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broadinstitute
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genetic-prevalence-estimator
https://genie.broadinstitute.org/
BSD 3-Clause "New" or "Revised" License
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Allow tagging variants
#125
nawatts
opened
1 year ago
0
Allow deleting variants from a list
#124
nawatts
opened
1 year ago
1
Configure Dataproc clusters with max idle
#123
nawatts
closed
1 year ago
0
Allow external users to log in
#122
nawatts
closed
1 year ago
2
Print version cutting off Population and subpopulation inference and Limitations
#121
sambaxter
closed
1 year ago
1
Change library used for authentication
#120
nawatts
closed
1 year ago
0
Website text
#119
sambaxter
closed
1 year ago
0
Remove any subpopulations with <2,000 alleles
#118
sambaxter
closed
1 year ago
10
Set document title for each page
#117
nawatts
closed
1 year ago
0
Change text for ClinVar variant options in recommended list creation
#116
sambaxter
opened
1 year ago
2
Move "Create a new variant list" button top of list
#115
sambaxter
closed
1 year ago
0
Include Gene Name as well as ENSEMBL ID
#114
sambaxter
closed
1 year ago
2
Subpopulations display changes
#113
sambaxter
closed
1 year ago
0
Add select all option to populations menu
#112
nawatts
closed
2 years ago
0
Remove distinction between recommended and custom variant lists
#111
nawatts
closed
2 years ago
0
Error when selecting including all variant regardless of significance
#110
sambaxter
closed
2 years ago
1
Add a column for loss of function curation
#109
sambaxter
closed
1 year ago
4
Add a flag for genomes only
#108
sambaxter
closed
2 years ago
2
Add per-user overrides for limit on number of variant lists
#107
nawatts
opened
2 years ago
0
Disable create variant list when limit on number of variant lists is reached
#106
nawatts
closed
2 years ago
0
Unclear error message when limit on number of variant lists is reached
#105
nawatts
closed
2 years ago
0
Getting an "unknown" error when trying to create variant lists
#104
sambaxter
closed
2 years ago
4
Maintenance mode
#103
nawatts
opened
2 years ago
0
Apply selected display format to graph axis
#102
nawatts
closed
2 years ago
1
Run pip-compile in Docker
#101
nawatts
closed
1 year ago
0
Add configuration file with data URLs
#100
nawatts
opened
2 years ago
0
Support tablet screen size
#99
nawatts
closed
1 year ago
1
Support gnomAD SVs in custom variant lists
#98
nawatts
closed
1 month ago
2
Elaborate on tooltip for filtered variants
#97
nawatts
closed
2 years ago
1
Hide filtered variants by default
#96
sambaxter
closed
2 years ago
4
Allow users to add additional variants to list after calculations
#95
sambaxter
closed
1 year ago
3
Add tests for worker
#94
nawatts
opened
2 years ago
1
Display gene/transcript in variant table
#93
nawatts
closed
2 years ago
0
Store gene symbol with variant lists
#92
nawatts
closed
2 years ago
0
Add activity log for variant lists
#91
nawatts
opened
2 years ago
0
Add variant-level notes
#90
nawatts
closed
1 year ago
1
Save which variants are selected in a variant list
#89
nawatts
opened
2 years ago
4
Remove dependency on gnomAD browser API
#88
nawatts
opened
2 years ago
0
Switch Cloud Build triggers to manual triggers
#87
nawatts
closed
1 year ago
0
Adding star status to ClinVar classification
#86
sambaxter
closed
2 years ago
0
"Included from" column blank
#85
sambaxter
closed
2 years ago
1
Conflicting levels of pathogenicity pulling more than it should
#84
sambaxter
closed
2 years ago
1
Add Allele frequency to download
#83
sambaxter
closed
2 years ago
0
Being able to change/save variant lists after creation
#82
sambaxter
closed
1 year ago
1
Including subcontinental ancestries
#81
sambaxter
closed
2 years ago
1
Changing label for “scientific”
#80
sambaxter
closed
2 years ago
0
Add filtering of columns for variant table
#79
sambaxter
closed
1 year ago
4
Version defaulting
#78
sambaxter
closed
2 years ago
0
Add sorting functionality to variant list
#77
sambaxter
closed
2 years ago
0
Change "username" to "email"
#76
sambaxter
closed
2 years ago
0
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