ArticleBriefings in bioinformatics2025
Enhancing LncRNA-miRNA interaction prediction with multimodal contrastive representation learning.
Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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
1 citing paper in PubMed.
- MCOAN: multimodal contrastive representation learning for cross-omics adaptive disease regulatory network prediction.Bioinformatics (Oxford, England) · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
Interactions between long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) play an important role in the development of complex human diseases by collaboratively regulating gene transcription and expression. Therefore, identifying lncRNA-miRNA interactions (LMIs) is essential for diagnosing and treating complex human diseases. Because identifying LMIs with wet experiments is time-consuming and labor-intensive, some computational methods have been developed to infer LMIs. However, these approaches excel at utilizing single-modal information but struggle to integrate multimodal data from lncRNAs and miRNAs, which is essential for uncovering complex patterns in LMIs, ultimately limiting their performance. Therefore, this article proposes a novel multimodal contrastive representation learning model (MCRLMI) for LMI predictions. The model fully integrates multi-source similarity information and sequence encodings of lncRNAs and miRNAs. It leverages a graph convolutional network (GCN) and a Transformer to capture local neighborhood structural features and long-distance dependencies, respectively, enabling the collaborative modeling of structural and semantic information. Subsequently, to effectively integrate multimodal characteristics with encoded information, a multichannel attention mechanism and contrastive learning are introduced to fuse the extracted features. Finally, a Kolmogorov-Arnold Network (KAN) is trained with the optimized embeddings to predict LMIs. Extensive experiments show that the proposed MCRLMI consistently outperforms existing methods. Moreover, case studies further validate the potential of MCRLMI to identify novel LMIs in practical applications.
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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 Socratic graph.