Thank you, Peter! I think I should put more detailed information here.
What I'm doing is piRNA data. Two groups of piRNA (named sense and
antisense)are in the library. As I said, they are complementary to
each other for about 10 nt, while the whole length is about 30nt. For
the sense group, they share the feature of having an "A" at their 10th.
In this case, how can I deal with it? One possible way come up is
inverting all sequences and aligning them.
Quoting "Peter Cock" <p.j.a.c...@googlemail.com>:
On Mon, Nov 26, 2012 at 6:47 PM, Zhiqiang Shu <z...@bio.fsu.edu> wrote:
Hi, Galaxy users!
I have a question on how to find out sense and antisense sequence. I've got
RNA seq data in the fastq format. The sequences inside are partially
complementary to each other (complementary is 10nt, while entire is about
30nt). How can I separate these sequences into two groups: sense and
Depending on how your sequences were prepared, you might be able to
look for a poly-A tail as a clue to orientation. Another approach is to
compare the (assembled) transcripts to known genes and if you only
get matches on one strand that is probably the correct orientation.
(one thing I know is for the sense sequence the 10th nucleotide is
Why is that? Is this related to your library preparation?
Zhiqiang Shu/Deng Lab
Department of Biological Science
Florida State University
319 Stadium Dr.
Tallahassee, FL, USA, 32306-4295
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