Releases: frankligy/SNAF
Releases · frankligy/SNAF
zenodo_version
This is the zenodo version for publication
Version 0.7.0
This is a release since the paper's original resubmission, in the past year, we added a ton of new features, main changes are briefly summarized below:
- differential gene analysis, differential splicing analysis, gene enrichment analysis
- hla coverage analysis, for each pHLA, what percentage of the population it can cover (benefit)
- enhanced and more flexible control database, adding two normal cohorts by default, and allowing user to add customized
- improved algorithms for MLE tumor specificity score, and external BayesTS score (https://github.com/frankligy/BayesTS)
- improved output for both T and B antigens
- fix multiple bugs
Version 0.6.0
Adding New functionalities:
- report B and T antigen in a more readable format
2.allow users to add all info to the frequency table at once
- add long_read mode for B antigen when inferring full-length isoform and update the B viewer codebase as well
version 0.5.2
Fixed multiple bugs:
-
scratch folder cleaning issue and multiprocessing conflist issues resolved
-
tumor_specificity issue resolved
-
fix docstring displacement
-
In test folder, contain a complete testing case.
Version 0.5.1
Fixed two bugs:
- Weckzueg can not be version 2.1.1, force it to be 2.0.2
- expose add_coord_frequency_table to snaf namespace
Version 0.0.5
First release (alpha version)