.:. is not the value for the GT field. Given that FORMAT is : separated, the GT value is just ., which is a no-call/unknown, like williamsbrian5064 says.
Am a beginner to genomics etc, so apologies for a trivial/strange question. When looking at a 23andMe dataset, the first variant listed was the following: …
Hi everyone: I have a VCF file having multiple population samples. Is there any way to calculate the observed counts of genotypes called and observed …
I think that is a no-call. I have that issue when I have a low depth of coverage in that particular variant location
.:.is not the value for the GT field. Given that FORMAT is:separated, the GT value is just., which is a no-call/unknown, like williamsbrian5064 says.