Description Usage Arguments Details Author(s) See Also Examples
For each position within the matrix of aligned sequences, the probability corresponding to each nucleotide is estimated. Missing values are imputed to a multistate nucleotide with probabilities corresponding to the frequency of each nucleotide in the corresponding organism.
1 | missing.fun(x, symbols, R, Prob)
|
x |
Position k of the training set (a set of aligned nucleotide sequence) |
symbols |
Number of each nucleotide |
R |
Number of missing values for position |
Prob |
Probability of each base within genome |
This function is included on probability function. Missing.fun has to be different NULL
Joan Maynou <joan.maynou@upc.edu>
probability
1 2 3 4 5 6 7 8 9 10 11 | data(TranscriptionFactor)
data(BackgroundOrganism)
x<-TranscriptionFactor[,1]
resum<-table(x)
A<-resum["A"];T<-resum["T"];C<-resum["C"];G<-resum["G"];R<-resum["-"]
symbols <- c(A,T,C,G)
names(symbols) <- c("A","T","C","G")
symbols[which(is.na(symbols))] <- 0
if(is.na(R)) R <- 0
prepm<-missing.fun(x,symbols,R,Prob)
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