Evidence map›Paper›PMID 20815886›Full record

ArticleBMC genomics2010

Comparison of information-theoretic to statistical methods for gene-gene interactions in the presence of genetic heterogeneity.

Lara Sucheston, Pritam Chanda, Aidong Zhang, David Tritchler, Murali Ramanathan

Abstract readComparative Study
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Genomics in the post-GWAS era.Seminars in liver disease · 2011
    Review
  8. Dark matters in AMD genetics: epigenetics and stochasticity.Investigative ophthalmology & visual science · 2011
    Review
  9. Information metrics in genetic epidemiology.Statistical applications in genetics and molecular biology · 2011
    Article
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

5 authors.

Lara SuchestonDepartment of Biostatistics, State University of New York, Buffalo, NY 14260, USA.
Pritam Chanda
Aidong Zhang
David Tritchler
Murali Ramanathan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultifactorial diseases such as cancer and cardiovascular diseases are caused by the complex interplay between genes and environment. The detection of these interactions remains challenging due to computational limitations. Information theoretic approaches use computationally efficient directed search strategies and thus provide a feasible solution to this problem. However, the power of information theoretic methods for interaction analysis has not been systematically evaluated. In this work, we compare power and Type I error of an information-theoretic approach to existing interaction analysis methods.

methodsThe k-way interaction information (KWII) metric for identifying variable combinations involved in gene-gene interactions (GGI) was assessed using several simulated data sets under models of genetic heterogeneity driven by susceptibility increasing loci with varying allele frequency, penetrance values and heritability. The power and proportion of false positives of the KWII was compared to multifactor dimensionality reduction (MDR), restricted partitioning method (RPM) and logistic regression.

resultsThe power of the KWII was considerably greater than MDR on all six simulation models examined. For a given disease prevalence at high values of heritability, the power of both RPM and KWII was greater than 95%. For models with low heritability and/or genetic heterogeneity, the power of the KWII was consistently greater than RPM; the improvements in power for the KWII over RPM ranged from 4.7% to 14.2% at for α = 0.001 in the three models at the lowest heritability values examined. KWII performed similar to logistic regression.

conclusionsInformation theoretic models are flexible and have excellent power to detect GGI under a variety of conditions that characterize complex diseases.

Indexed as

Epistasis, GeneticGenetic HeterogeneityInformation TheoryModels, StatisticalComputer SimulationDatabases, GeneticFalse Positive ReactionsGenotypeHumansLogistic ModelsModels, GeneticMultifactor Dimensionality ReductionPenetranceROC Curve

Identifiers

PMID20815886
PMCPMC2996983

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Registered trials

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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.