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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/11181?offset=650</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29305/miro-mirna-omics</guid>
	<pubDate>Tue, 04 Oct 2016 14:50:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29305/miro-mirna-omics</link>
	<title><![CDATA[MIRO : miRNA omics]]></title>
	<description><![CDATA[<p><span>The MIRO (the miRNA omics) pipeline is a flexible and powerful tool for the analysis of miRNA (or more generall short RNA) expression using short-read deep sequencing data. In its present implementation MIRO is especially adapted for the analysis of reads generated with the Illumina sequencing platform. MIRO allows to preprocess the Solexa-reads, map them flexibly to several reference genomes using one of four different mappers, create differential gene (miRNA) expression profiles and cluster reads using one of several algorithm. MIRO output is furthermore compatible with software such as genome browsers and miRDeep.</span></p><p>Address of the bookmark: <a href="http://seq.crg.es/download/software/Miro/" rel="nofollow">http://seq.crg.es/download/software/Miro/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/29601/statistics-using-r-with-biological-examples</guid>
	<pubDate>Thu, 03 Nov 2016 04:55:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/29601/statistics-using-r-with-biological-examples</link>
	<title><![CDATA[Statistics Using R   with Biological Examples]]></title>
	<description><![CDATA[<p>This book is a manifestation of my desire to teach researchers in biology a bit more about statistics than an ordinary introductory course covers and to introduce the utilization of R as a tool for analyzing their data. My goal is to reach those with little or no training in higher level statistics so that they can do more of their own data analysis, communicate more with statisticians, and appreciate the great potential statistics has to offer as a tool to answer biological questions. </p><p>This is necessary in light of the increasing use of higher level statistics in biomedical research. I hope it accomplishes this mission and encourage its free distribution and use as a course text or supplement.</p><p>K Seefeld, May 2007</p>]]></description>
	<dc:creator>Neel</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/29601" length="4581031" type="application/pdf" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30012/swalo</guid>
	<pubDate>Wed, 30 Nov 2016 05:06:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30012/swalo</link>
	<title><![CDATA[SWALO]]></title>
	<description><![CDATA[<p>SWALO (scaffolding with assembly likelihood optimization) is a method for scaffolding based on likelihood of genome assemblies computed using generative models for sequencing.</p>
<p><a href="https://atifrahman.github.io/SWALO/swalo-0.9.7-beta.tar.gz"><strong>Download</strong></a></p>
<p><strong>Git repository of SWALO is at <a href="https://github.com/atifrahman/SWALO">https://github.com/atifrahman/SWALO</a>.</strong></p><p>Address of the bookmark: <a href="https://atifrahman.github.io/SWALO/" rel="nofollow">https://atifrahman.github.io/SWALO/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30140/cutadapt</guid>
	<pubDate>Wed, 14 Dec 2016 09:59:52 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30140/cutadapt</link>
	<title><![CDATA[Cutadapt]]></title>
	<description><![CDATA[<p>Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.</p>
<p>Cutadapt helps with these trimming tasks by finding the adapter or primer sequences in an error-tolerant way. It can also modify and filter reads in various ways. Adapter sequences can contain IUPAC wildcard characters. Also, paired-end reads and even colorspace data is supported. If you want, you can also just demultiplex your input data, without removing adapter sequences at all.</p>
<p>Cutadapt comes with an extensive suite of automated tests and is available under the terms of the MIT license.</p>
<p>If you use cutadapt, please cite&nbsp;<a href="http://dx.doi.org/10.14806/ej.17.1.200">DOI:10.14806/ej.17.1.200</a>&nbsp;.</p>
<p>More at&nbsp;https://github.com/marcelm/cutadapt</p><p>Address of the bookmark: <a href="http://cutadapt.readthedocs.io/en/stable/guide.html" rel="nofollow">http://cutadapt.readthedocs.io/en/stable/guide.html</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30102/prism</guid>
	<pubDate>Sat, 10 Dec 2016 15:19:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30102/prism</link>
	<title><![CDATA[PRISM]]></title>
	<description><![CDATA[<p><span>PRISM is a software for split read (reads which span across a structrual variant -- SV ) mapping and SV calling from the mapping result. PRISM is able to detect small insertions and abitrary size deletions, inversions and tandom duplications with the direction of discordant read pairs. PRISM_CTX is a tool for detecting inter-chromosome trans-location events.&nbsp;</span><br><br><span>PRISM and PRISM_CTX were originally designed and written by&nbsp;</span><a href="http://www.cs.toronto.edu/~brudno">Michael Brudno</a><span>&nbsp;and Yue Jiang, The original PRISM publication can be found&nbsp;</span><a href="http://bioinformatics.oxfordjournals.org/content/early/2012/07/31/bioinformatics.bts484.abstract">here</a><span>.&nbsp;</span><br><br><span>The authors may be contacted via e-mail at:&nbsp;</span><em>prism at cs.toronto.edu</em><span>.&nbsp;</span><br><br><span>Additional information is available in the&nbsp;</span><a href="http://compbio.cs.toronto.edu/prism/PRISM_README">PRISM README</a><span>&nbsp;file and&nbsp;</span><a href="http://compbio.cs.toronto.edu/prism/PRISM_CTX_README">PRISM_CTX README</a><span>&nbsp;file.&nbsp;</span></p>
<p>http://compbio.cs.toronto.edu/prism/</p><p>Address of the bookmark: <a href="http://compbio.cs.toronto.edu/prism/" rel="nofollow">http://compbio.cs.toronto.edu/prism/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30153/e-mem-efficient-computation-of-maximal-exact-matches</guid>
	<pubDate>Thu, 15 Dec 2016 09:30:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30153/e-mem-efficient-computation-of-maximal-exact-matches</link>
	<title><![CDATA[E-MEM: Efficient computation of Maximal Exact Matches]]></title>
	<description><![CDATA[<p>E-MEM is a C++/OpenMP program designed to efficiently compute MEMs between large genomes. See the README file for instructions on how to use E-MEM.&nbsp;<br><br>E-MEM source code</p>
<p>The source code can be downloaded&nbsp;<a href="http://www.csd.uwo.ca/~ilie/E-MEM/e-mem.zip">here</a>.&nbsp;<br><br>If you use E-MEM, please cite:</p>
<ul>
<li>N. Khiste, L. Ilie, E-MEM: Efficient computation of Maximal Exact Matches for very large genomes,&nbsp;<a href="http://bioinformatics.oxfordjournals.org/content/31/4/509.short">Bioinformatics</a>&nbsp;<strong>31</strong>(4) (2015) 509 -- 514.</li>
</ul>
<p>For any questions, please contact Lucian Ilie:&nbsp;<a href="mailto:ilie@uwo.ca">ilie@uwo.ca</a>&nbsp;</p><p>Address of the bookmark: <a href="http://www.csd.uwo.ca/~ilie/E-MEM/" rel="nofollow">http://www.csd.uwo.ca/~ilie/E-MEM/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30212/pear</guid>
	<pubDate>Mon, 19 Dec 2016 09:28:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30212/pear</link>
	<title><![CDATA[PEAR]]></title>
	<description><![CDATA[<p><strong>PEAR</strong>&nbsp;is an ultrafast, memory-efficient and highly accurate pair-end read merger. It is fully parallelized and can run with as low as just a few kilobytes of memory.</p>
<p>PEAR evaluates all possible paired-end read overlaps and without requiring the target fragment size as input. In addition, it implements a statistical test for minimizing false-positive results. Together with a highly optimized implementation, it can merge millions of paired end reads within a couple of minutes on a standard desktop computer.</p><p>Address of the bookmark: <a href="http://sco.h-its.org/exelixis/web/software/pear/doc.html" rel="nofollow">http://sco.h-its.org/exelixis/web/software/pear/doc.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30555/yaha</guid>
	<pubDate>Fri, 20 Jan 2017 05:38:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30555/yaha</link>
	<title><![CDATA[YAHA]]></title>
	<description><![CDATA[<p>YAHA, a fast and flexible hash-based aligner. YAHA is as fast and accurate as BWA-SW at finding the single best alignment per query and is dramatically faster and more sensitive than both SSAHA2 and MegaBLAST at finding all possible alignments. Unlike other aligners that report all, or one, alignment per query, or that use simple heuristics to select alignments, YAHA uses a directed acyclic graph to find the optimal set of alignments that cover a query using a biologically relevant breakpoint penalty. YAHA can also report multiple mappings per defined segment of the query. We show that YAHA detects more breakpoints in less time than BWA-SW across all SV classes, and especially excels at complex SVs comprising multiple breakpoints.</p>
