| getting_started | R Documentation |
getting_started is a simulated dataset created to demonstrate the use of
the sme() function for genome-wide interaction analyses. It contains
results from a simulated analysis involving additive genetic effects and
gene-by-gene (GxG) interactions.
data("getting_started")
A list with results from sme(), including the following components:
summaryA data frame summarizing the analysis results, including
p-values for SNP associations (p).
pveA data frame containing the per SNP variance component estimates normalized to phenotypic variance explained (PVE).
vcA data frame containing the per SNP variance component estimates.
gxg_snpsA vector containing the indices of the SNPs assigned to have epistatic interactions in the trait simulations.
The dataset was generated as follows:
Genotype Simulation: Genotype data for 5000 individuals and 6,000 SNPs was simulated with synthetic allele counts.
Phenotype Simulation: Phenotypic values were simulated with an additive heritability of 0.3 and a GxG interaction heritability of 0.25. A set of 100 SNPs were selected for additive effects, and two groups of 5 SNPs each were used for GxG interactions.
PLINK-Compatible Files:
The simulated data was saved in PLINK-compatible .bed, .fam,
and .bim files.
Interaction Analysis:
The sme() function was used to perform genome-wide interaction analyses
on a subset of SNP indices, including the GxG SNP groups and 100 additional
additive SNPs. Memory-efficient computation parameters
(e.g., chun_ksize, n_randvecs, and n_blocks) were applied.
Additive Heritability: 0.3
GxG Heritability: 0.25
Number of Samples: 5000
Number of SNPs: 6,000
Selected Additive SNPs: 100
Selected GxG SNP Groups:
Group 1: 5 SNPs
Group 2: 5 SNPs
data-raw/getting_started.R
sme
data("getting_started")
head(getting_started$summary)
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