The script for running LD calculations is very specific for 1000G haplotype data. However, recently published reports (PMID: 28942963) show that using small external reference panels for summary statistics from large GWAS can negatively affect fine-mapping results.
Would there be a quick way to adapt the LD script for a different reference panel (like HRC)? From my naive reading of the script, it seems like just eliminating filtering on pop_ids might do the trick.
Hello,
The script for running LD calculations is very specific for 1000G haplotype data. However, recently published reports (PMID: 28942963) show that using small external reference panels for summary statistics from large GWAS can negatively affect fine-mapping results.
Would there be a quick way to adapt the LD script for a different reference panel (like HRC)? From my naive reading of the script, it seems like just eliminating filtering on pop_ids might do the trick.
Paul