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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/30168?offset=130</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29658/bookmarks-biostatistics-materials-and-books</guid>
	<pubDate>Tue, 08 Nov 2016 07:42:42 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29658/bookmarks-biostatistics-materials-and-books</link>
	<title><![CDATA[Bookmarks Biostatistics materials and books]]></title>
	<description><![CDATA[<p>Biostatistics did not spring fully formed from the brow of R. A. Fisher, but evolved over many years. This process is continuing, although it may not be obvious from the outside. It has been ten years since the first edition of this book appeared (and rather longer since it was begun). Over this time, new areas of biostatistics have been developed and emphases and interpretations have changed</p>
<p>Please bookmarks your favourate biostatistics&nbsp;books in commend sectons ...</p><p>Address of the bookmark: <a href="http://www.cos.ufrj.br/~bioestatistica/livros/Introduction%20to%20Biostatistics.pdf" rel="nofollow">http://www.cos.ufrj.br/~bioestatistica/livros/Introduction%20to%20Biostatistics.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29917/gojs</guid>
	<pubDate>Tue, 22 Nov 2016 08:25:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29917/gojs</link>
	<title><![CDATA[GoJS]]></title>
	<description><![CDATA[<p><strong>GoJS</strong> is a feature-rich JavaScript library for implementing custom interactive diagrams and complex visualizations across modern web browsers and platforms. <strong>GoJS</strong> makes constructing JavaScript diagrams of complex nodes, links, and groups easy with customizable templates and layouts.</p>
<p><strong>GoJS</strong> offers many advanced features for user interactivity such as drag-and-drop, copy-and-paste, in-place text editing, tooltips, context menus, automatic layouts, templates, data binding and models, transactional state and undo management, palettes, overviews, event handlers, commands, and an extensible tool system for custom operations.</p>
<p><strong>GoJS</strong> is pure JavaScript, so users get interactivity without requiring round-trips to servers and without plugins. <strong>GoJS</strong> normally runs completely in the browser, rendering to an HTML5 Canvas element or SVG without any server-side requirements. <strong>GoJS</strong> does not depend on any JavaScript libraries or frameworks, so it should work with any HTML or JavaScript framework or with no framework at all. &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</p>
<p>More at&nbsp;http://gojs.net/latest/index.html</p><p>Address of the bookmark: <a href="http://gojs.net/latest/index.html" rel="nofollow">http://gojs.net/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30074/minia</guid>
	<pubDate>Thu, 08 Dec 2016 05:07:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30074/minia</link>
	<title><![CDATA[Minia]]></title>
	<description><![CDATA[<p>Minia is a short-read assembler based on a de Bruijn graph, capable of assembling a human genome on a desktop computer in a day. The output of Minia is a set of contigs. Minia produces results of similar contiguity and accuracy to other de Bruijn assemblers (e.g. Velvet).</p>
<h3>Download</h3>
<p><a href="https://github.com/GATB/minia/releases/download/v2.0.7/minia-v2.0.7-bin-Linux.tar.gz">Minia 2.0.7 Linux 64-bits binaries</a>&nbsp;(<a href="https://github.com/GATB/minia/releases/download/v2.0.7/minia-v2.0.7-Source.tar.gz">Source code</a>)&nbsp;<span>(<a href="http://minia.genouest.org/files/minia-1.6906.tar.gz">Legacy codebase</a>)</span></p>
<h3>For the impatient</h3>
<p>A typical Minia command line looks like:</p>
<pre>./minia -in <span>reads.fa</span> -kmer-size <span>31</span> -abundance-min <span>3</span> -out <span>output_prefix</span></pre>
<p>Type</p>
<pre>./minia</pre>
<p><span>for a quick explanation of the parameters.</span></p>
<p>For more information, refer to the&nbsp;<a href="http://minia.genouest.org/files/minia.pdf">manual</a>.</p>
<p><a href="http://kmergenie.bx.psu.edu/">KmerGenie</a>&nbsp;can be used to determine the best k-mer size, minimum abundance of correct k-mers, and genome size estimation for your dataset.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://minia.genouest.org/" rel="nofollow">http://minia.genouest.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30093/velvet-tutorial</guid>
	<pubDate>Fri, 09 Dec 2016 04:19:07 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30093/velvet-tutorial</link>
