Dear Jen,
I am not much of a Galaxy user yet. Some days ago I know something about Galaxy
and found it a really wonderful tool. And I am confused by a simple question
regarding how to extract intron sequences from [gtf file];
Here is a simple of a gtf file:
1 Cufflinks transcript322
Dear Galaxy develop team:
As the subject said, I need to obtain random regions which are 1000-bb, and
then filter these regions to remove regions overlapping a specific [gtf] file.
So can I obtain random regions with Galaxy?
I found (Regional Variation)->Make windows may help me, but the tool
Hi Jen,
Thank you very much!
Best,
John
From: Jennifer Jackson
Sent: Friday, August 23, 2013 12:21 AM
To: 师云
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] How to get random region of 1000-bp window in the
chromosome not overlapping specific [gtf] file
Hello John,
Use "
Hello everyone,
I found regular expression could be available in the tool (filter and sort)
->Filter. I wonder whether it could be the same in the tool (Text
Manipulation) ->Compute. I have checked that the fuction "len(c4.split('_'))"
would return error. So, could anyone tell me if it was pos
Hi Jen,
Thank you for your help. The Galaxy tools can do many things!
From: Jennifer Jackson
Sent: Friday, August 30, 2013 8:31 AM
To: 师云
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] Question about expression in Galaxy tools
Hello,
There are some tools in the group '
Hi everyone,
I want to calculate GC content of transcripts in the gtf file like this:
chr1 Cufflinks transcript 3 22 1000 + . gene_id "CUFF.23955"; transcript_id
"CUFF.23955.1";
chr1 Cufflinks exon 3 10 1000 + . gene_id "CUFF.23955"; transcript_id
"CUFF.23955.1"; exon_number "1";
chr1 Cufflin
hello, jen
Thank you for your reply. I though it will return the GC content of each exon.
I try it and find that the Galaxy will interpret features.
Thank you.
John
From: Jennifer Jackson
Sent: Wednesday, September 18, 2013 6:38 AM
To: 师云
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re
Hi Jen,As the title, I have a [fasta] file that obtained from a [gtf] file,
>cuff102.1atcgtaaagggcgat>cuff103.1gtcgttgactgtc
and I want to get the output like this to filter the sequences that contain any
not[ATCG] character?
>cuff102.1atcgtaaagggcgat
I have a large of sequences to filter.
d use something like this, with the Select
tool and "Matching":
^..*\t[ATCGatcg]+$
(Only one dot is really required, this is just how I always do it.
Adds a bit of a format sanity check into the filter).
Hope this helps!
Jen
Galaxy
urious, I didn't try it that way. There are usually a few ways to
do the same thing when using a regex.
But, I am glad that this helped a bit and good luck with the query,
Jen
Galaxy team
On 12/9/13 7:06 AM, 朱师云 wrote:
Hi,
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