Im going to try that on a minimal example VCF and give a feedback. Thanks
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Hello everyone! I'm trying to use CNVkit, which uses b-allele frequency to find LoH
For this program, my somatic mutations must be tagged "SOMATIC" in the INFO field.
I have an annotated VCF with my somatic mutations with different tags.
How could I add another flag to my INFO field, after all the tags that are already there?
For example, the header for this new field would be
##INFO=<ID=SOMATIC,Number=0,Type=Flag,Description="Somatic event">
And the value would be
MVSDULK=0,0,0,1,0,0,0;NUM_TOOLS=1;LC=12.4;SOMATIC
My original VCF already had:
MVSDULK=0,0,0,1,0,0,0;NUM_TOOLS=1;LC=12.4
In the INFO field.
Any help is appreciated,
hum.. something like
awk '/^##/ {print;next;} /^#CHROM/ {printf("##INFO=<ID=SOMATIC,Number=0,Type=Flag,Description=\"Somatic event\">\n");print;next;} {OFS="\t";$8=sprintf("%s;SOMATIC",$8);print;}' in.vcf
?
Im going to try that on a minimal example VCF and give a feedback. Thanks
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