ldsc_rg | R Documentation |
Imported here to help estimate sample overlap between studies
ldsc_rg(id1, id2, ancestry = "infer", snpinfo = NULL, splitsize = 20000)
id1 |
ID 1 to analyse |
id2 |
ID 2 to analyse |
ancestry |
ancestry of traits 1 and 2 (AFR, AMR, EAS, EUR, SAS) or 'infer' (default) in which case it will try to guess based on allele frequencies |
snpinfo |
Output from |
splitsize |
How many SNPs to extract at one time. Default= |
model fit
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