Hi All,
I have a count alleles by Genes table for a vcf. Taking into account that variants stand for the total number of variants for the current sample in each gene and allele count stands for the total number of non-reference alleles for the current sample in each gene, could you please advise me on how to interpret this?
Gene Names # Variants Allele Count # Het # Hemi # HomoVars A1BG 9 13 5 4
I cannot understand how is it possible that in genes the allele count can be major than variants.
Thanks
patrick.mackay : Can you clarify if the following edit is appropriate and matches the header?
Hi Genomax.
Yes. This is the right edit.
Thanks for the clarification
Hi Igor,
i didn't' get it. Could you please advise by explaining with a practical example? I am just entering that field that extremely fascinates me but of course, I am encountering some hurtles.
Thanks in advance
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Hi Igor,
i didn't' get it. Could you please advise by explaining with a practical example? I am just entering that field that extremely fascinates me but of course, I am encountering some hurtles.
Let's say your reference sequence is:
AAA
.You have two reads:
AAG
andAAT
. Thus, you have a mutation at position 3. That is sometimes counted as 1 mutation since it is 1 position. However, if you look at the alleles, you have 2 (G and T).