powered by
makeGphmmPerRead returns a function to compute gphmm probabilities for each row of the csv file.
makeGphmmPerRead
makeGphmmPerRead(seqs, csv)
- DNAStringSet with DNA sequences used for the training.
- data.frame with first column = queries, second column = reference sequences, third column = qv
# NOT RUN { library(Biostrings) seqs <- DNAStringSet(c(a='ATGC', b = 'ATGG', c = 'ATGT')) csv <- data.frame(queries = c('a', 'b'), refs = c('c', 'c')) makeGphmmPerRead(seqs, csv) # }
Run the code above in your browser using DataLab