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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36806?offset=40</link>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45212/assistant-professor-in-rapid-marine-adaptation-uvienna</guid>
  <pubDate>Mon, 03 Aug 2026 06:52:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor in Rapid Marine Adaptation @ UVienna]]></title>
  <description><![CDATA[
<p>The University of Vienna invites applications for a Tenure Track Professorship in the field of Rapid Marine Adaptation. We seek a scientist with an outstanding record in marine evolutionary genomics who investigates rapid evolutionary responsesâ€”such as evolutionary rescueâ€”through field studies and/or experimental evolution in the laboratory. Preferred model systems should be eukaryotic marine organisms that have vital roles in oceanic or coastal ecosystems. The successful candidate will cooperate with physiologists, ecologists, biochemists, systems biologists and evolutionary biologists in Vienna to link genomic targets of selection to organismal phenotypes and local environmental conditions. This integrative work will advance mechanistic understanding and predictive modeling of rapid adaptation to climate change in marine environments and inform effective marine conservation strategies across Europe.<br />For more information see: https://jobs.univie.ac.at/job/Tenure-Track-Professorship-in-Rapid-Marine-Adaptation/1417563233/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/2518/genome-browsers</guid>
	<pubDate>Fri, 16 Aug 2013 19:04:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/2518/genome-browsers</link>
	<title><![CDATA[Genome Browsers]]></title>
	<description><![CDATA[<p>Genome Browser is the platform/database used for searching and retreiving sequences and annotation of genomes belong to various eukaryotes, prokaryotes, etc.</p><p>Following are the weblink for different available browsers:</p><p><a href="http://www.ensembl.org/index.html">http://www.ensembl.org/index.html</a></p><p><a href="http://ensemblgenomes.org/">http://ensemblgenomes.org/</a></p><p><a href="http://genome.ucsc.edu/">http://genome.ucsc.edu/</a></p><p><a href="http://www.ncbi.nlm.nih.gov/genome">http://www.ncbi.nlm.nih.gov/genome</a></p><p><a href="http://www.ebi.ac.uk/genomes/">http://www.ebi.ac.uk/genomes/</a></p><p><a href="http://flybase.org/">http://flybase.org/</a></p><p><a href="http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi">http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi</a></p><p><a href="http://www.sanger.ac.uk/resources/databases/">http://www.sanger.ac.uk/resources/databases/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4164/two-major-breakthrough</guid>
	<pubDate>Mon, 02 Sep 2013 10:18:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4164/two-major-breakthrough</link>
	<title><![CDATA[Two major breakthrough!!]]></title>
	<description><![CDATA[<p>"Scientists in Uruguay in colloboration with European partners sequenced the genome of the high-value Tannat grape, from which "the most healthy of red wines" are fermented.</p><p>A quick, $1 syphilis&nbsp;test in development by researchers from UNU-BIOLAC."</p><p><strong>Source</strong>:</p><p><a href="http://www.sciencedaily.com/releases/2013/09/130902101846.htm">http://www.sciencedaily.com/releases/2013/09/130902101846.htm</a></p><p><a href="http://www.eurekalert.org/pub_releases/2013-09/tca-ssg082613.php">http://www.eurekalert.org/pub_releases/2013-09/tca-ssg082613.php</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/9032/encode-sequencing-data-freely-available-to-download-and-use-for-academic-means</guid>
	<pubDate>Thu, 13 Mar 2014 18:18:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/9032/encode-sequencing-data-freely-available-to-download-and-use-for-academic-means</link>
	<title><![CDATA[Encode sequencing data freely available to download and use for academic means]]></title>
