Data Efficiency Semi-Supervised Meta-Learning Elucidates Understudied Interspecies Molecular Interactions
Wu, Y.; Xie, L.; Liu, Y.; Xie, L.
Show abstract
Many biological problems are understudied due to experimental limitations and human biases. Although deep learning is promising in accelerating scientific discovery, its power compromises when applied to problems with scarcely labeled data and data distribution shifts. We developed a semi-supervised meta learning framework Meta Model Agnostic Pseudo Label Learning (MMAPLE) to address these challenges by effectively exploring out-of-distribution (OOD) unlabeled data when transfer learning fails. The power of MMAPLE is demonstrated in multiple applications: predicting OOD drug-target interactions, hidden human metabolite-enzyme interactions, and understudied interspecies microbiome metabolite-human receptor interactions, where chemicals or proteins in unseen data are dramatically different from those in training data. MMAPLE achieves 11% to 242% improvement in the prediction-recall on multiple OOD benchmarks over baseline models. Using MMAPLE, we reveal novel interspecies metaboliteprotein interactions that are validated by bioactivity assays and fill in missing links in microbiome-human interactions. MMAPLE is a general framework to explore previously unrecognized biological domains beyond the reach of present experimental and computational techniques.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- GexMolGen: Cross-modal Generation of Hit-like Molecules via Large Language Model Encoding of Gene Expression Signatures 98%
- Interpretable and Generalizable Attention-Based Model for Predicting Drug-Target Interaction Using 3D Structure of Protein Binding Sites: SARS-CoV-2 Case Study and in-Lab Validation 97%
- Guided Diffusion for molecular generation with interaction prompt 97%
Similar papers in this journal
- Chemical-induced Gene Expression Ranking and its Application to Pancreatic Cancer Drug Repurposing 96%
- Functional microRNA-Targeting Drug Discovery by Graph-Based Deep Learning 95%
- Discovering nuclear localization signal universe through a novel deep learning model with interpretable attention units 94%
Similar papers in this journal
- A Graph-Attention-Based Deep Learning Network for Predicting Biotech-Small-Molecule Drug Interactions 97%
- Improving protein function prediction by learning and integrating representations of protein sequences and function labels 96%
- FLONE: fully Lorentz network embedding for inferring novel drug targets 95%
Similar papers in this journal
- G-PLIP: Knowledge graph neural network for structure-free protein-ligand bioactivity prediction 96%
- DrugForm-DTA: Towards real-world drug-target binding Affinity Model 96%
- DeepNeuropePred: a robust and universal tool to predict cleavage sites from neuropeptide precursors by protein language model 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.