| Name | Version | Summary | date |
| scout-browser |
4.94.1 |
Clinical DNA variant visualizer and browser |
2024-12-20 16:20:01 |
| sc-echidna |
1.0.2 |
Mapping genotype to phenotype through joint probabilistic modeling of single-cell gene expression and chromosomal copy number variation. |
2024-12-16 18:35:46 |
| 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 |
| hiscanner |
0.2a0 |
High-resolution copy number variant calling in single-cell whole-genome sequencing. |
2024-04-11 15:38:05 |
| sequana-multicov |
1.1.1 |
Parallelise version of sequana_coverage standalone application. |
2023-05-23 21:28:34 |