Evidence map›Paper›PMID 15457343›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2004

Genetic structure of the LXS panel of recombinant inbred mouse strains: a powerful resource for complex trait analysis.

Robert W Williams, Beth Bennett, Lu Lu, Jing Gu, John C DeFries, Phyllis J Carosone-Link, Brad A Rikke, John K Belknap, Thomas E Johnson

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
4.0field-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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
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  4. Estimating Genetic Variance in Life-Span Response to Diet: Insights From Statistical Simulation.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
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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

9 authors at 3 institutions in 1 country.

Robert W WilliamsPortland Alcohol Research Center, Oregon Health Sciences University, 97239, USA.
Beth Bennett
Lu Lu
Jing Gu
John C DeFries
Phyllis J Carosone-Link
Brad A Rikke
John K Belknap
Thomas E Johnson
University of Colorado Boulder · USOregon Health & Science University · USUniversity of Tennessee Health Science Center · US

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Suzanne S. Fei · 2006 to 2026
$34.5M
INFORMATICS CENTER FOR MOUSE NEUROGENETICSP20MH062009 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WILLIAMS, ROBERT W. W · 2000 to 2004
$5.9M
HIGH EFFICIENCY MAPPING OF ALCOHOL SENSITIVITY GENESR01AA011984 · NIAAA · UNIVERSITY OF COLORADO AT BOULDER · PI JOHNSON, THOMAS E. · 2000 to 2003
$1.2M
NIAAA NIH HHS KO1 AA00195NIAAA NIH HHS P50 AA13755NIAAA NIH HHS P60 AA010760NIAAA NIH HHS R01 AA11984NIAAA NIH HHS U24AA13513NIMH NIH HHS P20-MH 62009
6 · The paper itself

Abstract

The set of LXS recombinant inbred (RI) strains is a new and exceptionally large mapping panel that is suitable for the analysis of complex traits with comparatively high power. This panel consists of 77 strains-more than twice the size of other RI sets--and will typically provide sufficient statistical power (beta = 0.8) to map quantitative trait loci (QTLs) that account for approximately 25% of genetic variance with a genomewide p < 0.05. To characterize the genetic architecture of this new set of RI strains, we genotyped 330 MIT microsatellite markers distributed on all autosomes and the X Chromosome and assembled error-checked meiotic recombination maps that have an average F2-adjusted marker spacing of approximately 4 cM. The LXS panel has a genetic structure consistent with random segregation and subsequent fixation of alleles, the expected 3-4 x map expansion, a low level of nonsyntenic association among loci, and complete independence among all 77 strains. Although the parental inbred strains-Inbred Long-Sleep (ILS) and Inbred Short-Sleep (ISS)--were derived originally by selection from an 8-way heterogeneous stock selected for differential sensitivity to sedative effects of ethanol, the LXS panel is also segregating for many other traits. Thus, the LXS panel provides a powerful new resource for mapping complex traits across many systems and disciplines and should prove to be of great utility in modeling the genetics of complex diseases in human populations.

Indexed as

Chromosome MappingAllelesAnimalsChromosome SegregationGenetic MarkersGenotypeMiceMice, Inbred StrainsMicrosatellite RepeatsMultifactorial InheritanceSyntenyGenetic Markers

Identifiers

PMID15457343
OpenAlexW2033296058

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.