Evidence map›Paper›PMID 29760201›Full record

ArticleG3 (Bethesda, Md.)2018

A High-Resolution Genetic Map for the Laboratory Rat.

John Littrell, Shirng-Wern Tsaih, Amelie Baud, Pasi Rastas, Leah Solberg-Woods, Michael J Flister

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 4 institutions in 3 countries.

John LittrellGenomic Sciences and Precision Medicine Center.
Shirng-Wern TsaihGenomic Sciences and Precision Medicine Center.
Amelie BaudEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, CB10 1SD Hinxton, Cambridge, UK.ORCID 0000-0003-2448-0283
Pasi RastasInstitute of Biotechnology, University of Helsinki, Finland.
Leah Solberg-WoodsDepartment of Internal Medicine, Wake Forest Baptist Medical Center, Winston-Salem, NC 27157.
Michael J FlisterGenomic Sciences and Precision Medicine Center mflister@mcw.edu.ORCID 0000-0001-8030-7739
Medical College of Wisconsin · USAtrium Health Wake Forest Baptist · USEuropean Bioinformatics Institute · GBUniversity of Helsinki · FI

Funding

Leveraging genetic mapping for personalized targeting of breast cancer microenvironmentR01CA193343 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amit Joshi · 2015 to 2026
$3.5M
Systems Genetics of Adiposity Traits in Outbred RatsR01DK106386 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SOLBERG WOODS, LEAH CATHERINE · 2015 to 2018
$2.6M
Genome-wide fine-mapping of metabolic traits in heterogeneous stock ratsR01DK088975 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI SOLBERG WOODS, LEAH CATHERINE · 2010 to 2014
$1.9M
NCI NIH HHS R01 CA193343NIDDK NIH HHS R01 DK088975NIDDK NIH HHS R01 DK106386Wellcome TrustWellcome Trust 089269/Z/09/Z
6 · The paper itself

Abstract

An accurate and high-resolution genetic map is critical for mapping complex traits, yet the resolution of the current rat genetic map is far lower than human and mouse, and has not been updated since the original Jensen-Seaman map in 2004. For the first time, we have refined the rat genetic map to sub-centimorgan (cM) resolution (<0.02 cM) by using 95,769 genetic markers and 870 informative meioses from a cohort of 528 heterogeneous stock (HS) rats. Global recombination rates in the revised sex-averaged map (0.66 cM/Mb) did not differ compared to the historical map (0.65 cM/Mb); however, substantial refinement was made to the localization of highly recombinant regions within the revised map. Also for the first time, sex-specific rat genetic maps were generated, which revealed both genomewide and fine-scale variation in recombination rates between male and female rats. Reanalysis of multiple quantitative trait loci (QTL) using the historical and refined rat genetic maps demonstrated marked changes to QTL localization, shape, and effect size. As a resource to the rat research community, we have provided revised centimorgan positions for all physical positions within the rat genome and commonly used genetic markers for trait mapping, including 44,828 SSLP markers and the RATDIV genotyping array. Collectively, this study provides a substantial improvement to the rat genetic map and an unprecedented resource for analysis of complex traits and recombination in the rat.

Indexed as

Chromosome MappingGenetic MarkersGenomeGenomicsAnimalsAnimals, LaboratoryChromosomes, MammalianGenotypeMicrosatellite RepeatsQuantitative Trait LociRatsRecombination, GeneticGenetic Markersgenetic mapratrecombination

Identifiers

PMID29760201
PMCPMC6027877
OpenAlexW2951638329

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.