Hello,

My lab has some candidate SNPs for skin diseases. we want to go backward and see which of these SNPs are present in the same patients and have a more accurate list of SNPs to study.

DOES anyone have any experience going backward on the SNP GWAS data set and deconvoluting the information and asking in which patients studied, these SNPs are present at the same time?

I know I need to request the original data, but then any help would be greatly appreciated.

OR is it easier to get new samples and genotypes each patient?

Alessandro

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