Re: [galaxy-user] fastqc and blast? trinity?

2013-12-16 Thread Jennifer Jackson

  
  
Hi Jorge,

I see that Peter helped with the Blast question (thanks Peter!), but
you are having trouble with Trinity, too.

Trinity should work without any issues to my knowledge. Make sure
that you are running the latest distribution (or cloudman) and have
all of the dependencies set up. Then, if you are still having
problems, send details "to" the "galaxy-...@bx.psu.edu" mailing list
only (not to a team member, and please start a new thread - not a
reply the galaxy-user list). This way our development team/community
will see the thread and can help you troubleshoot the install. 
https://wiki.galaxyproject.org/MailingLists#The_lists

Thanks!

Jen
Galaxy team


--
Hello,
of course, Jennifer
  is right for the first question  . For the second question about  blast ... I wonder if running after blast in galaxy I can remove sequences that
  can contaminate
  the data. It's possible?
  
  Last question,
  trinity is 100%
  operational in galaxy?
  Because trinity
  ran but the result was
  empty, and
I think the script failure .Py
  
  Thanks Jennifer and
colleagues for your patience and solutions

  
-- 
Jennifer Hillman-Jackson
http://galaxyproject.org
  

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Re: [galaxy-user] fastqc and blast? trinity?

2013-12-14 Thread Peter Cock
On Sat, Dec 14, 2013 at 8:52 AM, Jorge Braun  wrote:
>
> Hello, of course, Jennifer is right for the first question . For
> the second question about  blast ... I wonder if running after
> blast in galaxy I can remove sequences that can contaminate
> the data. It's possible?
>

The BLAST suite is not available on the public Galaxy
server at http://usegalaxy.org but is available from the
Galaxy Tool Shed if you have a local Galaxy instance:

http://toolshed.g2.bx.psu.edu/view/devteam/ncbi_blast_plus/

One way to filter your FASTA file based on BLAST hits
would be to use the tabular output from BLAST with
this sequence filtering tool:

http://toolshed.g2.bx.psu.edu/view/peterjc/seq_filter_by_id

e.g. If you want to remove transcripts which seem
to be mitochondria, you could BLAST against a
mitochondrial database, and take only the sequence
with no hits.

Regards,

Peter
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[galaxy-user] fastqc and blast? trinity?

2013-12-14 Thread Jorge Braun
Hello, of course, Jennifer is right for the first question 😊 . For the second 
question about  blast ... I wonder if running after blast in galaxy I can 
remove sequences that can contaminate the data. It's possible?

Last question, trinity is 100% operational in galaxy? Because trinity ran but 
the result was empty, and I think the script failure .Py

Thanks Jennifer and colleagues for your patience and solutions

Date: Fri, 13 Dec 2013 08:53:31 -0800
From: j...@bx.psu.edu
To: braun_...@hotmail.com; galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] fastqc and blast?


  

  
  
Hello,



For the first question, make sure that you are running the groomer
with the correction options. In almost all cases for Illumina data
this will mean leaving all but one setting at default. The setting
to change is "Input FASTQ quality scores type:". The results of
FastQC will inform you about how to set this. An example is in this
wiki section's screencast plus the first bullet point:

https://wiki.galaxyproject.org/Support#Dataset_special_cases

http://vimeo.com/galaxyproject/fastqprep



For the second, I am not sure what you mean by 'different'. Do you
mean the data may have contamination from another species? Or that
the the data content may be different with respect to quality? 



In short, to filter based on quality as reported in the FastQC
report, try tools in the same tool group such as "FASTQ Trimmer" or
"FASTQ Quality Trimmer". 



The protocols included in our RNA-seq pipeline help start out with
some quality steps:

https://wiki.galaxyproject.org/Support#Tools_on_the_Main_server:_RNA-seq



And many from our community have contributed RNA-seq tutorials:

https://wiki.galaxyproject.org/Learn#Other_Tutorials



Hopefully this helps!



Jen

Galaxy team




On 12/13/13 7:05 AM, Jorge Braun wrote:



  
  Hello
  mates,

  

  I have two doubts
  galaxy:

  

  a) I have rna-seq data
from Illumina and do fastqc ... the results are good but
when I fastgroomer to Sanger format and then fastqc
  ... the results
are bad. Does anyone
know the cause? I do not understand
why.

  

  b) With
  the same sequences can
  know if they are different
  Rna and eliminate
  those that do not want
to examine?

  

  merry christmas :)
  
  

  
  

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-- 
Jennifer Hillman-Jackson
http://galaxyproject.org  ___
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