Hi,
I've performed SNP calling from exome seq data followed by association testing (case-control), so I now have a p-value for each identified SNP.
I would like to some how summarise the p-values for SNPs identified in the same gene, so that I get a p-value for each gene (for use in downstream analysis).
So far I have been using the lowest p-value for each gene, but I wonder if this is really the best method..?
So, what is the preferred method for this? And are there any tools for doing this?
I hope someone can be helpful with this
Best regards,
Sara
I've performed SNP calling from exome seq data followed by association testing (case-control), so I now have a p-value for each identified SNP.
I would like to some how summarise the p-values for SNPs identified in the same gene, so that I get a p-value for each gene (for use in downstream analysis).
So far I have been using the lowest p-value for each gene, but I wonder if this is really the best method..?
So, what is the preferred method for this? And are there any tools for doing this?
I hope someone can be helpful with this

Best regards,
Sara