A world-first scientific study has shown that whole-genome sequencing (WGS) improves diagnosis of rare diseases and shortens diagnostic journeys for […]
Whole-genome sequencing (WGS) shows promise as a first-line genetic test for acutely ill infants. However, before wide-spread adoption and implementation, […]
The genetic basis for schizophrenia has long been studied since the first major study was released over 70 years ago, […]
With the falling cost of genome sequencing, it comes as no surprise that there is a growing interest in expanding the availability and accessibility of genomics via consumer testing. Now, Nebula Genomics has entered the market by launching a comprehensive at-home test that analyses the whole genome for just $299.
Sinan Yavuz, Senior Bioinformatics Scientist from Seven Bridges spoke at the Festival of Genomics 2020
Genomics England have partnered with the NHS to implement the Newborn Genomes Programme. Whole genome sequencing (WGS) will be used […]
Genomics has the ability to transform our understanding of cancer, providing researchers with increasingly complex information on tumour heterogeneity and […]
New research, led by scientists at The Institute of Cancer Research, the Human Technopole in Milan, and Queen Mary University […]
After taking things digital for the past 2 years, the UK’s largest genomics event is back – and back to […]
