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samtools idxstats not removing ChrM

I am trying to remove ChrM from my ChIP-seq data. Below is my pipeline for one sample up to where I am having the issue (samtools idxstats). The output file from samtools idxstats is the same size as the input so it doesn't look like it is removing anything. I've used this before with success so I have no idea what I am doing wrong this time around. Any help is appreciated.

#Align to genome using bowtie2
bowtie2 -p 8 -q --local \
-x chipseq/reference_data/mm10/mm10 \
-U chipseq/raw_data/PPARg/PPARg_Input_1.fastq.gz \
-S chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_unsorted.sam

#Changing file format from SAM to BAM 
samtools view -h -S -b \
-o chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_unsorted.bam \
chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_unsorted.sam

#Sort BAM 
sambamba sort -t 8 \
-o chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam \
chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_unsorted.bam 

#Index BAM (need .bai for remove ChrM reads)
samtools index chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam

#Remove reads mapping to mitochondria
samtools idxstats chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam | cut -f 1 | grep -v chrM | xargs samtools view -b chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam > chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted_woChrM.bam
samtools chip-seq
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updated by Ram Ram • written by Jen • Jen

can we see the output from this? samtools idxstats chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam

conversely just as an experiment try isolating the mitochondrial alignments: samtools idxstats chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam | cut -f 1 | grep chrM | xargs samtools view -b chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam > chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted_onlyChrM.bam

• 0 views • link
written by Jeremy Leipzig Jeremy Leipzig

i'm not sure this is doing what you expect?

you should try filtering your bam directly and then running idx stats

samtools view -h your.bam | awk '{if($3 != "chrM"){print $0}}' | samtools view -Shb - > filter.bam
• 0 views • link
written by benformatics benformatics

enter image description here

I think I got it to work using "MT" rather than "ChrM" (code below)

samtools idxstats chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam | cut -f 1 | grep -v MT | xargs samtools view -b chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted.bam > chipseq/results/bowtie2/PPARg/PPARg_Input_Rep1_aln_sorted_woMT.bam

enter image description here

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written by Jen • Jen

1 answer

You mitochondrial genome is named MT not chrM...

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written by Pierre Lindenbaum Pierre Lindenbaum

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