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ncRNA genes and the clinical filter
enhancement
Under discussion
#4609
opened May 6, 2024 by
ielvers
Flag coverage dropouts induced by repeat expansions in long-read data
enhancement
LRS
#4597
opened Apr 29, 2024 by
fellen31
"Classify-link" on the Clinical Structural variants-variant page
Customer Request
enhancement
Intermediate
#4596
opened Apr 29, 2024 by
SofieCMD
Parse new format for pipeline info?
enhancement
nf-core/raredisease
Task
#4523
opened Mar 21, 2024 by
dnil
nf-core raredisease VEP 110 parsing
enhancement
nf-core/raredisease
#4446
opened Feb 20, 2024 by
dnil
1 task
Can we add more information for CNVs uploaded to Scout?
Cancer
enhancement
#4444
opened Feb 20, 2024 by
mathiasbio
Connection failure warning when you run scout --help command
#4408
opened Feb 6, 2024 by
northwestwitch
Block and then refactor submission of somatic variants to ClinVar
enhancement
#4400
opened Feb 2, 2024 by
northwestwitch
Unable to parse HGNC ID due to presence of 'HGNC:' prefix
nf-core/raredisease
#4397
opened Feb 2, 2024 by
lfearnley
Stop supporting ClinVar submission using CSV files and submit only using the API
Future ideas
QualityOfLife
Refactor
Task
#4387
opened Jan 31, 2024 by
northwestwitch
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