Skip to content

Issues: monarch-initiative/genophenocorr

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

25 Open 62 Closed
25 Open 62 Closed
Author
Filter by author
Label
Filter by label
Use alt + click/return to exclude labels
or ⇧ + click/return for logical OR
Projects
Filter by project
Milestones
Filter by milestone
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

Also add similar code for genomic visualization of variants
#172 opened May 28, 2024 by pnrobinson
@frehburg
add key with colors and names of protein ffeatures
#171 opened May 28, 2024 by pnrobinson
@frehburg
4
ProteinMetadata
#164 opened May 19, 2024 by pnrobinson
2
structural variant enhancement New feature or request
#156 opened May 9, 2024 by pnrobinson
PLA2G6 - correlations story An issue with a high-level user story
#152 opened May 3, 2024 by pnrobinson
@pnrobinson
RERE -- case story An issue with a high-level user story
#147 opened Apr 20, 2024 by pnrobinson
Provide documentation for key methods documentation Improvements or additions to documentation
#142 opened Mar 7, 2024 by pnrobinson Manuscript
@lnrekerle
Beta statistical significance testing enhancement New feature or request
#139 opened Feb 27, 2024 by ielis Manuscript
Help user to retieve the clinical transcript enhancement New feature or request
#134 opened Feb 20, 2024 by pnrobinson Manuscript
Review the API enhancement New feature or request
#133 opened Feb 20, 2024 by ielis
@graefea
1
Multiple testing correction strategy enhancement New feature or request
#126 opened Jan 3, 2024 by ielis Manuscript
@ielis
2
Draw variants, transcript and protein. enhancement New feature or request
#124 opened Dec 19, 2023 by ielis
9 of 10 tasks
Manuscript
@frehburg
3
Handling phenopackets with legacy CNV enhancement New feature or request
#119 opened Dec 14, 2023 by ielis
"toString" for Variant enhancement New feature or request
#109 opened Dec 7, 2023 by pnrobinson
1
Report the number of performed tests in GenotypePhenotypeAnalysisResult enhancement New feature or request
#98 opened Nov 16, 2023 by ielis Manuscript
Allow the user to limit the tested phenotypic features enhancement New feature or request
#97 opened Nov 16, 2023 by ielis Manuscript
1
Support numerical tests for GA4GH measurements enhancement New feature or request
#95 opened Oct 26, 2023 by ielis Nice to have
Enable comparison between diseases story An issue with a high-level user story
#69 opened Sep 29, 2023 by pnrobinson
@lnrekerle
1
method names should be unambiguous enhancement New feature or request
#59 opened Sep 26, 2023 by pnrobinson Manuscript
1
Available transcript viewer enhancement New feature or request
#58 opened Sep 26, 2023 by pnrobinson Manuscript
@pnrobinson
Divide by 0 error with HPO HP:0000276, not included in this analysis. bug Something isn't working
#54 opened Sep 20, 2023 by pnrobinson
Consider allowing to coordinate sort variants when summarizing cohort enhancement New feature or request
#49 opened Sep 18, 2023 by ielis Nice to have
Consider adding a step for inferring excluded features for a cohort enhancement New feature or request
#48 opened Sep 18, 2023 by ielis Nice to have
Add figure for showing distribution of phenotypic feature counts enhancement New feature or request
#44 opened Sep 14, 2023 by ielis
Show counts of monoallelic and biallelic variants enhancement New feature or request
#43 opened Sep 14, 2023 by ielis
1
ProTip! Find all open issues with in progress development work with linked:pr.