Evidence map›Paper›PMID 18510743›Full record

ArticleBMC bioinformatics2008

Variable selection for large p small n regression models with incomplete data: mapping QTL with epistases.

Min Zhang, Dabao Zhang, Martin T Wells

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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  14. Mapping and validation of quantitative trait loci associated with concentrations of 16 elements in unmilled rice grain.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2014
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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

3 authors.

Min ZhangDepartment of Statistics, Purdue University, West Lafayette, IN 47907, USA. minzhang@stat.purdue.edu
Dabao Zhang
Martin T Wells

Funding

Association Mapping in Structured PopulationsR01GM083606 · NIGMS · STANFORD UNIVERSITY · PI BUSTAMANTE, CARLOS DANIEL · 2007 to 2010
$1.3M
NIGMS NIH HHS 1R01GM083606-01NIGMS NIH HHS R01 GM083606
6 · The paper itself

Abstract

backgroundIdentifying quantitative trait loci (QTL) for both additive and epistatic effects raises the statistical issue of selecting variables from a large number of candidates using a small number of observations. Missing trait and/or marker values prevent one from directly applying the classical model selection criteria such as Akaike's information criterion (AIC) and Bayesian information criterion (BIC).

resultsWe propose a two-step Bayesian variable selection method which deals with the sparse parameter space and the small sample size issues. The regression coefficient priors are flexible enough to incorporate the characteristic of "large p small n" data. Specifically, sparseness and possible asymmetry of the significant coefficients are dealt with by developing a Gibbs sampling algorithm to stochastically search through low-dimensional subspaces for significant variables. The superior performance of the approach is demonstrated via simulation study. We also applied it to real QTL mapping datasets.

conclusionThe two-step procedure coupled with Bayesian classification offers flexibility in modeling "large p small n" data, especially for the sparse and asymmetric parameter space. This approach can be extended to other settings characterized by high dimension and low sample size.

Indexed as

Epistasis, GeneticModels, GeneticRegression AnalysisChromosome MappingComputer SimulationDatabases, GeneticData Interpretation, StatisticalModels, StatisticalQuantitative Trait LociSample Size

Identifiers

PMID18510743
PMCPMC2435550

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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.