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	<title><![CDATA[BOL: Related items]]></title>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/19560/alien-genome</guid>
	<pubDate>Sat, 13 Dec 2014 00:24:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/19560/alien-genome</link>
	<title><![CDATA[Alien Genome !!!]]></title>
	<description><![CDATA[<p>Genome sequencing, analysis and expression of Alien genome.</p><p>Note: This image/cartoon is create only for fun. It has nothing to do with any scientific findings.</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/19560" length="40389" type="image/jpeg" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27839/lorma-a-tool-for-correcting-sequencing-errors-in-long-reads-such-those-produced-by-pacific-biosciences-sequencing-machines</guid>
	<pubDate>Wed, 15 Jun 2016 17:18:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27839/lorma-a-tool-for-correcting-sequencing-errors-in-long-reads-such-those-produced-by-pacific-biosciences-sequencing-machines</link>
	<title><![CDATA[LoRMA: a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines]]></title>
	<description><![CDATA[<p>LoRMA is a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines.</p>
<p>Publication:</p>
<ul>
<li>L. Salmela, R. Walve, E. Rivals, and E. Ukkonen: Accurate selfcorrection of errors in long reads using de Bruijn graphs. Accepted to RECOMB-Seq 2016.</li>
</ul>
<p>Download:</p>
<ul>
<li><a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/LoRMA-0.3.tar.gz">LoRMA 0.3 source files</a></li>
<li><a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/README.txt">README</a></li>
</ul><p>Address of the bookmark: <a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/" rel="nofollow">https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32946/grass-a-generic-algorithm-for-scaffolding-next-generation-sequencing-assemblies</guid>
	<pubDate>Tue, 23 May 2017 05:20:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32946/grass-a-generic-algorithm-for-scaffolding-next-generation-sequencing-assemblies</link>
	<title><![CDATA[GRASS: a generic algorithm for scaffolding next-generation sequencing assemblies.]]></title>
	<description><![CDATA[<p><span>GRASS (GeneRic ASsembly Scaffolder)-a novel algorithm for scaffolding second-generation sequencing assemblies capable of using diverse information sources. GRASS offers a mixed-integer programming formulation of the contig scaffolding problem, which combines contig order, distance and orientation in a single optimization objective. The resulting optimization problem is solved using an expectation-maximization procedure and an unconstrained binary quadratic programming approximation of the original problem. We compared GRASS with existing HTS scaffolders using Illumina paired reads of three bacterial genomes. Our algorithm constructs a comparable number of scaffolds, but makes fewer errors. This result is further improved when additional data, in the form of related genome sequences, are used.</span></p><p>Address of the bookmark: <a href="https://github.com/AlexeyG/GRASS" rel="nofollow">https://github.com/AlexeyG/GRASS</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35055/jabba-hybrid-error-correction-for-long-sequencing-reads</guid>
	<pubDate>Fri, 05 Jan 2018 03:58:14 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35055/jabba-hybrid-error-correction-for-long-sequencing-reads</link>
	<title><![CDATA[Jabba: Hybrid Error Correction for Long Sequencing Reads]]></title>
	<description><![CDATA[<p>Jabba is a hybrid error correction tool to correct third generation (PacBio / ONT) sequencing data, using second generation (Illumina) data.</p>
<p>Input</p>
<p>Jabba takes as input a concatenated de Bruijn graph and a set of sequences:</p>
<p>the de Bruijn graph should appear in fasta format with 1 entry per node, the meta information should be in the format:<br>&gt;NODE <br>the set of sequences should be in fasta or fastq format. These sequences will be corrected (e.g. PacBio reads). The corrections will be written to a file Jabba fasta.<br>The output is a file in fasta format with corrections of the long reads, and additionally a file in the input format containing uncorrected reads.</p>
<p>https://github.com/biointec/jabba/wiki</p>
<p>https://almob.biomedcentral.com/articles/10.1186/s13015-016-0075-7</p><p>Address of the bookmark: <a href="https://github.com/biointec/jabba" rel="nofollow">https://github.com/biointec/jabba</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43892/choosing-the-right-ngs-sequencing-instrument-for-your-study</guid>
	<pubDate>Wed, 15 Jun 2022 00:37:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43892/choosing-the-right-ngs-sequencing-instrument-for-your-study</link>
	<title><![CDATA[Choosing the Right NGS Sequencing Instrument for Your Study]]></title>
	<description><![CDATA[<p>The right sequencing instrument for your study depends on your project goal. Setting aside turnaround time and price, it essentially comes down to the numbers of reads and read length you need for your experiment. Below, we've described and compared metrics for each of the instruments available. If you&rsquo;re new to high-throughput sequencing and have questions about how you should design your sequencing run, fill out our&nbsp;<a href="https://genohub.com/ngs-consultation/"><span>free consultation form</span></a>&nbsp;and we'll get in touch with you to help.</p>
