Semantic Versioning definition

Semantic Versioning means a versioning scheme where a version is identified by the version number MAJOR.MINOR.PATCH, where:
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Semantic Versioning means the determination or interpretation of the version number of a specification in accordance with the provisions of Semantic Versioning 2.0.0 (▇▇▇▇▇://▇▇▇▇▇▇.▇▇▇/spec/v2.0.0.html)
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Examples of Semantic Versioning in a sentence

  • All releases should be appropriately tagged; ● Adopt best practices: ○ Defining and enforcing code style guidelines; ○ Using Semantic Versioning; ○ Using a Configuration Management frameworks such as Ansible; ○ Taking security aspects into consideration through at every point in time; ○ Having automated testing in place; ○ Using code reviewing; ○ Treating documentation as code; ○ Documentation should be available for Developers, administrators and end users.

  • It is important that libraries conform to the Semantic Versioning Standard.

  • This version numbers will following Semantic Versioning rules 2.0.0, as described at https:// ▇▇▇▇▇▇.▇▇▇/.

  • The version number is based on the "Semantic Versioning" concept.

Related to Semantic Versioning

  • Biomarker testing means the analysis of an Insured’s tissue, blood, or other biospecimen for the presence of a Biomarker. "Biomarker testing" includes but is not limited to single-analyte tests, multi-plex panel tests, protein expression, whole exome, whole genome, and whole transcriptome sequencing.

  • Bioassay means the determination of kinds, quantities or concentrations, and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these regulations, "radiobioassay" is an equivalent term.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Phase I Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of a Product in subjects or that would otherwise satisfy requirements of 21 C.F.R. 312.21(a), or its foreign equivalent.

  • Genetic testing means an analysis of genetic markers to exclude or identify a man as the father or a woman as the mother of a child. The term includes an analysis of one or a combination of the following: