Description Usage Arguments Value Author(s) Examples
View source: R/ADDO_Heterotic2_Pvalue.r
P-value Calculation and Verfication of overdominance (or heterotic) QTLs (1) Run the whole PLINK file or Run the separated PLINK files ("Run_separated = F"); (2) Indicate Reocde Model (AA:1 0 0/AB:0 1 0/BB:0 0 1) without the "1" column of covariance matrix; (3) Estimate two T-statistics (t(AB-AA) and t(AB-BB)) to measure the deviation between the effect of heterozygote (AB) and that of two homozygotes (AA and BB); (4) Generate the P-value based on MVN distribution using the minor(abs(t(AB-AA)),abs(t(AB-BB))) from SNPs with t(AB-AA)*t(AB-BB)>0.
1 2 3 4 5 6 | ADDO_Heterotic2_Pvalue(indir = indir, outdir = outdir,
Input_name = Input_name, Kinship_type = Kinship_type,
VarComponent_Method = VarComponent_Method, PheList_Choose = F,
PheList = PheList, Phe_HistogramPlot = F, Run_separated = F,
covariates_sum = covariates_sum, Phe_IndMinimum = 200,
GT_IndMinimum = 10, num_nodes = 10)
|
indir |
A character. The input directory where contains the input bPLINK or GenABEL data. |
outdir |
A character. The output directory where generates the folder: "2_Pvalue". |
Input_name |
A character. The prefixes of the input files. |
Kinship_type |
A character. The method to generate kinship matrix. Please select from "GenABEL","EMMA","EMMAX","GEMMA", "GCTA", "GCTA_ad", "HOMEBREW_AFW" or "HOMEBREW_AS". |
VarComponent_Method |
A character. The method to estimate variance components. Please select from "EMMA_a", "GCTA_a" or "GCTA_ad" (When VarComponent_Method is "GCTA_ad", the Kinship_type must be "GCTA_ad"). |
PheList_Choose |
A logic variable. T: Just investigate specified phenotypes; F: Investigate all phenotypes. |
PheList |
A vector of character. When choose "PheList_Choose=F", the specified phenotype list must be specified. |
Phe_HistogramPlot |
A logic variable. T: Draw the histogram plots for all phenotypes; F: Aviod the histogram plots. |
Run_separated |
A logic variable. T: Run the separated genotype files; F: Run the whole genotype file. |
covariates_sum |
A numeric variable. The sum of all covariates. |
Phe_IndMinimum |
A numeric variable. Remove phenotypes without enough available individuals. |
GT_IndMinimum |
A numeric variable. Remove loci with available individuals <GT_IndMinimum for all three genotypes. |
num_nodes |
A numeric variable. The number of cores used parallelly. |
a folder named "2_Pvalue" with various statistics of each significant SNP for all phenotypes.
Leilei Cui and Bin Yang
1 | ADDO_Heterotic2_Pvalue(indir=indir, outdir=outdir, Input_name="TEST", Kinship_type="GCTA_ad", VarComponent_Method="GCTA_ad", covariates_sum=2)
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