Evidence map›Paper›PMID 23708188›Full record

ArticleNature genetics2013

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats.

Rat Genome Sequencing and Mapping Consortium, Amelie Baud, Roel Hermsen, Victor Guryev, Pernilla Stridh, Delyth Graham, Martin W McBride, Tatiana Foroud, Sophie Calderari, Margarita Diez and 61 more

Abstract read
In one paragraph

Article in Nature genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 1 pooled it
–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

111 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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51 more citing papers are in PubMed but not listed here.

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

71 authors.

Rat Genome Sequencing and Mapping ConsortiumWellcome Trust Centre for Human Genetics, Oxford, UK.
Amelie Baud
Roel Hermsen
Victor Guryev
Pernilla Stridh
Delyth Graham
Martin W McBride
Tatiana Foroud
Sophie Calderari
Margarita Diez
Johan Ockinger
Amennai D Beyeen
Alan Gillett
Nada Abdelmagid
Andre Ortlieb Guerreiro-Cacais
Maja Jagodic
Jonatan Tuncel
Ulrika Norin
Elisabeth Beattie
Ngan Huynh
William H Miller
Daniel L Koller
Imranul Alam
Samreen Falak
Mary Osborne-Pellegrin
Esther Martinez-Membrives
Toni Canete
Gloria Blazquez
Elia Vicens-Costa
Carme Mont-Cardona
Sira Diaz-Moran
Adolf Tobena
Oliver Hummel
Diana Zelenika
Kathrin Saar
Giannino Patone
Anja Bauerfeind
Marie-Therese Bihoreau
Matthias Heinig
Young-Ae Lee
Carola Rintisch
Herbert Schulz
David A Wheeler
Kim C Worley
Donna M Muzny
Richard A Gibbs
Mark Lathrop
Nico Lansu
Pim Toonen
Frans Paul Ruzius
Ewart de Bruijn
Heidi Hauser
David J Adams
Thomas Keane
Santosh S Atanur
Tim J Aitman
Paul Flicek
Tomas Malinauskas
E Yvonne Jones
Diana Ekman
Regina Lopez-Aumatell
Anna F Dominiczak
Martina Johannesson
Rikard Holmdahl
Tomas Olsson
Dominique Gauguier
Norbert Hubner
Alberto Fernandez-Teruel
Edwin Cuppen
Richard Mott
Jonathan Flint

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
GENETIC ANALYSIS OF HIP FRAGILITYR01AR047822 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FOROUD, TATIANA M. · 2003 to 2010
$2.1M
British Heart Foundation BHFRG/07/005/23633British Heart Foundation RG/07/005/23633Cancer Research UK 13031Cancer Research UK A10976Medical Research Council G0900084Medical Research Council G9900061Medical Research Council MC_U120061454NHGRI NIH HHS U54 HG003273NIAMS NIH HHS R01 AR047822Wellcome Trust 083573Wellcome Trust 083573/Z/07/ZWellcome Trust 089269Wellcome Trust 089269/Z/09/ZWellcome Trust 090532Wellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

Genetic mapping on fully sequenced individuals is transforming understanding of the relationship between molecular variation and variation in complex traits. Here we report a combined sequence and genetic mapping analysis in outbred rats that maps 355 quantitative trait loci for 122 phenotypes. We identify 35 causal genes involved in 31 phenotypes, implicating new genes in models of anxiety, heart disease and multiple sclerosis. The relationship between sequence and genetic variation is unexpectedly complex: at approximately 40% of quantitative trait loci, a single sequence variant cannot account for the phenotypic effect. Using comparable sequence and mapping data from mice, we show that the extent and spatial pattern of variation in inbred rats differ substantially from those of inbred mice and that the genetic variants in orthologous genes rarely contribute to the same phenotype in both species.

Indexed as

AnimalsAnimals, Outbred StrainsAnxietyChromosome MappingGenetic VariationGenotypeHeart DiseasesHumansMiceMice, Inbred C57BLModels, MolecularMultiple SclerosisPhenotypePolymorphism, Single NucleotideQuantitative Trait LociRats

Identifiers

PMID23708188
PMCPMC3821058

What OpenQuestion holds

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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.