Evidence map›Paper›PMID 33785770›Full record

ArticleScientific reports2021

A domestic cat whole exome sequencing resource for trait discovery.

Alana R Rodney, Reuben M Buckley, Robert S Fulton, Catrina Fronick, Todd Richmond, Christopher R Helps, Peter Pantke, Dianne J Trent, Karen M Vernau, John S Munday and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. SomaticHypertension (Dallas, Tex. : 1979) · 2024
    Article
  8. Review
  9. Article
  10. Journal of feline medicine and surgery · 2023
    Article
  11. Article
  12. Article
  13. Genes · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

14 authors.

Alana R Rodney *Department of Animal Sciences, College of Agriculture, Department of Surgery, School of Medicine, Institute for Data Science and Informatics, University of Missouri, Columbia, MO, 65211, USA.
Reuben M Buckley *Department of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO, 65211, USA.
Robert S FultonMcDonnell Genome Institute, Washington University, School of Medicine, St Louis, MO, 63108, USA.
Catrina FronickMcDonnell Genome Institute, Washington University, School of Medicine, St Louis, MO, 63108, USA.
Todd RichmondRoche Sequencing Solutions, Pleasanton, CA, 94588, USA.
Christopher R HelpsLangford Vets, University of Bristol, Langford, Bristol, BS40 5DU, UK.
Peter PantkeAniCura Bielefeld GmbH, Tierärztliche Klinik für Kleintiere, 33719, Bielefeld, Germany.
Dianne J TrentDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, Knoxville, TN, 37996, USA.
Karen M VernauSchool of Veterinary Medicine, University of California Davis, Davis, CA, 95616, USA.
John S MundaySchool of Veterinary Science, Massey University, Palmerston North, New Zealand.
Andrew C LewinDepartment of Veterinary Clinical Sciences, Louisiana State University, Baton Rouge, LA, 70803, USA.
Rondo MiddletonNestlé Purina Research US, Saint Louis, MO, 63164, USA.
Leslie A LyonsDepartment of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO, 65211, USA.
Wesley C WarrenDepartment of Animal Sciences, College of Agriculture, Department of Surgery, School of Medicine, Institute for Data Science and Informatics, University of Missouri, Columbia, MO, 65211, USA. warrenwc@missouri.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over 94 million domestic cats are susceptible to cancers and other common and rare diseases. Whole exome sequencing (WES) is a proven strategy to study these disease-causing variants. Presented is a 35.7 Mb exome capture design based on the annotated Felis_catus_9.0 genome assembly, covering 201,683 regions of the cat genome. Whole exome sequencing was conducted on 41 cats with known and unknown genetic diseases and traits, of which ten cats had matching whole genome sequence (WGS) data available, used to validate WES performance. At 80 × mean exome depth of coverage, 96.4% of on-target base coverage had a sequencing depth > 20-fold, while over 98% of single nucleotide variants (SNVs) identified by WGS were also identified by WES. Platform-specific SNVs were restricted to sex chromosomes and a small number of olfactory receptor genes. Within the 41 cats, we identified 31 previously known causal variants and discovered new gene candidate variants, including novel missense variance for polycystic kidney disease and atrichia in the Peterbald cat. These results show the utility of WES to identify novel gene candidate alleles for diseases and traits for the first time in a feline model.

Indexed as

Exome SequencingGenetic Predisposition to DiseaseAnimalsCat DiseasesCatsExomeFemaleMalePolymorphism, Single Nucleotide

Identifiers

PMID33785770
PMCPMC8009874

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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.