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Related Concept Videos

Genome-wide Association Studies-GWAS01:11

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Updated: Sep 19, 2025

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
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Higher-Order Weighted Perturbation-Based Multilevel Information Fusion Model for Predicting CircRNA-Disease

Shanchen Pang1,2,3, Zheqi Song1, Yunyin Li1

  • 1College of Computer Science and Technology, Qingdao Institute of Software, China University of Petroleum (East China), Qingdao 266580, China.

Journal of Chemical Information and Modeling
|June 17, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces a new model for predicting disease-associated circular RNAs (circRNAs). The high-order weighted perturbation-based multilevel information fusion model (HWP-MIFM) effectively captures complex relationships for improved disease mechanism understanding.

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In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Circular RNAs (circRNAs) play a role in disease initiation and progression.
  • Current computational methods often miss higher-order circRNA-disease associations and multilevel features.

Purpose of the Study:

  • To develop a novel computational model for predicting circRNA-disease associations.
  • To address limitations in existing methods by capturing higher-order and multilevel features.

Main Methods:

  • Proposed the high-order weighted perturbation-based multilevel information fusion model (HWP-MIFM).
  • Employed higher-order weighted perturbation for dynamic weight adjustment and higher-order association extraction.
  • Utilized dual-stage matrix factorization for multilayer structure construction and linear feature extraction.
  • Incorporated a dual-path feature learning module to capture complex nonlinear relationships.

Main Results:

  • HWP-MIFM demonstrated superior overall performance compared to seven state-of-the-art methods in 5-fold cross-validation across four datasets.
  • Ablation studies and case analyses validated the model's accuracy and practical utility.

Conclusions:

  • The HWP-MIFM model offers a more comprehensive approach to predicting circRNA-disease associations.
  • This advancement aids in understanding disease mechanisms and identifying potential therapeutic targets.