Evidence map›Paper›PMID 16542433›Full record

ArticleBMC genomics2006

Linkage disequilibrium interval mapping of quantitative trait loci.

Simon Boitard, Jihad Abdallah, Hubert de Rochambeau, Christine Cierco-Ayrolles, Brigitte Mangin

Abstract readComparative Study
In one paragraph

Article in BMC genomics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Meta-analysis of QTL involved in silage quality of maize and comparison with the position of candidate genes.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2010
    Article
  2. Article
  3. Article
  4. Linear models for joint association and linkage QTL mapping.Genetics, selection, evolution : GSE · 2009
    Article
  5. 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.

Simon BoitardUnité de Biométrie et Intelligence Artificielle, Institut National de la Recherche Agronomique, BP 52627, 31326 Castanet-Tolosan Cedex, France. simon.boitard@toulouse.inra.fr
Jihad Abdallah
Hubert de Rochambeau
Christine Cierco-Ayrolles
Brigitte Mangin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor many years gene mapping studies have been performed through linkage analyses based on pedigree data. Recently, linkage disequilibrium methods based on unrelated individuals have been advocated as powerful tools to refine estimates of gene location. Many strategies have been proposed to deal with simply inherited disease traits. However, locating quantitative trait loci is statistically more challenging and considerable research is needed to provide robust and computationally efficient methods.

resultsUnder a three-locus Wright-Fisher model, we derived approximate expressions for the expected haplotype frequencies in a population. We considered haplotypes comprising one trait locus and two flanking markers. Using these theoretical expressions, we built a likelihood-maximization method, called HAPim, for estimating the location of a quantitative trait locus. For each postulated position, the method only requires information from the two flanking markers. Over a wide range of simulation scenarios it was found to be more accurate than a two-marker composite likelihood method. It also performed as well as identity by descent methods, whilst being valuable in a wider range of populations.

conclusionOur method makes efficient use of marker information, and can be valuable for fine mapping purposes. Its performance is increased if multiallelic markers are available. Several improvements can be developed to account for more complex evolution scenarios or provide robust confidence intervals for the location estimates.

Indexed as

Linkage DisequilibriumQuantitative Trait LociAnimalsChromosome MappingComputer SimulationGenetic MarkersHaplotypesHumansLikelihood FunctionsModels, TheoreticalGenetic Markers

Identifiers

PMID16542433
PMCPMC1559614

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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.