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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/26322?offset=230</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30015/scripts</guid>
	<pubDate>Wed, 30 Nov 2016 10:35:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30015/scripts</link>
	<title><![CDATA[Scripts]]></title>
	<description><![CDATA[<p>Useful script for NGS analysis.</p><p>Address of the bookmark: <a href="http://augustus.gobics.de/binaries/scripts/" rel="nofollow">http://augustus.gobics.de/binaries/scripts/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30203/e-rga-enhanced-reference-guided-assembly-of-complex-genomes</guid>
	<pubDate>Mon, 19 Dec 2016 05:56:14 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30203/e-rga-enhanced-reference-guided-assembly-of-complex-genomes</link>
	<title><![CDATA[e-RGA: enhanced Reference Guided Assembly of Complex Genomes]]></title>
	<description><![CDATA[<p><span>Next Generation Sequencing has totally changed genomics: we are able to produce huge amounts of data at an incredibly low cost compared to Sanger sequencing. Despite this, some old problems have become even more difficult, de novo assembly being on top of this list. Despite efforts to design tools able to assemble, de novo, an organism sequenced with short reads, the results are still far from those achievable with long reads. In this paper, we propose a novel method that aims to improve de novo assembly in the presence of a closely related reference. The idea is to combine de novo and reference-guided assembly in order to obtain enhanced results.</span></p><p>Address of the bookmark: <a href="http://journal.embnet.org/index.php/embnetjournal/article/view/208" rel="nofollow">http://journal.embnet.org/index.php/embnetjournal/article/view/208</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30111/eager</guid>
	<pubDate>Sat, 10 Dec 2016 18:07:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30111/eager</link>
	<title><![CDATA[EAGER]]></title>
	<description><![CDATA[<p><span>The automated reconstruction of genome sequences in ancient genome analysis is a multifaceted process.</span></p>
<p><span>EAGER encompasses both state-of-the-art tools for each step as well as new complementary tools tailored for ancient DNA data within a single integrated solution in an easily accessible format.</span></p>
<p>https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-0918-z</p><p>Address of the bookmark: <a href="https://github.com/apeltzer/EAGER-GUI" rel="nofollow">https://github.com/apeltzer/EAGER-GUI</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</guid>
	<pubDate>Thu, 22 Dec 2016 03:53:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</link>
	<title><![CDATA[MCscan]]></title>
	<description><![CDATA[<p><span>MCscan is a computer program that can simultaneously scan multiple genomes to identify homologous chromosomal regions and subsequently align these regions using genes as anchors. This is the toolset for generating the synteny correspondences in&nbsp;</span><a href="http://chibba.agtec.uga.edu/duplication">Plant Genome Duplication Database</a><span>. It is intended as an easy-to-use and quick way to identify conserved gene arrays both within the same genome and across different genomes.</span></p>
<p><span>More at&nbsp;http://chibba.agtec.uga.edu/duplication/mcscan/</span></p><p>Address of the bookmark: <a href="http://chibba.agtec.uga.edu/duplication/mcscan/" rel="nofollow">http://chibba.agtec.uga.edu/duplication/mcscan/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30538/gkno</guid>
	<pubDate>Tue, 17 Jan 2017 03:35:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30538/gkno</link>
	<title><![CDATA[GKNO]]></title>
	<description><![CDATA[<p><span>gkno opens the world of complex bioinformatic analysis to people of all level of computational expertise. This site contains documentation, tutorials and information on all the tools that comprise gkno.</span></p>
<p><span>More at&nbsp;http://gkno.me/</span></p><p>Address of the bookmark: <a href="http://gkno.me/" rel="nofollow">http://gkno.me/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30557/speedseq</guid>
	<pubDate>Fri, 20 Jan 2017 06:05:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30557/speedseq</link>
	<title><![CDATA[SpeedSeq]]></title>
	<description><![CDATA[<p>A flexible framework for rapid genome analysis and interpretation</p>
<p>C Chiang, R M Layer, G G Faust, M R Lindberg, D B Rose, E P Garrison, G T Marth, A R Quinlan, and I M Hall. SpeedSeq: ultra-fast personal genome analysis and interpretation. Nat Meth (2015). doi:10.1038/nmeth.3505.</p>
<p><a href="http://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.3505.html">http://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.3505.html</a></p><p>Address of the bookmark: <a href="https://github.com/hall-lab/speedseq" rel="nofollow">https://github.com/hall-lab/speedseq</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</guid>
