ArticleInterdisciplinary sciences, computational life sciences2023
LDAEXC: LncRNA-Disease Associations Prediction with Deep Autoencoder and XGBoost Classifier.
Article in Interdisciplinary sciences, computational life sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- LDA-SCGB: inferring lncRNA-disease associations based on condensed gradient boosting.BMC bioinformatics · 2025Article
- HGCMLDA: predicting lncRNA-disease associations using hypergraph contrastive learning and multi-scale attentional feature fusion.Briefings in bioinformatics · 2025Article
- Predicting noncoding RNA and disease associations using multigraph contrastive learning.Scientific reports · 2025Article
- MORE: a multi-omics data-driven hypergraph integration network for biomedical data classification and biomarker identification.Briefings in bioinformatics · 2024Article
- LDAGM: prediction lncRNA-disease asociations by graph convolutional auto-encoder and multilayer perceptron based on multi-view heterogeneous networks.BMC bioinformatics · 2024Article
- GEnDDn: An lncRNA-Disease Association Identification Framework Based on Dual-Net Neural Architecture and Deep Neural Network.Interdisciplinary sciences, computational life sciences · 2024Article
- Finding potential lncRNA-disease associations using a boosting-based ensemble learning model.Frontiers in genetics · 2024Article
- A stacked machine learning-based classification model for endometriosis and adenomyosis: a retrospective cohort study utilizing peripheral blood and coagulation markers.Frontiers in digital health · 2024Article
- Applying negative sample denoising and multi-view feature for lncRNA-disease association prediction.Frontiers in genetics · 2023Article
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2 authors.
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Abstract
Numerous scientific evidences have revealed that long non-coding RNAs (lncRNAs) are involved in the progression of human complex diseases and biological life activities. Therefore, identifying novel and potential disease-related lncRNAs is helpful to diagnosis, prognosis and therapy of many human complex diseases. Since traditional laboratory experiments are cost and time-consuming, a great quantity of computer algorithms have been proposed for predicting the relationships between lncRNAs and diseases. However, there are still much room for the improvement. In this paper, we introduce an accurate framework named LDAEXC to infer LncRNA-Disease Associations with deep autoencoder and XGBoost Classifier. LDAEXC utilizes different similarity views of lncRNAs and human diseases to construct features for each data sources. Then, the reduced features are obtained by feeding the constructed feature vectors into a deep autoencoder, and at last an XGBoost classifier is leveraged to calculate the latent lncRNA-disease-associated scores using reduced features. The fivefold cross-validation experiments on four datasets showed that LDAEXC reached AUC scores of 0.9676 ± 0.0043, 0.9449 ± 0.022, 0.9375 ± 0.0331 and 0.9556 ± 0.0134, respectively, significantly higher than other advanced similar computer methods. Extensive experiment results and case studies of two complex diseases (colon and breast cancers) further indicated the practicability and excellent prediction performance of LDAEXC in inferring unknown lncRNA-disease associations. TLDAEXC utilizes disease semantic similarity, lncRNA expression similarity, and Gaussian interaction profile kernel similarity of lncRNAs and diseases for feature construction. The constructed features are fed to a deep autoencoder to extract reduced features, and an XGBoost classifier is used to predict the lncRNA-disease associations based on the reduced features. The fivefold and tenfold cross-validation experiments on a benchmark dataset showed that LDAEXC could achieve AUC scores of 0.9676 and 0.9682, respectively, significantly higher than other state-of-the-art similar methods.
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