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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37574?offset=210</link>
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<item>
  <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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<item>
	<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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/19560/alien-genome</guid>
	<pubDate>Sat, 13 Dec 2014 00:24:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/19560/alien-genome</link>
	<title><![CDATA[Alien Genome !!!]]></title>
	<description><![CDATA[<p>Genome sequencing, analysis and expression of Alien genome.</p><p>Note: This image/cartoon is create only for fun. It has nothing to do with any scientific findings.</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/19560" length="40389" type="image/jpeg" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32862/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</guid>
	<pubDate>Fri, 19 May 2017 07:44:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32862/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</link>
	<title><![CDATA[GAM-NGS: genomic assemblies merger for next generation sequencing]]></title>
	<description><![CDATA[<p><span>GAM-NGS is a tool able to merge two or more assemblies in order to improve contiguity and correctness. It can be used on all NGS-based assembly projects and it shows its full potential with multi-library Illumina-based projects. With more than 20 available assemblers it is hard to select the best tool. In this context we propose a tool that improves assemblies (and, as a by-product, perhaps even assemblers) by merging them and selecting the generating that is most likely to be correct.</span></p><p>Address of the bookmark: <a href="https://github.com/vice87/gam-ngs" rel="nofollow">https://github.com/vice87/gam-ngs</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41452/apollo-a-sequencing-technology-independent-scalable-and-accurate-assembly-polishing-algorithm</guid>
	<pubDate>Mon, 16 Mar 2020 10:09:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41452/apollo-a-sequencing-technology-independent-scalable-and-accurate-assembly-polishing-algorithm</link>
	<title><![CDATA[Apollo: A Sequencing-Technology-Independent, Scalable, and Accurate Assembly Polishing Algorithm]]></title>
	<description><![CDATA[<p><span>Apollo is an assembly polishing algorithm that attempts to correct the errors in an assembly. It can take multiple set of reads in a single run and polish the assemblies of genomes of any size. Described by Firtina et al. (preliminary version at&nbsp;</span><a href="https://arxiv.org/pdf/1902.04341.pdf">https://arxiv.org/pdf/1902.04341.pdf</a></p>
<p>More at&nbsp;<a href="https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa179/5804978?rss=1">https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa179/5804978?rss=1</a></p><p>Address of the bookmark: <a href="https://github.com/CMU-SAFARI/Apollo" rel="nofollow">https://github.com/CMU-SAFARI/Apollo</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4210/uni-computing-bergen-norway</guid>
  <pubDate>Tue, 03 Sep 2013 18:40:50 -0500</pubDate>
  <link></link>
  <title><![CDATA[Uni Computing Bergen Norway]]></title>
  <description><![CDATA[
<p>Info on Uni Computing (Webpage: http://www.bccs.uni.no/) :</p>

<p>Uni Computing (formerly Uni BCCS) is a department of Uni Research, affiliated with the University of Bergen.</p>

<p>5 groups in this lab works on computational resources, methods, algorithms, and software.</p>

<p>Following two bioinformatics groups are:</p>

<p>The Computational Biology Unit (CBU) provides education and research in bioinformatics focused on functional genomics.</p>

<p>The Computational Ecology Unit (CEU) is basically deal with population fluctuations, behavioural patterns and the ways life cycles emerge.</p>
]]></description>
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<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/news/view/2991/illumina-reveals-first-dataset-of-long-reads</guid>
	<pubDate>Fri, 23 Aug 2013 06:29:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/2991/illumina-reveals-first-dataset-of-long-reads</link>
	<title><![CDATA[Illumina reveals first dataset of long reads]]></title>
	<description><![CDATA[<p>With the help of Moleculo technology , acquired by Illumina releases new service for long reads sequencing i.e., &nbsp;<a href="http://www.illumina.com/services/long-read-sequencing-service.ilmn">FastTrack Long Reads</a>.</p><p>Average read length is around<span>&nbsp;8,500 base pairs in release dataset.</span>&nbsp;Best thing about this, there is not much effect on cost and quality of data.</p><p>You can also check following pages for publications on long reads and more:</p><p><a href="http://www.illumina.com/services/long-read-sequencing-service.ilmn">http://www.illumina.com/services/long-read-sequencing-service.ilmn</a></p><p><a href="http://blog.basespace.illumina.com/2013/07/22/first-data-set-from-fasttrack-long-reads-early-access-service/">http://blog.basespace.illumina.com/2013/07/22/first-data-set-from-fasttrack-long-reads-early-access-service/</a></p><p>&nbsp;</p><p>&nbsp;</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>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4591/the-breitbart-lab</guid>
  <pubDate>Tue, 17 Sep 2013 18:19:49 -0500</pubDate>
  <link></link>
  <title><![CDATA[The Breitbart lab]]></title>
  <description><![CDATA[
<p>Breitbart’s lab has created a new branch of biology called metagenomics in which one can sample and sequence genetic material collected from the environment.</p>

<p>Breitbart lab is located in the College of Marine Science at the University of South Florida. She is chosen as top "10 Brilliant" scientist by Popular Science magazine.<br />http://www.popsci.com/science/article/2013-09/mya-breitbart</p>

<p>Lab Link:<br />https://sites.google.com/site/breitbartgenomicslab/<br />http://www.marine.usf.edu/faculty/mya-breitbart.shtml</p>
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