Hi, there
I'm new to this field and have a question when using Galaxy. I have
RNA sequence data. How can I plot the graph of the length of sequence
with Galaxy.
Thanks!
___
The Galaxy User list should be used for the discussion of
Gal
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
g
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.
Thanks!
Best,
Zhiqiang
Quoting "Peter Cock" :
On Mon, Nov 26, 2012 at 6:47 PM, Zhiqiang Shu wro
ice (and more
complicated). Tools in "Interval Operation" group will be of help if
you go down that path.
Best,
Jen
Galaxy team
On 11/26/12 10:47 AM, Zhiqiang Shu wrote:
Hi, Galaxy users!
I have a question on how to find out sense and antisense sequence.
I've got RNA seq
ns to this and other Galaxy lists,
please use the interface at:
http://lists.bx.psu.edu/
----------
Zhiqiang Shu/Deng Lab
Department of Biological Science
Florida State University
319 Stadium Dr.
Tallahassee, FL, USA, 32306-4
Hi, all!
I have a maybe naive question that might be not so related to Galaxy
usage. So I got the RNA seq data from Illumina Hiseq. Do I need to get
rid of the adapter manually? If so, is it "clip adapter" that I should
use? It should only have one adapter sequence or maybe more than one?
Hi,
I have two simple questions related to manipulating step history. So,
how to change the order of steps, for example, put step 7 right after
step 3. Second question is related, how to re-order steps, for
instance, I deleted step 4 and 5 and want the next step (step 6) to
take the order
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