Scientists have compiled data from induced pluripotent stem cells to link genetic variants to many different diseases. Linking variants Researchers […]
Researchers have assembled 64 haplotypes from 32 diverse human genomes in order to serve as a new reference for genetic […]
The growing epidemic of “The Silent Liver Disease” Non-alcoholic fatty liver disease (NAFLD) is experiencing a meteoric rise globally. NAFLD […]
Advancements in technologies, including single cell and spatial transcriptomics, have provided us with a finer view of our complex biology […]
“A genetic counsellor is like air conditioning. When you do not have it, you do not realise you are missing […]
In this new age of genomic epidemiology, so-called “Microbe Hunters” are combining whole genome sequencing technology with epidemiological data. This […]
Pre-conception Expanded Carrier Screening is a technology that uses whole genome sequencing to screen prospective parents as potential carriers of […]
Researchers from Donnelly Centre for Cellular and Biomolecular Research at the University of Toronto, have mapped the genes that allow […]
Researchers at the Wellcome Sanger Institute, the University of Cambridge and the KEMRI-Wellcome Trust Research Programme, Kenya, have revealed for […]
As part of the 20th anniversary of Nature Reviews Genetics, Professor Ambroise Wonkam from the University of Cape Town has […]
