I have 156 SNP markers and I would like to do an association analysis for some traits. And which is better? FDR or Bonferroni corrections?
I have read a paper published in Genome and the authors used 20% of FDR. Don't you think that's so high?
Bonferroni correlation is much conserved, I would suggested 5% or 10% in GWAS for following up validations.
5% or 10% FDR????
I used 5% in my projects. Just realized you have 156 SNPs, I think Bonferroni correction is reasonable, FDR or Q value is usually used at genome-wide level.
thank you
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