It’s clear that CRISPR-Cas9 technology has really changed the game for anyone looking to quickly and easily manipulate specific genes. But what if you want to study genes all across the genome? Two new human lentiviral CRISPR library systems described in companion papers in Science in December were developed as an answer to that question. Additionally, a concurrent Nature Biotechnology article describes the development of a mouse lentiviral CRISPR library.
“This enables you to do customized genetic modification on a scale that was really not possible before,” said the Broad Institute's Ophir Shalem. “Whole regions of the genome which were not accessible before are now accessible using this technology.”