News

An international team of scientists together with the University of Bonn Hospital have taken a new path in the research into causes of epilepsy: The researchers determined the networks of the active genes and, like a dragnet, looked for the "main perpetrators" using a computer model.

Researchers at the University of East Anglia are developing a simple blood test to diagnose bone cancer thanks to funding from the Big C.

Sequenom to apply Cypher's Mantis technology for advanced genome interpretation in NIPT.

European consortium will use 3D liver tissues to better predict drug-induced liver injury.

A research article published in Science presents the first major analysis based on the Human Protein Atlas, including a detailed picture of the proteins that are linked to cancer, the number of proteins present in the bloodstream, and the targets for all approved drugs on the market.

A single gene that coordinates a network of about 400 genes involved in epilepsy could be a target for new treatments, according to research.

Researchers used a genetic technique called whole-exome sequencing to examine tumour samples.

Study tested the potential of denoising autoencoders to identify and extract complex patterns from genomic data.

Culturing of mini-guts from single mouse intestine stem cells.

The identity of eight common mutations may one day reveal more about Alzheimer’s, autism and other neurological disorders.