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Mutect 2 on WGS data takes too long to run

I used Mutect2 on human exome sequencing (30x) data before and without parallel processing, it took me 5.5 days. That was still doable - However, now I am trying to run Mutect2 on my human WGS data (30x, bqsr bam file size ~120G), the estimation tells me 500+ weeks at the start!

I feel like even I split on regions, or use Queue offered by GATK will not improve the situation to a satisfying level... Here is my code:

java -jar $GATK -T MuTect2 -R $REF -I:tumor $BQSRTBam -I:normal $BQSRNBam --dbsnp $DBSNP --cosmic $cosmicData -o $mutect2VCF

I tried different memory, and with/without dbsnp/cosmic... going without cosmic seems to let Mutect2 give a longer estimation.

Anyone experience similar issues? Any suggestion is appreciated. Thank you very much in advance.

mutect wgs
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updated by donfreed donfreed • written by DVA DVA

2 answers

Varscan2 instead is another choice, much faster.

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written by chen chen

I had a little experience with VarScan2 - don't you need to use samtools pileup? I recall the pileup procedure to be painfully long too... Maybe I did not do it correctly, but please comment on it. Thank you.

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written by DVA DVA

Yes, you are right, samtools mipileup is needed. But samtools mpileup + VarScan2 is still much much faster than MuTect2.

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written by chen chen

It is possible to pipe a few process to avoid creating the intermediate files. 

samtools view -b -L region.bed  $bam  | samtools mpileup --reference $ref  - |  java -jar  VarScan.v2.4.4.jar mpileup2snp --output-vcf --min-var-freq 0.01  --variants  - > out.vcf
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written by Hideo • Hideo

You can try the Sentieon Genomic Tools: http://www.biorxiv.org/content/early/2017/05/12/115717. We provide a variant caller (TNhaplotyper, part of TNseq) that provides matching results to MuTect2 with a substantial performance improvement. You can request a free trial from https://www.sentieon.com/home/free-trial/.

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written by donfreed donfreed

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