v2.2.8

What's Changed

🚀 New Features

• Introduce MyDisease.info integration by @acoffman in #755
• Introduce MyChem.info integration by @acoffman in #758

🎉 Enhancements to Existing Features

• add entrez symbol filtering support for single gene query by @acoffman in #766
• add top bar link to docs by @acoffman in #768

🐛 Bug Fixes

• dont display a broken link when transcript is missing by @acoffman in #767

Full Changelog: v2.2.7...v2.2.8

v2.2.7

What's Changed

🐛 Bug Fixes

• Handle cases where none of the allele registry transcripts are tagged as MANE select by @susannasiebert in #754
• Handle revision popover for revisions without creation comment by @susannasiebert in #746
• Long evidence and assertion descriptons will overflow into scroll by @acoffman in #751

Full Changelog: v2.2.6...v2.2.7

v2.2.6

What's Changed

🐛 Bug Fixes

• Handle MANE transcript for variants without allele registry ID by @susannasiebert in #743

Full Changelog: v2.2.5...v2.2.6

v2.2.5

What's Changed

🚀 New Features

• Allow moving of variants between genes in variant revise form by @susannasiebert in #735

🎉 Enhancements to Existing Features

• Add creation comment to the revision popover by @susannasiebert in #742
• Add MANE select transcript by @susannasiebert in #739

🐛 Bug Fixes

• Fix horizontal scrolling issues in various tables by @susannasiebert in #741
• Update formatting of MyGeneInfo Overview to avoid overlap on smaller screens by @susannasiebert in #740
• Lookup Variant by alias before creating a new one by @susannasiebert in #738
• Remove nzLabel on the quicksearch dropdown options to remove tooltip by @susannasiebert in #737
• Fix flickering comment-popover by @susannasiebert in #736

Full Changelog: v2.2.4...v2.2.5

v2.2.4

What's Changed

🎉 Enhancements to Existing Features

• show OpenCRAVAT url on MP page Variant cards by @acoffman in #732

🐛 Bug Fixes

• Don't fuzzy match MP names in the MP menu by @acoffman in #733
• Fix guideline version not being picked up in assertion revisions

🧹 Housekeeping

• display molecular profile count on more popovers and tables by @acoffman in #727

Full Changelog: v2.2.3...v2.2.4

v2.2.3

What's Changed

🚀 New Features

• Link out to OpenCRAVAT variant report on CIViC variant pages when an Allele Registry ID is present.

Full Changelog: v2.2.2...v2.2.3

v2.2.2

What's Changed

🐛 Bug Fixes

• Fix a few more places where we were using the eid -> variant association by @susannasiebert in #722

Full Changelog: v2.2.1...v2.2.2

v2.2.1

What's Changed

🎉 Enhancements to Existing Features

• Scrape abstract text for ASH sources by @acoffman in #702
• Browse table updates by @acoffman in #703
• Update materialized views to use MP connections and remove variant_id and gene_id tables on eids and assertions by @susannasiebert in #706
• Show all MPs unless deprecated in browse views. Show all sources in Source browse view by @acoffman in #707
• Add Variant Type filtering and configurable page sizes to Variant Menu by @acoffman in #718

🐛 Bug Fixes

• Fixes for Source Browse Table by @acoffman in #695
• do not attempt to look for misspellings unless there are no matches by @acoffman in #701
• Accomodate Leading Zeroes in DOID entry by @acoffman in #704
• Validate Citation ID formatting by @acoffman in #708

🧹 Housekeeping

• Backend Field Renames by @acoffman in #694
• Rename drugs to therapies on the backend. by @acoffman in #700
• Remove variant_id on evidence item by @susannasiebert in #711

Full Changelog: v2.2.0...v2.2.1

v.2.2.0

What's Changed

🧨 Breaking Changes

We aim to roll out breaking changes as infrequently as possible to our users. As such this release bundles several breaking changes to be aware of, all at once.

• Evidence Items and Assertions are no longer attached to Variants. They are attached to the new Molecular Profile concept.
• The Clinical Significance Field has been renamed to Significance.
• Drugs are now referred to as Therapies, and Drug Interaction Type is now Therapy Interaction Type. As a result, Evidence Items and Assertions are linked to Therapies instead of Drugs.
• Variant Description, Sources, and Evidence Score have been moved from Variants to Molecular Profiles

🚀 New Features

• Molecular profiles by @acoffman in #580
• Add mechanism for deprecating variants and molecular profiles by @susannasiebert in #599
• Support ASH Abstracts as a Source by @acoffman in #619

🎉 Enhancements to Existing Features

• updated evidence, assertion tag status styles by @jmcmichael in #579
• updated tag status styles, new icon badges by @jmcmichael in #583
• add badges to entity icons by @jmcmichael in #587
• provides evidenceLevelBrief option for evidenceEnumTooltip pipe by @jmcmichael in #595
• Clicking a revision tag takes you to the the revision set regardless of status by @acoffman in #606
• Allow admins to set a parent organization when editing orgs in the admin UI by @acoffman in #610
• Add missing clinical trial links to source and eid summary gql by @susannasiebert in #616
• Add alert banner to rejected evidence and assertion summary pages by @susannasiebert in #618
• Make source tags on Source Suggestions table linkable by @acoffman in #617
• Give the user feedback when no new revisions are created by @acoffman in #613
• Provide user feedback when proposed revisions would have resulted in duplicates. by @acoffman in #639
• Link out to OpenCRAVAT from variant pages where possible. by @acoffman in #637

🐛 Bug Fixes

• Fix variant menu behavior by @acoffman in #577
• Remove total from table counts since it's unreliable by @susannasiebert in #589
• fixes app header and entity home page header wrapping at narrow window widths by @jmcmichael in #590
• fixes the event icon's twotone background color by @jmcmichael in #594
• fix org-selector-btn synchronization of class, disabled, hidden by @jmcmichael in #598
• Display unregistered allele registry variants correctly by @susannasiebert in #593
• Make variant name search in browse table wildcard match in both directions by @acoffman in #605
• Add special handling for NCCN guideline revisions by @susannasiebert in #626
• Fix method name typo by @acoffman in #641
• Various Org Page Fixes by @acoffman in #645
• Reload submit source form on navigation to same route. by @acoffman in #678
• fix clinvar linkout in the NONE FOUND case by @acoffman in #679
• distinguish between false and undefined by @acoffman in #682
• Don't delete Disease entries that have revisions linked to them by @susannasiebert in #689

🧹 Housekeeping

• removes entity table title icons, entity icons in col headers switched to monochrome by @jmcmichael in #592
• Author list improvements for sources by @acoffman in #604
• build client when tests are run by @acoffman in #612
• Remove "Does Not Support" option for Predisposing and Oncogenic Assertions by @acoffman in #636
• Rename myvariant.info CADD tab to "Conservation Analysis Tools" by @susannasiebert in #643
• Rename various fields (including drug->therapy), additional MP fixes by @acoffman in #675
• Rename CIViC Evidence Score to Molecular Profile Score by @acoffman in #684
• Remove sources from variants in gql schema by @acoffman in #690

Other Changes

• Variant and MP popover fixes by @acoffman in #685

Full Changelog: v2.1.2...v2.2.0

v2.1.2

Other Changes

• Adds GCBR inclusion announcement to Welcome page news feed by @jmcmichael in #683

Full Changelog: v2.1.1...v2.1.2