Evidence map›Paper›PMID 28819774›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2017

Whole exome sequencing of wild-derived inbred strains of mice improves power to link phenotype and genotype.

Peter L Chang, Emily Kopania, Sara Keeble, Brice A J Sarver, Erica Larson, Annie Orth, Khalid Belkhir, Pierre Boursot, François Bonhomme, Jeffrey M Good and 1 more

Abstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Genetic variation in the Y chromosome and sex-biased DNA methylation in somatic cells in the mouse.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    Article
  10. Article
  11. Meiotic drive in house mice: mechanisms, consequences, and insights for human biology.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Review
  12. Molecular Evolution across Mouse Spermatogenesis.Molecular biology and evolution · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Phenotypic characteristics of commonly used inbred mouse strains.Journal of molecular medicine (Berlin, Germany) · 2020
    Review
  18. Article
  19. Genome-wide association for testis weight in the diversity outbred mouse population.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Article
  20. 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

11 authors.

Peter L ChangMolecular and Computational Biology, University of Southern California, 1050 Childs Way, Los Angeles, CA, 90089, USA.
Emily KopaniaMolecular and Computational Biology, University of Southern California, 1050 Childs Way, Los Angeles, CA, 90089, USA.
Sara KeebleMolecular and Computational Biology, University of Southern California, 1050 Childs Way, Los Angeles, CA, 90089, USA.
Brice A J SarverDivision of Biological Sciences, University of Montana, Missoula, MT, USA.
Erica LarsonDivision of Biological Sciences, University of Montana, Missoula, MT, USA.
Annie OrthInstitut des Sciences de l'Evolution, CNRS UMR554, Université de Montpellier, Montpellier, France.
Khalid BelkhirInstitut des Sciences de l'Evolution, CNRS UMR554, Université de Montpellier, Montpellier, France.
Pierre BoursotInstitut des Sciences de l'Evolution, CNRS UMR554, Université de Montpellier, Montpellier, France.
François BonhommeInstitut des Sciences de l'Evolution, CNRS UMR554, Université de Montpellier, Montpellier, France.
Jeffrey M GoodDivision of Biological Sciences, University of Montana, Missoula, MT, USA.
Matthew D DeanMolecular and Computational Biology, University of Southern California, 1050 Childs Way, Los Angeles, CA, 90089, USA. matthew.dean@usc.edu.

Funding

Evolutionary and Functional Genetics of Male Reproduction using Wild Mice as a MoR01GM098536 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DEAN, MATTHEW D · 2012 to 2016
$1.5M
Meiotic sex chromosome inactivation and the developmental basis of hybrid male stR01HD073439 · NICHD · UNIVERSITY OF MONTANA · PI GOOD, JEFFREY · 2012 to 2016
$1.5M
Division of Environmental Biology 1146525National Institute of General Medical Sciences GM098536NICHD NIH HHS R01 HD073439NIGMS NIH HHS R01 GM098536
6 · The paper itself

Abstract

The house mouse is a powerful model to dissect the genetic basis of phenotypic variation, and serves as a model to study human diseases. Despite a wealth of discoveries, most classical laboratory strains have captured only a small fraction of genetic variation known to segregate in their wild progenitors, and existing strains are often related to each other in complex ways. Inbred strains of mice independently derived from natural populations have the potential to increase power in genetic studies with the addition of novel genetic variation. Here, we perform exome-enrichment and high-throughput sequencing (~8× coverage) of 26 wild-derived strains known in the mouse research community as the "Montpellier strains." We identified 1.46 million SNPs in our dataset, approximately 19% of which have not been detected from other inbred strains. This novel genetic variation is expected to contribute to phenotypic variation, as they include 18,496 nonsynonymous variants and 262 early stop codons. Simulations demonstrate that the higher density of genetic variation in the Montpellier strains provides increased power for quantitative genetic studies. Inasmuch as the power to connect genotype to phenotype depends on genetic variation, it is important to incorporate these additional genetic strains into future research programs.

Indexed as

Exome SequencingGenotypePhenotypeAnimalsAnimals, WildCodon, TerminatorComputer SimulationCrosses, GeneticFemaleGenetic VariationHigh-Throughput Nucleotide SequencingMiceMice, Inbred StrainsPhylogenyPolymorphism, Single NucleotideSequence Analysis, DNACodon, Terminator

Identifiers

PMID28819774
PMCPMC5693759

What OpenQuestion holds

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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.