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DNI-MDCAP: improvement of causal MiRNA-disease association prediction based on deep network imputation.
Han, Yu; Zhou, Qiong; Liu, Leibo; Li, Jianwei; Zhou, Yuan.
Afiliación
  • Han Y; Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Zhou Q; Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Liu L; Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Li J; Institute of Computational Medicine, School of Artificial Intelligence, Hebei University of Technology, Tianjin, China.
  • Zhou Y; Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China. zhouyuanbioinfo@hsc.pku.edu.cn.
BMC Bioinformatics ; 25(1): 22, 2024 Jan 12.
Article en En | MEDLINE | ID: mdl-38216907
ABSTRACT

BACKGROUND:

MiRNAs are involved in the occurrence and development of many diseases. Extensive literature studies have demonstrated that miRNA-disease associations are stratified and encompass ~ 20% causal associations. Computational models that predict causal miRNA-disease associations provide effective guidance in identifying novel interpretations of disease mechanisms and potential therapeutic targets. Although several predictive models for miRNA-disease associations exist, it is still challenging to discriminate causal miRNA-disease associations from non-causal ones. Hence, there is a pressing need to develop an efficient prediction model for causal miRNA-disease association prediction.

RESULTS:

We developed DNI-MDCAP, an improved computational model that incorporated additional miRNA similarity metrics, deep graph embedding learning-based network imputation and semi-supervised learning framework. Through extensive predictive performance evaluation, including tenfold cross-validation and independent test, DNI-MDCAP showed excellent performance in identifying causal miRNA-disease associations, achieving an area under the receiver operating characteristic curve (AUROC) of 0.896 and 0.889, respectively. Regarding the challenge of discriminating causal miRNA-disease associations from non-causal ones, DNI-MDCAP exhibited superior predictive performance compared to existing models MDCAP and LE-MDCAP, reaching an AUROC of 0.870. Wilcoxon test also indicated significantly higher prediction scores for causal associations than for non-causal ones. Finally, the potential causal miRNA-disease associations predicted by DNI-MDCAP, exemplified by diabetic nephropathies and hsa-miR-193a, have been validated by recently published literature, further supporting the reliability of the prediction model.

CONCLUSIONS:

DNI-MDCAP is a dedicated tool to specifically distinguish causal miRNA-disease associations with substantially improved accuracy. DNI-MDCAP is freely accessible at http//www.rnanut.net/DNIMDCAP/ .
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: MicroARNs Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido