ArticlebioRxiv : the preprint server for biology2025
Qimai: a multi-agent framework for zero-shot DNA-protein interaction prediction.
Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Accurate prediction of DNA-protein interactions, a fundamental task in genomics, is limited by the poor generalization of existing models to novel proteins not seen during training. To address this challenge, we introduce Qimai, a modular AI agent framework that integrates deep learning predictions with biological evidence using Large Language Model (LLM) as reasoning engine. Qimai combines direct motif evidence from the query protein, indirect motif evidence from its interactors, and quantitative prediction from a new transformer-based DPI model to produce explainable predictions with confidence scores. On a benchmark of 78 unseen proteins, Qimai consistently outperforms standalone deep learning models across all metrics, increasing the Area Under Curve of the Precision-Recall (AUC-PR), the Area Under Curve of the Receiver Operating Characteristic (AUC-ROC), and Matthews Correlation Coefficient (MCC) by 17.6%, 15.6%, and 244% respectively compared to the best standalone model. Ablation analyses reveal that this gain is driven by the LLM's ability to dynamically weigh diverse evidence, with indirect motif evidence of co-factors particularly critical for unseen proteins. Qimai establishes a generalizable and interpretable paradigm for integrating heterogeneous data in predictive genomics. This framework is accessible via the Qimai web portal (https://qimai.wanglab.ucsd.edu/).
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.