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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31087?offset=1500</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44474/claw-chloroplast-long-read-assembly-workflow</guid>
	<pubDate>Wed, 21 Feb 2024 12:37:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44474/claw-chloroplast-long-read-assembly-workflow</link>
	<title><![CDATA[CLAW: Chloroplast Long-read Assembly Workflow]]></title>
	<description><![CDATA[<p dir="auto">CLAW (Chloroplast Long-read Assembly Workflow) is an mostly-automated Snakemake-based workflow for the assembly of chloroplast genomes. CLAW uses chloroplast long-reads, which are baited out of larger read libraries (e.g., an Oxford Nanopore Technologies MinION read library derived from photosynthetic tissue), for assembly with Flye and/or Unicycler. CLAW was designed with the novice bioinformatician in mind - it is easy to install and easy to use, requiring only minimal user input.</p><p>Address of the bookmark: <a href="https://github.com/aaronphillips7493/CLAW" rel="nofollow">https://github.com/aaronphillips7493/CLAW</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45133/postdoctoral-position-in-evolutionary-genomics-and-bioinformatics-at-the-center-for-interdisciplinary-neuroscience-at-university-of-valparaiso-valparaiso-chile</guid>
  <pubDate>Wed, 22 Apr 2026 02:36:00 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Position in Evolutionary Genomics and Bioinformatics, at the Center for Interdisciplinary Neuroscience at University of Valparaiso, Valparaiso, Chile.]]></title>
  <description><![CDATA[
<p>The Center for Interdisciplinary Neuroscience of Valparaiso (CINV)<br />in Valparaiso, Chile, invites postdoctoral researchers to apply for<br />a Postdoctoral Fellowship focusing on understanding the evolution of<br />genes and molecular pathways that play a role on inflammatory processes<br />driving diseases affecting the central nervous system.</p>

<p>The postdoctoral researcher will contribute to this project using<br />a combination of evolutionary and comparative genomics, as well as a<br />diverse set of bioinformatic approaches for data analysis and integration<br />(e.g., transcriptomics, genomics, phenotypic data). This position offers<br />a unique opportunity to integrate diverse state-of-the-art genomic and<br />phenotypic datasets across different model organisms to understand the<br />role of genes, molecular pathways in the origin of complex diseases.</p>

<p>CINV provides a highly collaborative and multidisciplinary environment<br />using a variety of computational and experimental approaches,<br />including genetically tractable animal models as well as expertise in<br />genetics, behavior, glia-neuron communication, metabolism, biophysics,<br />genomics, bioinformatics, host-microbe communication, and biomolecular<br />modelling. The new postdoc will be part of one of our labs which focuses<br />more generally on the intersection between molecular evolution and<br />disease biology.</p>

<p>Required qualifications are a PhD in evolutionary biology, computational<br />biology, bioinformatics, or closely related fields. Candidates must have<br />excellent verbal and written communication skills (working language<br />is English), as well as an established record of productivity (e.g.,<br />at least one previous peer-reviewed publication). Candidates with a<br />past record of publications in bioinfomatics, computational biology,<br />population genetics or evolutionary genomics are strongly preferred. Ideal<br />candidates should have experience in analyzing genomic and phenomic<br />data, performing comparative evolution or population genomic analyses,<br />as well as in collaborating with experimentalists.</p>

<p>Interested candidates should first contact Evandro Ferrada at<br />. Please include the following: (1) a cover<br />letter addressing your interest in the position and how your expertise<br />meets the position requirements, (2) a CV, (3) contact information of<br />at least 2 references. A short online interview will follow to discuss<br />specific proposals. Candidate materials will be reviewed as soon as<br />possible until the position is filled.</p>

<p>For further information, please visit:<br />https://cinv.uv.cl/cinv-postdoctoral-fellowship-program-2026/</p>

