Expansion in situ Genome Sequencing: A New Tool for Studying Nuclear Abnormalities
The investigation of nuclear anomalies and how they influence the regulation of genes warrants analysis of various cellular functions and diseases. The researchers from MIT, Harvard, and the University of California San Francisco describe a new approach, Expansion in situ Genome Sequencing (ExIGS), that allows, for the first time, to unravel the relationship between nuclear…
