MERGE is a comprehensive artificial intelligence framework that integrates the most advanced unsupervised and self-supervised genomic foundation models. By avoiding clinical data circularity, MERGE provides robust and highly accurate pathogenicity predictions for coding, non-coding, and splice region variants.
Disclaimer
This tool is provided for basic academic research purposes only and must not be used for commercial purposes. Results are for reference only and do not constitute clinical diagnostic or medical advice. Users assume all responsibility for any use of the outputs.