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Assembling the cause of phenotypes and genotypes from NGS data

Home Page: https://sanger-pathogens.github.io/plasmidtron/

License: GNU General Public License v3.0

Python 96.73% Shell 2.93% Dockerfile 0.34%
genomics sequencing next-generation-sequencing research bioinformatics bioinformatics-pipeline global-health infectious-diseases pathogen

plasmidtron's Issues

run error of plasmidtron 0.4.1

Academic tradition requires you to cite works you base your article on.
When using programs that use GNU Parallel to process data for publication
please cite:

O. Tange (2011): GNU Parallel - The Command-Line Power Tool,
;login: The USENIX Magazine, February 2011:42-47.

This helps funding further development; AND IT WON'T COST YOU A CENT.
If you pay 10000 EUR you should feel free to use GNU Parallel without citing.

To silence this citation notice: run 'parallel --citation'.

/bin/sh: line 1: 7651 已放弃 kmc_tools -t4 complex traits_config_file > /dev/null 2>&1
Traceback (most recent call last):
File "/hwfssz1/ST_CANCER/CVD/USER/lindechun/software/anaconda2/envs/py3/bin/plasmidtron", line 46, in
plasmid_tron.run()
File "/hwfssz1/ST_CANCER/CVD/USER/lindechun/software/anaconda2/envs/py3/lib/python3.6/site-packages/plasmidtron/PlasmidTron.py", line 244, in run
kmc_complex.run()
File "/hwfssz1/ST_CANCER/CVD/USER/lindechun/software/anaconda2/envs/py3/lib/python3.6/site-packages/plasmidtron/KmcComplex.py", line 113, in run
subprocess.check_call(self.kmc_complex_command('traits_config_file'), shell=True)
File "/hwfssz1/ST_CANCER/CVD/USER/lindechun/software/anaconda2/envs/py3/lib/python3.6/subprocess.py", line 291, in check_call
raise CalledProcessError(retcode, cmd)
subprocess.CalledProcessError: Command 'kmc_tools -t4 complex traits_config_file > /dev/null 2>&1' returned non-zero exit status 134.

Input files for plasmidtron

Hello,
I have installed plasmidtron plus its dependencies as described in the readme file. However, I do not understand what input files should be. specifically, what are file_of_traits and file_of_nontraits?

I have 3 bacteria genomes reads and I would like to pull out the plasmids so that I can study them. How do I format the genomes so that they can satisfy input requirements?

Best regards,
Clabe Wekesa

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