	<title><![CDATA[Velvet tutorial]]></title>
	<description><![CDATA[<p><span>The objective of this activity is to help you understand how to run&nbsp;</span><a href="http://evomics.org/resources/software/genomics-software/assembly/velvet/" title="Velvet">Velvet</a><span>&nbsp;in general, how to accurately estimate the insert size of a paired-end library through the use of&nbsp;</span><a href="http://evomics.org/resources/software/genomics-software/assembly/bowtie/" title="Bowtie">Bowtie</a><span>, the primary parameters of velvet, and the process involved in producing a&nbsp;</span><em>de novo</em><span>&nbsp;assembly from Illumina reads.</span></p>
<p>http://evomics.org/learning/assembly-and-alignment/velvet/</p><p>Address of the bookmark: <a href="http://evomics.org/learning/assembly-and-alignment/velvet/" rel="nofollow">http://evomics.org/learning/assembly-and-alignment/velvet/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</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/30214/megamerge-a-tool-to-merge-assembled-contigs-long-reads-from-metagenomic-sequencing-runs</guid>
	<pubDate>Mon, 19 Dec 2016 09:42:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30214/megamerge-a-tool-to-merge-assembled-contigs-long-reads-from-metagenomic-sequencing-runs</link>
	<title><![CDATA[MeGAMerge: A tool to merge assembled contigs, long reads from metagenomic sequencing runs]]></title>
	<description><![CDATA[<p>MeGAMerge</p>
<p>MeGAMerge (A tool to merge assembled contigs, long reads from metagenomic sequencing runs)</p>
<p>Description</p>
<p>MeGAMerge is a perl based wrapper/tool that can accept any number of sequence (FASTA) files containing assembled contigs of any length in Multi-FASTA format to produce an improved contig set based on OLC based assembly. All overlap parameters (Minimum Overlap Length, Identity, etc) are user-declarable at runtime. It is written to run on Linux.</p>
<p>Requirements:</p>
<p>You will need to have the following tools installed and in $PATH, or added to $binpath in the tool:</p>
<p>Newbler (specifically runAssembly)<br>Minimus2 (part of AMOS, also requires MUMmer)</p><p>Address of the bookmark: <a href="https://github.com/LANL-Bioinformatics/MeGAMerge" rel="nofollow">https://github.com/LANL-Bioinformatics/MeGAMerge</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30355/meme-suite</guid>
	<pubDate>Fri, 23 Dec 2016 08:49:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30355/meme-suite</link>
	<title><![CDATA[MEME suite]]></title>
	<description><![CDATA[<p>Motif based sequence analysis suits&nbsp;</p>
<p>The MEME Suite allows the biologist to discover novel motifs in collections of unaligned nucleotide or protein sequences, and to perform a wide variety of other motif-based analyses.</p>
<p>The MEME Suite supports motif-based analysis of DNA, RNA and protein sequences. It provides motif discovery algorithms using both probabilistic (MEME) and discrete models (MEME), which have complementary strengths. It also allows discovery of motifs with arbitrary insertions and deletions (GLAM2). In addition to motif discovery, the MEME Suite provides tools for scanning sequences for matches to motifs (FIMO, MAST and GLAM2Scan), scanning for clusters of motifs (MCAST), comparing motifs to known motifs (Tomtom), finding preferred spacings between motifs (SpaMo), predicting the biological roles of motifs (GOMo), measuring the positional enrichment of sequences for known motifs (CentriMo), and analyzing ChIP-seq and other large datasets (MEME-ChIP).</p>
<p>The MEME Suite is comprised of a collection of tools that work together, as shown below. Not all the tools are available as webservices, so to get the full power of the MEME Suite you will need to&nbsp;<a href="http://meme-suite.org/doc/download.html">download</a>&nbsp;and&nbsp;<a href="http://meme-suite.org/doc/install.html">install</a>&nbsp;a local copy of the software. To see what has changed recently you can peruse the&nbsp;<a href="http://meme-suite.org/doc/release-notes.html">release notes</a>.</p>
<p>http://meme-suite.org/</p><p>Address of the bookmark: <a href="http://meme-suite.org/" rel="nofollow">http://meme-suite.org/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30540/progressive-cactus</guid>
	<pubDate>Tue, 17 Jan 2017 03:40:06 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30540/progressive-cactus</link>
	<title><![CDATA[Progressive Cactus]]></title>
