Entering edit mode
4.2 years ago
r00628112
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10
For GWAS analysis, we get different significant points on SNP-based, and Indel-based GWAS. In my opinion, it is understandable, because we conducted exome sequencing. The associated SNP or Indel are dependent event, thus the different pattern are normal. But I got the comments, the variant are just as genetic markers. Either SNP or Indel based GWAS, the significant peaks will not be different.
Actually, I can not understand why? The marker density, marker type and marker locations are totally different.
😆
If it is QTL analysis, I can understand why.
Why not treat them as the same variable type for the purpose of the GWAS / eQTL? I see no reason to perform an analysis stratified by SNP and indel.