Assemble mitochondrial genomes from short read data: Difference between revisions
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#SBATCH --ntasks=8 | #SBATCH --ntasks=8 | ||
#SBATCH --nodes=1 | #SBATCH --nodes=1 | ||
#SBATCH --constraint= | #SBATCH --constraint=4gpercpu | ||
#SBATCH --output=output_%j.txt | #SBATCH --output=output_%j.txt | ||
#SBATCH --error=error_output_%j.txt | #SBATCH --error=error_output_%j.txt | ||
#SBATCH --job-name=assemble_mito | #SBATCH --job-name=assemble_mito | ||
#SBATCH --mail-type=ALL | #SBATCH --mail-type=ALL | ||
#SBATCH --mail-user=hendrik-jan.megens@wur.nl | #SBATCH --mail-user=hendrik-jan.megens@wur.nl | ||
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bowtie2 --phred$2 --local -p 8 -x mt_pig.fa -1 $3 -2 $4 | awk '$5>0' | head -10000 >>$1_mito_align.sam | bowtie2 --phred$2 --local -p 8 -x mt_pig.fa -1 $3 -2 $4 | awk '$5>0' | head -10000 >>$1_mito_align.sam | ||
java7 -jar | java7 -jar /shared/apps/SHARED/picard-tools/picard-tools-1.109/SamToFastq.jar I=$1_mito_align.sam F=fq1.fq F2=fq2.fq INCLUDE_NON_PF_READS=True | ||
SOAPdenovo-63mer all -K 63 -p 4 -s soapdenovo.config -o $1_mito_assembly.fa | SOAPdenovo-63mer all -K 63 -p 4 -s soapdenovo.config -o $1_mito_assembly.fa | ||
Latest revision as of 09:58, 16 June 2023
A simple procedure for assembling mitochondrial genomes based on whole-genome re-sequencing data. The first step is to extract reads from the sequence library based on a closely related entirely assembled genome (e.g., for pig, the MT genome as present in the genome build, but could also be of a related species). The genome is then assembled using SOAPdenovo.
- a reference genome of a closely related population or species.
- a bowtie2 index (make with bowtie2_build)
- a blastable db of the reference mitochondrial genome
- a SOAPdenovo configuration file:
soapdenovo.config
[LIB] avg_ins=450 reverse_seq=0 asm_flags=1 rank=3 q1=fq1.fq q2=fq2.fq
Note that the avg_ins flag may vary between libraries; may have an effect on assembly efficiency.
<source lang='bash'>
- !/bin/bash
- SBATCH --time=1000
- SBATCH --mem=16000
- SBATCH --ntasks=8
- SBATCH --nodes=1
- SBATCH --constraint=4gpercpu
- SBATCH --output=output_%j.txt
- SBATCH --error=error_output_%j.txt
- SBATCH --job-name=assemble_mito
- SBATCH --mail-type=ALL
- SBATCH --mail-user=hendrik-jan.megens@wur.nl
module load bowtie/2-2.2.1 SOAPdenovo2/r240 BLAST+/2.2.28 MUMmer/3.23
bowtie2 --phred$2 --local -p 8 -x mt_pig.fa -1 $3 -2 $4 | head -2 >$1_mito_align.sam bowtie2 --phred$2 --local -p 8 -x mt_pig.fa -1 $3 -2 $4 | awk '$5>0' | head -10000 >>$1_mito_align.sam
java7 -jar /shared/apps/SHARED/picard-tools/picard-tools-1.109/SamToFastq.jar I=$1_mito_align.sam F=fq1.fq F2=fq2.fq INCLUDE_NON_PF_READS=True
SOAPdenovo-63mer all -K 63 -p 4 -s soapdenovo.config -o $1_mito_assembly.fa
blastn -query $1_mito_assembly.fa.scafSeq -db mt_pig.fa -outfmt 6
mummer -mum -b -c mt_pig.fa $1_mito_assembly.fa.scafSeq > mummer.mums mummerplot -postscript -p mummer mummer.mums </source>
Invoke like this: <source lang='bash'> sbatch do_mtalign_bowtie_pig.sh MA01F18 33\
/lustre/nobackup/WUR/ABGC/shared/Pig/ABGSA/ABGSA0071/ABGSA0071_MA01F18_R1.PF.fastq.gz\ /lustre/nobackup/WUR/ABGC/shared/Pig/ABGSA/ABGSA0071/ABGSA0071_MA01F18_R2.PF.fastq.gz