Evidence map›Paper›PMID 18648990›Full record

ArticleGenetica2009

A new Bayesian automatic model selection approach for mapping quantitative trait loci under variance component model.

Ming Fang, Dan Jiang, Huijiang Gao, Dongxiao Sun, Runqing Yang, Qin Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Genetica, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Ming FangLife Science College, Heilongjiang August First Land Reclamation University, Daqing, 163319, People's Republic of China. fangming618@126.com
Dan Jiang
Huijiang Gao
Dongxiao Sun
Runqing Yang
Qin Zhang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bayesian variable selection implemented via reversible jump Markov chain Monte Carlo (RJMCMC) is an effective method for mapping multiple QTL. Recently, it has been used for QTL mapping both in inbred line crosses and in outbred populations. However, by RJMCMC, since the model-dimension is variable, the parameters are usually subject to poor mixing and difficult to converge. In inbred lines, the fixed effect model is used for mapping QTL, various approaches which keep the model-dimension unchanged have been proposed, and it is proved that the mixing properties of Markov chains is substantially improved compared with RJMCMC. In outbred populations, the random effect model is used and the implementation via RJMCMC for variable selection still is the mainstream to map multiple QTL. Due to the poor performance RJMCMC has, it is meaningful to develop a model-dimension fixed approach for mapping QTL under random effect model. In this article, we proposed a new model-dimension fixed approach called Bayesian automatic model selection method for mapping multiple QTL under random effect model. By the new approach, all variances of QTL are subject to estimate, in which the variance of zero-effect QTL will exactly converge to zero, and those of non-zero effect QTL will be estimated precisely. Therefore, no special model selection is required. A series of simulation experiments have been conducted to investigate the performance of the method, the result showed that the new approach is very efficient for mapping multiple QTL. A computer program written in FORTRAN is available to interested users on request.

Indexed as

Genetic VariationModels, GeneticBayes TheoremChromosome MappingComputer SimulationQuantitative Trait Loci

Identifiers

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.