Evidence map›Paper›PMID 39345458›Full record

ArticlebioRxiv : the preprint server for biology2024

The Unified Phenotype Ontology (uPheno): A framework for cross-species integrative phenomics.

Nicolas Matentzoglu, Susan M Bello, Ray Stefancsik, Sarah M Alghamdi, Anna V Anagnostopoulos, James P Balhoff, Meghan A Balk, Yvonne M Bradford, Yasemin Bridges, Tiffany J Callahan and 36 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

46 authors.

Nicolas MatentzogluSemanticly, Athens, Greece.ORCID 0000-0002-7356-1779
Susan M BelloThe Jackson Laboratory, Bar Harbor, ME.ORCID 0000-0003-4606-0597
Ray StefancsikEMBL-EBI, Hinxton, UK.ORCID 0000-0001-8314-2140
Sarah M AlghamdiKing Abdullah University of Science and Technology (KAUST).ORCID 0000-0001-8314-2140
Anna V AnagnostopoulosThe Jackson Laboratory, Bar Harbor, ME.ORCID 0000-0002-6490-7723
James P BalhoffRenaissance Computing Institute, University of North Carolina, Chapel Hill, NC USA.ORCID 0000-0002-8688-6599
Meghan A BalkNatural History Museum, University of Oslo, Oslo, Norway.ORCID 0000-0003-2699-3066
Yvonne M BradfordUniversity of Oregon, Eugene, OR.ORCID 0000-0002-9900-7880
Yasemin BridgesQueen Mary University of London.ORCID 0009-0002-1371-3782
Tiffany J CallahanDepartment of Biomedical Informatics, Columbia University Irving Medical Center.ORCID 0000-0002-8169-9049
Harry CaufieldLawrence Berkeley National. Laboratory, Berkeley, CA, USA.ORCID 0000-0001-5705-7831
Alayne CuzickRothamsted Research.ORCID 0000-0001-8941-3984
Leigh C CarmodyThe Jackson Laboratory, Bar Harbor, ME.ORCID 0000-0001-7941-2961
Anita R CaronEMBL-EBI, Hinxton, UK.ORCID 0000-0002-6523-4866
Vinicius de SouzaEMBL-EBI, Hinxton, UK.ORCID 0000-0003-3961-0247
Stacia R EngelStanford University, Palo Alto, CA, 94304.ORCID 0000-0001-5472-917X
Petra FeyNorthwestern University, Chicago.ORCID 0000-0002-4532-2703
Malcolm FisherCincinnati Children's Hospital Medical Center, Cincinnati, OH, US.ORCID 0000-0003-1074-8103
Sarah GehrkeUniversity of North Carolina at Chapel Hill.ORCID 0000-0003-3245-2880
Christian GroveCalifornia Institute of Technology, Pasadena, CA 91125.ORCID 0000-0001-9076-6015
Peter HansenBerlin Institute of Health at Charité.ORCID 0000-0001-5535-2845
Nomi L HarrisLawrence Berkeley National. Laboratory, Berkeley, CA, USA.ORCID 0000-0001-6315-3707
Midori A HarrisUniversity of Cambridge.ORCID 0000-0003-4148-4606
Laura HarrisEMBL-EBI, Hinxton, UK.ORCID 0000-0003-4312-7223
Arwa IbrahimEMBL-EBI, Hinxton, UK.ORCID 0000-0001-6757-4744
Julius O B JacobsenQueen Mary University of London.ORCID 0000-0002-3265-1591
Sebastian KöhlerAda Health GmbH.ORCID 0000-0002-5316-1399
Julie A McMurryUniversity of North Carolina at Chapel Hill.ORCID 0000-0002-9353-5498
Violeta Munoz-FuentesUNEP-WCMC.ORCID 0000-0003-3574-546X
Monica C Munoz-TorresUniversity of Colorado Anschutz Medical Campus.ORCID 0000-0001-8430-6039
Helen ParkinsonEMBL-EBI, Hinxton, UK.ORCID 0000-0003-3035-4195
Zoë M PendlingtonEMBL-EBI, Hinxton, UK.ORCID 0000-0002-4071-8397
Clare PilgrimUniversity of Cambridge.ORCID 0000-0002-1373-1705
Sofia Mc RobbStowers Institute for Medical Research.ORCID 0000-0002-3528-5267
Peter N RobinsonBerlin Institute of Health at Charité.ORCID 0000-0002-0736-9199
James SeagerRothamsted Research.ORCID 0000-0001-7487-610X
Erik SegerdellCincinnati Children's Hospital Medical Center, Cincinnati, OH, US.ORCID 0000-0002-9611-1279
Damian SmedleyQueen Mary University of London.ORCID 0000-0002-5836-9850
Elliot SollisEMBL-EBI, Hinxton, UK.ORCID 0000-0003-1322-388X
Sabrina ToroUniversity of North Carolina at Chapel Hill.ORCID 0000-0002-4142-7153
Nicole VasilevskyCritical Path Institute.ORCID 0000-0001-5208-3432
Valerie WoodUniversity of Cambridge.ORCID 0000-0001-6330-7526
Melissa A HaendelUniversity of North Carolina at Chapel Hill.ORCID 0000-0001-9114-8737
Christopher J MungallLawrence Berkeley National. Laboratory, Berkeley, CA, USA.ORCID 0000-0002-6601-2165
James A McLaughlinEMBL-EBI, Hinxton, UK.ORCID 0000-0002-8361-2795
David Osumi-SutherlandWellcome Sanger Institute.ORCID 0000-0002-7073-9172