<p><strong>Availability:</strong> YAHA is currently supported on 64-bit Linux systems. Binaries and sample data are freely available for download from <a href="http://faculty.virginia.edu/irahall/YAHA" target="pmc_ext">http://faculty.virginia.edu/irahall/YAHA</a>.</p>
<p><strong>Contact:</strong></p>
<p>http://genome.wustl.edu/people/groups/detail/hall-lab/</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463118/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463118/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30696/many-core-engine-mce-for-perl-example</guid>
	<pubDate>Tue, 31 Jan 2017 05:37:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30696/many-core-engine-mce-for-perl-example</link>
	<title><![CDATA[Many-Core Engine (MCE) for Perl example]]></title>
	<description><![CDATA[<p><span>MCE spawns a pool of workers and therefore does not fork a new process per each element of data. Instead, MCE follows a bank queuing model. Imagine the line being the data and bank-tellers the parallel workers. MCE enhances that model by adding the ability to chunk the next n elements from the input stream to the next available worker.</span></p>
<p>CORE MODULES</p>
<p>Three modules make up the core engine for MCE.</p>
<dl><dt id="MCE::Core"><a href="https://metacpan.org/pod/MCE#MCE::Core"><span></span></a><a></a><a href="https://metacpan.org/pod/distribution/MCE/lib/MCE/Core.pod">MCE::Core</a></dt><dd>
<p>Provides the Core API for Many-Core Engine. The various MCE options are described here.</p>
</dd><dt id="MCE::Signal"><a href="https://metacpan.org/pod/MCE#MCE::Signal"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Signal">MCE::Signal</a></dt><dd>
<p>Temporary directory creation, cleanup, and signal handling.</p>
</dd><dt id="MCE::Util"><a href="https://metacpan.org/pod/MCE#MCE::Util"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Util">MCE::Util</a></dt><dd>
<p>Utility functions for Many-Core Engine.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MCE-EXTRAS"><span></span></a><a></a>MCE EXTRAS</p>
<p>There are 4 add-on modules for use with MCE.</p>
<dl><dt id="MCE::Candy"><a href="https://metacpan.org/pod/MCE#MCE::Candy"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Candy">MCE::Candy</a></dt><dd>
<p>Provides a collection of sugar methods and output iterators for preserving output order.</p>
</dd><dt id="MCE::Mutex"><a href="https://metacpan.org/pod/MCE#MCE::Mutex"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Mutex">MCE::Mutex</a></dt><dd>
<p>Provides a simple semaphore implementation supporting threads and processes.</p>
</dd><dt id="MCE::Queue"><a href="https://metacpan.org/pod/MCE#MCE::Queue"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Queue">MCE::Queue</a></dt><dd>
<p>Provides a hybrid queuing implementation for MCE supporting normal queues and priority queues from a single module. MCE::Queue exchanges data via the core engine to enable queuing to work for both children (spawned from fork) and threads.</p>
</dd><dt id="MCE::Relay"><a href="https://metacpan.org/pod/MCE#MCE::Relay"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Relay">MCE::Relay</a></dt><dd>
<p>Enables workers to receive and pass on information orderly with zero involvement by the manager process while running.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MCE-MODELS"><span></span></a><a></a>MCE MODELS</p>
<p>The models take Many-Core Engine to a new level for ease of use. Two options (chunk_size and max_workers) are configured automatically as well as spawning and shutdown.</p>
<dl><dt id="MCE::Loop"><a href="https://metacpan.org/pod/MCE#MCE::Loop"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Loop">MCE::Loop</a></dt><dd>
<p>Provides a parallel loop utilizing MCE for building creative loops.</p>
</dd><dt id="MCE::Flow"><a href="https://metacpan.org/pod/MCE#MCE::Flow"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Flow">MCE::Flow</a></dt><dd>
<p>A parallel flow model for building creative applications. This makes use of user_tasks in MCE. The author has full control when utilizing this model. MCE::Flow is similar to MCE::Loop, but allows for multiple code blocks to run in parallel with a slight change to syntax.</p>