<p>More at&nbsp;https://genohub.com/ngs-instrument-guide/</p><p>Address of the bookmark: <a href="https://genohub.com/ngs-instrument-guide/" rel="nofollow">https://genohub.com/ngs-instrument-guide/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/1956/structure-of-binary-files-used-for-storing-sequencing-data-bam-and-sff</guid>
	<pubDate>Sun, 11 Aug 2013 14:29:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/1956/structure-of-binary-files-used-for-storing-sequencing-data-bam-and-sff</link>
	<title><![CDATA[Structure of Binary files used for storing sequencing data-bam and sff]]></title>
	<description><![CDATA[<p>Many times bioinformatician needs to parse binary files like bam and sff. Advantage of binary files is that they occupy less space in memory with maximum information content.</p><p>Link for those who looking for structure of Bam and sff file:</p><p>Bam:</p><p><a href="http://samtools.sourceforge.net/SAMv1.pdf">http://samtools.sourceforge.net/SAMv1.pdf</a>&nbsp;(from page 12)</p><p>sff file (for Ion torrent and 454 files):</p><p><a href="http://www.ncbi.nlm.nih.gov/Traces/trace.cgi?cmd=show&amp;f=formats&amp;m=doc&amp;s=format#sff">http://www.ncbi.nlm.nih.gov/Traces/trace.cgi?cmd=show&amp;f=formats&amp;m=doc&amp;s=format#sff</a></p><p>Binary file Editor and Viewer:</p><p><a href="http://mh-nexus.de/en/hxd/">http://mh-nexus.de/en/hxd/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/3889/bioinformatics-and-sequencing-courses-and-workshops</guid>
	<pubDate>Sat, 24 Aug 2013 16:41:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/3889/bioinformatics-and-sequencing-courses-and-workshops</link>
	<title><![CDATA[Bioinformatics and Sequencing Courses and Workshops]]></title>
	<description><![CDATA[<p>Swiss Institute of Bioinformatics (SIB) organises lots of bioinformatics courses covering wide range of topics:</p><p><a href="http://www.isb-sib.ch/education/training-courses.html">http://www.isb-sib.ch/education/training-courses.html</a></p><p>Canadian bioinformatics also organises various bioinformatics and sequencing courses:</p><p><a href="http://bioinformatics.ca/workshops">http://bioinformatics.ca/workshops</a></p><p>In addition to above two, EMBI&nbsp;Europe, EMBO Europe, Cold Spring Harbour USA, Wellcome Trust UK and NOVA&nbsp;Europe&nbsp;also organise bioinformatics and sequencing courses annually:</p><p><a href="http://www.embl.de/training/events/index.php?p_outstation=ALL">http://www.embl.de/training/events/index.php?p_outstation=ALL</a></p><p><a href="http://www.embo.org/funding-awards/courses-workshops">http://www.embo.org/funding-awards/courses-workshops</a></p><p><a href="http://meetings.cshl.edu/courses.html">http://meetings.cshl.edu/courses.html</a></p><p><a href="http://www.wellcome.ac.uk/Education-resources/Courses-and-conferences/Advanced-Courses-and-Scientific-Conferences/Advanced-Courses/index.htm">http://www.wellcome.ac.uk/Education-resources/Courses-and-conferences/Advanced-Courses-and-Scientific-Conferences/Advanced-Courses/index.htm</a></p><p><a href="http://www.nova-university.org/pagetop.cfm?MenySidorTop_id=2&amp;open=7">http://www.nova-university.org/pagetop.cfm?MenySidorTop_id=2&amp;open=7</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/3030/illuminating-next-generation-sequencing-data-with-go</guid>
	<pubDate>Fri, 23 Aug 2013 07:13:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/3030/illuminating-next-generation-sequencing-data-with-go</link>
	<title><![CDATA[Illuminating next generation sequencing data with Go]]></title>
	<description><![CDATA[<p>Another good lecture for Illumina sequencing data analysis from&nbsp;</p>
<p>Dan Kortschak,&nbsp;Bioinformatics Group,&nbsp;School of Molecular and Biomedical Science ,The University of Adelaide</p><p>Address of the bookmark: <a href="http://talks.biogo.googlecode.com/git/illumination/illumination.pdf" rel="nofollow">http://talks.biogo.googlecode.com/git/illumination/illumination.pdf</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4591/the-breitbart-lab</guid>
  <pubDate>Tue, 17 Sep 2013 18:19:49 -0500</pubDate>
  <link></link>
  <title><![CDATA[The Breitbart lab]]></title>
  <description><![CDATA[
<p>Breitbart’s lab has created a new branch of biology called metagenomics in which one can sample and sequence genetic material collected from the environment.</p>

<p>Breitbart lab is located in the College of Marine Science at the University of South Florida. She is chosen as top "10 Brilliant" scientist by Popular Science magazine.<br />http://www.popsci.com/science/article/2013-09/mya-breitbart</p>

<p>Lab Link:<br />https://sites.google.com/site/breitbartgenomicslab/<br />http://www.marine.usf.edu/faculty/mya-breitbart.shtml</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/5402/key-bioinformatics-scientists</guid>
	<pubDate>Wed, 09 Oct 2013 13:37:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/5402/key-bioinformatics-scientists</link>
	<title><![CDATA[Key Bioinformatics Scientists]]></title>
	<description><![CDATA[<p>Address of the bookmark: <a href="http://www.iscb.org/iscb-leadership-a-staff-/officers-and-board-directors" rel="nofollow">http://www.iscb.org/iscb-leadership-a-staff-/officers-and-board-directors</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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