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<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Recent changes to support-requests</title><link>https://sourceforge.net/p/prinseq/support-requests/</link><description>Recent changes to support-requests</description><atom:link href="https://sourceforge.net/p/prinseq/support-requests/feed.rss" rel="self"/><language>en</language><lastBuildDate>Fri, 20 Jan 2012 20:08:49 -0000</lastBuildDate><atom:link href="https://sourceforge.net/p/prinseq/support-requests/feed.rss" rel="self" type="application/rss+xml"/><item><title>Turn off duplicate removal</title><link>https://sourceforge.net/p/prinseq/support-requests/4/</link><description>&lt;div class="markdown_content"&gt;&lt;p&gt;I am working with illumina metatranscriptomic fastq files at around 8 GB. The vast majority of my exact duplicates are ribosomal sequences that I would like to keep in my quality filtered dataset with prinseq. Is there a way to turn off the duplicate removal in the standalone version?&lt;/p&gt;&lt;/div&gt;</description><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anonymous</dc:creator><pubDate>Fri, 20 Jan 2012 20:08:49 -0000</pubDate><guid>https://sourceforge.net8a193c1e95d578da4f7d5621e087d442baa5b7bf</guid></item><item><title>processing after analysis on webversion</title><link>https://sourceforge.net/p/prinseq/support-requests/3/</link><description>&lt;div class="markdown_content"&gt;&lt;p&gt;I really really like your site. I've a rather silly question though. After uploading a fasta file I get all the stats but I don't understand how to run the file with the filter and trim options. So I'd like to analyze a fasta file and then do some seperate sessions of trimming.&lt;br /&gt;
best regards and thanks foor your support!&lt;/p&gt;&lt;/div&gt;</description><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anonymous</dc:creator><pubDate>Tue, 18 Oct 2011 07:06:10 -0000</pubDate><guid>https://sourceforge.net39a018969bc43890a78b83670cf5aae653837c52</guid></item><item><title>problems with large files</title><link>https://sourceforge.net/p/prinseq/support-requests/1/</link><description>&lt;div class="markdown_content"&gt;&lt;p&gt;We are using prinseq-lite to filter fastq files with the parameters -derep 1. The function works fine with files less that 3 GB, but I have problems when filtering largest files (I think that the computer is probably out of memory). I have a computer with a i7 intel processor and 16 GB RAM. The host OS is Windows 7 and I run prinseq on a Virtual Machine (VMware) loaded with Centos 5. I have assigned 8 GB RAM to the Virtual Machine. Could it be a problem of memory?&lt;br /&gt;
Thank you very much in advance&lt;/p&gt;&lt;/div&gt;</description><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Javier Alonso</dc:creator><pubDate>Thu, 13 Oct 2011 13:21:48 -0000</pubDate><guid>https://sourceforge.netcf8a0cc806ebd44c567f94e6076f66a5e0897153</guid></item></channel></rss>