The tool detects chromosomal mutations predictive of drug resistance based on WGS data.
Contact Jeevan in slack if you have any issues or further assistance (F. ex. run the tool for multiple isolates).
https://bitbucket.org/genomicepidemiology/pointfinder
Important rules to follow
- Refer the user manual for all the parameters in the tool
- Keep your data in /project/nn9305k/
- Store your resutls also in /project/nn9305k/
- Execute the script from your home directory
#!/bin/bash
#SBATCH --job-name=DontKillMe
#SBATCH --account=nn9305k
#SBATCH --time=01:00:00
#SBATCH --mem-per-cpu=32G
## Set up job environment:
source /cluster/bin/jobsetup
conda activate PointFinder
# Database location
PointFinder_DB="/work/projects/nn9305k/src/PointFinder_DB/src/"
python PointFinder.py -p $PointFinder_DB -i input_file -o output_file
conda deactivate