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SPAdes

SPAdes is a short read assembler for small genomes. SPAdes works with Illumina or IonTorrent reads and is capable of providing hybrid assemblies using PacBio, Oxford Nanopore and Sanger reads.

SPAdes (spades.py) includes several separate modules:

  • BayesHammer – read error correction tool for Illumina reads, which works well on both single-cell and standard datasets.
  • IonHammer – read error correction tool for IonTorrent data, which also works on both types of data.
  • SPAdes – iterative short-read genome assembly module; values of K are selected automatically based on the read length and dataset type.
  • MismatchCorrector – a tool which improves mismatch and short indel rates in resulting contigs and scaffolds; this module uses the BWA tool [Li H. and Durbin R., 2009]; MismatchCorrector is turned off by default, but we recommend turning it on.

We recommend running SPAdes with BayesHammer/IonHammer to obtain high-quality assemblies. However, if you use your own read correction tool, it is possible to turn error correction module off. It is also possible to use only the read error correction stage if you wish to use another assembler.

In addition to the general purpose SPAdes there are specific SPAdes parameter sets for:

  • Coronaspades (coronaspades.py)
  • Metaviralspades (metaviralspades.py)
  • Rnaviralspades (rnaviralspades.py)
  • Metagenomics (metaspades.py)
  • Plasmid assembly (plasmidspades.py)
  • RNA-Seq assembly (rnaspades.py)

See the SPAdes documentation for more details.

License

Free to use and open source under GNU GPLv2.

Available

  • Puhti: 3.15.5, 4.0.0

Usage

On Puhti, SPAdes is activated by loading the spades module.

module load spades/<version>

For usage help, use command:

spades.py -h

Assembly tasks can be very resource demanding and, therefore, you should never run real SPAdes jobs on the login nodes of Puhti. For any real analysis task, we recommend running SPAdes as a batch job.

Sample SPAdes batch job file:

#!/bin/bash
#SBATCH --job-name=SPAdes
#SBATCH --account=<project>
#SBATCH --time=12:00:00
#SBATCH --ntasks=1
#SBATCH --nodes=1
#SBATCH --output==spades_out
#SBATCH --error=sprdes_err
#SBATCH --cpus-per-task=8
#SBATCH --mem=32G
#SBATCH --partition=small

module load biokit
export OMP_NUM_THREADS=$SLURM_CPUS_PER_TASK 
srun spades.py --pe1-1 reads_R1.fastq.gz --pe1-2 reads_R2.fastq.gz -t $SLURM_CPUS_PER_TASK -o SpadesResult

In the example above <project> should be replaced with your project name. You can use csc-projects to check your CSC projects. Maximum running time is set to 12 hours (--time=12:00:00). As SPAdes uses thread-based parallelization, the process is considered as one job that should be executed within one node (--ntasks=1, --nodes=1). The job reserves eight cores --cpus-per-task=8 that can use in total up to 32 GB of memory (--mem=32G). Note that the number of cores to be used needs to be defined with both $OMP_NUM_THREADS environment variable and in the actual spades.py command (option -t). In this case, we use $SLURM_CPUS_PER_TASK variable that contains the --cpus-per-task value. We could as well use export OMP_NUM_THREADS=8 and -t 8, but then we have to remember to change the values if the number of the reserved CPUs is changed.

The job is submitted to the batch job system with sbatch command. For example, if the batch job file is named spades_job.sh, then the submission command is: 

sbatch spades_job.sh

More information about running batch jobs can be found from the batch job section of the Puhti user guide.

More information