<p>Dr. Evandro Ferrada<br />Associate Profesor</p>

<p>Centro Interdisciplinario de Neurociencia (CINV)</p>

<p>Facultad de Ciencias, Universidad de Valpara�so.</p>

<p>Pasaje Harrington 287, Playa Ancha, Valpara�so, Chile.</p>

<p>Tel.  +56 (32) 250 8453</p>

<p>www.cinv.cl</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35286/alfred-bam-statistics-and-feature-counting</guid>
	<pubDate>Tue, 23 Jan 2018 05:28:38 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35286/alfred-bam-statistics-and-feature-counting</link>
	<title><![CDATA[Alfred: BAM Statistics and Feature Counting]]></title>
	<description><![CDATA[<p>The easiest way to get Alfred is to download a statically linked binary from the&nbsp;<a href="https://github.com/tobiasrausch/alfred/releases/">Alfred github release page</a>. Alternatively, you can build Alfred from source. Alfred dependencies are included as submodules so you need to do a recursive clone.</p>
<p><code>git clone --recursive https://github.com/tobiasrausch/alfred.git</code></p>
<p><code>cd alfred/</code></p>
<p><code>make all</code></p>
<p>https://github.com/tobiasrausch/alfred/</p><p>Address of the bookmark: <a href="https://gear.embl.de/alfred" rel="nofollow">https://gear.embl.de/alfred</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2631/what-junk-dna-it%E2%80%99s-an-operating-system</guid>
	<pubDate>Mon, 19 Aug 2013 15:24:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2631/what-junk-dna-it%E2%80%99s-an-operating-system</link>
	<title><![CDATA[What Junk DNA? It’s an Operating System]]></title>
	<description><![CDATA[<p>The report adds to growing experimental support for the idea that all that extra stuff in the human genes, once referred to as &ldquo;junk DNA,&rdquo; is more than functionless, space-filling material that happens to make up nearly 98% of the genome. The paper adds to a growing body of knowledge establishing a considerable role for this material in the regulation of gene expression and its potential role in human disease.</p><p>Address of the bookmark: <a href="http://www.genengnews.com/keywordsandtools/print/3/32115/" rel="nofollow">http://www.genengnews.com/keywordsandtools/print/3/32115/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40251/mosdepth-fast-bamcram-depth-calculation-for-wgs-exome-or-targeted-sequencing</guid>
	<pubDate>Wed, 13 Nov 2019 22:20:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40251/mosdepth-fast-bamcram-depth-calculation-for-wgs-exome-or-targeted-sequencing</link>
	<title><![CDATA[mosdepth: fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing]]></title>
	<description><![CDATA[<p>mosdepth can output:</p>
<p>per-base depth about 2x as fast samtools depth--about 25 minutes of CPU time for a 30X genome.<br>mean per-window depth given a window size--as would be used for CNV calling.<br>the mean per-region given a BED file of regions.<br>a distribution of proportion of bases covered at or above a given threshold for each chromosome and genome-wide.<br>quantized output that merges adjacent bases as long as they fall in the same coverage bins e.g. (10-20)<br>threshold output to indicate how many bases in each region are covered at the given thresholds.<br>A summary of mean depths per chromosome and within specified regions per chromosome.</p><p>Address of the bookmark: <a href="https://github.com/brentp/mosdepth" rel="nofollow">https://github.com/brentp/mosdepth</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/3029/bioinformatics-market-in-india</guid>
	<pubDate>Fri, 23 Aug 2013 07:08:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/3029/bioinformatics-market-in-india</link>
	<title><![CDATA[Bioinformatics market in India]]></title>
	<description><![CDATA[<div><strong>Key Topics Covered in the Report:</strong></div>
<ul>
<li>The market size of the Indian Bioinformatics Industry , FY&rsquo;2007-FY&rsquo;2013</li>
<li>Market segmentation of India bioinformatics industry by application by sectors, FY&rsquo;2007-FY&rsquo;2013</li>
<li>Market Segmentation of India bioinformatics industry by products and services,FY&rsquo;2007-FY&rsquo;2013</li>
<li>Market Segmentation of India bioinformatics industry by applications of bioinformatics ,FY&rsquo;2007-FY&rsquo;2013</li>
<li>India bioinformatics industry trends and developments</li>
<li>Government regulations and initiatives of India bioinformatics industry</li>
<li>Major bioinformatics research institutes in India</li>
<li>Market Share of leading players in bioinformatics industry in India,FY&rsquo;2013</li>
<li>Company profiles of major players in India bioinformatics industry</li>
<li>Future outlook and projections on the basis of revenue in India bioinformatics market, FY&rsquo;2014-FY&rsquo;2018</li>
</ul>
<p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;(Source: Ken Research)</p><p>Address of the bookmark: <a href="http://www.kenresearch.com/healthcare/biotechnology/india-bioinformatics-industry-research-report/392-91.html" rel="nofollow">http://www.kenresearch.com/healthcare/biotechnology/india-bioinformatics-industry-research-report/392-91.html</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4212/eivind-hovigs-lab</guid>
  <pubDate>Tue, 03 Sep 2013 19:06:29 -0500</pubDate>
  <link></link>
  <title><![CDATA[Eivind Hovig's Lab]]></title>
  <description><![CDATA[
<p>Bioinformatics relevant research topics are:</p>