	<description><![CDATA[<p>In <span style="text-decoration: underline;"><strong>Encode</strong></span>,&nbsp;<span>regulatory elements investigated via DNA hypersensitivity assays, assays of DNA methylation, and chromatin immunoprecipitation (ChIP) of proteins that interact with DNA, including modified histones and transcription factors, followed by sequencing (ChIP-Seq).</span></p>
<p><span>More information:</span></p>
<p><span>https://genome.ucsc.edu/ENCODE/pilot.html</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://genome.ucsc.edu/ENCODE/" rel="nofollow">https://genome.ucsc.edu/ENCODE/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10238/tsetse-fly-genome-sequenced</guid>
	<pubDate>Fri, 25 Apr 2014 10:48:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10238/tsetse-fly-genome-sequenced</link>
	<title><![CDATA[Tsetse Fly Genome sequenced]]></title>
	<description><![CDATA[<p><span><span>As it&nbsp;</span><a href="http://www.sciencemag.org/content/344/6182/380" target="_blank">reported online today</a><span>&nbsp;in&nbsp;</span><em>Science</em><span>, the team used several sequencing approaches to tackle the tsetse fly's 366 million base genome.</span></span></p><p><span>The current study, and companion articles slated to appear in&nbsp;</span><em>PLOS One</em><span>,&nbsp;</span><em>PLOS Genetics</em><span>, and&nbsp;</span><em>PLOS Neglected Tropic Diseases</em><span>, are the result of &nbsp;nearly 150 researchers based in 18 countries.</span></p><p><span>Source:</span></p><p><span>http://www.genomeweb.com/sequencing/international-team-sequences-tsetse-fly-genome</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/10739/science-for-life-laboratory-scilifelab-sweden</guid>
  <pubDate>Sat, 10 May 2014 06:22:30 -0500</pubDate>
  <link></link>
  <title><![CDATA[Science for Life Laboratory (SciLifeLab)-Sweden]]></title>
  <description><![CDATA[
<p>Science for Life Laboratory (SciLifeLab) is a national center for molecular biosciences with focus on health and environmental research. The center combines frontline technical expertise with advanced knowledge of translational medicine and molecular bioscience. SciLifeLab is a national resource and a collaboration between four universities: Karolinska Institutet, KTH Royal Institute of Technology, Stockholm University and Uppsala University.</p>

<p>Webpage : https://www.scilifelab.se/about-us/<br />Opportunity: https://www.scilifelab.se/about-us/career/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/11644/mirna-database-and-tools</guid>
	<pubDate>Mon, 09 Jun 2014 07:58:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/11644/mirna-database-and-tools</link>
	<title><![CDATA[miRNA database and tools]]></title>
	<description><![CDATA[<p>Since few years miRNA has shown to play important role in therapeutic related research and also known to play vital role in controlling gene expression specifically at transcriptional and post-transcription levels. Here are some important DBs and tools related with miRNA:</p><p><strong>miRNA Sequencing data analysis</strong> :&nbsp;http://tools.genxpro.net/omiras/</p><p><strong>miRNApath( R based tool)&nbsp;</strong>: &nbsp;<a href="http://www.bioconductor.org/packages/release/bioc/html/miRNApath.html">http://www.bioconductor.org/packages/release/bioc/html/miRNApath.html</a></p><p><strong>miRWalk DB</strong> :&nbsp;http://www.umm.uni-heidelberg.de/apps/zmf/mirwalk/</p><p><strong>TargetScanHuman</strong> :&nbsp;http://www.targetscan.org/</p><p><strong>RNAhybrid</strong> :&nbsp;http://bibiserv.techfak.uni-bielefeld.de/rnahybrid/welcome.html</p><p><strong>RNA22 predictor</strong> :&nbsp;http://cbcsrv.watson.ibm.com/rna22.html</p><p><strong>miRNA predictor</strong> :&nbsp;http://www.microrna.org/microrna/home.do</p><p><strong>Plant miRNA DB</strong> :http://bioinformatics.cau.edu.cn/PMRD/</p><p><strong>miRBASE DB</strong>:&nbsp;http://www.mirbase.org/</p><p><strong>Plant RNA