This function takes in the final data object and writes the variant influences that are at or below the specified significance level.
write_variant_influences(
data_obj,
p_or_q = 0.05,
include_main_effects = TRUE,
filename = "Variant.Influences.csv",
delim = ",",
mark_covar = FALSE,
write_file = TRUE
)
If write_file is TRUE, this function writes the results table to a file and invisibly returns the table. If write_file is FALSE, the function returns the results table without writing to file.
a Cape
object
A threshold indicating the maximum adjusted p value considered significant. If an FDR method has been used to correct for multiple testing, this value specifies the maximum q value considered significant.
Whether to include main effects (TRUE) or only interaction effects (FALSE) in the output table.
A character vector specifying the name of the file.
A character string indicating the delimiter in the data file. The default indicates a comma-separated file (",").
A logical value. If TRUE, an asterisk is appended the names of markers used as covariates in the pair scan.
A logical value indicating whether the table should be written to a file or simply returned.
The columns of the output file are the following: Source: The marker that is the source of the directed interaction Chr: The chromosome on which the source marker lives Position: The genomic position of the source marker Target: If the effect is an interaction, this column lists the marker that is the target of the directed interaction. If the effect is a main effect, this column lists the trait that is the target of the main effect. Chr: The chromosome on which the target marker lives. If the effect is a main effect, this is listed as 0. Position: The genomic position of the target marker. If the effect is a main effect, this is listed as 1. Conditioning: If the effect is a main effect, this column identifies the marker on which the main effect marker was conditioned when it had it's largest main effect. Chr: If the effect is a main effect, this column lists the chromosome on which the conditioning marker lives Position: If the effect is a main effect, this column lists the genomic position of the conditioning marker. Effect: The effect size of the effect, either main effect or interaction. SE: The standard error of the effect, either main effect or interaction. |Effect|/SE: The standardized effect P_empirical: The empirical p value calculated from permutations p_adjusted: The p value adjusted by the method specified in the parameter file.
if (FALSE) {
inf_table <- write_variant_influences(data_obj)
}
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