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Deep learning algorithm used to pinpoint potential disease-causing variants in non-coding regions of the human genome. ScienceDaily . Retrieved July 24, 2025 from www.sciencedaily.com / releases ...
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Researchers use algorithm to pinpoint disease risk mutations in ...Researchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of Pennsylvania (Penn Medicine) have successfully employed an algorithm to ...
Journal reference: Dudek, M. F., et al. (2025). Characterization of non-coding variants associated with transcription-factor binding through ATAC-seq-defined footprint QTLs in liver.
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