FDR_IQT.Rd
FDR_IQT
is a function which uses summary statistics to reduce Winner's
Curse bias in SNP-trait association estimates, obtained from a discovery GWAS.
The function implements the FDR Inverse Quantile Transformation method
described in
Bigdeli et
al. (2016), which was established for this purpose.
FDR_IQT(summary_data, min_pval = 1e-300)
A data frame containing summary statistics from the
discovery GWAS. It must have three columns with column names rsid
,
beta
and se
, respectively, and columns beta
and
se
must contain numerical values. Each row must correspond to a
unique SNP, identified by the numerical value rsid
.
A numerical value whose purpose is to avoid zero
\(p\)-values as this introduces issues when qnorm()
is applied. Any
SNP for which its computed \(p\)-value is found to be less than
min_pval
is merely re-assigned min_pval
as its \(p\)-value
and the method proceeds. By definition, the method makes no adjustment to
the association estimate of a SNP for which this has occurred with the
presumption that in general, estimates of SNPs with \(z > 37\) are not
biased. The default value is min_pval = 1e-300
.
A data frame with the inputted summary data occupying the first three
columns. The new adjusted association estimates for each SNP are returned in
the fourth column, namely beta_FIQT
. The SNPs are contained in this
data frame according to their significance, with the most significant SNP,
i.e. the SNP with the largest absolute \(z\)-statistic, now located in the
first row of the data frame.
Bigdeli, T. B., Lee, D., Webb, B. T., Riley, B. P., Vladimirov, V. I., Fanous, A. H., Kendler, K. S., & Bacanu, S. A. (2016). A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans. Bioinformatics (Oxford, England), 32(17), 2598\(-\)2603. doi:10.1093/bioinformatics/btw303
https://amandaforde.github.io/winnerscurse/articles/winners_curse_methods.html
for illustration of the use of FDR_IQT
with a toy data set and further
information regarding the computation of the adjusted SNP-trait association
estimates.