ArticleBioinformatics (Oxford, England)2026
DeepLMI: deep feature mining with a globally enhanced graph convolutional network for robust lncRNA-miRNA interaction prediction.
Article in Bioinformatics (Oxford, England), 2026. 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
8 authors.
Funding
Abstract
motivationInteractions between long noncoding RNAs (lncRNAs) and microRNAs (miRNAs) play pivotal roles in gene regulation and disease progression, notably through mechanisms such as competitive miRNA sponging. Accurate identification of lncRNA-miRNA interactions is therefore essential for understanding disease mechanisms and discovering therapeutic targets. However, current knowledge is largely derived from labor-intensive and costly biological experiments, underscoring the need for reliable computational approaches.
resultsWe propose DeepLMI, a novel deep learning framework for lncRNA-miRNA interaction prediction that integrates deep feature mining with a globally enhanced graph convolutional network. To effectively capture the distinct properties of lncRNAs and miRNAs, DeepLMI employs specialized feature extraction modules: for lncRNAs, we combine sequence pretraining with self-attention mechanisms to learn multiscale semantic representations; for miRNAs, we fuse heterogeneous features through a graph convolutional encoder. To further address the sparsity and structural complexity of known RNA interaction networks, we design a Global-Enhanced Graph Convolutional Network that jointly models local neighborhood information and global topological signals. The embeddings learned for lncRNAs and miRNAs are then integrated to infer interaction probabilities. Extensive experiments across multiple datasets and evaluation settings demonstrate that DeepLMI consistently outperforms existing state-of-the-art methods and exhibits strong robustness, highlighting its potential as a valuable tool for RNA interaction analysis and disease research. AVAILABILITY AND IMPLEMENTATION: The codes and data are publicly available at https://github.com/Hhhzj-7/DeepLMI.
Indexed as
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.