Hi, Zhili.
I am currently running SBayeRC for the first time on a phenotype of Anorexia Nervosa. The GWAS dataset I am utilizing is from 2019, which I have used in other approaches. However, I have encountered an issue as the dataset does not include information on the allele frequency of the effect variant, an information that SBayesRC used as input. I would like to know how to deal with this situation, is it possible to obtain the beta effect without the allele frequency data?
The allele frequency is only used for the QC purpose. If you are sure about the quality, you can fill the allele frequency with our LD information (LD_folder/snp.info).
Hi, Zhili. I am currently running SBayeRC for the first time on a phenotype of Anorexia Nervosa. The GWAS dataset I am utilizing is from 2019, which I have used in other approaches. However, I have encountered an issue as the dataset does not include information on the allele frequency of the effect variant, an information that SBayesRC used as input. I would like to know how to deal with this situation, is it possible to obtain the beta effect without the allele frequency data?