Clinical-Genomics / cgbeacon2

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• version_1
• info_endpoint
• master
• parse_vcf
• add_dataset
• update_dataset
• delete-dataset
• save_variants
• update_variants
• delete_variants
• panel_filter
• query_endpoint
• query_beacon
• codeowners
• expand_snv_query
• check_build_against_dsets
• parse_svs
• non_specific_queries
• negative_responses
• simple_query_interface
• run_post_queries
• auth_levels
• query_with_authlevel
• enforce_json
• results_by_authlevel
• no_content_type_check
• load_demo
• minimal_readme
• extensive_docs
• some_fixes
• variantype_snv
• fix_#57
• snvs_variantTypes
• update_alleleCount_varCount
• v1
• bugfixes_1.0.1
• version_1.1
• v1.1
• northwestwitch-patch-1
• bnd_variants
• add_mkdocs
• genes_to_panel
• add_variants_api
• variants_remove_api
• version_1.2
• 1.2
• create_wsgi
• require_cython
• set_cython_version
• dockerfile
• github_actions

Build # 359

Build Type

Pull #64

travis-ci-com

Committed by web-flow

Commit Message

Merge 809269df7 into d04f94fea

Pull Request Pull Request #64: Major release 1.0

Run Details

1 of 1 new or added line in 1 file covered. (100.0%)

832 of 857 relevant lines covered (97.08%)

0.97 hits per line