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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/45093?offset=350</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29210/cgview-circular-genome-viewer</guid>
	<pubDate>Mon, 19 Sep 2016 07:52:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29210/cgview-circular-genome-viewer</link>
	<title><![CDATA[CGView - Circular Genome Viewer]]></title>
	<description><![CDATA[<p>GView is a Java package used to display and navigate bacterial genomes. GView is useful for producing high-quality genome maps for use in publications and websites, or as a visualization tool in a sequence annotation pipeline. Users can interact with the genome using a powerful pan-and-zoom interface, or GView can write static images of a genome to a file. GView can draw a genome using either circular or linear layouts. For examples of some of the images GView can produce, see the <a href="https://www.gview.ca/bin/view/GView/ImageGallery">Image Gallery</a>. GView is a re-write of <a href="http://wishart.biology.ualberta.ca/cgview/" target="_top">CGView</a>, a circular genome viewer written by Paul Stothard. The goal of GView is to provide greater user interaction, and more flexibility in how the genome map is rendered. To aid with easily configuring the display of a genome, a style editor has been included to provide an intuitive, user-friendly graphical user interface for customizing genome maps. Styling attributes such as colours or fonts for the various map elements can be adjusted in real time. Customized styles can be saved for later use or for application to other genome maps using GView's <a href="https://www.gview.ca/bin/view/GViewDocumentation/GViewGSS">custom file format</a>.</p><p>Address of the bookmark: <a href="http://wishart.biology.ualberta.ca/cgview/" rel="nofollow">http://wishart.biology.ualberta.ca/cgview/</a></p>]]></description>
	<dc:creator>Jit</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/29280/nemo-%E2%80%93-a-stochastic-individual-base-genetically-explicit-simulation-platform</guid>
	<pubDate>Sat, 01 Oct 2016 14:45:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29280/nemo-%E2%80%93-a-stochastic-individual-base-genetically-explicit-simulation-platform</link>
	<title><![CDATA[Nemo – A stochastic, individual-base, genetically explicit simulation platform]]></title>
	<description><![CDATA[<ul>
<li>
<p>A&nbsp;<strong>recombination map</strong>&nbsp;has been added for all multi-locus traits. The map positions (chromosomal) for neutral markers (e.g. SNPs) and loci under selection (QTLs, deleterious mutations, DMIs) can now be specified explicitly, or set at random. The map can hold an unlimited number of loci of different types jointly, at any recombination scale (cM or lower). The effects of linkage can thus be finely explored.</p>
</li>
<li>
<p>A new trait coding for (Bateson-)<strong>Dobzhansky-Muller incompatibility loci</strong>. Multiple haploid or diploid pairs of incompatible loci can be spread throughout the genome and affect individual fitness.</p>
</li>
<li>
<p><strong>Multi-type selection</strong>:&nbsp;<a href="http://nemo2.sourceforge.net/classIndividual.html" title="This class contains traits along with other individual information (sex, pedigree, etc. ).">Individual</a>&nbsp;fitness can be jointly determined by different types of loci under selectinon, such as QTLs coding for quantitative traits under spatially variable selection, universally deleterious mutations, and Dobzhansky-Muller incompatibility loci.</p>
</li>
<li>
<p><strong>An unlimited number of quantitative traits</strong>&nbsp;under different forms of selection can be modelled, based on universally pleiotropic loci with several bi- or multi-allelic models.</p>
</li>
<li>
<p><strong>Spatial and temporal variation of selection</strong>&nbsp;on quantitative traits is possible, modelling shifts of environmental conditions over time.</p>
