Foundation models, data platforms, tools, and publications for multimodal AI research in Type 1 Diabetes — all in one place.
MAI-T1D is a five-institution project building multimodal AI foundation models for type 1 diabetes, trained and benchmarked across genomics, single-cell, spatial, and immunological data from existing T1D resources to comprehensively characterize disease progression. We also study the ethical side of this work — participation leakage, content leakage, and safeguards such as split learning for private whole-genome sequencing data. See the publications below.
This hub hosts the consortium's public output: the models, the data platforms behind them, the governance tooling that tracks how training data evolves, and the publications. Everything is openly available or points to the access process for controlled data.
This work used resources developed by the MAI-T1D consortium, supported by the National Institutes of Health Office of Data Science Strategy through the Advancing Health Research through Multimodal AI program under award OT2OD038003.
Predicts epigenomic profiles and chromatin organization from DNA sequences. Core genomic FM of the MAI-T1D foundation stack.
Foundation model for single-cell transcriptomics and epigenomics analysis. Supports cell-type annotation, gene program discovery, and perturbation prediction.
Foundation model for spatial transcriptomics. Models tissue architecture and cell–cell interactions in pancreatic islet microenvironments.
Vision–omics foundation model that predicts single-cell gene expression directly from H&E morphology, trained contrastively on 23M cells paired with Xenium data. Combines direct regression with retrieval from reference cells, weighted per gene.
PubMed-integrated knowledge platform with ML-enhanced search, agentic Q&A in biomedicine, and AI-driven hypothesis generation.
Curated, AI-ready datasets derived from the Human Pancreas Analysis Program — preprocessed and standardized for direct use in MAI-T1D foundation model training and benchmarking.
Training and evaluation data behind the Genomics Foundation Model (EPCOT v2), which predicts cell-type- and context-specific regulatory signals from ATAC-seq data and DNA sequences.
Showcased applications and end-to-end workflows demonstrating how MAI-T1D models and data platforms can be applied to real-world T1D research questions.
Central GitHub repository that integrates the genomics, single-cell, spatial transcriptomics, and spatial omics foundation models into one pipeline for T1D research.
PROV-inspired knowledge graph for automated governance of evolving multimodal AI training data across the MAI-T1D consortium. Interactive demo with provenance graph, impact analysis, and governance agent views.
Participation leakage — whether an individual's presence in the training data can be inferred from a trained model. We audit MAI-T1D models for this risk and quantify how much it grows as modalities are combined.
Content leakage — whether original training records can be reconstructed out of a trained model. We test how much of a donor's multimodal record a model memorizes, and what limits that memorization.
A safeguard rather than a risk — the model is partitioned across sites so private whole-genome sequencing data stays protected during training. Quantized-TinyLLaVA compresses the intermediate features exchanged between partitions, cutting communication ~87.5% at 2-bit.
Consortium work on type 1 diabetes data, biomedical models, and the platforms listed on this hub.
Aligns cell-centered H&E morphology with single-cell expression embeddings by contrastive learning over 23M cells, then predicts expression through a direct-regression branch and a retrieval branch fused with per-gene weights — generalizing to held-out patients, slides, and partially overlapping Xenium panels.
Optimal-transport integration method that aligns scRNA-seq with spatial proteomics even when features link weakly and cell populations are imbalanced, enabling cross-modal imputation for multimodal foundation models.
Multi-task genomic model (EPCOT) that takes ATAC-seq and DNA sequence as input and predicts nascent RNA, high-resolution chromatin organization, and non-coding variant effects across human and mouse.
GLKB is a knowledge graph of 14.6M relationships over 3.2M entities drawn from 33M PubMed abstracts; the paired agent lifts eight state-of-the-art LLMs by up to 27.5% on PubMedQA.
Builds a local knowledge graph from retrieved documents using propositional claims, then layerwise-summarizes it to contextualize a small language model — matching or beating RAG baselines on biomedical QA.
Prompt-based phenotype concept recognition that generalizes to new ontologies and unseen text without ontology-specific training, with an optional self-supervised boost.
Quantizes the intermediate features exchanged between split-learning partitions into discrete codes, cutting communication overhead ~87.5% at 2-bit while matching the 16-bit model across five benchmarks.
Builds the UMLS-derived Medical Knowledge Judgment Dataset to isolate factual medical recall from multi-hop reasoning, exposing weak recall on rare conditions and poor calibration.
Machine-learning methods work by MAI-T1D investigators. These papers are not T1D-specific, but the techniques feed the models and evaluation pipelines above.
Identifies a contamination effect where an LLM judge systematically favors student models trained on synthetic data from a related generator, quietly inflating evaluation scores.
Traces reward over-optimization to misspecification at the high-reward tail, then uses off-policy examples in a rubric-based reward workflow to separate "excellent" from merely "great" and curb reward hacking.
REFRAIN decides when to stop chain-of-thought reasoning, pairing a two-stage stop discriminator with a sliding-window bandit that adapts the threshold to problem difficulty — no training required.
A 4,000-prompt benchmark across 10 cultures showing LLMs write as cultural insiders for the US but default to an outsider stance elsewhere, plus prompt- and agent-based mitigations.
Recasts unlearning as bi-level optimization — lower level minimizes forget loss, upper level preserves utility — instead of the usual weighted sum, yielding better forget/retain trade-offs.
Deep Policy Research drafts a full content-moderation policy from seed domain information alone, iteratively proposing web queries, distilling sources into rules, and indexing them into a policy document.
Treats the model's own parametric knowledge as a first-class retrieval source, jointly training source selection, verbalization, and generation — ~29% fewer retrievals at ~5.1% higher accuracy.
Literature review and data explorer for TEDDY metabolomics and lipidomics datasets — supporting multimodal T1D research and biomarker discovery.
Literature review of the TrialNet data cohort — covering natural history studies, autoantibody screening, and intervention trials in T1D progression.
Internal knowledge base covering project protocols, data dictionaries, onboarding guides, and cross-institutional coordination documentation.
Central code repository for all MAI-T1D foundation models, analysis pipelines, governance tools, and shared utilities.