	<description><![CDATA[<h1><em style="font-size: 12.8px; font-weight: normal;">v0.0 by Glenn Hickey (<a href="mailto:hickey@soe.ucsc.edu">hickey@soe.ucsc.edu</a>)</em></h1>
<p>Progressive Cactus is a whole-genome alignment package.</p>
<h3><a href="https://github.com/glennhickey/progressiveCactus#requirements"></a>Requirements</h3>
<ul>
<li>git</li>
<li>gcc 4.2 or newer</li>
<li>python 2.7</li>
<li>wget</li>
<li>64bit processor and build environment</li>
<li>150GB+ of memory on at least one machine when aligning mammal-sized genomes; less memory is needed for smaller genomes.</li>
<li>Parasol or SGE for cluster support.</li>
<li>750M disk space</li>
</ul>
<h3><a href="https://github.com/glennhickey/progressiveCactus#instructions"></a>Instructions</h3>
<p>IMPORTANT NOTE: Progressive Cactus does not presently support installation into paths that contain spaces. Until this is resolved, you can use a softlink as a workaround: ln -s "path with spaces" "installation path without spaces"</p>
<p>In the parent directory of where you want Progressive Cactus installed:</p>
<pre><code>git clone git://github.com/glennhickey/progressiveCactus.git
cd progressiveCactus
git pull
git submodule update --init
make
</code></pre>
<p>It is also convenient to add the location of&nbsp;<code>progressiveCactus/bin</code>&nbsp;to your PATH environment variable. In order to run the included tools (ex hal2maf) in the submodules/ directory structure, first source&nbsp;<code>progressiveCactus/environment</code>&nbsp;to load the installed environment.</p>
<p>If any errors occur during the build process, you are unlikely to be able to use the tool. Please submit a GitHub issue so we can help out: not only will you help yourself, but others who wish to use the tool as well.</p>
<p><em>Note that all dependencies are also built and included in the submodules/ directory. This increases the size and build time but greatly simplifies installation and version management. The installation does not create or modify any files outside the progressiveCactus/ directory.</em></p><p>Address of the bookmark: <a href="https://github.com/glennhickey/progressiveCactus" rel="nofollow">https://github.com/glennhickey/progressiveCactus</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30833/dnasp-v5-a-software-for-comprehensive-analysis-of-dna-polymorphism-data</guid>
	<pubDate>Mon, 06 Feb 2017 04:45:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30833/dnasp-v5-a-software-for-comprehensive-analysis-of-dna-polymorphism-data</link>
	<title><![CDATA[DnaSP v5: a software for comprehensive analysis of DNA polymorphism data]]></title>
	<description><![CDATA[<p><span>DnaSP is a software package for a comprehensive analysis of DNA polymorphism data. Version 5 implements a number of new features and analytical methods allowing extensive DNA polymorphism analyses on large datasets. Among other features, the newly implemented methods allow for: (i) analyses on multiple data files; (ii) haplotype phasing; (iii) analyses on insertion/deletion polymorphism data; (iv) visualizing sliding window results integrated with available genome annotations in the UCSC browser.</span></p><p>Address of the bookmark: <a href="http://www.ub.edu/dnasp/" rel="nofollow">http://www.ub.edu/dnasp/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</guid>
	<pubDate>Fri, 24 Feb 2017 04:50:44 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</link>
	<title><![CDATA[bedtools]]></title>
	<description><![CDATA[<p>Collectively, the&nbsp;<strong>bedtools</strong>&nbsp;utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable&nbsp;<em>genome arithmetic</em>: that is, set theory on the genome. For example,&nbsp;<strong>bedtools</strong>&nbsp;allows one to<em>intersect</em>,&nbsp;<em>merge</em>,&nbsp;<em>count</em>,&nbsp;<em>complement</em>, and&nbsp;<em>shuffle</em>&nbsp;genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g.,&nbsp;<em>intersect</em>&nbsp;two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line.</p>
<p><strong>bedtools</strong>&nbsp;is developed in the&nbsp;<a href="http://quinlanlab.org/">Quinlan laboratory</a>&nbsp;at the&nbsp;<a href="http://www.utah.edu/">University of Utah</a>&nbsp;and benefits from fantastic contributions made by scientists worldwide.</p><p>Address of the bookmark: <a href="http://bedtools.readthedocs.io/en/latest/index.html" rel="nofollow">http://bedtools.readthedocs.io/en/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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