| PathoScope takes next-generation sequencing reads from a mixture sample and predicts which genomes are present. We use a Bayesian framework combined with an initial reference-based alignment to assign reads to the correct genome of origin. |
hg clone https://toolshed.g2.bx.psu.edu/repos/jasper/pathoscope_id
| Name | Description | Version | Minimum Galaxy Version |
|---|---|---|---|
| Pathoscope ID | 0.1.0 | any | |