Evidence map›Paper›PMID 32398234›Full record

ArticleG3 (Bethesda, Md.)2020

Adapting Genotyping-by-Sequencing and Variant Calling for Heterogeneous Stock Rats.

Alexander F Gileta, Jianjun Gao, Apurva S Chitre, Hannah V Bimschleger, Celine L St Pierre, Shyam Gopalakrishnan, Abraham A Palmer

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

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

  1. Pooled it
  2. Article
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  5. Low-coverage whole-genome sequencing facilitates accurate and cost-effective haplotype reconstruction in complex mouse crosses.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
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  14. Genomic Loci Influencing Cue-Reactivity in Heterogeneous Stock Rats.bioRxiv : the preprint server for biology · 2024
    Article
  15. Article
  16. Article
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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

7 authors.

Alexander F GiletaDepartment of Psychiatry.ORCID 0000-0002-7793-8043
Jianjun GaoDepartment of Psychiatry.
Apurva S ChitreDepartment of Psychiatry.ORCID 0000-0003-1709-9214
Hannah V BimschlegerDepartment of Psychiatry.
Celine L St PierreDepartment of Psychiatry.ORCID 0000-0001-5465-6601
Shyam GopalakrishnanDepartment of Human Genetics, University of Chicago, Chicago, Illinois, 60637, and.ORCID 0000-0002-2004-6810
Abraham A PalmerDepartment of Psychiatry, aapalmer@ucsd.edu.ORCID 0000-0003-3634-0747

Funding

Sequencing CoreP50DA037844 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2014 to 2023
$27.4M
PREDOCTORAL TRAINING IN GENETICS AND REGULATIONT32GM007197 · NIGMS · UNIVERSITY OF CHICAGO · PI ROTHMAN-DENES, LUCIA B. B · 1985 to 2020
$17.0M
Use of Next-Gen Sequencing to Identify Genetic Variants that Influence compulsiveOxycodone Intake in Outbred RatsU01DA044451 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Olivier George, Abraham A Palmer · 2018 to 2026
$7.3M
GWAS for Goal Versus Sign Tracking in Genetically Heterogeneous RatsR21DA036672 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2014 to 2015
$445k
GWAS for the attribution of incentive salience in outbred ratsF31DA039638 · NIDA · UNIVERSITY OF CHICAGO · PI GILETA, ALEXANDER · 2015 to 2017
$117k
NIDA NIH HHS F31 DA039638NIDA NIH HHS P50 DA037844NIDA NIH HHS R21 DA036672NIDA NIH HHS U01 DA044451NIGMS NIH HHS T32 GM007197
6 · The paper itself

Abstract

The heterogeneous stock (HS) is an outbred rat population derived from eight inbred rat strains. HS rats are ideally suited for genome wide association studies; however, only a few genotyping microarrays have ever been designed for rats and none of them are currently in production. To address the need for an efficient and cost effective method of genotyping HS rats, we have adapted genotype-by-sequencing (GBS) to obtain genotype information at large numbers of single nucleotide polymorphisms (SNPs). In this paper, we have outlined the laboratory and computational steps we took to optimize double digest genotype-by-sequencing (ddGBS) for use in rats. We evaluated multiple existing computational tools and explain the workflow we have used to call and impute over 3.7 million SNPs. We have also compared various rat genetic maps, which are necessary for imputation, including a recently developed map specific to the HS. Using our approach, we obtained concordance rates of 99% with data obtained using data from a genotyping array. The principles and computational pipeline that we describe could easily be adapted for use in other species for which reliable reference genome sets are available.

Indexed as

Genotyping TechniquesHigh-Throughput Nucleotide SequencingAnimalsGenome, PlantGenome-Wide Association StudyGenotypePolymorphism, Single NucleotideRatsgenotyping-by-sequencingheterogeneous stockimputationrat

Identifiers

PMID32398234
PMCPMC7341140

What OpenQuestion holds

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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.