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

Genomics02:02

Genomics

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...
Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scaleĀ  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...
Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.

You might also read

Related Articles

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

Sort by
Same author

The effect of acute fatigue on somatosensory function differs between trained and untrained individuals.

Scientific reportsĀ·2026
Same author

Macromolecular crowding reshapes the conformational landscapes of intrinsically disordered proteins: mechanisms, cellular contexts, and functional consequences.

Current opinion in structural biologyĀ·2026
Same author

Force Field Evaluation for an Intrinsically Disordered Domain: MD-NMR-FCS Benchmarking of Protein 4.1G Headpiece Ensembles.

Journal of chemical information and modelingĀ·2026
Same author

Hydrogen-bonded Organic Frameworks Decorated Polymeric High Internal Phase Emulsions as Adsorbents for Solid-Phase Extraction of Estrogens.

Journal of separation scienceĀ·2026
Same author

Profiling of porcine B-cell receptor heavy-chain repertoires indicates the development of a wide public pseudorabies virus-specific immune response after vaccination and challenge.

Discovery immunologyĀ·2026
Same author

Concanavalin A targets phylogenetically conserved N-linked glycans on coronavirus spike proteins for broad-spectrum antiviral activity.

Journal of virologyĀ·2026
Same journal

SNPio: a Python interface for population genomic data processing.

BMC bioinformaticsĀ·2026
Same journal

SpaHNR: a spatial domain identification method via sparse attention-based hierarchical node representation and multi-view contrastive learning.

BMC bioinformaticsĀ·2026
Same journal

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry.

BMC bioinformaticsĀ·2026
Same journal

NAP: an open source pipeline for cross-domain microbiome profiling using Nanopore sequencing-derived amplicon data.

BMC bioinformaticsĀ·2026
Same journal

SurvGME: an R package for survival analysis with graphical and measurement error models.

BMC bioinformaticsĀ·2026
Same journal

SimMapNet: a Bayesian framework for gene regulatory network inference using gene ontology similarities as external hint.

BMC bioinformaticsĀ·2026
See all related articles

Related Experiment Video

Updated: Jun 17, 2026

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization
03:08

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization

Published on: October 3, 2025

Gene prioritization and clustering by multi-view text mining.

Shi Yu1, Leon-Charles Tranchevent, Bart De Moor

  • 1Bioinformatics Group, Department of Electrical Engineering, Katholieke Universiteit Leuven, Kasteelpark Arenberg 10, Heverlee B3001, Belgium. shi.yu@esat.kuleuven.be

BMC Bioinformatics
|January 16, 2010
PubMed
Summary
This summary is machine-generated.

Integrating multiple text mining models improves disease gene identification. A novel multi-view approach enhances accuracy in gene prioritization and clustering, outperforming individual models for better biomedical knowledge discovery.

More Related Videos

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets
03:37

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets

Published on: March 1, 2024

Related Experiment Videos

Last Updated: Jun 17, 2026

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization
03:08

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization

Published on: October 3, 2025

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets
03:37

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets

Published on: March 1, 2024

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Text mining aids biologists in understanding disease genetics and identifying candidate genes.
  • Existing text mining models show variable effectiveness in disease-gene identification.
  • Combining multiple text mining models is challenging but potentially beneficial for refined knowledge.

Purpose of the Study:

  • To present a multi-view approach for biomedical knowledge retrieval using diverse controlled vocabularies.
  • To investigate the integration of multiple text mining views for disease gene identification tasks.
  • To evaluate the performance of the multi-view approach against existing methods.

Main Methods:

  • Utilized nine bio-ontologies to select controlled vocabularies for indexing MEDLINE gene-based text.
  • Treated text mining results from each vocabulary as a separate 'view'.
  • Integrated multiple views using multi-source learning algorithms for gene prioritization and clustering.

Main Results:

  • The multi-view approach demonstrated significantly superior performance in both gene prioritization and gene clustering tasks.
  • Systematic evaluation on real benchmark datasets confirmed the enhanced accuracy of the proposed method.
  • The integrated model outperformed individual text mining models and other comparative methods.

Conclusions:

  • Multi-view text mining is a superior and promising strategy for text-based disease gene identification.
  • This approach is particularly valuable when the relevance of specific vocabularies is unknown in practical research.
  • The findings support the integration of diverse data sources for robust biomedical knowledge discovery.