MakeCounts | R Documentation |
MakeCounts
creates a matrix of genotype counts, with one row for
each bi-allelic marker, containing 4 columns with the counts AA, AB, BB
and NA (missings) respectively
MakeCounts(X, alleles, pos1 = 1, pos2 = 3, coding = c(AA=0,AB=1,BB=2), sep = "")
X |
A matrix or dataframe with bi-allelic genotyping information, markers in columns, individuals in rows |
alleles |
a vector of alleles for each marker
(e.g. c("A/T","A/G",...)). Only relevanit if |
pos1 |
position of the first allele in the allele string (1 by default) |
pos2 |
position of the second allele in the allele string (3 by default) |
coding |
indicates how homozygotes and heterozygote are coded as
numbers. Only relevant if |
sep |
allele separator character for genotype data in text format ("" for AA; "/" for "A/A") |
MakeCounts
is thought for bi-allelic marker data only. Missings
are should be coded by NA. It produces the right input for
HWTernaryPlot
.
Heterozygotes may be coded in the data as "AB" or "BA". Both entries will be counted as a heterozygote.
A matrix of 4 columns
Jan Graffelman jan.graffelman@upc.edu
HWTernaryPlot
SNP1 <- c("GG","GG","GG","GG","GG","GG","GG","GG","GG")
SNP2 <- c("CG","GG","CC","GG","GG","CG","CG","CG","CG")
SNP3 <- c("AA","AA","AA","AG","AA","AG","AA","AA","AA")
SNP4 <- c("GG","GG","GG","GG","GG","GG","GG","GG","GG")
SNP5 <- c("CC","CC","CC","CC","CC","CC","CT","CT","CT")
X <- cbind(SNP1,SNP2,SNP3,SNP4,SNP5)
Y <- MakeCounts(X,c("A/G","C/G","A/G","A/G","C/T"))
print(Y)
W <- matrix(sample(c(0,1,2,NA),100,replace=TRUE),ncol=5)
Z <- MakeCounts(W,coding=c(0,1,2))
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