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	<title><![CDATA[BOL: Anjana's bookmarks]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/owner/anjana?</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29410/entrez-direct-e-utilities-on-the-unix-command-line</guid>
	<pubDate>Wed, 19 Oct 2016 08:06:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29410/entrez-direct-e-utilities-on-the-unix-command-line</link>
	<title><![CDATA[Entrez Direct: E-utilities on the UNIX Command Line]]></title>
	<description><![CDATA[<p>Entrez Direct (EDirect) is an advanced method for accessing the NCBI's suite of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. Functions take search terms from command-line arguments. Individual operations are combined to build multi-step queries. Record retrieval and formatting normally complete the process.</p>
<p>EDirect also provides an argument-driven function that simplifies the extraction of data from document summaries or other results that are returned in structured XML format. This can eliminate the need for writing custom software to answer ad hoc questions. Queries can move seamlessly between EDirect commands and UNIX utilities or scripts to perform actions that cannot be accomplished entirely within Entrez.</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/books/NBK179288/" rel="nofollow">https://www.ncbi.nlm.nih.gov/books/NBK179288/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29276/murasaki</guid>
	<pubDate>Fri, 30 Sep 2016 10:22:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29276/murasaki</link>
	<title><![CDATA[Murasaki]]></title>
	<description><![CDATA[<p>Murasaki is an anchor alignment program that is</p>
<ul style="margin-left: 16px;">
<li>exteremely fast (17 CPU hours for whole Human x Mouse genome (with 40 nodes: 35 wall minutes), or 8 mammals in 21 CPU hours (42 wall minutes))</li>
<li>scalable (Arbitrarily parallelizable across multiple nodes using MPI)</li>
<li>memory efficient. (Even a single node with 16GB of ram can handle over 1Gbp of sequence)</li>
<li>unlimited by pattern length or selection</li>
<li>repeat tolerant</li>
</ul>
<p><img src="http://murasaki.dna.bio.keio.ac.jp/9mammals-small.png" width="500" height="375" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="http://murasaki.dna.bio.keio.ac.jp/wiki/index.php?Murasaki" rel="nofollow">http://murasaki.dna.bio.keio.ac.jp/wiki/index.php?Murasaki</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29274/strudel</guid>
	<pubDate>Fri, 30 Sep 2016 09:47:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29274/strudel</link>
	<title><![CDATA[Strudel]]></title>
	<description><![CDATA[<p>Strudel is our graphical tool for visualizing genetic and physical maps of genomes for comparative purposes. The application aims to let the user examine their data at a variety of different levels of resolution, from entire maps to individual markers, and explore syntenic relationships between genomes. All browsing and interaction with Strudel happens in real-time &ndash; there is no need to wait while the maps are generated. It is built using Java 1.6 and ships with its own JRE, so there is no need for users to install or update Java.</p><p>Address of the bookmark: <a href="https://ics.hutton.ac.uk/strudel/" rel="nofollow">https://ics.hutton.ac.uk/strudel/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29272/decipher</guid>
	<pubDate>Fri, 30 Sep 2016 09:33:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29272/decipher</link>
	<title><![CDATA[DECIPHER]]></title>
	<description><![CDATA[<p>DECIPHER is a software toolset that can be used to maintain, analyze, and decipher large amounts of DNA sequence data. To install DECIPHER, see the <a href="http://DECIPHER.cee.wisc.edu/Download.html">Downloads</a> page.<br><br> To begin using DECIPHER read the "Getting Started DECIPHERing" tutorial. Refer to the PDF documents below for instructions on how to use DECIPHER for various tasks.</p><p>Address of the bookmark: <a href="http://decipher.cee.wisc.edu/Documentation.html" rel="nofollow">http://decipher.cee.wisc.edu/Documentation.html</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29270/blast-ring-image-generator-brig</guid>
	<pubDate>Fri, 30 Sep 2016 09:18:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29270/blast-ring-image-generator-brig</link>
	<title><![CDATA[BLAST Ring Image Generator (BRIG)]]></title>
	<description><![CDATA[<p>BRIG is a free cross-platform (Windows/Mac/Unix) application that can display circular comparisons between a large number of genomes, with a focus on handling genome assembly data. The application is available at: <a href="http://sourceforge.net/projects/brig">http://sourceforge.net/projects/brig</a></p>
<p>If you have any questions or comments, post them on <a href="http://sourceforge.net/tracker/?group_id=328245">one of the trackers</a> on BRIG&rsquo;s SourceForge page: <a href="http://sourceforge.net/tracker/?group_id=328245">http://sourceforge.net/tracker/?group_id=328245</a>.</p>
