I am trying to convert DNAbin files to fasta format. Rationale: I want to use the fasta file to calculate non-synonymous/synonymous mutation rate.
my_dnabin1 is a DNAbin file of 55 samples and I am using the following code to convert it into a fasta file.
dnabin_to_fasta <- lapply(my_dnabin1, function(x) as.character(x[1:length(x)]))
This generates a list of 55 samples which looks like:
$SS.11.01
[1] "t" "t" "a" "c" "c" "t" "a" "a" "a" "a" "a" "g" "c" "c" "g" "c" "t" "t" "c" "c" "c" "t" "c" "c" "a" "a" [27] "c" "c" "c" "t" "a" "g" "a" "a" "g" "c" "a" "a" "a" "c" "c" "t" "t" "t" "c" "a" "a" "c" "c" "c" "c" "a"
$SS.11.02
[1] "t" "t" "a" "c" "c" "t" "a" "a" "a" "a" "a" "g" "c" "c" "g" "c" "t" "t" "c" "c" "c" "t" "c" "c" "a" "a" [27] "c" "c" "c" "t" "a" "g" "a" "a" "g" "c" "a" "a" "a" "c" "c" "t" "t" "t" "c" "a" "a" "c" "c" "c" "c" "a"
and so on...
However, I want a fasta formatted file as the output that may look something like:
>SS.11.01 ttacctga
>SS.11.02 ttacctga
catwith thefileoption, it's probably saving somewhere. You can find out where by using thegetwd()command. – gringer Aug 30 '17 at 14:18