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update MSP+SM and rebuild
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larrybabb committed Sep 9, 2024
1 parent 2774737 commit ca65cd0
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2 changes: 1 addition & 1 deletion .requirements.txt
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Expand Up @@ -2,6 +2,6 @@ pytest
sphinx ~= 7.2
sphinx-rtd-theme ~= 1.2
pyyaml
ga4gh.gks.metaschema==0.3.0b12
ga4gh.gks.metaschema==0.3.0b13
jsonschema
referencing
6 changes: 3 additions & 3 deletions schema/cat-vrs/cat-vrs-source.yaml
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Expand Up @@ -49,7 +49,7 @@ $defs:
A change that occurs in a protein sequence as a result of genomic changes. Due to the degenerate nature
of the genetic code, there are often several genomic changes that can cause a protein sequence consequence.
The protein sequence consequence, like a :ref:`CanonicalAllele`, is defined by an
`Allele <https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#>`
`Allele <https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#>`_
that is representative of a collection of congruent Protein Alleles that share the same altered codon(s).
properties:
type:
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inherits: CategoricalVariation
maturity: draft
description: >-
A categorical variation domain is defined first by a sequence derived from a canonical `SequenceLocation
<https://vrs.ga4gh.org/en/2.x/concepts/LocationAndReference/SequenceLocation.html>`_ ,
A categorical variation domain is defined first by a sequence derived from a canonical
`SequenceLocation <https://vrs.ga4gh.org/en/2.x/concepts/LocationAndReference/SequenceLocation.html>`_ ,
which is representative of a collection of congruent Locations. The change or count of this sequence is
also described, either by a numeric value (e.g. "3 or more copies") or categorical representation
(e.g. "high-level gain"). Categorical CNVs may optionally be defined by rules specifying the location
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2 changes: 1 addition & 1 deletion schema/cat-vrs/def/ProteinSequenceConsequence.rst
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**Computational Definition**

A change that occurs in a protein sequence as a result of genomic changes. Due to the degenerate nature of the genetic code, there are often several genomic changes that can cause a protein sequence consequence. The protein sequence consequence, like a :ref:`CanonicalAllele`, is defined by an `Allele <https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#>` that is representative of a collection of congruent Protein Alleles that share the same altered codon(s).
A change that occurs in a protein sequence as a result of genomic changes. Due to the degenerate nature of the genetic code, there are often several genomic changes that can cause a protein sequence consequence. The protein sequence consequence, like a :ref:`CanonicalAllele`, is defined by an `Allele <https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#>`_ that is representative of a collection of congruent Protein Alleles that share the same altered codon(s).

**Information Model**

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2 changes: 1 addition & 1 deletion schema/cat-vrs/json/ProteinSequenceConsequence
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"title": "ProteinSequenceConsequence",
"type": "object",
"maturity": "draft",
"description": "A change that occurs in a protein sequence as a result of genomic changes. Due to the degenerate nature of the genetic code, there are often several genomic changes that can cause a protein sequence consequence. The protein sequence consequence, like a CanonicalAllele, is defined by an `Allele <https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#>` that is representative of a collection of congruent Protein Alleles that share the same altered codon(s).",
"description": "A change that occurs in a protein sequence as a result of genomic changes. Due to the degenerate nature of the genetic code, there are often several genomic changes that can cause a protein sequence consequence. The protein sequence consequence, like a CanonicalAllele, is defined by an [Allele](https://vrs.ga4gh.org/en/2.x/concepts/MolecularVariation/Allele.html#) that is representative of a collection of congruent Protein Alleles that share the same altered codon(s).",
"properties": {
"id": {
"type": "string",
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2 changes: 1 addition & 1 deletion submodules/vrs

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