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Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

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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.
GWAS does not require the identification of the target gene involved in...
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Related Experiment Video

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Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
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Convolution Neural Networks Using Deep Matrix Factorization for Predicting Circrna-Disease Association.

Zhi-Hao Liu, Cun-Mei Ji, Jian-Cheng Ni

    IEEE/ACM Transactions on Computational Biology and Bioinformatics
    |December 24, 2021
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a novel computational model, DMFCNNCD, to predict associations between circular RNAs (circRNAs) and diseases. The method efficiently identifies potential links, aiding in disease diagnosis and biomarker discovery.

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    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Genomics

    Background:

    • Circular RNAs (circRNAs) possess stable structures, making them promising for disease diagnosis.
    • Identifying circRNA-disease associations through biological experiments is costly and time-consuming.
    • There is a critical need for efficient computational models to predict these associations.

    Purpose of the Study:

    • To develop a novel deep matrix factorization with convolution neural networks framework (DMFCNNCD) for predicting circRNA-disease associations.
    • To leverage circRNA and disease features for accurate association prediction.
    • To overcome the limitations of traditional experimental methods.

    Main Methods:

    • Matrix decomposition of the circRNA-disease association matrix to extract inherent features.
    • Utilizing a mapping module to capture potential nonlinear features.
    • Integrating extracted features with similarity information to create a comprehensive training dataset.
    • Applying convolution neural networks (CNNs) for prediction of unknown circRNA-disease associations.

    Main Results:

    • The DMFCNNCD framework successfully predicts circRNA-disease associations.
    • Experimental results demonstrate the efficacy of the proposed method.
    • The model outperforms existing state-of-the-art methods in prediction accuracy.

    Conclusions:

    • The DMFCNNCD model offers an efficient and achievable computational approach for predicting circRNA-disease associations.
    • This method can accelerate the discovery of novel circRNA biomarkers for various diseases.
    • The findings contribute to advancing the application of circRNAs in clinical diagnostics.