Hi Mark,
I'm happy to help. The programs have evolved faster than the documentation. Here is how to run it to accomplish what you desire:
Input files:
1. known GWAS hits: knownhits.lst
2. association results: results.txt
3. genotypes used for LD: genotypes.lbat (most any format will work)
Run:
glu ld.surrogates results.txt --haystack=knownhits.lst genotypes.lbat -o surrogates.txt
The SNPs listed without a surrogate are not known hits or in LD with one or more known hit.
-Kevin
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