CLQD | R Documentation |
CLQD
partitioning the given data into subgroups that contain SNPs which are highly correlated.
CLQD(subgeno, subSNPinfo, CLQcut = 0.5, clstgap = 40000, CLQmode = c("Density", "Maximal"), codechange = FALSE)
subgeno |
A data frame or matrix of additive genotype data, each column is additive genotype of each SNP. |
subSNPinfo |
A data frame or matrix of SNPs information. 1st column is rsID and 2nd column is bp position. |
CLQcut |
A numeric value of threshold for the correlation value |r|, between 0 to 1. |
clstgap |
An integer value to specifing the threshold of physical distance (bp) between two consecutive SNPs
which do not belong to the same clique, i.e., if a physical distance between two consecutive SNPs in a clique
greater than |
CLQmode |
A character string to specify the way to give priority among detected cliques.
if |
codechange |
If |
A vector of cluster numbers of all SNPs (NA
represents singleton cluster)
Sun-Ah Kim <sunny03@snu.ac.kr>, Yun Joo Yoo <yyoo@snu.ac.kr>
data(geno) data(SNPinfo) CLQD(geno,SNPinfo,CLQcut = 0.5, clstgap= 40000, CLQmode = 'Maximal', codechange = FALSE) CLQD(geno,SNPinfo,CLQcut = 0.5, clstgap= 40000, CLQmode = 'Density', codechange = FALSE)
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