Name | Version | Summary | date |
scout-browser |
4.104.0 |
Clinical DNA variant visualizer and browser |
2025-09-03 10:37:23 |
hiscanner |
1.6 |
High-resolution single-cell copy number analysis. |
2025-08-12 13:18:41 |
sc-echidna |
1.0.3 |
Mapping genotype to phenotype through joint probabilistic modeling of single-cell gene expression and chromosomal copy number variation. |
2025-07-24 18:39:45 |
echidna-sc |
1.0.0 |
Mapping genotype to phenotype through joint probabilistic modeling of single-cell gene expression and chromosomal copy number variation. |
2024-12-16 00:57:32 |
scechidna |
1.0.0 |
Mapping genotype to phenotype through joint probabilistic modeling of single-cell gene expression and chromosomal copy number variation. |
2024-12-16 00:50:28 |
hmmCNV |
1.1.6 |
Python package for Copy-Number Variation calling |
2024-11-20 22:35:22 |
sequana-multicov |
1.1.1 |
Parallelise version of sequana_coverage standalone application. |
2023-05-23 21:28:34 |