Human Genome Project Completion
Genetics & Genomics
2003
Featured
Discoverers: Francis Collins, Craig Venter
Overview
The full sequencing of the approximately 3 billion base pairs of the human genome, identifying around 20,500 protein-coding genes.
Significance
Provided a reference map of the entire human genetic blueprint, transforming biomedical research, diagnostics, and personalised medicine.
Methodology
Combination of hierarchical shotgun sequencing by the public consortium and whole-genome shotgun sequencing by Celera Genomics, with computational assembly.
Impact
- Accelerated gene discovery for thousands of diseases
- Enabled pharmacogenomics and precision medicine
- Drove down DNA sequencing costs by six orders of magnitude