Dear all
I must admit that I'm a newbie in the snp calling practice. I used samtools in my analysis trying to identify SNPs from 3 human samples (belong to the same group)
I used the example code from samtools mpileup synopsis and modified it to suit my computational environment. However, the final output vcf file gave me more than 500,000 identified SNPs which really puzzled me. Then I tried it on a single sample, samtools got me more than 70,000 snps this time.
Is this normal?
Should I merge all 3 samples before I run samtools or I just treat them separately in samtools mpileup code?
Thanks a lot
I must admit that I'm a newbie in the snp calling practice. I used samtools in my analysis trying to identify SNPs from 3 human samples (belong to the same group)
I used the example code from samtools mpileup synopsis and modified it to suit my computational environment. However, the final output vcf file gave me more than 500,000 identified SNPs which really puzzled me. Then I tried it on a single sample, samtools got me more than 70,000 snps this time.
Is this normal?
Should I merge all 3 samples before I run samtools or I just treat them separately in samtools mpileup code?
Thanks a lot
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