Evidence map›Paper›PMID 23975245›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2013

Combined linkage and linkage disequilibrium QTL mapping in multiple families of maize (Zea mays L.) line crosses highlights complementarities between models based on parental haplotype and single locus polymorphism.

N Bardol, M Ventelon, B Mangin, S Jasson, V Loywick, F Couton, C Derue, P Blanchard, A Charcosset, Laurence Moreau

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Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  8. Multi-parent multi-environment QTL analysis: an illustration with the EU-NAM Flint population.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2020
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  17. MAGIC populations in crops: current status and future prospects.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2015
    Review
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4 · The record

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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

10 authors at 3 institutions in 1 country.

N BardolUMR0320/UMR8120 de Génétique Végétale, INRA, Université Paris-Sud, CNRS, Ferme du Moulon, 91190, Gif-sur-Yvette, France.
M Ventelon
B Mangin
S Jasson
V Loywick
F Couton
C Derue
P Blanchard
A Charcosset
Laurence Moreau
Domain Therapeutics (France) · FRUniversité Paris-Sud · FRDépartement Mathématiques et Informatique Appliquées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advancements in genotyping are rapidly decreasing marker costs and increasing marker density. This opens new possibilities for mapping quantitative trait loci (QTL), in particular by combining linkage disequilibrium information and linkage analysis (LDLA). In this study, we compared different approaches to detect QTL for four traits of agronomical importance in two large multi-parental datasets of maize (Zea mays L.) of 895 and 928 testcross progenies composed of 7 and 21 biparental families, respectively, and genotyped with 491 markers. We compared to traditional linkage-based methods two LDLA models relying on the dense genotyping of parental lines with 17,728 SNP: one based on a clustering approach of parental line segments into ancestral alleles and one based on single marker information. The two LDLA models generally identified more QTL (60 and 52 QTL in total) than classical linkage models (49 and 44 QTL in total). However, they performed inconsistently over datasets and traits suggesting that a compromise must be found between the reduction of allele number for increasing statistical power and the adequacy of the model to potentially complex allelic variation. For some QTL, the model exclusively based on linkage analysis, which assumed that each parental line carried a different QTL allele, was able to capture remaining variation not explained by LDLA models. These complementarities between models clearly suggest that the different QTL mapping approaches must be considered to capture the different levels of allelic variation at QTL involved in complex traits.

Indexed as

Chromosome MappingModels, GeneticPolymorphism, GeneticAllelesCluster AnalysisCrosses, GeneticGenetic LociGenome, PlantHaplotypesInheritance PatternsLinkage DisequilibriumQuantitative Trait LociZea mays

Identifiers

PMID23975245
OpenAlexW2070348747

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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.