predictor</strong> : http://plantgrn.noble.org/psRNATarget/</p><p><strong>miRNA Interaction DB</strong> :&nbsp;http://starbase.sysu.edu.cn/</p><p><strong>Sequencing based miRNA DB</strong> :&nbsp;http://mirgator.kobic.re.kr/</p><p><strong>predicted A-to-I edited miRNA DB </strong>:&nbsp;http://microrna.osumc.edu/mireditar/</p><p><strong>Animal, plant and virus miRNA DB</strong> :&nbsp;http://lemur.amu.edu.pl/share/php/mirnest/</p><p><strong>Atlantic Salmon&nbsp;miRNAs DB </strong>:<strong>&nbsp;</strong>http://www.molgenv.com/ssa_mirnas_db_home.php</p><p><strong>miRNA prediction on UTRs</strong> :&nbsp;http://genie.weizmann.ac.il/pubs/mir07/mir07_prediction.html</p><p><span style="text-decoration: underline;"><strong>Idea of analysing miRNA Sequencing data</strong></span> :</p><p>http://www.illumina.com/applications/epigenetics/small_rna_analysis.ilmn</p><p><strong>More:</strong></p><p><a href="http://www.bioconductor.org/help/search/index.html?q=miRNA+target">http://www.bioconductor.org/help/search/index.html?q=miRNA+target</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/23167/graphmap-a-highly-sensitive-and-accurate-mapper-for-long-error-prone-reads</guid>
	<pubDate>Mon, 06 Jul 2015 08:46:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/23167/graphmap-a-highly-sensitive-and-accurate-mapper-for-long-error-prone-reads</link>
	<title><![CDATA[GraphMap - A highly sensitive and accurate mapper for long, error-prone reads]]></title>
	<description><![CDATA[<p>GraphMap is a novel mapper targeted at aligning long, error-prone third-generation sequencing data.<br>It is&nbsp;<strong>designed to handle Oxford Nanopore MinION 1d and 2d reads</strong>&nbsp;with very high sensitivity and accuracy, and also presents a significant improvement over the state-of-the-art for PacBio read mappers.</p>
<p>GraphMap was also designed for ease-of-use: the&nbsp;<strong>default parameters</strong>&nbsp;can handle a wide range of read lengths and error profiles, including:&nbsp;<em>Illumina</em>,&nbsp;<em>PacBio</em>&nbsp;and&nbsp;<em>Oxford Nanopore</em>.<br>This is an especially important feature for technologies where the error rates and error profiles can vary widely across, or even within, sequencing runs.</p>
<p><a href="http://biorxiv.org/content/early/2015/06/10/020719">http://biorxiv.org/content/early/2015/06/10/020719</a></p><p>Address of the bookmark: <a href="https://github.com/isovic/graphmap" rel="nofollow">https://github.com/isovic/graphmap</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27841/covcal-coverage-read-count-calculator</guid>
	<pubDate>Wed, 15 Jun 2016 18:08:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27841/covcal-coverage-read-count-calculator</link>
	<title><![CDATA[CovCal: Coverage / Read Count Calculator]]></title>
	<description><![CDATA[<h2>Coverage / Read Count Calculator</h2>
<h4>Calculate how much sequencing you need to hit a target depth of coverage (or vice versa).</h4>
<p><span>Instructions:</span> set the read length/configuration and genome size, then select what you want to calculate.</p>
<p>Written by <a href="http://stephenturner.us/" target="blank">Stephen Turner</a>, based on the <a href="http://www.ncbi.nlm.nih.gov/pubmed/3294162" target="_blank">Lander-Waterman formula</a>, inspired by <a href="http://core-genomics.blogspot.com/2016/05/how-many-reads-to-sequence-genome.html" target="_blank">a similar calculator</a> written by James Hadfield. Coverage is calculated as <em>C=LN/G</em> and reads as <em>N=CG/L</em> where <em>C</em> = Coverage (X),<em>L</em> = Read length (bp), <em>G</em> = Haploid genome size (bp), and <em>N</em> = Number of reads. Source code <a href="https://github.com/stephenturner/covcalc" target="_blank">on GitHub</a>.</p><p>Address of the bookmark: <a href="http://apps.bioconnector.virginia.edu/covcalc/" rel="nofollow">http://apps.bioconnector.virginia.edu/covcalc/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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