Evidence map›Paper›PMID 36330959›Full record

ArticleNucleic acids research2023

Mouse Phenome Database: towards a more FAIR-compliant and TRUST-worthy data repository and tool suite for phenotypes and genotypes.

Molly A Bogue, Robyn L Ball, Vivek M Philip, David O Walton, Matthew H Dunn, Georgi Kolishovski, Anna Lamoureux, Matthew Gerring, Hongping Liang, Jake Emerson and 9 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Mouse phenome database: curated data repository with interactive multi-population and multi-trait analyses.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    Pooled it
  3. Article
  4. Article
  5. The power of mouse models in the diagnostic odyssey of patients with rare congenital anomalies.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
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  20. The Ontology of Biological Attributes (OBA)-computational traits for the life sciences.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    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

19 authors.

Molly A BogueThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.ORCID 0000-0001-6624-9261
Robyn L BallThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Vivek M PhilipThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
David O WaltonThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Matthew H DunnThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Georgi KolishovskiThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Anna LamoureuxThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Matthew GerringThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Hongping LiangThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Jake EmersonThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Tim StearnsThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Hao HeThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Gaurab MukherjeeThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.ORCID 0000-0002-1473-4174
John BluisThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Sejal DesaiThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Beth SundbergThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Beena KadakkuzhaThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Govindarajan Kunde-RamamoorthyThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.
Elissa J CheslerThe Jackson Laboratory, Bar Harbor Maine, 04609, USA.

Funding

Project 5: Circadian RhythmsP50DA039841 · NIDA · JACKSON LABORATORY · PI LAURA G REINHOLDT · 2016 to 2026
$26.2M
The Jackson Laboratory Center for Precision GeneticsU54OD030187 · OD · JACKSON LABORATORY · PI Cathleen M Lutz · 2020 to 2026
$17.2M
Mouse Phenome ProjectR01DA028420 · NIDA · JACKSON LABORATORY · PI Elissa J Chesler · 2010 to 2026
$9.5M
Mouse Phenome Database: NIA Interventions Testing Program Data Coordinating CenterU24AG066346 · NIA · JACKSON LABORATORY · PI Elissa J Chesler · 2019 to 2026
$1.7M
NIA NIH HHS U24 AG066346NIDA NIH HHS P50 DA039841NIDA NIH HHS R01 DA028420
6 · The paper itself

Abstract

The Mouse Phenome Database (MPD; https://phenome.jax.org; RRID:SCR_003212), supported by the US National Institutes of Health, is a Biomedical Data Repository listed in the Trans-NIH Biomedical Informatics Coordinating Committee registry. As an increasingly FAIR-compliant and TRUST-worthy data repository, MPD accepts phenotype and genotype data from mouse experiments and curates, organizes, integrates, archives, and distributes those data using community standards. Data are accompanied by rich metadata, including widely used ontologies and detailed protocols. Data are from all over the world and represent genetic, behavioral, morphological, and physiological disease-related characteristics in mice at baseline or those exposed to drugs or other treatments. MPD houses data from over 6000 strains and populations, representing many reproducible strain types and heterogenous populations such as the Diversity Outbred where each mouse is unique but can be genotyped throughout the genome. A suite of analysis tools is available to aggregate, visualize, and analyze these data within and across studies and populations in an increasingly traceable and reproducible manner. We have refined existing resources and developed new tools to continue to provide users with access to consistent, high-quality data that has translational relevance in a modernized infrastructure that enables interaction with a suite of bioinformatics analytic and data services.

Indexed as

Databases, GeneticPhenomicsAnimalsGenotypeMiceMice, Inbred StrainsPhenotype

Identifiers

PMID36330959
PMCPMC9825561

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.