Open jianvhuang opened 1 year ago
Yes. We check for complement too. We flip by changing the allele dosage. 0 1 2 to 2 1 0
On Wed, May 3, 2023, 3:42 AM jianhuang @.***> wrote:
Hi
I wonder how PRSice deals with inconsistent strand and allele coding between the base GWAS and the target sample. I found a statement from the webpage that PRSsice performs strand flip automatically. Does it also deal with complimentary allele coding (e.g., EffectAllele.base="C", NonEffectAllele.base="T", A1.target="G", A2.target="A")? In this example, I suppose no flipping of beta is needed.
It will be very helpful if you could elaborate what PRSice checks for this QC step. Thank you very much.
Regards, Jian
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Do you think this could be very different from flipping the effect allele and non effect allele (along with the +/- sign of beta) in the base GWAS?
Could you point out which part of the code in the below file deal with the harmonisation issue? I would like to learn more about this. Thank you very much.
https://github.com/choishingwan/PRSice/blob/master/PRSice.R
Hi
I wonder how PRSice deals with inconsistent strand and allele coding between the base GWAS and the target sample. I found a statement from the webpage that PRSsice performs strand flip automatically. Does it also deal with complimentary allele coding (e.g.,
EffectAllele.base="C", NonEffectAllele.base="T", A1.target="G", A2.target="A"
)? In this example, I suppose no flipping of beta is needed.It will be very helpful if you could elaborate what PRSice checks for this QC step. Thank you very much.
Regards, Jian