Hi everyone,
I have a problem calling indels with samtools. Up to now, I called variants with the following command:
samtools pileup -vcf ref.fasta mapping.bam > raw_variants.var
and created the pileup file with:
samtools pileup -cf ref.fasta mapping.bam > mapping.pileup
After that I added the filter steps. But for my last samples I didn't receive any indels (just SNPs). In the mapping I can see indels, but neither in the pileup-file nor in the variance-files are indels. Are there any parameter to include/exclude indels? Or do I have to do anything different for Solid-reads mapped with Bioscope in comparision to Illumina-reads?
Thanks for your help!
I have a problem calling indels with samtools. Up to now, I called variants with the following command:
samtools pileup -vcf ref.fasta mapping.bam > raw_variants.var
and created the pileup file with:
samtools pileup -cf ref.fasta mapping.bam > mapping.pileup
After that I added the filter steps. But for my last samples I didn't receive any indels (just SNPs). In the mapping I can see indels, but neither in the pileup-file nor in the variance-files are indels. Are there any parameter to include/exclude indels? Or do I have to do anything different for Solid-reads mapped with Bioscope in comparision to Illumina-reads?
Thanks for your help!
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