<p>genomic scale studies<br />endogenous mechanisms of mutations, germ line and somatic <br />computational aspects of immunology in cancer <br />signalling networks<br />three-dimensional organization of information in the nucleus<br />gene silencing<br />metastatic cross-talk<br />kinase signaling<br />personalized medicine<br />detection of biomarkers in cancer <br />historical DNA variation</p>

<p>From : http://www.ous-research.no/hovig/</p>

<p>Group address:<br />Eivind Hovig, The Norwegian Radium Hospital, Montebello, 0310 Oslo,Norway<br />Email: ehovig@radium.uio.no</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/87/linux-cheat-sheet</guid>
	<pubDate>Tue, 09 Jul 2013 17:30:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/87/linux-cheat-sheet</link>
	<title><![CDATA[Linux Cheat Sheet]]></title>
	<description><![CDATA[<p><span>In an attempt to find a good Linux reference for bioinformatician and BOL readers, I was unsuccessful at finding a decent one on the Internet. So, we decided to make a cheat sheet for biological programmers.</span></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/87" length="81260" type="application/pdf" />
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/6130/rna-bioinformatics-and-high-throughput-analysis-jena</guid>
  <pubDate>Sat, 09 Nov 2013 20:03:56 -0600</pubDate>
  <link></link>
  <title><![CDATA[RNA Bioinformatics and High Throughput Analysis Jena]]></title>
  <description><![CDATA[
<p>Research Topics:</p>

<p>High Throughput Sequencing Analysis<br />Comparative Genomics<br />Identification and Annotation of Non-coding RNAs<br />Bioinformatic Analysis and System Biology of Viruses<br />Coevolution of Proteins and RNAs<br />Algorithmic Bioinformatics<br />Phylogenetic Analysis</p>

<p>http://www.rna.uni-jena.de/index.php</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/396/bioinformatics-introduction-to-perl</guid>
	<pubDate>Thu, 11 Jul 2013 09:49:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/396/bioinformatics-introduction-to-perl</link>
	<title><![CDATA[Bioinformatics: Introduction to PERL]]></title>
	<description><![CDATA[<p>This course is aimed at those new to programming and provides an introduction to programming using <strong>Perl</strong>. By the end of this course, attendees should be able to write simple <strong>Perl</strong> programs and to understand more complex <strong>Perl</strong> programs written by others. The course will be taught using the online <a href="http://sofiarobb.com/learning-perl-toc/" title="http://sofiarobb.com/learning-perl-toc/">Learning Perl</a> materials created by <a href="http://stajich.bioinformatics.ucr.edu/members/sofia-robb" title="http://stajich.bioinformatics.ucr.edu/members/sofia-robb">Sofia Robb</a> of the <a href="http://www.ucr.edu/" title="http://www.ucr.edu/">University of California Riverside</a>. Further information is <a href="http://ruddles.bio.cam.ac.uk/%7Edpjudge/Descriptions/PERL.php" title="http://ruddles.bio.cam.ac.uk/~dpjudge/Descriptions/PERL.php">available</a>.</p>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
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