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ZENODO
Dataset . 2020
Data sources: Datacite
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2020
Data sources: ZENODO
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OMOP2OBO Measurement Mappings -- WRONG DATA FILE UPLOADED IGNORE THIS VERSION

Authors: Callahan, Tiffany J; Vasilevsky, Nicole A; Bennett, Tellen D; Martin, Blake; Feinstein, James A; Baumgartner, William A; Hunter, Lawrence D; +1 Authors

OMOP2OBO Measurement Mappings -- WRONG DATA FILE UPLOADED IGNORE THIS VERSION

Abstract

OMOP2OBO Measurement Mappings V1.0 The mappings in this repository were created between OMOP standard measurement concepts (i.e., LOINC) to the Human Phenotype Ontology (HPO), Chemical Entities of Biological Interest (CheBI), Vaccine Ontology (VO), National Center for Biotechnology Information Taxon Ontology (NCBITaxon), Protein Ontology (PRO), Cell Ontology (CL), and the Uber-anatomy Ontology (UBERON). For each measurement, all levels of the test result (results above, below, and within a reference range) were mapped, not only those deemed clinically relevant. Results outside of a reference range, but not currently deemed clinically relevant (as advised by the literature or consultation via domain expert), were annotated to the nearest relevant ontology concept ancestor. For example, when annotating the results of a test for Asparagus IgE Ab RAST class [Presence] in Serum (LOINC:15547-3), a result above a reference range would be annotated with an increased anti-plant-based food allergen IgE antibody level (HP:0410228). While a low level of this antibody may not be deemed clinically relevant, it is still outside of the provided reference range and thus was annotated to the nearest applicable concept ancestor, abnormal immunoglobulin level (HP:0010701). There is one exception to this rule: all measured drugs and toxins (entities not normally found in the human body) with normal results (results that were not outside of a given reference range) were annotated to the same HP concept as the clinically relevant result and logically negated. For example, Amphetamine [Presence] in Urine by Screen (LOINC:19343-3), a positive finding was mapped to a positive urine amphetamine test (HP:0500112) and a negative finding was mapped to a positive urine amphetamine test and logically negated (NOT HP:0500112). LOINC2HPO currently aligns LOINC to HP. The current work extends existing LOINC2HPO annotations to match the OMOP2OBO mappings in the following two ways: (1) annotations were updated if new and/or more specific concepts had been added to the HP; and (2) existing mappings were expanded to include the measurement substance (body fluids, tissues, and organs via Uberon), the entity being measured (chemicals, metabolites, or hormones via ChEBI; cell types via CL; and proteins and protein complexes via PR), and the species of the measured entities (organism taxonomy via NCBITaxon). Consistent with LOINC2HPO, all measurements lacking sufficient specimen detail (those measured in non-specific body substances) were annotated as “Unspecified Sample” and all measurements without a valid result type were annotated as “Not Mapped test Type”. All modifications to the original LOINC2HPO annotations were meticulously recorded in the mapping evidence field enabling users to easily identify when an original LOINC2HPO annotation had been updated. For this OMOP domain, the owl:complementOf (“not” and was used to model normal test results), owl:intersectionOf (“and”), and owl:unionOf (“or”) constructors were used to construct semantically expressive mappings. Mapping Details Mappings included in this set were generated automatically using OMOP2OBO or through the use of a Bag-of-words embedding model using TF-IDF. Cosine similarity is used to compute similarity scores between all pairwise combinations of OMOP and OBO concepts and ancestor concepts. To improve the efficiency of this process, the algorithm searches only the top 𝑛 most similar results and keeps the top 75th percentile among all pairs with scores >= 0.25. Manually created mappings are also included. Mapping Categories Automatic One-to-One Concept: Exact label or synonym, dbXRef, or expert validated mapping @ concept-level; 1:1 Automatic One-to-One Ancestor: Exact label or synonym, dbXRef, or expert validated mapping @ concept ancestor-level; 1:1 Automatic One-to-Many Concept: Exact label or synonym, dbXRef, cosine similarity, or expert validated mapping @ concept-level; 1:Many Automatic One-to-Many Ancestor: Exact label or synonym, dbXRef, cosine similarity, or expert validated mapping @ concept-level; 1:Many Manual One-to-One: Hand mapping created using expert suggested resources; 1:1 Manual One-to-Many: Hand mapping created using expert suggested resources; 1:Many Cosine Similarity: score suggested mapping -- manually verified UnMapped: No suitable mapping or not mapped type Mapping Statistics Additional statistics have been provided for the mappings and are shown in the table below. This table presents the counts of OMOP concepts by mapping category and ontology: Mapping Category HPO UBERON ChEBI CL PR NCBITaxon Automatic One-to-One Concept 20 1981 268 129 19 286 Automatic One-to-Many Concept 49 5 0 24 0 0 Automatic One-to-One Ancestor 43 426 1149 5 5 207 Automatic Constructor - Ancestor 0 1 12 1 0 0 Cosine Similarity 113 50 160 35 45 56 Manual 10663 319 1446 185 1590 2357 Manual One-to-Many 49 1118 528 18 133 196 UnMapped 184 184 529 3688 2296 982 Provenance and Versioning: The V1.0 deposited mappings were created by OMOP2OBO v1.0.0 on October 2022 using the OMOP Common Data Model V5.0 and OBO Foundry ontologies downloaded on September 14, 2020. Caveats: Please note that these are the original mappings that were created for the preprint. They have not been updated to current versions of the ontologies. In our experience, this should result in very few errors, but we do suggest that you check the ontology concepts used against current versions of each ontology before using them. Important Resources and Documentation GitHub: OMOP2OBO Project Wiki: OMOP2OBO - wiki Zenodo Community: OMOP2OBO Preprint Manuscript: 10.5281/zenodo.5716421

Keywords

Observational Medical Outcome Partnership, PRO, Protein Ontology, Uber-anatomy Ontology, UBERON, OMOP2OBO, Human Phenotype Ontology, Cell Ontology, Concept Mappings, Open Biomedical Foundry, Uberon Multi-Species Anatomy Ontology, NCBITaxon, Open Biomedical Foundry Ontologies, OBO, CL, National Center for Biotechnology Information Taxon Ontology, HPO, Chemical Entities of Biological Interest, CHEBI, OMOP

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average