KAT (K-mer Analysis Toolkit) provides a suite of tools that, through the use of k-mer counts, help the user address or identify issues such as determining sequencing completeness for assembly, assessing sequencing bias, identifying contaminants, validating genomic assemblies and filtering content. KAT is geared primarily to work with high-coverage genomic reads from Illumina devices, although can work with any fasta or fastq sequence file.
Allocate an interactive session and run the program.
Sample session (user input in bold):
[user@biowulf]$ sinteractive salloc.exe: Pending job allocation 46116226 salloc.exe: job 46116226 queued and waiting for resources salloc.exe: job 46116226 has been allocated resources salloc.exe: Granted job allocation 46116226 salloc.exe: Waiting for resource configuration salloc.exe: Nodes cn3144 are ready for job [user@cn3144 ~]$ module load kat [user@cn3144 ~]$ kat hist /fdb/app_testdata/fastq/H_sapiens/hg100_1m_pe?.fq.gz [user@cn3144 ~]$ exit salloc.exe: Relinquishing job allocation 46116226 [user@biowulf ~]$
Create a batch input file (e.g. KAT.sh). For example:
#!/bin/bash set -e module load kat kat hist /fdb/app_testdata/fastq/H_sapiens/hg100_1m_pe?.fq.gz
Submit this job using the Slurm sbatch command.
sbatch [--cpus-per-task=#] [--mem=#] KAT.sh
Create a swarmfile (e.g. kat.swarm). For example:
kat hist sample1.fastq kat hist sample2.fastq kat hist sample3.fastq kat hist sample4.fastq
Submit this job using the swarm command.
swarm -f kat.swarm [-g #] [-t #] --module katwhere
-g # | Number of Gigabytes of memory required for each process (1 line in the swarm command file) |
-t # | Number of threads/CPUs required for each process (1 line in the swarm command file). |
--module kat | Loads the KAT module for each subjob in the swarm |