Entering edit mode
Kristian Ullrich
▴
10
@kristian-ullrich-4698
Last seen 10.2 years ago
Hello Biostrings curators,
again the question to you:
Is there an easier way to solve the follwing:
R-code:
####################
####################
library(Biostrings)
#example sequence
seq.list=list()
seq.list[1]="AAAAAAAAAATTTTTTTTTTGGGGGGGGGGCCCCCCCCCC"
seq.list[2]="TTTTTTTTTTGGGGGGGGGGCCCCCCCCCCAAAAAAAAAA"
fas.seq = DNAStringSet(unlist(seq.list))
#defining start and end points of subseq
start1 = 1
end1 = 10
start2 = 21
end2 = 25
#creating first and second subseq
first.subseq = subseq(fas.seq,start1,end1)
second.subseq = subseq(fas.seq,start2,end2)
new.seq =
DNAStringSet(apply(sapply(list(first.subseq,second.subseq),as.characte
r),1,function(x)
paste(x,collapse="")))
names(new.seq) = names(fas.seq)
####################
####################
I basically want to combine subseqs from one DNAStringset, something
like:
subseq(DNAStringSet, start = c(start1,start2), end = c(end1,end2))
would be nice.
Thank you in anticipation
Kristian Ullrich
--
Kristian Ullrich
Leibniz Institute of Plant Biochemistry
Weinberg 3
D-06120 Halle (Saale), Germany
phone +49 345 5582 1221
fax +49 345 5582 1209
mail kullrich at ipb-halle.de