s_hat_bigsnp.Rd
Step Two of bigsnp2mashr
s_hat_bigsnp(
path,
gwas_rds,
phenotype,
top_set,
random_sample,
scaled = TRUE,
markers = NULL,
markers2 = NULL,
model = c("linear", "logistic"),
clump = TRUE
)
Path
RDS file with gwas results
Character vector. Single phenotype name
Top markers chosen
Numeric vector. Random sample of SNPs
Logical. Should effect sizes and std errors be scaled?
Marker names for the GWAS you ran
Markers to include if SNPs are LD clumped.
One of linear or logistic. Type of GWAS model.
Logical. Clump SNPs?