Closed zyxNo1 closed 3 months ago
What's more, I am unsure about how to call somatic variants. I have 2 bam files, one for the tumor and one for the control. My goal is to generate a typical somatic vcf output with only one sample column (instead of displaying tumor and control at the same time). Is there any related documentation available for this? Alternatively, what steps should I take to accomplish this?
There is a typo in your set print merged_calls
command; it should be print merged_calls
.
Currently, only the calls output of a single Pytor file can be saved in VCF format. For merged output, it can be saved in XLSX, TSV, or other similar formats.
The following command can be used to generate VCF output of a sample using VIEW
mode:
set print_filename test1.vcf
print calls
Thank you, Arijit
I encountered a problem when I run cnvpytor for multiple samples analysis. Firstly, I followed the basic process outlined in the guide for every bam file:
Next, I executed a command similar to the one provided in CNVpytor's examples/merging.md file:
cnvpytor -root sample1.pytor sample2.pytor sample3.pytor sample4.pytor -view 10000
And there are 2 important things I think:And I made the following adjustment as I desired a VCF file:
However, I got nothing. No ouput file at all. But if I change it into other format like tsv:
I can get correctly formated output.
Why did the result turn out this way? And if I want to get merged vcf, how should I do that?