Funding

SOFTWARE AND DATABASE SYSTEM DEVELOPMENTP41HG000330 · NHGRI · JACKSON LABORATORY · PI EPPIG, JANAN T. · 1995 to 2010
$72.1M
Text mining in the CloudU24HG010859 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAROL J BULT, PAUL Warren STERNBERG · 2019 to 2026
$42.0M
Resource ProjectU41HG002273 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHERRY, J. MICHAEL, MUNGALL, CHRISTOPHER J · 2012 to 2021
$34.7M
Genomic Resource for the Yeast SaccharomycesU41HG001315 · NHGRI · STANFORD UNIVERSITY · PI CHERRY, J. MICHAEL · 2011 to 2020
$26.4M
Xenbase: the Xenopus Model Organism KnowledgebaseP41HD064556 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Aaron M Zorn · 2010 to 2026
$24.9M
Mouse Phenotyping Informatics Infrastructure - MP12UM1HG006370 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI Pilar Cacheiro Martinez, Helen Elizabeth Parkinson · 2016 to 2026
$20.4M
The Jackson Laboratory Center for Precision GeneticsU54OD030187 · OD · JACKSON LABORATORY · PI Cathleen M Lutz · 2020 to 2026
$17.2M
The Monarch Initiative: Linking Diseases to Model Organism ResourcesR24OD011883 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2012 to 2024
$16.0M
ZFIN: The Zebrafish Model Organism DatabaseU24HG002659 · NHGRI · UNIVERSITY OF OREGON · PI WESTERFIELD, MONTE · 2021 to 2025
$10.8M
Improvements to the LinkML framework to support the Phenomics First open science resourceRM1HG010860 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2020 to 2024
$10.3M
Mouse Phenome ProjectR01DA028420 · NIDA · JACKSON LABORATORY · PI Elissa J Chesler · 2010 to 2026
$9.5M
The Human Phenotype Ontology: Accelerating Computational Integration of Clinical Data for GenomicsU24HG011449 · NHGRI · JACKSON LABORATORY · PI Peter Nicholas Robinson · 2021 to 2026
$6.7M
NHGRI NIH HHS P41 HG000330NHGRI NIH HHS RM1 HG010860NHGRI NIH HHS U24 HG002659NHGRI NIH HHS U24 HG010859NHGRI NIH HHS U24 HG011449NHGRI NIH HHS U24 HG012542NHGRI NIH HHS U41 HG001315NHGRI NIH HHS U41 HG002273NHGRI NIH HHS UM1 HG006370NICHD NIH HHS P41 HD064556NIDA NIH HHS R01 DA028420NIH HHS R24 OD011883NIH HHS U54 OD030187Wellcome Trust
6 · The paper itself

Abstract

Phenotypic data are critical for understanding biological mechanisms and consequences of genomic variation, and are pivotal for clinical use cases such as disease diagnostics and treatment development. For over a century, vast quantities of phenotype data have been collected in many different contexts covering a variety of organisms. The emerging field of phenomics focuses on integrating and interpreting these data to inform biological hypotheses. A major impediment in phenomics is the wide range of distinct and disconnected approaches to recording the observable characteristics of an organism. Phenotype data are collected and curated using free text, single terms or combinations of terms, using multiple vocabularies, terminologies, or ontologies. Integrating these heterogeneous and often siloed data enables the application of biological knowledge both within and across species. Existing integration efforts are typically limited to mappings between pairs of terminologies; a generic knowledge representation that captures the full range of cross-species phenomics data is much needed. We have developed the Unified Phenotype Ontology (uPheno) framework, a community effort to provide an integration layer over domain-specific phenotype ontologies, as a single, unified, logical representation. uPheno comprises (1) a system for consistent computational definition of phenotype terms using ontology design patterns, maintained as a community library; (2) a hierarchical vocabulary of species-neutral phenotype terms under which their species-specific counterparts are grouped; and (3) mapping tables between species-specific ontologies. This harmonized representation supports use cases such as cross-species integration of genotype-phenotype associations from different organisms and cross-species informed variant prioritization.

Identifiers

PMID39345458
PMCPMC11429889

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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.