Clinical-Genomics / cgbeacon2

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LAST BUILD ON BRANCH update_alleleCount_varCount

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

Build # 356

Build Type

Pull #63

travis-ci-com

Committed by web-flow

Commit Message

Merge 61558d9d5 into 877313697

Pull Request Pull Request #63: Update datasets variantCount and alleleCount when variant content changes

Run Details

48 of 48 new or added lines in 5 files covered. (100.0%)

832 of 857 relevant lines covered (97.08%)

0.97 hits per line