What if you could harness the power of everything that makes you biologically you—your sex, ancestry, genetic minutiae—to help accelerate drug discovery and prevent and cure diseases? The health care ...

Scientists first read the human genome, a three-billion-letter biological book, in April 2003. Since then, researchers have steadily advanced the ability to write DNA, moving far beyond single-gene ...

The ability to sequence and edit human DNA has revolutionized biomedicine. Now a new consortium wants to take the next step and build human genomes from scratch. The Human Genome Project was one of ...

The holidays bring out the wishful thinker in all of us. Some of us pine for that car that folds up into a suitcase. Others hope for something more eco-friendly, like a matter transporter. A few ...

In its effort to correlate genomic structure with gene function, the 4D Nucleome Consortium (4DN), led by Job Dekker, Ph.D., ...

NIH funding has allowed scientists to see the DNA blueprints of human life—completely. In 2022, the Telomere-to-Telomere Consortium, a group of NIH-funded scientists from research institutions around ...

July 2025 will mark the 25th anniversary of the UC Santa Cruz Genome Browser, one of the most widely used resources for genomics worldwide. Originally built to allow researchers to explore a single ...

New analysis of the 1000 Genomes sample set yields brand new insights, providing a more complete view of human genetic variation than ever before. Completed in 2003, the Human Genome Project gave us ...

The UC Santa Cruz Genomics Institute has received a $2 million grant from the W. M. Keck Foundation for ongoing research to develop a comprehensive map of human genetic variation. The Human Genome ...

In January 2025, the government of India announced the completion of the GenomeIndia Project, which entailed sequencing the genomes of 10,000 Indians across 83 communities. The project, launched in ...

The GoE project was initiated in response to the rapidly growing use of genetic data in research and clinical applications, and the lack of a whole genome sequence (WGS) reference dataset for Europe.