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Thread | Thread Starter | Forum | Replies | Last Post |
Free & Open Environment for RNA-seq analysis: Galaxy (http://usegalaxy.org) | jgoecks | RNA Sequencing | 27 | 11-07-2016 12:02 AM |
NAR: PileLineGUI a desktop environment for handling NGS genome position files. | gonvader | Literature Watch | 0 | 06-09-2011 02:59 AM |
Free Partek RNA-Seq & ChIP-Seq Data Analysis Workshops | mgabrielli@partek.com | Events / Conferences | 0 | 04-05-2011 07:28 AM |
Free Avadis NGS webinar on 23 February 2011 | Strand SI | Events / Conferences | 4 | 03-15-2011 01:54 AM |
ChIP-Seq: The Poisson Margin Test for Normalization-Free Significance Analysis of NGS | Newsbot! | Literature Watch | 0 | 03-10-2011 02:00 AM |
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#21 | |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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- gzip them - put them to a web-accessible loocation - paste a URL pointing to your files to upload tool as shown in the attached image Aspera is incredibly expensive to license, and we're not convinced it really accelerates things that much. There are some open source alternative we will be taking a look at Yes, blasting against custom db is on the to do list as numerous people want this to happen. |
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#22 |
Junior Member
Location: boston, usa Join Date: Aug 2008
Posts: 3
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Hi,
Have you looked at open source alternative such as UDT to address the data transfer bottleneck? Also, is there a limit on how much data that I can save in my galaxy account? Thanks! |
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#23 |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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#24 | |
Junior Member
Location: Cardiff Join Date: Dec 2009
Posts: 9
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Ben |
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#25 |
Senior Member
Location: SEA Join Date: Nov 2009
Posts: 203
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I have uploaded a gzipped 300 MB .qual file and it works for doing box plot.
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__________________
http://kevin-gattaca.blogspot.com/ |
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#26 |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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Yes, you can. The best way to get data in is to upload gzipped files via URL (http and ftp both work). See post #21 in the thread (scroll up).
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#27 |
Member
Location: Cardiff Join Date: Mar 2010
Posts: 23
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I'm having a similar problem to Ben, I have illumina fastq files that are gzipped. I can upload them in a few minutes but then when I try to do the groomer i get this error:
An error occurred running this job: Traceback (most recent call last): File "/galaxy/home/g2main/galaxy_main/tools/fastq/fastq_groomer.py", line 37, in <module> if __name__ == "__main__": main() File "/galaxy/home/g2main/galaxy_main/tools/fastq/fastq_groomer.py", line 18, in main Is there some sort of facility to unzip gz files? Thanks, J |
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#28 | ||
Junior Member
Location: Penn State Join Date: Mar 2010
Posts: 4
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Galaxy does not yet accept .tar(.gz) nor .zip files. Each file needs to be gzip'd individually (without tar'ing) in order for it it work with the upload tool at this time. Support for .tar(.gz) and .zip files is being investigated. Please don't hesitate to let us know if we can be of further help. Thanks for using Galaxy. |
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#29 |
Member
Location: Houston Join Date: Jan 2010
Posts: 13
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Is there any way that Galaxy can be used to analyze data from a Helicos machine?
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#30 |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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#31 |
Member
Location: Houston Join Date: Jan 2010
Posts: 13
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Not yet, but I am about to subject some samples to Helicos sequencing.
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#32 | |
Senior Member
Location: Southern France Join Date: Aug 2009
Posts: 269
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#33 |
Member
Location: Melbourne, Australia Join Date: Jan 2009
Posts: 37
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Problem with Helicos is that it doesn't come as FASTQ (quality scores are assigned to reads, not nucleotides within the reads). The best (only?) way to handle this is to convert the original format to FASTA after filtering at a given quality cutoff and take it from there. There are also tools to create 'fake' FASTQ files by setting the quality score to a uniform value if a tool absolutely requires FASTQ.
You almost need to use their filtering workflow anyway as it gets rid of a number of artifacts which are otherwise difficult to remove. |
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#34 | |
Junior Member
Location: Chicago Join Date: Apr 2010
Posts: 1
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UDT (udt.sf.net) should work. It is a library with C++/JNI/.net API and only has a simple command line tool. You can also look at HSCP (http://sourceforge.net/projects/hscp/), which is a SCP-like tool but uses UDT for data transfer. Both UDT and HSCP are open source and free to use.
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#35 | |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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#36 |
Nils Homer
Location: Boston, MA, USA Join Date: Nov 2008
Posts: 1,285
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I have been playing with Galaxy on my local machine for the past few days. It is great piece of software, and was relatively easy to plug in new tools. Thank-you again.
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#37 |
Member
Location: Penn State Join Date: Apr 2009
Posts: 22
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Nils:
Thanks for sending us your wrappers. They will be on public site shortly! |
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#38 |
Junior Member
Location: usa Join Date: Jan 2022
Posts: 2
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If there is anything the site or community can do to support this effort, don't hesitate
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#39 |
Junior Member
Location: usa Join Date: Jan 2022
Posts: 2
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I think it is important to include bfast as perm/bowtie do not do gapped alignment.
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