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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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deselect of all variants doesn't work - reverts to selecting all each time
#268
sambaxter
opened
3 weeks ago
0
Feasibility of using custom allele frequency data
#267
aymanm
opened
3 weeks ago
1
Remove gnomAD HC LoF variants with B/LB ClinVar classification
#266
rileyhgrant
closed
4 weeks ago
0
Add FAQ question
#265
rileyhgrant
closed
4 weeks ago
0
Create LICENSE
#264
rileyhgrant
closed
4 weeks ago
0
Move Dashboard to navigation header
#263
rileyhgrant
closed
4 weeks ago
0
Clarify that Dashboard lists are unreviewed
#262
rileyhgrant
closed
4 weeks ago
0
Make it more obvious the preliminary estimates are not manually reviewed
#261
sambaxter
closed
4 weeks ago
0
ClinVar "Risk factors" should be removed from being brought in
#260
sambaxter
opened
4 weeks ago
2
Add dashboard download
#259
rileyhgrant
closed
4 weeks ago
0
Fix NA in ClinVar input
#258
rileyhgrant
closed
1 month ago
0
Add new clinvar category in second dict
#257
rileyhgrant
closed
1 month ago
0
Add new ClinVar 0 star category
#256
rileyhgrant
closed
1 month ago
0
Update dashboard pipeline
#255
rileyhgrant
closed
1 month ago
0
Add hover overs to emails
#254
rileyhgrant
closed
1 month ago
0
Reword representivity -> dashboard
#253
rileyhgrant
closed
1 month ago
0
Add help text popovers
#252
rileyhgrant
closed
1 month ago
0
Replace usage of "population" in methods text
#251
rileyhgrant
closed
1 month ago
0
Update FAQ text
#250
rileyhgrant
closed
1 month ago
0
Update copy in variant list creation and terminology used
#249
rileyhgrant
closed
1 month ago
0
Add better supporting document handling
#248
rileyhgrant
closed
1 month ago
0
Make AF column fit into default variant list view
#247
rileyhgrant
closed
1 month ago
0
Add homozygote counts to v2 dataset
#246
rileyhgrant
closed
1 month ago
0
Add gnomAD v2 SV support
#245
rileyhgrant
closed
1 month ago
0
Edit wording regarding representative variant lists
#244
rileyhgrant
closed
1 month ago
0
Various minor copy edits
#243
rileyhgrant
closed
1 month ago
0
feat(worker): remove filtering of malformed SVids
#242
rileyhgrant
closed
1 month ago
0
Hotfixes to return functionality of v2 lists
#241
rileyhgrant
closed
1 month ago
0
Add new genetic prevalence model
#240
rileyhgrant
closed
1 month ago
0
Allow removal of homozygotes from calculations
#239
rileyhgrant
closed
1 month ago
0
Add supporting_document to variant list
#238
rileyhgrant
closed
1 month ago
0
Add homozygote flag
#237
rileyhgrant
closed
1 month ago
0
Modify Dashboard list page
#236
rileyhgrant
closed
1 month ago
0
Include "D", "I" flags on Dashboard
#235
rileyhgrant
closed
1 month ago
0
Allow adding of Structural Variants to Variant Lists
#234
rileyhgrant
closed
1 month ago
0
Add generic text field to Variant Lists
#233
rileyhgrant
closed
1 month ago
0
PR Release
#232
rileyhgrant
closed
4 weeks ago
3
Dashboard flags
#231
sambaxter
closed
1 month ago
0
Update FAQ text
#230
sambaxter
closed
1 month ago
1
Bug in the allele frequency brought into GeniE
#229
sambaxter
closed
1 month ago
1
ClinVar variant incorrectly included in Variant List
#228
sambaxter
opened
2 months ago
1
Check conditional re-rendering of BarGraph
#227
rileyhgrant
opened
2 months ago
0
Fix incorrect bar graph frequencies with subpops
#226
rileyhgrant
closed
2 months ago
0
Bug in prevalence/carrier charts when uncheck "include subcontinental populations"
#225
sambaxter
closed
2 months ago
1
fix(app): move logic to update v4.0.0 to v4.1.0 in metadata
#224
rileyhgrant
closed
2 months ago
0
fix(frontend): correct v4.1.0 variant links to gnomad
#223
rileyhgrant
closed
2 months ago
0
feat(calculator): add 4.1.0_non-ukb to dictionary
#222
rileyhgrant
closed
2 months ago
0
feat(pipeline): add gnomad v4.1 support
#221
rileyhgrant
closed
2 months ago
0
Add v4.1 support
#220
rileyhgrant
closed
2 months ago
0
Add low AN flag
#219
rileyhgrant
closed
1 month ago
0
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