Iteratively run susie and estimate parameters
susieI(
pgenfs,
exprfs,
Y,
regionlist,
niter = 20,
L = 1,
group_prior = NULL,
group_prior_var = NULL,
estimate_group_prior = T,
estimate_group_prior_var = T,
use_null_weight = T,
coverage = 0.95,
standardize = T,
ncore = 1,
outputdir = getwd(),
outname = NULL,
report_parameters = T
)
A character vector of .pgen or .bed files. One file for one chromosome, in the order of 1 to 22. Therefore, the length of this vector needs to be 22. If .pgen files are given, then .pvar and .psam are assumed to present in the same directory. If .bed files are given, then .bim and .fam files are assumed to present in the same directory.
a vector of length n, phenotype, the same order as provided by `.pgenfs` (defined in .psam or .fam files).
a list object indexing regions, variants and genes. The output of
index_regions
the number of iterations of the E-M algorithm to perform
the number of effects for susie
a vector of two prior inclusion probabilities for SNPs and genes. This is ignored
if estimate_group_prior = T
a vector of two prior variances for SNPs and gene effects. This is ignored
if estimate_group_prior_var = T
TRUE/FALSE. If TRUE, the prior inclusion probabilities for SNPs and genes are estimated
using the data. If FALSE, group_prior
must be specified
TRUE/FALSE. If TRUE, the prior variances for SNPs and genes are estimated
using the data. If FALSE, group_prior_var
must be specified
TRUE/FALSE. If TRUE, allow for a probability of no effect in susie
A number between 0 and 1 specifying the “coverage” of the estimated confidence sets
TRUE/FALSE. If TRUE, all variables are standardized to unit variance
The number of cores used to parallelize susie over regions
a string, the directory to store output
a string, the output name
TRUE/FALSE. If TRUE, estimated parameters are reported at the end of iteration
character vector of .`expr` or `.expr.gz` files. One file for one chromosome, in the order of 1 to 22. Therefore, the length of this vector needs to be 22. `.expr.gz` file is gzip compressed `.expr` files. `.expr` is a matrix of imputed expression values, row is for each sample, column is for each gene. Its sample order is same as in files provided by `.pgenfs`. We also assume corresponding `.exprvar` files are present in the same directory. `.exprvar` files are just tab delimited text files, with columns:
chromosome number, numeric
gene boundary position, the smaller value
gene boundary position, the larger value
gene id
Its rows should be in the same order as the columns for corresponding `.expr` files.