Scientists using TwinsUK data and ultra‑precise DNA sequencing have uncovered rare DNA mutations in healthy tissue that could ...

The global next generation sequencing (NGS) market is expected to register a robust CAGR of around 15% over the next five years. This growth is primarily driven by the rising adoption of precision ...

Researchers at UW’s School of Medicine and the Institute for Research in Biomedicine Barcelona may have found an additional ...

Roche’s SBX sequencing achieved a world record for the fastest human genome analysis and is driving breakthroughs in ...

This insightful review explores key areas of cancer genetic research, focusing on genes that may benefit from ...

New research using data from the TwinsUK cohort has helped reveal how naturally occurring DNA mutations in healthy tissue may ...

Every time a doctor orders a CT scan, or a child receives a lifesaving vaccine, or your phone’s GPS corrects itself by the ...

ETH Zurich scientists have created “MetaGraph,” a revolutionary DNA search engine that functions like Google for genetic data. By compressing global genomic datasets by a factor of 300, it allows ...

Standard laboratory tests can fail to detect many disease-causing DNA changes. Now, a novel 3D chromosome mapping method can ...

Decades of research has viewed DNA as a sequence-based instruction manual; yet every cell in the body shares the same genes – so where is the language that writes the memory of cell identities?

Objective: To describe the joint manifestations associated with clonal haematopoiesis and to compare patients with and ...

Researchers have developed a new technique for tagging senescent cells with DNA aptamers to identify and characterize these ...