</li>
<li>
<p>The dispersal matrix describing the movement of individuals among sub-populations can be replaced by a connectivity matrix and a reduced dispersal matrix describing migration only among the connected sub-populations. This offers a substantial gain in computing time and system memory when simulating very large grids.</p>
</li>
<li>
<p>Input parameters' arguments may be specified in separate files. This is particularly convenient when specifying large matrices.</p>
</li>
<li>
<p>Many adjustments have been made for refined control of the input of parameters and data output. See updates in the manual.</p>
</li>
</ul><p>Address of the bookmark: <a href="http://nemo2.sourceforge.net/index.html" rel="nofollow">http://nemo2.sourceforge.net/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29379/bbmap-help</guid>
	<pubDate>Mon, 10 Oct 2016 06:29:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29379/bbmap-help</link>
	<title><![CDATA[BBMap help]]></title>
	<description><![CDATA[<div>
<div>BBMAP <span> &bull; <span>a solution for everything</span></span><a href="https://www.biostarhandbook.com/"><span></span></a></div>
<div>That content has been reformatted and it is being expanded to include more information.<span><span></span></span></div>
</div>
<hr>
<p>There are common options for most BBMap suite programs and depending on the file extension the input/output format is automatically chosen/set.</p>
<hr>
<h3>Using BBMap</h3>
<h4>Mapping Nanopore reads</h4>
<p>BBMap.sh has a length cap of 6kbp. Reads longer than this will be broken into 6kbp pieces and mapped independently.</p>
<p>More at https://www.biostarhandbook.com/tools/bbmap/bbmap-help.html</p><p>Address of the bookmark: <a href="https://www.biostarhandbook.com/tools/bbmap/bbmap-help.html" rel="nofollow">https://www.biostarhandbook.com/tools/bbmap/bbmap-help.html</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/29479/how-to-install-perl-modules-on-mac-os-x-in-easy-steps</guid>
	<pubDate>Thu, 20 Oct 2016 07:26:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/29479/how-to-install-perl-modules-on-mac-os-x-in-easy-steps</link>
	<title><![CDATA[How to install Perl modules on Mac OS X in easy steps !!]]></title>
	<description><![CDATA[<p>Today at work, I learned how to install Perl modules using&nbsp;<a href="http://en.wikipedia.org/wiki/CPAN">CPAN</a>. It&rsquo;s a lot easier than I thought.</p><p>You see, for the past couple of years, I&rsquo;ve been a bit frustrated because OS X does not come with a whole lot of Perl modules pre-installed, and for all I googled, I couldn&rsquo;t find an &ldquo;idiot&rsquo;s&rdquo; guide for moderately-savvy-but-not-expert users like myself to install modules and dependencies on demand.</p><p>The only instructions I could find point to&nbsp;<a href="http://fink.sourceforge.net/">Fink</a>, which basically installs modules in a path that isn&rsquo;t included in the Perl @INC variable, meaning you have to manually specify the full path to the modules in every script &mdash; which is not a lot of fun if you&rsquo;re developing on OS X and deploying on Red Hat, for instance.</p><p>Moreover, Fink doesn&rsquo;t seem to make every module available, and it&rsquo;s not very easy to determine which Fink package you need to install if you need a particular module.</p><p>So, with a script that called on several apparently unavailable modules, and a deadline looming, I finally decided to suck it up and figure out how to use CPAN to install them:</p><h4>1) Make sure you have the Apple Developer Tools (XCode) installed.</h4><p>These are on one of your install discs, or available as a huge but free download from the&nbsp;<a href="https://developer.apple.com/xcode/">Apple Developer Connection</a>&nbsp;[free registration required] or the Mac App Store. I thought I had them, but apparently when we upgraded that computer to Tiger, they went missing.