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

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

As questions surrounding paternity fraud and DNA disputes gain prominence, experts maintain that despite the introduction of Next Generation Sequencing [NGS] Capillary Electrophoresis [CE] precision, ...

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

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

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

Roche has put forward a new approach to genetic analysis, which it describes as sequencing-by-expansion—a proprietary method that pulls apart the DNA molecule and amplifies the signal of each ...

The findings show that disease-causing mutations were found in around 2% of the sperm from men in their early 30s, increasing ...

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

Researchers at the University of Toronto have invented a new method that uses DNA sequencing to measure metabolites. This enables rapid and precise analysis of biological compounds, such as sugars, ...

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 ...

A team led by the Wellcome Sanger Institute, in collaboration with the TwinsUK study at King’s College London, has refined nanorate sequencing (NanoSeq) a method allowing scientists to study genetic ...