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 Experiment Videos

Supervised learning-based tagSNP selection for genome-wide disease classifications.

Qingzhong Liu1, Jack Yang, Zhongxue Chen

  • 1Department of Computer Science, New Mexico Institute of Mining and Technology, Socorro, NM 87801, USA. liu@cs.nmt.edu

BMC Genomics
|April 17, 2008
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Designing 2D Metal-Semiconductor Junctions for Optoelectronics: A Comprehensive Consideration of Static Electronic Structures and Excited-State Carrier Dynamics.

The journal of physical chemistry letters·2026
Same author

Training for the Digital Clinical Environment: Preliminary Findings in Implementation of Electronic Health Record Platform in Medical Education.

Journal of medical systems·2026
Same author

Flaxseed globulin versus albumin proteins - Interfacial assembly and nonlinear rheology at the air-water interface.

Journal of colloid and interface science·2026
Same author

Global burden of antimicrobial-resistant Staphylococcus aureus lower respiratory tract infections in older adults: a secondary analysis of the MICROBE database (1990-2021).

BMC infectious diseases·2026
Same author

A Multidimensional Strategy of Flavor Evaluation Linking Yeast-Driven Chemical Networks to Sensory Attributes of Cherry Wine.

Journal of food science·2026
Same author

Causal association between gastroesophageal reflux disease and anemia: Mendelian randomization analysis.

Annals of medicine and surgery (2012)·2026
Same journal

pGWAS-Portal: a comprehensive online platform for integrative post-genome-wide association study analysis.

BMC genomics·2026
Same journal

Physiological and transcriptomic analyses of Rosa persica in response to drought stress and functional validation of the transcription factor RpERF113-like.

BMC genomics·2026
Same journal

Integrated analysis of chromatin accessibility and transcriptome profiles in granulosa cells of sheep with different FecB genotypes.

BMC genomics·2026
Same journal

Correction: TB-DROP: deep learning-based drug resistance prediction of Mycobacterium tuberculosis utilizing whole genome mutations.

BMC genomics·2026
Same journal

Chromosomal scale genome assembly of medicinal plant Sophora tonkinensis.

BMC genomics·2026
Same journal

Variant-specific RNA testing resolves variants of uncertain significance in exome testing.

BMC genomics·2026
See all related articles

We developed Supervised Recursive Feature Addition (SRFA) and Support Vector based Recursive Feature Addition (SVRFA) for selecting single nucleotide polymorphisms (SNPs) to predict complex diseases. These methods improve classification accuracy in genetic association studies.

Area of Science:

  • Human Genome Research
  • Genetic Epidemiology
  • Computational Biology

Background:

  • Genome-wide association studies (GWAS) aim to identify single nucleotide polymorphisms (SNPs) linked to complex diseases.
  • A key challenge is selecting optimal SNP subsets for accurate disease prediction.
  • Reducing study costs and time involves managing redundant SNP information.

Purpose of the Study:

  • To develop and evaluate novel feature selection methods for SNP-disease association studies.
  • To improve the accuracy of disease classification using genetic markers.
  • To reconcile information redundancy among SNP markers.

Main Methods:

  • Developed Supervised Recursive Feature Addition (SRFA), combining supervised learning and statistical measures.

Related Experiment Videos

  • Proposed Support Vector based Recursive Feature Addition (SVRFA) for SNP-disease association analysis.
  • Applied SRFA and SVRFA to complex disease datasets for SNP selection and classification.
  • Main Results:

    • SRFA and SVRFA demonstrated improved classification performance compared to existing methods like Support Vector Machine Recursive Feature Elimination and logic regression.
    • The proposed methods effectively reconciled redundant information among SNP markers.
    • Achieved superior disease classification accuracy in genetic association studies.

    Conclusions:

    • SRFA and SVRFA are effective for SNP selection and disease classification in genetic association studies.
    • These methods outperform established techniques like SVM-RFE and logic regression.
    • Accurate prediction of complex diseases requires considering both genetic and environmental factors, especially those involving gene-environment interactions.