A new bioinformatics tool, MHcut reveals that a natural repair system for DNA damage, microhomology-mediated end joining, is probably far more common in humans than originally assumed. Using MHcut and commercial genome-editing technology, the researchers created mutations in iPS cells with extraordinary precision to model diseases without the need of patient samples. The tool is expected to make it easier to study diseases even when patients are rare or unavailable.
Transforming DNA repair errors into assets
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