</p><p>If you don&rsquo;t have this stuff installed, your installation will fail with errors about unavailable commands.</p><h4>1.5) Install Command Line Tools (Recent XCode versions only)</h4><p>(Thank you to Tom Marchioro for informing me about this step.)</p><p>Older versions of XCode installed the command line tools (which are required to properly install CPAN modules) by default, but apparently newer ones do not. To check whether you have the command line tools already installed, run the following from the Terminal:</p><p><code>$ which make</code></p><p>This command checks the system for the &ldquo;<code>make</code>&rdquo; tool. If it spits out something like&nbsp;<code>/usr/bin/make</code>&nbsp;you&rsquo;re golden and can skip ahead to Step 2. If you just get a new prompt and no output, you&rsquo;ll need to install the tools:</p><ol>
<li>Launch XCode and bring up the Preferences panel.</li>
<li>Click on the Downloads tab</li>
<li>Click to install the Command Line Tools</li>
</ol><p>If you like, you can run&nbsp;<code>which make</code>&nbsp;again to confirm that everything&rsquo;s installed correctly.</p><h4>2) Configure CPAN.</h4><p><code>$ sudo perl -MCPAN -e shell</code></p><p><code>perl&gt; o conf init</code></p><p>This will prompt you for some settings. You can accept the defaults for almost everything (just hit &ldquo;return&rdquo;). The two things you must fill in are the path to&nbsp;<code>make</code>&nbsp;(which should be&nbsp;<code>/usr/bin/make</code>&nbsp;or the value returned when you run&nbsp;<code>which make</code>&nbsp;from the command line) and your choice of CPAN mirrors (which you actually choose don&rsquo;t really matter, but it won&rsquo;t let you finish until you select at least one). If you use a proxy or a very restrictive firewall, you may have to configure those settings as well.</p><p>If you skip Step 2, you may get errors about&nbsp;<code>make</code>&nbsp;being unavailable.</p><h4>3) Upgrade CPAN</h4><p><code>$ sudo perl -MCPAN -e 'install Bundle::CPAN'</code></p><p>Don&rsquo;t forget the&nbsp;<code>sudo</code>, or it&rsquo;ll fail with permissions errors, probably when doing something relatively unimportant like installing&nbsp;<code>man</code>&nbsp;files.</p><p>This will spend a long time downloading, testing, and compiling various files and dependencies. Bear with it. It will prompt you a few times about dependencies. You probably want to enter &ldquo;yes&rdquo;. I agreed to everything it asked me, and everything turned out fine. YMMV of course. If everything installs properly, it&rsquo;ll give you an &ldquo;OK&rdquo; at the end.</p><h4>4) Install your modules. For each module&hellip;.</h4><p><code>$ sudo perl -MCPAN -e 'install Bundle::Name'</code></p><p>or</p><p><code>$ sudo perl -MCPAN -e 'install Module::Name'</code></p><p>This will install the module&nbsp;<em>and</em>&nbsp;its dependencies. Nice, eh? Again, don&rsquo;t forget the&nbsp;<code>sudo</code>.</p><p>The first time you run this after upgrading CPAN, it may prompt you to configure again (see Step 2). If you accept its offer to try to configure itself automatically, it may just run through everything without a problem.</p><p>There are a couple of potential pitfalls with specific modules (such as the<code>LWP::UserAgent</code>&nbsp;/&nbsp;<code>HEAD</code>&nbsp;issue), but most have workarounds, and I haven&rsquo;t run into anything that wasn&rsquo;t easily recoverable.</p><p>And that&rsquo;s it!</p><p>Did you find this useful? Is there anything I missed?</p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29953/traineeship-at-jawaharlal-nehru-tropical-botanic-garden-and-research-institute</guid>
  <pubDate>Fri, 25 Nov 2016 08:07:59 -0600</pubDate>
  <link></link>
  <title><![CDATA[Traineeship at JAWAHARLAL NEHRU TROPICAL BOTANIC GARDEN AND RESEARCH INSTITUTE]]></title>
  <description><![CDATA[
<p>JAWAHARLAL NEHRU TROPICAL BOTANIC GARDEN AND RESEARCH INSTITUTE</p>

