Evidence map›Paper›PMID 15534693›Full record

ArticlePLoS biology2004

Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse.

Mathew T Pletcher, Philip McClurg, Serge Batalov, Andrew I Su, S Whitney Barnes, Erica Lagler, Ron Korstanje, Xiaosong Wang, Deborah Nusskern, Molly A Bogue and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
18.0field-weighted citation impact, top 1% 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

119 citing papers in PubMed, 226 citations in OpenAlex.

  1. Article
  2. Genetic determinants of ammonia-induced acute lung injury in mice.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  3. Article
  4. In silico mapping of quantitative trait loci (QTL) regulating the milk ionome in mice identifies a milk iron locus on chromosome 1.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    Article
  10. Article
  11. Genome-wide association mapping of acute lung injury in neonatal inbred mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
  12. Article
  13. Article
  14. Article
  15. Functional genomic assessment of phosgene-induced acute lung injury in mice.American journal of respiratory cell and molecular biology · 2013
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

59 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

13 authors at 2 institutions in 1 country.

Mathew T PletcherGenomics Institute of the Novartis Research Foundation, San Diego, California, USA.
Philip McClurg
Serge Batalov
Andrew I Su
S Whitney Barnes
Erica Lagler
Ron Korstanje
Xiaosong Wang
Deborah Nusskern
Molly A Bogue
Richard J Mural
Beverly Paigen
Tim Wiltshire
Genomics Institute of the Novartis Research Foundation · USJackson Laboratory · US

Funding

COGNITIVE DEFICITS RELATED TO CHRONIC ALCOHOLISMR01AA000187 · NIAAA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MCGLINCHEY, REGINA · 1985 to 2001
$192k
NIAAA NIH HHS R01 AA000187-20Wellcome Trust
6 · The paper itself

Abstract

Rapid expansion of available data, both phenotypic and genotypic, for multiple strains of mice has enabled the development of new methods to interrogate the mouse genome for functional genetic perturbations. In silico mapping provides an expedient way to associate the natural diversity of phenotypic traits with ancestrally inherited polymorphisms for the purpose of dissecting genetic traits. In mouse, the current single nucleotide polymorphism (SNP) data have lacked the density across the genome and coverage of enough strains to properly achieve this goal. To remedy this, 470,407 allele calls were produced for 10,990 evenly spaced SNP loci across 48 inbred mouse strains. Use of the SNP set with statistical models that considered unique patterns within blocks of three SNPs as an inferred haplotype could successfully map known single gene traits and a cloned quantitative trait gene. Application of this method to high-density lipoprotein and gallstone phenotypes reproduced previously characterized quantitative trait loci (QTL). The inferred haplotype data also facilitates the refinement of QTL regions such that candidate genes can be more easily identified and characterized as shown for adenylate cyclase 7.

Indexed as

Chromosome MappingPolymorphism, Single NucleotideAdenylyl CyclasesAllelesAnimalsComputational BiologyCrosses, GeneticGallstonesGenomeHaplotypesLinkage DisequilibriumLipoproteins, HDLLogistic ModelsMiceMice, Inbred C57BLMice, Inbred DBAAdenylyl CyclasesLipoproteins, HDL

Identifiers

PMID15534693
PMCPMC526179
OpenAlexW2050499823

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.