	<pubDate>Fri, 24 Feb 2017 08:56:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</link>
	<title><![CDATA[VAGUE:Velvet Assembler Graphical Front End]]></title>
	<description><![CDATA[<p>VAGUE is a vague acronym for "Velvet Assembler Graphical Front End", which means it is a GUI for the Velvet <em>de novo</em> assembler. The command line version of Velvet can be complicated for beginners to use, but VAGUE makes it clear and simple</p>
<p>More at&nbsp;http://www.vicbioinformatics.com/software.vague.shtml</p><p>Address of the bookmark: <a href="http://www.vicbioinformatics.com/software.vague.shtml" rel="nofollow">http://www.vicbioinformatics.com/software.vague.shtml</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31105/understanding-pacbio</guid>
	<pubDate>Fri, 24 Feb 2017 10:17:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31105/understanding-pacbio</link>
	<title><![CDATA[Understanding PacBio]]></title>
	<description><![CDATA[<p>This tutorial includes resources for learning more about PacBio data and bioinformatics analysis, and includes content suitable for both beginners and experts. Below are links to training modules (webinars and PowerPoint presentations) to help you get started with your data processing, as well as information for specialized applications.</p>
<p>Training Resources:</p>
<ul>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Bioinformatics-Workshop">Bioinformatics Workshop (Webinars)</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Bioinformatics-Training-Slides">Bioinformatics Training Slides</a></li>
</ul>
<p>Specialized Applications:</p>
<ul>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/De-Novo-Assembly">De Novo Assembly</a></li>
<li><a href="https://github.com/PacificBiosciences/cDNA_primer/wiki">Transcriptome analysis</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Base-modification-analysis">Base Modification Analysis</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Barcoding">Barcoding</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Data-Analysis-Tools">Data Analysis Tools</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Minor-Variants-and-Phasing-Analysis">Minor Variants and Phasing Analysis</a></li>
</ul><p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki" rel="nofollow">https://github.com/PacificBiosciences/Bioinformatics-Training/wiki</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</guid>
	<pubDate>Mon, 06 Mar 2017 03:44:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</link>
	<title><![CDATA[MetaBAT:  An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities]]></title>
	<description><![CDATA[<p>MetaBAT, An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities</p>
<p>Grouping large genomic fragments assembled from shotgun metagenomic sequences to deconvolute complex microbial communities, or metagenome binning, enables the study of individual organisms and their interactions. Here we developed an automated metagenome binning software, called MetaBAT, which integrates empirical probabilistic distances of genome abundance and tetranucleotide frequency. Tested on both synthetic and real metagenome datasets, MetaBAT outperforms alternative methods in both accuracy and computational efficiency. Applying MetaBAT to an assembly from 1,704 human gut samples formed 1,634 genome bins (&gt;200kb) in 3 hours, where 621 genome bins are &gt;50% complete with &lt;5% contamination from other species. Further analysis shows that the quality of these genome bins approaches manually curated genomes.</p><p>Address of the bookmark: <a href="https://bitbucket.org/berkeleylab/metabat" rel="nofollow">https://bitbucket.org/berkeleylab/metabat</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30973/abacas</guid>
	<pubDate>Thu, 16 Feb 2017 12:15:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30973/abacas</link>
	<title><![CDATA[ABACAS]]></title>
	<description><![CDATA[<p><span>ABACAS is intended to rapidly contiguate (align, order, orientate) , visualize and design primers to close gaps on shotgun assembled contigs based on a reference sequence. It uses MUMmer to find alignment positions and identify syntenies of assembly contigs against the reference. The output is then processed to generate a pseudomolecule taking overlaping contigs and gaps in to account. MUMmer's alignment generating programs, Nucmer and Promer are used followed by the 'delta-filter' utility function. Users could also run tblastx on contigs that are not used to generate the pseudomolecule.&nbsp;</span></p><p>Address of the bookmark: <a href="http://abacas.sourceforge.net/Manual.html#9._Colour_code" rel="nofollow">http://abacas.sourceforge.net/Manual.html#9._Colour_code</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
</item>

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