Issues
- 0
Clear cache not clearing loaded variants
#795 opened by tonydisera - 0
Clinvar pathogenic variant not showing up in eutils for variant in clinvar vcf
#794 opened by tonydisera - 3
Min number or min percent of alt counts
#792 opened by mvelinder - 1
Adding DECIPHER gene page links
#793 opened by mvelinder - 7
Add DGIdb data to gene information
#791 opened by mvelinder - 3
- 0
Prompt user if relatedness in trio is suspicious
#789 opened by mvelinder - 1
Collapse introns
#788 opened by AlistairNWard - 1
Exon colouring on low coverage
#787 opened by AlistairNWard - 0
Exon colouring on low coverage
#786 opened by AlistairNWard - 4
SCN8A missing likely pathogenic ClinVar annotaiton
#785 opened by tonydisera - 1
Remove BRCA1 as startup gene
#784 opened by AlistairNWard - 0
When user entered affected sib, then uaffected sib row shows up in Ranked Variants Table
#783 opened by tonydisera - 0
- 0
Link out UCSC browser, show conservation, maybe phenotype tracks, reference sequence [gene]
#782 opened by tonydisera - 0
Remove VCF filter status field
#781 opened by tonydisera - 0
- 0
Zooming not obvious
#779 opened by tonydisera - 0
Only report back top n number of genes from phenolyzer (250?) -- some terms give back thousands
#778 opened by tonydisera - 0
Would like to see OMIM entry for gene (important to show mode of inheritance for associated disorders)
#776 opened by tonydisera - 0
OMIM clinical synopsis information (affected systems and their phenotypes) Compound het filters
#777 opened by tonydisera - 0
Find rare variants, bookmarks don't load
#773 opened by tonydisera - 1
- 0
Make it clear when a gene is on X or Y
#775 opened by AlistairNWard - 2
- 1
After selecting radio button 'Variants' in the Clinvar Variant card, switching genes resets to ClinVar 'counts.
#746 opened by tonydisera - 0
Endpoints
#754 opened by tonydisera - 1
- 0
- 0
EBF3 gene linking out to MAPRE3 on genecards
#770 opened by mvelinder - 0
Simplify loading display next to page controls
#768 opened by tonydisera - 0
Improve performance by increasing batch size for 'Analyze all' and increasing number of worker nodes
#767 opened by tonydisera - 0
Analyze with results from phenolyzer, not change phenotype term, add genes and analyze all. Gene now loses badge
#747 opened by tonydisera - 0
- 0
'Add or replace genes' prompts keeps reappearing on Phenolyzer search after user presses 'Keep genes' and phenolyzer is still pending.
#752 opened by tonydisera - 0
- 0
Phenolyzer - can't copy/paste separate terms or use copy/paste for typeahead
#750 opened by tonydisera - 0
Show OMIM entry for gene (important to show mode of inheritance for associated disorders)
#756 opened by tonydisera - 0
Show OMIM clinical synopsis information (affected systems and their phenotypes)
#757 opened by tonydisera - 0
Only report back top n number of genes from phenolyzer (250?) -- some terms give back thousands
#758 opened by tonydisera - 0
Remove VCF filter status field in variant card
#759 opened by tonydisera - 0
Chrome windows bug – filtering (toggling on/off inheritance causes browser crash)
#761 opened by tonydisera - 0
Variant card shows ‘NULL’ for proband
#760 opened by tonydisera - 0
X chromosome not flagging as X linked recessive
#762 opened by tonydisera - 0
- 0
Link out UCSC browser, show conservation, maybe phenotype tracks, reference sequence
#764 opened by tonydisera - 0
- 0
- 0
Include sibling symbols in legend
#751 opened by AlistairNWard - 0
Progress bars
#749 opened by AlistairNWard