A set of standalone application and pipelines dedicated to NGS (new generation sequencing) analysis
| Python version: | 3.5 (and 2.7 without snakemake) |
|---|---|
| Online documentation: | |
| On readthedocs | |
| Issues and bug reports: | |
| On github | |
| How to cite: | Desvillechabrol D, Bouchier C, Cokelaer T and Kennedy S. Sequana: a set of flexible genomic pipelines for processing and reporting NGS analysis [v1; no peer reviewed]. F1000Research 2016, 5:1767 (poster) (doi: 10.7490/f1000research.1112656.1) |
Sequana includes a set of pipelines related to NGS (new generation sequencing) including quality control, variant calling, coverage, taxonomy…
Please see the documentation for an up-to-date status and documentation.
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| File Name & Checksum SHA256 Checksum Help | Version | File Type | Upload Date |
|---|---|---|---|
| sequana-0.4.1.tar.gz (12.9 MB) Copy SHA256 Checksum SHA256 | – | Source | Jul 20, 2017 |
