CRISPR-Cas9 is the go-to technique for knocking out genes in human cell lines to discover what the genes do, but the efficiency with which it disables genes can vary immensely.
University of California, Berkeley researchers have now found a way to boost the efficiency with which CRISPR-Cas9 cuts and disables genes up to fivefold, in most types of human cells, making it easler to create and study knockout cell lines and, potentially, disable a mutant gene as a form of human therapy.
Scientists are constantly discovering new genes or the proteins they code for, but it's much harder to figure out their role in the body or in disease. Key to discovering this role is disabling the gene to see what happens when it's removed.