Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

13.8K
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...
13.8K
Multiple Allele Traits01:49

Multiple Allele Traits

34.4K
The Concept of Multiple Allelism
34.4K
Genomics02:02

Genomics

36.7K
Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
36.7K
Gene Families01:57

Gene Families

8.9K
Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
8.9K
Pleiotropy01:33

Pleiotropy

40.8K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.8K
DNA Microarrays02:34

DNA Microarrays

17.9K
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
17.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Purification, characterisation and antioxidant activities of chondroitin sulphate extracted from Raja porosa cartilage.

Carbohydrate polymers·2020
Same author

Comparison and evaluation of non-invasive models in predicting liver inflammation and fibrosis of chronic hepatitis B virus-infected patients with high hepatitis B virus DNA and normal or mildly elevated alanine transaminase levels.

Medicine·2020
Same author

miR-155 Accelerates the Growth of Human Liver Cancer Cells by Activating CDK2 via Targeting H3F3A.

Molecular therapy oncolytics·2020
Same author

Osteoclastogenesis Modulatory Steroids from the South China Sea Gorgonian Coral Iciligorgia sp.

Chemistry & biodiversity·2020
Same author

Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson's disease.

Scientific reports·2020
Same author

Do underlying cardiovascular diseases have any impact on hospitalised patients with COVID-19?

Heart (British Cardiac Society)·2020
Same journal

Corrigendum to "CFPNet-M: A light-weight encoder-decoder based network for multimodal biomedical image real-time segmentation" [Comput. Biol. Med. 154 (2023) 106579].

Computers in biology and medicine·2026
Same journal

ECG arrhythmia classification via wavelet-driven feature extraction and swarm-optimised gradient boosting.

Computers in biology and medicine·2026
Same journal

Electro-osmotic metachronal cilia transport of viscoelastic blood infused with penta-hybrid nanoparticles in an oviduct: Analytical and neural network modeling.

Computers in biology and medicine·2026
Same journal

sEEGnal: an automated EEG preprocessing pipeline evaluated against expert-driven preprocessing.

Computers in biology and medicine·2026
Same journal

Corrigendum to "Integrating experimental biology, computational methods, and artificial Intelligence in anticancer drug discovery: Bridging the translational Gap" [Comput. Biol. Med. 213 (2026) 111832].

Computers in biology and medicine·2026
Same journal

Organ dose optimization for a point-of-care forearm X-ray photon-counting CT.

Computers in biology and medicine·2026
See all related articles

Related Experiment Video

Updated: Aug 9, 2025

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
07:35

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports

Published on: October 13, 2023

1.7K

MGREL: A multi-graph representation learning-based ensemble learning method for gene-disease association prediction.

Ziyang Wang1, Yaowen Gu1, Si Zheng2

  • 1Institute of Medical Information IMI, Chinese Academy of Medical Sciences and Peking Union Medical College CAMS & PUMC, Beijing, 100020, China.

Computers in Biology and Medicine
|February 22, 2023
PubMed
Summary
This summary is machine-generated.

This study introduces MGREL, a novel computational model for predicting gene-disease associations by integrating genetic, therapeutic, and network data. MGREL significantly improves the accuracy of identifying potential disease-related genes and therapeutic targets.

Keywords:
Ensemble learningGene-disease association predictionMulti-graph representation learning

More Related Videos

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.6K
Constructing and Visualizing Models using Mime-based Machine-learning Framework
06:19

Constructing and Visualizing Models using Mime-based Machine-learning Framework

Published on: July 22, 2025

98

Related Experiment Videos

Last Updated: Aug 9, 2025

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
07:35

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports

Published on: October 13, 2023

1.7K
Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.6K
Constructing and Visualizing Models using Mime-based Machine-learning Framework
06:19

Constructing and Visualizing Models using Mime-based Machine-learning Framework

Published on: July 22, 2025

98

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Identifying gene-disease associations is crucial for understanding disease mechanisms and finding therapeutic targets.
  • Computational methods offer an effective approach but often overlook integrated data types.
  • Existing methods may not fully leverage genetic, therapeutic, and network topology information.

Purpose of the Study:

  • To develop an advanced computational model for predicting gene-disease associations.
  • To integrate diverse data sources including genetic, therapeutic, and network information.
  • To improve the accuracy and scope of gene-disease association prediction.

Main Methods:

  • Re-organized a benchmark dataset with updated gene-disease associations from the OMIM database.
  • Developed a multi-graph representation learning-based ensemble model (MGREL).
  • Integrated knowledge extraction and graph learning channels for feature generation, followed by a 5-model ensemble classifier.

Main Results:

  • MGREL demonstrated superior performance compared to five state-of-the-art methods.
  • Achieved high performance metrics: AUC = 0.925 and AUPR = 0.935.
  • Showcased significant improvements in predicting associations for novel genes and diseases, with relative gains of 3.24% (AUC) and 2.75% (AUPR).

Conclusions:

  • MGREL effectively integrates multi-modal data for accurate gene-disease association prediction.
  • The model shows promise for identifying novel therapeutic targets.
  • This approach advances computational strategies in precision medicine and disease research.