<p>THIRUVANANTHAPURAM - 695 562</p>

<p>Traineeship on Bioinformatics(2)</p>

<p>First class M.Sc. Bioinformatics/ Agriculture/ Botany/ Biotechnology @ Rs.8000</p>

<p>Those candidates who fulfill the above criteria may attend a walk PCC Coordinator in-interview on 28th November 2016 at Saraswathy Thangavelu center, JNTBGRI, Puthenthope, Thiruvananthapuram between at 10.00 am and 2.00 pm with all the relevant document and testimonials.</p>

<p>No TA/DA will be given to candidates for attending the interview.</p>

<p>More Info : http://jntbgri.res.in/downloads/traineeship_notification.pdf</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29583/graph-genome-suite</guid>
	<pubDate>Fri, 28 Oct 2016 07:59:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29583/graph-genome-suite</link>
	<title><![CDATA[Graph Genome Suite]]></title>
	<description><![CDATA[<p><span>Seven Bridges is the biomedical data analysis company accelerating breakthroughs in genomics research for cancer, drug development and precision medicine. We build self-improving systems to analyze millions of genomes, including the&nbsp;</span><strong>Graph Genome Suite</strong><span>&nbsp;&mdash; the most advanced population genomics tools in the world.</span></p><p>Address of the bookmark: <a href="https://www.sbgenomics.com/graph/" rel="nofollow">https://www.sbgenomics.com/graph/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29603/statistical-for-biological-research</guid>
	<pubDate>Thu, 03 Nov 2016 04:59:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29603/statistical-for-biological-research</link>
	<title><![CDATA[Statistical for biological research]]></title>
	<description><![CDATA[<p>There is no disputing the importance of statistical analysis in biological research, but too often it is considered only after an experiment is completed, when it may be too late.</p>
<p>This collection highlights important statistical issues that biologists should be aware of and provides practical advice to help them improve the rigor of their work.</p>
<p><em>Nature Methods</em>' <strong><a href="http://www.nature.com/collections/qghhqm/pointsofsignificance">Points of Significance</a></strong> column on statistics explains many key statistical and experimental design concepts. <strong><a href="http://www.nature.com/collections/qghhqm/resources">Other resources</a></strong> include an online plotting tool and links to statistics guides from other publishers.</p><p>Address of the bookmark: <a href="http://www.nature.com/collections/qghhqm" rel="nofollow">http://www.nature.com/collections/qghhqm</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29628/links</guid>
	<pubDate>Fri, 04 Nov 2016 06:19:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29628/links</link>
	<title><![CDATA[LINKS]]></title>
	<description><![CDATA[<p>LINKS is a genomics application for scaffolding genome assemblies with long reads, such as those produced by Oxford Nanopore Technologies Ltd. It can be used to scaffold high-quality draft genome assemblies with any long sequences (eg. ONT reads, PacBio reads, another draft genomes, etc)</p>
<p>Paper at&nbsp;https://gigascience.biomedcentral.com/articles/10.1186/s13742-015-0076-3</p><p>Address of the bookmark: <a href="https://github.com/warrenlr/LINKS/" rel="nofollow">https://github.com/warrenlr/LINKS/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29644/junior-research-fellow-at-rajiv-gandhi-centre-for-biotechnology-thiruvananthapuram</guid>
  <pubDate>Mon, 07 Nov 2016 10:27:06 -0600</pubDate>
  <link></link>
  <title><![CDATA[Junior Research Fellow at Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram]]></title>
  <description><![CDATA[
<p>Adv. # 22/ 2016<br />Applications are invited from suitable candidates for one position of Junior Research Fellow in a DST funded bioinformatics research project entitled "Major gene influxes in microbial genome evolution" in the Laboratory of Dr. Shijulal Nelson-Sathi at Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram.</p>

<p>ESSENTIAL QUALIFICATIONS:<br />We are looking for a motivated candidate with keen interest in bioinformatics and microbial genome evolution. The candidate must have a Master’s Degree in Bioinformatics, Computational Biology, Computer Science, Microbiology, Biology or a related field with good academic record.</p>

<p>DESIRABLE QUALIFICATIONS<br />Hands on research experience on handling next generation sequencing data and phylogenetic reconstruction methods. Excellent programming skills (Perl/Python/Java/Php) and experience in working on Unix/Linux platform is preferred. Furthermore; good knowledge is required in statistics (R/Matlab) and the application of bioinformatics analysis tools.</p>

<p>AGE:<br />Below 28 years as on 15th November, 2016.</p>

<p>EMOLUMENTS:<br />Rs. 25,000 + 20% HRA for NET/GATE qualified and Post Graduate in Professional Degree course qualified candidates and <br />Rs. 12,000/- + 20% HRA for others.</p>

<p>DURATION:<br />Initial appointment will be given for one year and further extension will be based on the performance till termination of the project.<br />Only those fulfilling the above criteria need apply and will be called for interview. In the event of more than 10 candidates being short-listed by screening the applications, a written test will be conducted before the selection interview and only those who are successful in the written test will be interviewed. No TA/ DA will be given for appearing in the interview.</p>

<p>Suitably qualified candidates may send applications in the prescribed format (Download here) with a photograph, a copy of full resume indicating the percentage of Marks obtained and attested photocopies of credentials &amp; experience to reach the undersigned on or before 15th November, 2016. Envelopes must be superscripted with abbreviated title of the project, advertisement number and job title. Selection to the position will not entitle the candidate to any future positions at RGCB (permanent or otherwise). As with all project positions at RGCB, the position will be co terminus with end of the project.</p>
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