Decoding the Impact of Mutations: Interface-Guided Phenotyping of RUNX1 Transcription Factor Reveals New Insights
Researchers from the University of California deploy SEUSS (scalable functional screening by sequencing), a perturb-seq method, to analyze single-gene missense mutations, which have been notoriously difficult to interpret. The study focused on mutations in the RUNX1 gene, which is associated with myelogenous leukemia. Using SEUSS, the team evaluated 115 mutations and categorized them into three…
