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