Hands-on training for analysing Oxford Nanopore Technologies (ONT) sequencing data for microbial pathogen detection
# login to unix environment in powershell (in windows)
wsl
# activate conda environment
conda activate cpgih_utility
Make sure that your data is on the DESKTOP in a folder labelled your RUN NAME.
In this folder, you will have a folder called ‘fastq_pass’, in which there will be folders named after the barcodes eg. ‘barcode01’, in which your fastq.gz files will reside.
Edit the RENAMING.TSV FILE (saved to share_file_templates directory on the desktop) to have the list of all the samples to be analysed (one per line)
The format is barcode## TAB samplename MAKE SURE THE SEPARATOR IS A TAB - example:
barcode25 Sample01
barcode26 Sample02
barcode27 Sample03
Edit the NAMES FILE (saved to share_file_templates directory on the desktop) to have the list of all the samples to be analysed (one per line, with no spaces) - example:
Sample01
Sample02
Run the following:
ont_seq [RUN_NAME]
#eg.
ont_seq ONT_test