<p>Features:</p>
<ul>
<li>Images show similarity between a central reference sequence and other sequences as concentric rings.</li>
<li>BRIG will perform all BLAST comparisons and file parsing automatically via a simple GUI.</li>
<li>Contig boundaries and read coverage can be displayed for draft genomes; customized graphs and annotations can be displayed.</li>
<li>Using a user-defined set of genes as input, BRIG can display gene presence, absence, truncation or sequence variation in a set of complete genomes, draft genomes or even raw, unassembled sequence data.</li>
<li>BRIG also accepts SAM-formatted read-mapping files enabling genomic regions present in unassembled sequence data from multiple samples to be compared simultaneously</li>
</ul><p>Address of the bookmark: <a href="http://brig.sourceforge.net/" rel="nofollow">http://brig.sourceforge.net/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27691/histonedb-20-%E2%80%93-with-variants</guid>
	<pubDate>Fri, 03 Jun 2016 05:06:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27691/histonedb-20-%E2%80%93-with-variants</link>
	<title><![CDATA[HistoneDB 2.0 – with variants]]></title>
	<description><![CDATA[<p><span>This histone database can be used to explore the diversity of histone proteins and their sequence variants in many organisms. The resource was established to better understand how sequence variation may affect functional and structural features of nucleosomes. To get started, select a histone type to explore its variants.</span></p>
<p><span>More at&nbsp;http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/</span></p><p>Address of the bookmark: <a href="http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/" rel="nofollow">http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27479/biogps</guid>
	<pubDate>Mon, 23 May 2016 03:15:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27479/biogps</link>
	<title><![CDATA[BioGPS]]></title>
	<description><![CDATA[<p>A free&nbsp;<em>extensible</em>&nbsp;and&nbsp;<em>customizable</em>&nbsp;<strong>gene annotation portal</strong>, a complete resource for learning about&nbsp;<strong>gene and protein function</strong>.</p>
<p>http://biogps.org/#goto=welcome</p><p>Address of the bookmark: <a href="http://biogps.org/#goto=welcome" rel="nofollow">http://biogps.org/#goto=welcome</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27477/cytoscape</guid>
	<pubDate>Mon, 23 May 2016 02:32:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27477/cytoscape</link>
	<title><![CDATA[Cytoscape]]></title>
	<description><![CDATA[<p>Cytoscape is an <a href="http://www.cytoscape.org/download.php">open source</a> software platform for visualizing complex networks and integrating these with any type of attribute data. A lot of <a href="http://apps.cytoscape.org/"><em>Apps</em></a> are available for various kinds of problem domains, including bioinformatics, social network analysis, and semantic web.</p><p>Address of the bookmark: <a href="http://www.cytoscape.org/" rel="nofollow">http://www.cytoscape.org/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</guid>
	<pubDate>Mon, 23 May 2016 02:27:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</link>
	<title><![CDATA[PolyPhen-2: Prediction of functional effects of human nsSNPs]]></title>
	<description><![CDATA[<p><strong>PolyPhen-2</strong> (<strong>Poly</strong>morphism <strong>Phen</strong>otyping v<strong>2</strong>) is a tool which predicts possible impact of an amino acid substitution on the structure and function of a human protein using straightforward physical and comparative considerations.</p><p>Address of the bookmark: <a href="http://genetics.bwh.harvard.edu/pph2/" rel="nofollow">http://genetics.bwh.harvard.edu/pph2/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27261/segemehl</guid>
	<pubDate>Tue, 10 May 2016 08:10:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27261/segemehl</link>
	<title><![CDATA[segemehl]]></title>
	<description><![CDATA[<p><span>segemehl is a software to map short sequencer reads to reference genomes. Unlike other methods, segemehl is able to detect not only mismatches but also insertions and deletions. Furthermore, segemehl is not limited to a specific read length and is able to map&nbsp;primer- or polyadenylation contaminated reads correctly.&nbsp; segemehl implements a matching strategy based on enhanced suffix arrays (ESA).&nbsp;</span></p>
<p><span>More at&nbsp;http://www.bioinf.uni-leipzig.de/Software/segemehl/</span></p>
<p><span>Manual&nbsp;http://www.bioinf.uni-leipzig.de/Software/segemehl/segemehl_manual_0_1_7.pdf</span></p><p>Address of the bookmark: <a href="http://hoffmann.bioinf.uni-leipzig.de/LIFE/segemehl.html" rel="nofollow">http://hoffmann.bioinf.uni-leipzig.de/LIFE/segemehl.html</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
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