nf-eresearch/ConsGenome: Nextflow based Genome Assembly, Variant Calling and building a Consensus Genome workflow

Goal

Enable the study of new strains of Dengue viruses by producing de novo assembled genomic scaffolds, comparison to reference genomes, variant calling and generation of a reference guided consensus genome.

Pre-requisites

• Nextflow NextFlow quick start

• Basic unix command line knowledge (example: Learning Resources: the Linux Command Line ; The Unix Shell: Summary and Setup )

• Familiarity with one unix text editors (example Vi/Vim or Nano):

  • VIM ( VIM Guide | Computational Biology Core ; Editors (Vim))

  • Nano (Basic tutorial for Nano users ; https://www.howtogeek.com/howto/42980/the-beginners-guide-to-nano-the-linux-command-line-text-editor/ )

ConsGenome workflow

Installing

The nextflow based ConsGenome workflow is available on the HPC. To download a copy of the workflow to your home folder the following steps are needed on the HPC

Running the pipeline

Step 1:

Create a folder to hold the output of the pipeline. The results folder will be created here.

Step 2:

Prepare the index.csv file. This file will contain a list of sample ids and the full path to the paired samples. Read 1 and Read 2 must be specified separately.

EG:

Step 3:

Create a nextflow.config file (if needed). If you need to override any of the pipeline defaults, put them in this file.

Step 4:

Create a PBS launch script. I.e.. Copy this into launch.pbs

If you wish to use the conda version of the pipeline use this script:

Step 5:

Launch the pipeline

see the progress of the job

Step 6:

Monitor on the Nextflow Tower

If you have previously enabled Nextflow Tower visit

https://nftower.qut.edu.au

Step 7:

Once finished, examine the results in the results folder.