Explore the decades-long journey to map the full human genome, from early breakthroughs to the first complete, gapless DNA sequence.

Increased adoption of clinical whole-genome sequencing is advancing diagnostics for rare diseases, which affect 15 million American children SAN DIEGO, Feb. 27, 2026 /PRNewswire/ -- Illumina, Inc.

Newborn babies admitted to the hospital's neonatal intensive care unit (NICU) rely on the quick decisions and rapid action of the medical team responsible for them. DNA testing is critical to ...

Miami University’s Center for Bioinformatics and Functional Genomics (CBFG) has become one of the first institutions in the region to acquire the PacBio VEGA Benchtop System — a cutting-edge DNA ...

Inocras and the Broad Institute analyzed 8,000+ TCGA cancer genomes to uncover new drivers and create a harmonized dataset ...

Please provide your email address to receive an email when new articles are posted on . Researchers identified new sites in the placenta where genomic imprinting occurs. This could find previously ...

Advances in DNA sequencing technology help forensic biologists identify suspects where traditional DNA profiling has failed, ...

Pages Latest Report] According to a market research study published by Healthcare Foresights, the demand analysis of Global ...

Pioneering scientist J. Craig Venter has died at 79. His "whole genome shotgun method" helped genome sequencing become faster ...

A renowned DNA expert believes genome sequencing opens the door in the Nancy Guthrie case ...