ArticleGenetica2009
A new Bayesian automatic model selection approach for mapping quantitative trait loci under variance component model.
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.
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.
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.
Who cites it
1 citing paper in PubMed.
- A new mapping method for quantitative trait loci of silkworm.BMC genetics · 2011Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
18648990What OpenQuestion holds
Registered trials
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.