Hi I want to do variant calling for more than 60 samples using haplotype caller. I want to know, I should do it with multiple samples using this command :
java -Xmx16g -jar GenomeAnalysisTK-3.8-0-ge9d806836/GenomeAnalysisTK.jar -R Equus_caballus.EquCab2.dna.toplevel.fa -T HaplotypeCaller -I sample-1.bam -I sample-2 -I sample-3 ......-I sample-60 -ERC GVCF -o output.vcf.gz
I want to know is it a true method?
You can call sample by sample and joint genotype - that way, you shouldn't lose cross-sample genotype information. Or, you could call all samples per region, where each region can be a chromosome or smaller so you reduce computational burden.
You'd just need different GATK tools to Combine/Cat Variants based on the division you choose.
You could even combine both if you'd like to. The choice is best made based on time and computational resources available to you.
so you mean my command is not a true way for all samples variant calling?
java -Xmx16g -jar GenomeAnalysisTK-3.8-0-ge9d806836/GenomeAnalysisTK.jar -R Equus_caballus.EquCab2.dna.toplevel.fa -T HaplotypeCaller -I sample-1.bam -I sample-2 -I sample-3 ......-I sample-60 -ERC GVCF -o output.vcf.gz
If you're looking for someone to give you the "right" command, sorry, I'm not that person. I've outlined possible approaches, and it is up to you to choose one and implement it.
What you're doing above is using neither of those approaches - you're calling all samples across all regions in a single thread with 16G RAM. That's fine as long as you're ready to wait a long time and risk everything on one thread.
what are you thinking if I increase my memory an thread (RAM 64 and 16 thread)?
what are you thinking
I think it will be faster. GATK has multiple levels of parallelism, multithreading is just one of them.
so, according to your comments, I can have 3 scenarios: 1. call sample by sample and joint genotype 2.call all samples per region 3. call all samples (all regions) using multithreading so, Are there any differences in the results (genotypes) of these scenarios?
We're getting into a rabbit hole now, where the principal question was something else and the discussion devolves into an one-on-one between OP and an answerer. This is not good and I cannot encourage this.
If you're really curious about this, search for posts that address this question. Better yet, Google it. The better you are at Google-ing stuff, the faster you can solve your problems.
sorry if bother you. Thanks
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What do you mean by "true method"? Also, please use the formatting bar (especially the
codeoption) to present your post better. I've done it for you this time.thank you for your attention. I mean can I do variant calling for 60 samples or I should do it separately for each sample? because when I do it separately for each sample, I have only two Genotypes per SNP (0/1 or 1/1) in g.vcf files.
Hi siyavash_damdar,
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Cheers,
Wouter
Hi Thank you for useful comment. Yes of course, I did it. The best, Siavash