</dd><dt id="MCE::Grep"><a href="https://metacpan.org/pod/MCE#MCE::Grep"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Grep">MCE::Grep</a></dt><dd>
<p>Provides a parallel grep implementation similar to the native grep function.</p>
</dd><dt id="MCE::Map"><a href="https://metacpan.org/pod/MCE#MCE::Map"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Map">MCE::Map</a></dt><dd>
<p>Provides a parallel map model similar to the native map function.</p>
</dd><dt id="MCE::Step"><a href="https://metacpan.org/pod/MCE#MCE::Step"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Step">MCE::Step</a></dt><dd>
<p>Provides a parallel step implementation utilizing MCE::Queue between user tasks. MCE::Step is a spin off from MCE::Flow with a touch of MCE::Stream. This model, introduced in 1.506, allows one to pass data from one sub-task into the next transparently.</p>
</dd><dt id="MCE::Stream"><a href="https://metacpan.org/pod/MCE#MCE::Stream"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Stream">MCE::Stream</a></dt><dd>
<p>Provides an efficient parallel implementation for chaining multiple maps and greps together through user_tasks and MCE::Queue. Like with MCE::Flow, MCE::Stream can run multiple code blocks in parallel with a slight change to syntax from MCE::Map and MCE::Grep.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MISCELLANEOUS"><span></span></a>MISCELLANEOUS</p>
<p>Miscellaneous additions included with the distribution.</p>
<dl><dt id="MCE::Examples"><a href="https://metacpan.org/pod/MCE#MCE::Examples"><span></span></a><a></a><a href="https://metacpan.org/pod/distribution/MCE/lib/MCE/Examples.pod">MCE::Examples</a></dt><dd>
<p>Describes various demonstrations for MCE including a Monte Carlo simulation.</p>
</dd><dt id="MCE::Subs"><a href="https://metacpan.org/pod/MCE#MCE::Subs"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Subs">MCE::Subs</a></dt><dd>
<p>Exports functions mapped directly to MCE methods; e.g. mce_wid. The module allows 3 options; :manager, :worker, and :getter.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#REQUIREMENTS"><span></span></a>REQUIREMENTS</p>
<p>Perl 5.8.0 or later. PDL::IO::Storable is required in scripts running PDL.</p>
<p><a href="https://metacpan.org/pod/MCE#SOURCE-AND-FURTHER-READING"><span></span></a><a></a>SOURCE AND FURTHER READING</p>
<p>The source, cookbook, and examples are hosted at GitHub.</p>
<ul>
<li>
<p><a href="https://github.com/marioroy/mce-perl">https://github.com/marioroy/mce-perl</a></p>
</li>
<li>
<p><a href="https://github.com/marioroy/mce-cookbook">https://github.com/marioroy/mce-cookbook</a></p>
</li>
<li>
<p><a href="https://github.com/marioroy/mce-examples">https://github.com/marioroy/mce-examples</a></p>
</li>
</ul>
<p><a href="https://metacpan.org/pod/MCE#SEE-ALSO"><span></span></a><a></a>SEE ALSO</p>
<p><code>MCE::Shared</code>&nbsp;provides data sharing capabilities for&nbsp;<code>MCE</code>. It includes&nbsp;<code>MCE::Hobo</code>&nbsp;for running code asynchronously.</p>
<ul>
<li>
<p><a href="https://metacpan.org/pod/MCE::Shared">MCE::Shared</a></p>
</li>
<li>
<p><a href="https://metacpan.org/pod/MCE::Hobo">MCE::Hobo</a></p>
</li>
</ul><p>Address of the bookmark: <a href="https://github.com/marioroy/mce-examples" rel="nofollow">https://github.com/marioroy/mce-examples</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30971/hiveplot</guid>
	<pubDate>Thu, 16 Feb 2017 11:39:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30971/hiveplot</link>
	<title><![CDATA[HivePlot]]></title>
	<description><![CDATA[<p>The&nbsp;<em>hive plot</em>&nbsp;is a rational visualization method for drawing networks. Nodes are mapped to and positioned on radially distributed linear axes &mdash; this mapping is based on network structural properties. Edges are drawn as curved links. Simple and interpretable.</p>
<p>The purpose of the hive plot is to establish a new baseline for visualization of large networks &mdash; a method that is both general and tunable and useful as a starting point in visually exploring network structure.</p>
<p>More at&nbsp;http://www.hiveplot.com/</p><p>Address of the bookmark: <a href="http://www.hiveplot.com/" rel="nofollow">http://www.hiveplot.com/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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