Evidence map›Paper›PMID 16722772›Full record

ArticleApplied bioinformatics2006

Machine learning for detecting gene-gene interactions: a review.

Brett A McKinney, David M Reif, Marylyn D Ritchie, Jason H Moore

Abstract read
In one paragraph

Article in Applied bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

92 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Machine learning approaches and genetic determinants that influence the development of type 2 diabetes mellitus: a genetic association study in Brazilian patients.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. In Silico Exploration ofBiomolecules · 2022
    Article
  19. Review
  20. Article

32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Brett A McKinneyDepartment of Molecular Physiology and Biophysics, Center for Human Genetics Research, Vanderbilt University Medical School, Nashville, Tennessee, USA.
David M Reif
Marylyn D Ritchie
Jason H Moore

Funding

VARIATION IN BIOACCUMULATION AND BIOMAGNIFICATION OF METALS IN NORTHERN US LAKESP42ES007373 · NIEHS · DARTMOUTH COLLEGE · PI STANTON, BRUCE A. · 1995 to 2019
$52.0M
THE ROLE OF CAL IN CIF-MEDIATED DEGRADATION OF CFTRP20RR018787 · NCRR · DARTMOUTH COLLEGE · PI TRAVISS, NORA · 2003 to 2011
$21.9M
Bioinformatics Strategies: Biodefense Vaccine ResearchR01AI059694 · NIAID · DARTMOUTH COLLEGE · PI MOORE, JASON H. · 2004 to 2012
$4.5M
Machine Learning Prediction of Cancer SusceptibilityR01LM009012 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H. · 2006 to 2014
$3.3M
Genetics Basis of Trauma RecoveryR01HD047447 · NICHD · DARTMOUTH COLLEGE · PI MOORE, JASON H. · 2005 to 2009
$1.8M
GENETIC ARCHITECTURE OF PLASMA T-PA AND PAI-1R01HL065234 · NHLBI · VANDERBILT UNIVERSITY · PI MOORE, JASON H. · 2000 to 2004
$1.7M
Cell-Mediated Immune Responses to Vaccinia VirusesR01AI057661 · NIAID · VANDERBILT UNIVERSITY · PI CROWE, JAMES E · 2003 to 2006
$1.2M
Cytokine Signaling Network Response to Smallpox VaccineK25AI064625 · NIAID · VANDERBILT UNIVERSITY · PI MCKINNEY, BRETT · 2006 to 2010
$534k
NCRR NIH HHS P20 RR018787NCRR NIH HHS RR018787NHLBI NIH HHS HL65234NHLBI NIH HHS R01 HL065234NIAID NIH HHS AI057661NIAID NIH HHS AI059694NIAID NIH HHS AI064625NIAID NIH HHS K25 AI064625NIAID NIH HHS R01 AI057661NIAID NIH HHS R01 AI059694NICHD NIH HHS HD047447NICHD NIH HHS R01 HD047447NIEHS NIH HHS ES007373NIEHS NIH HHS P42 ES007373NLM NIH HHS LM009012NLM NIH HHS R01 LM009012
6 · The paper itself

Abstract

Complex interactions among genes and environmental factors are known to play a role in common human disease aetiology. There is a growing body of evidence to suggest that complex interactions are 'the norm' and, rather than amounting to a small perturbation to classical Mendelian genetics, interactions may be the predominant effect. Traditional statistical methods are not well suited for detecting such interactions, especially when the data are high dimensional (many attributes or independent variables) or when interactions occur between more than two polymorphisms. In this review, we discuss machine-learning models and algorithms for identifying and characterising susceptibility genes in common, complex, multifactorial human diseases. We focus on the following machine-learning methods that have been used to detect gene-gene interactions: neural networks, cellular automata, random forests, and multifactor dimensionality reduction. We conclude with some ideas about how these methods and others can be integrated into a comprehensive and flexible framework for data mining and knowledge discovery in human genetics.

Indexed as

Artificial IntelligenceAlgorithmsAnimalsGenome, HumanGenomicsGenotypeHumansModels, GeneticModels, StatisticalNeural Networks, ComputerPolymorphism, Single Nucleotide

Identifiers

PMID16722772
PMCPMC3244050

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.