Digenic variant interpretation with hypothesis-driven explainable AI
The digenic inheritance hypothesis holds the potential to enhance diagnostic yield in rare diseases. Computational approaches capable of accurately interpreting and prioritizing digenic combinations of variants based on the proband's phenotypes and family information can provide valuable assistance during the diagnostic process. We developed diVas, a hypothesis-driven machine learning approach that interprets genomic variants across different gene pairs. DiVas demonstrates strong performance in both classifying and prioritizing causative digenic combinations of rare variants within the top positions across 11 cases with the complete list of variants available (73% sensitivity and a median ranking of 3). Furthermore, it achieves a sensitivity of 0.81 when applied to 645 published causative digenic combinations. Additionally, diVas leverages explainable artificial intelligence to elucidate the digenic disease mechanism for predicted positive pairs.
Authors
- Andrea Gazzo (ORCID: https://orcid.org/0009-0009-9282-4667)
- Giovanna Nicora (ORCID: https://orcid.org/0000-0001-7007-0862)
- Ettore Rizzo (ORCID: https://orcid.org/0000-0003-1631-9000)
- Riccardo Bellazzi (ORCID: https://orcid.org/0000-0002-6974-9808)
- Federica De Paoli (ORCID: https://orcid.org/0000-0002-8027-5666)
- Susanna Zucca (ORCID: https://orcid.org/0000-0001-8465-632X)
- Ivan Limongelli (ORCID: https://orcid.org/0000-0002-9781-2974)
- Paolo Magni (ORCID: https://orcid.org/0000-0002-8931-4676)
- Silvia Berardelli (ORCID: https://orcid.org/0009-0009-5468-1466)
Institutions
- Memorial Sloan Kettering Cancer Center (US)
- University of Pavia (IT)
Publication Details
- Journal
- NAR Genomics and Bioinformatics
- Published
- 2025-03-29
- DOI
- https://doi.org/10.1093/nargab/lqaf029
- Citations
- 1
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.82