Evidence map›Paper›PMID 32392208›Full record

ArticlePLoS genetics2020

Copy number variants and fixed duplications among 198 rhesus macaques (Macaca mulatta).

Marina Brasó-Vives, Inna S Povolotskaya, Diego A Hartasánchez, Xavier Farré, Marcos Fernandez-Callejo, Muthuswamy Raveendran, R Alan Harris, Douglas L Rosene, Belen Lorente-Galdos, Arcadi Navarro and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Genomic resources for rhesus macaques (Macaca mulatta).Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Article
  6. Gene editing monkeys: Retrospect and outlook.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. 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

13 authors at 8 institutions in 4 countries.

Marina Brasó-VivesInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0001-5007-5789
Inna S PovolotskayaVeltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University, Moscow, Russia.ORCID 0000-0001-6621-232X
Diego A HartasánchezInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0003-2596-6883
Xavier FarréInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0001-6838-9479
Marcos Fernandez-CallejoNational Centre for Genomic Analysis-Centre for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Catalonia, Spain.ORCID 0000-0002-9968-3766
Muthuswamy RaveendranHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
R Alan HarrisHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0002-7333-4752
Douglas L RoseneDepartment of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Belen Lorente-GaldosDepartment of Neuroscience, Yale School of Medicine, New Haven, Connecticut, United States of America.ORCID 0000-0001-5390-2452
Arcadi NavarroInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.
Tomas Marques-BonetInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0002-5597-3075
Jeffrey RogersHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0002-7374-6490
David JuanInstitut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Parc de Recerca Biomèdica de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0003-1912-9667
Baylor College of Medicine · USUniversitat Pompeu Fabra · ESInstitució Catalana de Recerca i Estudis Avançats · ESBoston University · USCentre for Genomic Regulation · ESPirogov Russian National Research Medical University · RUUniversité Claude Bernard Lyon 1 · FRYale University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Genomic Architecture of Common Disease in Diverse Populations: WGS of Ongoing Hemorrhagic Stroke Study SupplementUM1HG008898 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2016 to 2020
$77.0M
Genomic Sequencing to Establish a Macaque Genotype and Phenotype Research ResourceR24OD021324 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI BIMBER, BENJAMIN, WALL, JEFFREY D · 2016 to 2023
$7.7M
Large Scale Sequencing Variation in Rhesue Macaques - HIV Vaccine SupplementR24OD011173 · OD · BAYLOR COLLEGE OF MEDICINE · PI ROGERS, JEFFREY A. · 2012 to 2017
$3.7M
Biobehavioral characterization of infant rhesus monkeysR24OD010962 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CAPITANIO, JOHN P · 2012 to 2018
$2.5M
Howard Hughes Medical InstituteNHGRI NIH HHS UM1 HG008898NIH HHS P51 OD011092NIH HHS P51 OD011107NIH HHS R24 OD010962NIH HHS R24 OD011173NIH HHS R24 OD021324
6 · The paper itself

Abstract

The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for biomedical research due to its close phylogenetic relationship to humans. Copy number variation is one of the main sources of genomic diversity within and between species and a widely recognized cause of inter-individual differences in disease risk. However, copy number differences among rhesus macaques and between the human and macaque genomes, as well as the relevance of this diversity to research involving this nonhuman primate, remain understudied. Here we present a high-resolution map of sequence copy number for the rhesus macaque genome constructed from a dataset of 198 individuals. Our results show that about one-eighth of the rhesus macaque reference genome is composed of recently duplicated regions, either copy number variable regions or fixed duplications. Comparison with human genomic copy number maps based on previously published data shows that, despite overall similarities in the genome-wide distribution of these regions, there are specific differences at the chromosome level. Some of these create differences in the copy number profile between human disease genes and their rhesus macaque orthologs. Our results highlight the importance of addressing the number of copies of target genes in the design of experiments and cautions against human-centered assumptions in research conducted with model organisms. Overall, we present a genome-wide copy number map from a large sample of rhesus macaque individuals representing an important novel contribution concerning the evolution of copy number in primate genomes.

Indexed as

Chromosome MappingAnimalsDNA Copy Number VariationsFemaleGene DuplicationGenetics, PopulationGenomeHigh-Throughput Nucleotide SequencingHumansMacaca mulattaMaleOpen Reading FramesPhylogenySequence Analysis, DNASpecies Specificity

Identifiers

PMID32392208
PMCPMC7241854
OpenAlexW3023272815

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.