HL7 Terminology (THO)
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HL7 Terminology (THO), published by HL7 International - Vocabulary Work Group. This guide is not an authorized publication; it is the continuous build for version 7.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/UTG/ and changes regularly. See the Directory of published versions

Sequence Ontology Metadata Record

Metadata Record Information Version 20251031
Maintained By HL7 Terminology Services Management Group (TSMG)
Last Updated Date 31 October 2025
Responsible Organizations Sequence Ontology Roles
  • Code System Owner
  • Code System Maintainer (Steward)
  • Code System Publisher
Website http://www.sequenceontology.org/
Email address
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Address
Code System Names Formal name Sequence Ontology
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Code System Technical Identifiers Identification Record
TSMG-endorsed URI http://www.sequenceontology.org
TSMG-endorsed OID Not Assigned
Code System Information Links
Description
"The Sequence Ontology is a set of terms and relationships used to describe the features and attributes of biological sequence. SO includes different kinds of features which can be located on the sequence. Biological features are those which are defined by their disposition to be involved in a biological process." "The Sequence Ontologies are provided as a resource to the biological community. They have the following obvious uses: * To provide for a structured controlled vocabulary for the description of primary annotations of nucleic acid sequence, e.g. the annotations shared by a DAS server ([BioDAS](http://www.biodas.org/documents/das2/das2_protocol.html), [Biosapiens DAS](http://www.biosapiens.info/page.php?page=das_portal)), or annotations encoded by [GFF3](http://www.sequenceontology.org/gff3.shtml)." * To provide for a structured representation of these annotations within databases. Were genes within model organism databases to be annotated with these terms then it would be possible to query all these databases for, for example, all genes whose transcripts are edited, or trans-spliced, or are bound by a particular protein. One such genomic database is [Chado](http://www.gmod.org/wiki/Chado). * To provide a structured controlled vocabulary for the description of mutations at both the sequence and more gross level in the context of genomic databases." "The Sequence Ontology is part of [OBO](http://www.obofoundry.org/). It has close links to other ontology projects such as the [RNAO consortium](http://roc.bgsu.edu/), and the [Biosapiens polypeptide features](http://www.ebi.ac.uk/ontology-lookup/browse.do?ontName=BS)." The content can be browsed [here](http://www.sequenceontology.org/browser/obob.cgi) The content can be downloaded [here](https://github.com/The-Sequence-Ontology/SO-Ontologies) For information on contributing, please see [here](https://github.com/The-Sequence-Ontology/SO-Ontologies#contributing) To request a term or register feedback, see [here](https://github.com/The-Sequence-Ontology/SO-Ontologies/issues)
Arrangements or agreements with HL7 for use of content
Version management Version information
Code System Copyright, Intellectual Property and Licensing Copyright Statement
The Sequence Ontology: A tool for the unification of genome annotations. Eilbeck K., Lewis S.E., Mungall C.J., Yandell M., Stein L., Durbin R., Ashburner M. [Genome Biology (2005) 6:R44](http://genomebiology.com/2005/6/5/R44) Please also include the version of SO used. Sequence Ontology data and data products are licensed under the [Creative Commons Attribution 4.0 Unported License](https://creativecommons.org/licenses/by/4.0/legalcode).
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Intellectual Property Information
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