Evidence map›Paper›PMID 14975137›Full record

ArticleBMC genetics2003

Locating disease genes using Bayesian variable selection with the Haseman-Elston method.

Cheongeun Oh, Kenny Q Ye, Qimei He, Nancy R Mendell

Abstract read
In one paragraph

Article in BMC genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Identification of significant genes in genomics using Bayesian variable selection methods.Advances and applications in bioinformatics and chemistry : AABC · 2008
    Article
  3. Article
  4. Article
  5. Article
  6. 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

4 authors.

Cheongeun OhDepartment of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT, USA. cheongun.oh@yale.edu
Kenny Q Ye
Qimei He
Nancy R Mendell

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe applied stochastic search variable selection (SSVS), a Bayesian model selection method, to the simulated data of Genetic Analysis Workshop 13. We used SSVS with the revisited Haseman-Elston method to find the markers linked to the loci determining change in cholesterol over time. To study gene-gene interaction (epistasis) and gene-environment interaction, we adopted prior structures, which incorporate the relationship among the predictors. This allows SSVS to search in the model space more efficiently and avoid the less likely models.

resultsIn applying SSVS, instead of looking at the posterior distribution of each of the candidate models, which is sensitive to the setting of the prior, we ranked the candidate variables (markers) according to their marginal posterior probability, which was shown to be more robust to the prior. Compared with traditional methods that consider one marker at a time, our method considers all markers simultaneously and obtains more favorable results.

conclusionsWe showed that SSVS is a powerful method for identifying linked markers using the Haseman-Elston method, even for weak effects. SSVS is very effective because it does a smart search over the entire model space.

Indexed as

Genetic LinkageBayes TheoremChromosome MappingComputer SimulationEpistasis, GeneticFemaleGenetic MarkersGenetic Predisposition to DiseaseHumansLeast-Squares AnalysisMaleMatched-Pair AnalysisModels, GeneticQuantitative Trait, HeritableQuantitative Trait LociSiblingsGenetic Markers

Identifiers

PMID14975137
PMCPMC1866507

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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.