)
-
The conjugation-associated linear-BAC iterative assembling (CALBIA) method for cloning 2.1-Mb human chromosomal DNAs in bacteria
Cell Research (2025)
-
A roadmap to precision medicine through post-genomic electronic medical records
Nature Communications (2025)
-
PVGwfa: a multi-level parallel sequence-to-graph alignment algorithm
The Journal of Supercomputing (2025)
-
Overcoming barriers to single-cell RNA sequencing adoption in low- and middle-income countries
European Journal of Human Genetics (2024)