Evidence map›Paper›PMID 25057293›Full record

ArticleBioData mining2014

A classification and characterization of two-locus, pure, strict, epistatic models for simulation and detection.

Ryan J Urbanowicz, Ambrose Ls Granizo-Mackenzie, Jeff Kiralis, Jason H Moore

Abstract read
In one paragraph

Article in BioData mining, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Leveraging putative enhancer-promoter interactions to investigate two-way epistasis in Type 2 Diabetes GWAS.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018
    Article
  5. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ryan J UrbanowiczDepartment of Genetics, Dartmouth College, 1 Medical Center Dr., Lebanon, NH 05001, USA.
Ambrose Ls Granizo-MackenzieDepartment of Genetics, Dartmouth College, 1 Medical Center Dr., Lebanon, NH 05001, USA.
Jeff KiralisDepartment of Genetics, Dartmouth College, 1 Medical Center Dr., Lebanon, NH 05001, USA.
Jason H MooreDepartment of Genetics, Dartmouth College, 1 Medical Center Dr., Lebanon, NH 05001, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe statistical genetics phenomenon of epistasis is widely acknowledged to confound disease etiology. In order to evaluate strategies for detecting these complex multi-locus disease associations, simulation studies are required. The development of the GAMETES software for the generation of complex genetic models, has provided the means to randomly generate an architecturally diverse population of epistatic models that are both pure and strict, i.e. all n loci, but no fewer, are predictive of phenotype. Previous theoretical work characterizing complex genetic models has yet to examine pure, strict, epistasis which should be the most challenging to detect. This study addresses three goals: (1) Classify and characterize pure, strict, two-locus epistatic models, (2) Investigate the effect of model 'architecture' on detection difficulty, and (3) Explore how adjusting GAMETES constraints influences diversity in the generated models.

resultsIn this study we utilized a geometric approach to classify pure, strict, two-locus epistatic models by "shape". In total, 33 unique shape symmetry classes were identified. Using a detection difficulty metric, we found that model shape was consistently a significant predictor of model detection difficulty. Additionally, after categorizing shape classes by the number of edges in their shape projections, we found that this edge number was also significantly predictive of detection difficulty. Analysis of constraints within GAMETES indicated that increasing model population size can expand model class coverage but does little to change the range of observed difficulty metric scores. A variable population prevalence significantly increased the range of observed difficulty metric scores and, for certain constraints, also improved model class coverage.

conclusionsThese analyses further our theoretical understanding of epistatic relationships and uncover guidelines for the effective generation of complex models using GAMETES. Specifically, (1) we have characterized 33 shape classes by edge number, detection difficulty, and observed frequency (2) our results support the claim that model architecture directly influences detection difficulty, and (3) we found that GAMETES will generate a maximally diverse set of models with a variable population prevalence and a larger model population size. However, a model population size as small as 1,000 is likely to be sufficient.

Indexed as

Computational geometryConvex hullEpistasisGAMETESGeneticsModelsSimulation

Identifiers

PMID25057293
PMCPMC4094921

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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.