Clinical genome sequencing now delivers genetic diagnoses for about 1 in 4 suspected rare disease patients, guiding targeted ...

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

This illustration demonstrates how metapipeline-DNA processes raw genome sequencing data. It begins by aligning the sequence of DNA base pairs to a reference genome. Then produces sets of detected ...

The first human genome sequencing took 13 years and cost $3 billion. It can now be done in a matter of days, but drawing meaningful conclusions from millions of points of data is cumbersome. However, ...

Explore how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale.

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 ...

Dayhoff Health and AMD publish a joint white paper documenting up to 330× faster microbiome processing, 13–22× faster ...

What is Third-Generation Sequencing? Third-generation sequencing, also known as long-read sequencing, refers to the latest advancements in DNA sequencing technologies that enable the analysis of ...

Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative ...

In a way, sequencing DNA is very simple: There's a molecule, you look at it, and you write down what you find. You'd think it would be easy—and, for any one letter in the sequence, it is. The problem ...