The Unified Phenotype Ontology : a framework for cross-species integrative phenomics
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 contex...
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| Vydáno v: | Genetics (Austin) Ročník 229; číslo 3 |
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17.03.2025
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| ISSN: | 1943-2631, 1943-2631 |
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| 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. |
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| AbstractList | 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. 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.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. |
| Author | Ibrahim, Arwa Caufield, Harry Smedley, Damian Fey, Petra Pendlington, Zoë M Pilgrim, Clare Segerdell, Erik Fisher, Malcolm Harris, Nomi L Robb, Sofia M C Bridges, Yasemin Osumi-Sutherland, David Bradford, Yvonne M McLaughlin, James A Hansen, Peter Harris, Laura Caron, Anita R Parkinson, Helen Vasilevsky, Nicole Engel, Stacia R Sollis, Elliot Stefancsik, Ray Wood, Valerie Robinson, Peter N Matentzoglu, Nicolas de Souza, Vinicius Bello, Susan M Toro, Sabrina Haendel, Melissa A Callahan, Tiffany J Carmody, Leigh C Balhoff, James P Gehrke, Sarah Seager, James Köhler, Sebastian McMurry, Julie A Munoz-Torres, Monica C Alghamdi, Sarah M Munoz-Fuentes, Violeta Balk, Meghan A Anagnostopoulos, Anna V Cuzick, Alayne Harris, Midori A Mungall, Christopher J Jacobsen, Julius O B Grove, Christian |
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0000-0001-5472-917X surname: Engel fullname: Engel, Stacia R organization: Department of Genetics, Stanford University, Palo Alto, CA 94304, USA – sequence: 17 givenname: Petra surname: Fey fullname: Fey, Petra organization: Center for Genetic Medicine, Northwestern University, Chicago, IL 60611, USA – sequence: 18 givenname: Malcolm orcidid: 0000-0003-1074-8103 surname: Fisher fullname: Fisher, Malcolm organization: Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA – sequence: 19 givenname: Sarah surname: Gehrke fullname: Gehrke, Sarah organization: Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA – sequence: 20 givenname: Christian surname: Grove fullname: Grove, Christian organization: Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA – sequence: 21 givenname: Peter orcidid: 0000-0001-5535-2845 surname: Hansen fullname: 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Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, Cambridgeshire, CB10 1SD, UK – sequence: 32 givenname: Zoë M surname: Pendlington fullname: Pendlington, Zoë M organization: European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, Cambridgeshire, CB10 1SD, UK – sequence: 33 givenname: Clare surname: Pilgrim fullname: Pilgrim, Clare organization: Department of Biochemistry, University of Cambridge, Cambridge, CB21 TN, UK – sequence: 34 givenname: Sofia M C surname: Robb fullname: Robb, Sofia M C organization: Stowers Institute for Medical Research, Kansas City, MO 64110, USA – sequence: 35 givenname: Peter N surname: Robinson fullname: Robinson, Peter N organization: Universitätsmedizin Berlin, Berlin Institute of Health at Charité, Anna-Louisa-Karsch-Straße 2, Berlin 10178, Germany – sequence: 36 givenname: James orcidid: 0000-0001-7487-610X surname: Seager fullname: Seager, James organization: Department of 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Osumi-Sutherland, David organization: Wellcome Sanger Institute, Hinxton, Saffron Walden CB10 1RQ, UK |
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| Title | The Unified Phenotype Ontology : a framework for cross-species integrative phenomics |
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