There is a genetic feature known as a repeat expansion, in which short sequences are repeated continuously. Some of them ...

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 ...

The collection of high-quality genomic DNA remains a major barrier in pediatric and neurodevelopmental research, particularly ...

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St. Jude Children's Research Hospital. Significant amounts of time and resources ...

The completion of a South American lung fish genome sequencing represents one of the most remarkable moments within current genetic research. Because .

CHANGE-seq-BE was developed to enable scientists to better understand base editors, an important class of CRISPR precise genome editors.

A new study indicates that noninvasive prenatal screening (NIPS) performed using a low-cost form of whole genome sequencing can detect the risk in pregnant mothers of transmitting cytomegalovirus (CMV ...

Management of mitochondrial-related heart disease relies on multidisciplinary care and symptom control, as targeted gene-editing therapies are limited.

One-step Library Prep Workflow Designed to Address the Scalability, Performance, and Affordability Needs of Applied ...