Open Issues Need Help
View All on GitHub Classification stats - evidence key filter and stats about 1 month ago
good first issue
Auto detected bugs - variantopedia 4 months ago
bug good first issue
Auto detected bugs - ontology 5 months ago
bug good first issue
good first issue
Refactor - consolidate 'django_utils' 6 months ago
good first issue
good first issue
Auto detected bugs - library 7 months ago
bug good first issue
Auto detected bugs - upload 7 months ago
bug good first issue
Auto detected bugs - snpdb 7 months ago
bug good first issue
Auto detected bugs - Patients 7 months ago
bug good first issue
Auto detected bugs - seqauto 7 months ago
bug good first issue
Auto detected bugs - Annotation 7 months ago
bug good first issue
Auto detected bugs - genes 7 months ago
bug good first issue
ClinVarCitation Count 8 months ago
good first issue
Admin only - Server stats - duplicate SQL queries about 1 year ago
good first issue
Show g.HGVS in more places about 1 year ago
AI Summary: Implement a setting in the VariantGrid application to optionally display genomic coordinates in HGVS format (e.g., NC_000005.10:g.172454352T>A) instead of the internal format (e.g., 5:172454352 T>A) in search results and the HGVS tester. This involves modifying the display logic in these sections of the application to accommodate the new setting.
Complexity:
3/5
good first issue