v0.3.0: Merge pull request #259 from cancervariants/staging

• HGVS to relative / absolute copy number endpoints
• Remove unused methods from validator (human / concise description)
• Use uta-tools to handle MANE transcript work

v0.2.22

• Bump jupyter-server from 1.13.5 to 1.15.4

v0.2.21

• Add vrs-python's translate_from method (hgvs/spdi/beacon/gnomad --> VRS Allele object)

v0.2.20: Merge pull request #243 from cancervariants/staging

• Adds dockerfile
• Set variation descriptor's label to input query
• Replace pandas.read_sql in uta data source
• Add canonical spdi to categorical variation endpoint

v0.2.19: Merge pull request #238 from cancervariants/staging

• Remove normalized MANE Transcript response from toVRS

v0.2.18: Merge pull request #233 from cancervariants/staging

• Removes unused hgvs.parser from validator + mane transcript
• Fix bug in deletions state

v0.2.17: Merge pull request #227 from cancervariants/issue-226

• Add url to openapi contact info
• Always enable Try it out param in FastAPI
• Add citation
• Update dependencies
  • sqlalchemy
  • psycopg2-binary (dev)

VICC Variation Normalization

The January 2022 pre-release of the VICC variation normalization software, live instance available online at http://normalize.cancervariants.org/variation

v0.2.15

• Catches ValueError when creating a sequence location whose namespace can't be inferred

v0.2.14: Merge pull request #206 from cancervariants/staging

• Add translate_identifier endpoint
• Fix bug in UTA for ordering alt_ac by desc
• Add support for basic gnomad VCF substitution, insertion, and deletion
• Add support for gnomad VCF -> MANE p