Skip to content

Issues: Clinical-Genomics/scout

New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

Sign up for GitHub

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

214 Open 2,487 Closed
214 Open 2,487 Closed
Author
Filter by author
Loading
Label
Filter by label
Loading
Use alt + click/return to exclude labels
or ⇧ + click/return for logical OR
Projects
Filter by project
Loading
Milestones
Filter by milestone
Loading
Assignee
Filter by who’s assigned
Sort
Sort by
Newest Oldest Most commented Least commented Recently updated Least recently updated Best match
Most reactions
👍 👎 😄 🎉 😕 ❤️ 🚀 👀

Issues list

Marking a haplotype as causative in scout?
#5155 opened Jan 3, 2025 by alieden
Bayesian score classification on general report not matching score in Scout (when using "Evidence of benign impact")
#5153 opened Dec 30, 2024 by 1ctw
Improve matching causatives by not checking GT matching when matched case has just one sample Easy enhancement
#5152 opened Dec 20, 2024 by northwestwitch
1
RNA fusions parsing issue? question wontfix
#5148 opened Dec 20, 2024 by northwestwitch
@northwestwitch
2
Docker hub repo descriptions Task
#5146 opened Dec 20, 2024 by dnil
Long protein strings in hgvs description on e.g. cancer variantS page, summary etc enhancement QualityOfLife
#5144 opened Dec 19, 2024 by dnil
CCV bayesian score classifications (Ie cold VUS etc) on general report enhancement
#5143 opened Dec 19, 2024 by dnil
VariantS filtering with start 0 returns all variants for the chromsome enhancement QualityOfLife
#5142 opened Dec 19, 2024 by dnil
4
Add data- and library attribution to a live view enhancement
#5134 opened Dec 18, 2024 by dnil
info from CLinvar enhancement nf-core/raredisease
#5133 opened Dec 18, 2024 by 4WGH
2
ORPHA prevalences enhancement
#5130 opened Dec 18, 2024 by dnil
Write tests for the Clingen-CGC-VICC oncogenicity classification Easy enhancement
#5117 opened Dec 12, 2024 by northwestwitch
[obophenotype/human-phenotype-ontology] Release v2024-12-12 Task
#5116 opened Dec 12, 2024 by dnil
1
Slow tests - load research enhancement QualityOfLife
#5115 opened Dec 11, 2024 by dnil
More ACMG co-use warnings Customer Request enhancement Under discussion
#5101 opened Dec 5, 2024 by dnil
1
ACMG criteria modulation to very strong missing Customer Request enhancement
#5100 opened Dec 4, 2024 by 4WGH
2
load variants command has a parameter spelled wrong Refactor Scout5.0
#5090 opened Nov 29, 2024 by northwestwitch
3
Entry version has disappeared from gene panel lists question
#5082 opened Nov 28, 2024 by ielvers
4
Refactor general case report variant decoration Refactor
#5078 opened Nov 26, 2024 by dnil
Classify function in Clinical structural variants view enhancement Under discussion
#5074 opened Nov 26, 2024 by SofieCMD
2
Expand instructions on how to export data from scout docs QualityOfLife
#5051 opened Nov 20, 2024 by northwestwitch
MT DNA freq guesstimate on each variant
#5047 opened Nov 19, 2024 by dnil
1
Singleton RNA on DNA trio fallback is a bit dangerous blocked enhancement RNA-seq
#5046 opened Nov 19, 2024 by dnil
1
Sorting of variant table on other columns Under discussion wontfix
#5031 opened Nov 18, 2024 by molucorner
1
Are we interested in having a button for removing ClinVar deletions from Scout? question
#5029 opened Nov 18, 2024 by northwestwitch
1
ProTip! What’s not been updated in a month: updated:<2024-12-03.