ArticleFrontiers in genetics2020
Multiview Consensus Graph Learning for lncRNA-Disease Association Prediction.
Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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Who cites it
3 citing papers in PubMed.
- Self-supervised learning on graphs predicts non-coding RNA and disease associations.Scientific reports · 2026Article
- Artificial intelligence predictive system of individual survival rate for lung adenocarcinoma.Computational and structural biotechnology journal · 2022Article
- Bioinformatics Analysis of Long Non-coding RNA and Related Diseases: An Overview.Frontiers in genetics · 2021Review
Corrections and comments
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Authors and funding
7 authors.
Funding
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Abstract
Long noncoding RNAs (lncRNAs) are a class of noncoding RNA molecules longer than 200 nucleotides. Recent studies have uncovered their functional roles in diverse cellular processes and tumorigenesis. Therefore, identifying novel disease-related lncRNAs might deepen our understanding of disease etiology. However, due to the relatively small number of verified associations between lncRNAs and diseases, it remains a challenging task to reliably and effectively predict the associated lncRNAs for given diseases. In this paper, we propose a novel multiview consensus graph learning method to infer potential disease-related lncRNAs. Specifically, we first construct a set of similarity matrices for lncRNAs and diseases by taking advantage of the known associations. We then iteratively learn a consensus graph from the multiple input matrices and simultaneously optimize the predicted association probability based on a multi-label learning framework. To convey the utility of our method, three state-of-the-art methods are compared with our method on three widely used datasets. The experiment results illustrate that our method could obtain the best prediction performance under different cross validation schemes. The case study analysis implemented for uterine cervical neoplasms further confirmed the utility of our method in identifying lncRNAs as potential prognostic biomarkers in practice.
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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.