Researchers have refined the famous CRISPR-Cas method. Now, for the very first time, it is possible to modify dozens, if not hundreds, of genes in a cell simultaneously.
Using AI, researchers have succeeded in making the mass analysis of proteins from any organism significantly faster than before and almost error-free.
Engineers have combined CRISPR with electronic transistors made from graphene to create a new hand-held device that can detect specific genetic mutations in a matter of minutes.
Researchers use the analogy of raindrops on the sidewalk to explain their new method to identify genetic variations that cause severe pediatric diseases.
Scientists plan to edit their genomes to correct rare genetic mutations and slow or halt progression of their diseases.
Research project is aimed at improving therapeutic options for both rare and common diseases, including supporting methods to improve editing the human genome.