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Let’s create an NEW interactive session on the HPC:

qsub -I -S /bin/bash -l walltime=10:00:00 -l select=1:ncpus=2:mem=4gb

We will now create a new CONDA environment to install the tools needed for mapping. The reason we need to create a new a new environments is because the QC and mapping tools have no compatible dependencies.

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Alternative approach to create a conda env and install tools (we are not doing this - this just for your information) - installing all tools at once (slower option!)

Prepare the following environment.yml file:

name: ONTvariants_mapping
channels:
  - conda-forge
  - defaults
  - bioconda
dependencies:
  - samtools=1.20
  - minimap2=2.28

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As you have seen, we can search at anaconda.org for other tools that we might be interested to use.

Remember, if you run into compatibility issues or errors, you can always create a new conda environment for the tool of interest. NOTE: you can switch between conda environements as follows:

conda activate ONTvariants_QC
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conda deactivate
conda activate ONTvariants_mapping
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#!/bin/bash -l
#PBS -N run2_mapping
#PBS -l select=1:ncpus=8:mem=16gb
#PBS -l walltime=72:00:00
#PBS -m abe

cd $PBS_O_WORKDIR

#condaconda activate ONTvariants_QCmapping
conda
activate porechop

###############################################################
# Variables
###############################################################
FASTQ='/work/training/ONTvariants/data/runs/run1_QC/SRR17138639_1_porechop_abi_chopper_q10_300b.fastq'
GENOME='/work/training/ONTvariants/data/chr20.fasta'
SAMPLEID='SRR17138639'
GENOMEID='chr20'
###############################################################

#STEP1: Mapping preprocessed reads with minimap2 onto reference genome
minimap2#minimap2 -t 8 -a $GENOME $FASTQ | awk '$3!="*"'  > ${SAMPLEID}_mapped_${GENOMEID}.sam
minimap2 -t 8 -a $GENOME $FASTQ > ${SAMPLEID}_mapped_${GENOMEID}.sam

##STEP2: samtools - SAM to sorted BAM
samtools view -bS ${SAMPLEID}_mapped_${GENOMEID}.sam > ${SAMPLEID}_mapped_${GENOMEID}.bam
samtools sort -o ${SAMPLEID}_mapped_${GENOMEID}.sorted.bam ${SAMPLEID}_mapped_${GENOMEID}.bam
samtools index ${SAMPLEID}_mapped_${GENOMEID}.sorted.bam

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Monitor the progress of the job:

qjobs

Once the run has completed. The following files will be in the “run2_mapping” folder:

.
├── launch_ONTvariants_mapping.pbs
├── SRR17138639_mapped_chr20.bam
├── SRR17138639_mapped_chr20.sam
├── SRR17138639_mapped_chr20.sorted.bam
└── SRR17138639_mapped_chr20.sorted.bam.bai

To visualise the mapped reads (sorted BAM file) using IGV (see below), first we need to connect to the HPC using FileFinder:

NOTE: To proceed, you need to be on QUT’s WiFi network or signed via VPN.

To browse the working folder in the HPC type in the file finder:

Windows PC

\\hpc-fs\work\training\ONTvariants\runs\run2_mapping

Mac

smb://hpc-fs/work/training/ONTvariants\runs\run2_mapping

Visualisation of the alignment using IGV

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Zoom in a visualise the alignments:

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Next: ONTvariants - epi2me WF-Human Variation pipeline