Hello,
So, I have 8 normal sample and 8 tumor sample. Each normal and tumor group had been processed to get mpileup file by samtools. After that, I did the varscan2 soomatic function to call variation. After that, I got warning resetting normal and from what I found in the document, it's better to not call mpileup for each group. Instead, calling mpileup for 2 bam file, 1 normal and 1 tumor. So, I had finished doing this. I take 1 normal sample and 1 tumor sample for mpileup input to generate 1 mpileup file. After that, I use that mpileup file for varscan input. The result is no warning and seems no problem. My question is, how do I integrate the result for 8 normal/tumor pair varscan results? I figure if I proocess the data with 1 normal and 1 tumor, I will need to do varscan call 8 times and will get 8 results. Is there any method to join the results?
Thank you for your reply.
So, basically, you generate VCF file for each sample, not normal-tumor pair? Is the workflow like this:
1. Generate mplieup for each sample
2. Generate vcf for each mpileup
3. Merge vcf into bed
4. Use varscan validation to the bed
5. Merge the result
For each PATIENT I run varscan to generate a vcf; each run of varscan requires two samples: the tumour and the normal