Open beginner984 opened 4 years ago
I dont want to tell you how to do your thing, but if you can avoid parsing vcfs yourself, I think you should. Why not take one of the many libraries/modules available in basically any programming language to help you with it? For perl, which this script seesm to be vcftools provides a VCF.pm perl module, which could be very helpful. https://vcftools.github.io/perl_module.html
Thank you. In INDEL file there is not normal INFO
I noticed in some cases the frequency is above 100% or 1, is this because there is more information in support of the variant than there is read depth???. In these cases, could I consider the frequency to be around 1?
Hello
I have a script extracting some fields like
TumorReadCount
,tumorVariantAlleleCount
,TumorReferenceAlleleCount
,NormalReadCount
,NormalAlleleCount
,NormalReferenceCount
andVAF
from .vcf StrelkaThis is my script
This code works well on SNVs for example this file
https://sotonac-my.sharepoint.com/personal/fi1d18_soton_ac_uk/Documents/Microsoft%20Teams%20Chat%20Files/LP6008202-DNA_B03_vs_LP6008201-DNA_B03.snp.pass.vcf
But gives empty fields on INDELs like file
https://sotonac-my.sharepoint.com/personal/fi1d18_soton_ac_uk/Documents/Microsoft%20Teams%20Chat%20Files/LP6008202-DNA_B03_vs_LP6008201-DNA_B03.passed.somatic.indels.vcf
I really don't know how to change the code to work on INDELs
Can you please help me?
Thank you