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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/13852?offset=0</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43643/corona-virus-literature</guid>
	<pubDate>Sun, 12 Dec 2021 23:30:56 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43643/corona-virus-literature</link>
	<title><![CDATA[Corona Virus Literature !]]></title>
	<description><![CDATA[<p><span><span>LitCovid</span>&nbsp;is a curated literature hub for tracking up-to-date scientific information about the 2019 novel Coronavirus.</span><span>&nbsp;It is the most comprehensive resource on the subject, providing a central access to&nbsp;</span><span>201482</span><span>&nbsp;(and&nbsp;</span><span>growing</span><span>) relevant articles in PubMed. The articles are updated daily and are further categorized by different research topics (e.g.&nbsp;</span><span>Long Covid</span><span>) and geographic locations for improved access. You can learn more at&nbsp;</span><a href="https://www.nature.com/articles/d41586-020-00694-1" target="_blank">Chen et al. Nature</a><span>&nbsp;(2020) or our&nbsp;</span><span>FAQ</span><span>, and download our data&nbsp;</span><a href="https://www.ncbi.nlm.nih.gov/research/coronavirus/#data-download">here</a><span>.</span></p>
<p>https://www.ncbi.nlm.nih.gov/research/coronavirus/</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/research/coronavirus/" rel="nofollow">https://www.ncbi.nlm.nih.gov/research/coronavirus/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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  <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>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/11311/stephen-friend-the-hunt-for-unexpected-genetic-heroes</guid>
	<pubDate>Sat, 31 May 2014 14:31:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/11311/stephen-friend-the-hunt-for-unexpected-genetic-heroes</link>
	<title><![CDATA[Stephen Friend: The hunt for "unexpected genetic heroes"]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/Yagdvqn2YMU" frameborder="0" allowfullscreen></iframe>What can we learn from people with the genetics to get sick — who don't? With most inherited diseases, only some family members will develop the disease, while others who carry the same genetic risks dodge it. Stephen Friend suggests we start studying those family members who stay healthy. Hear about the Resilience Project, a massive effort to collect genetic materials that may help decode inherited disorders.

TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes (or less). Look for talks on Technology, Entertainment and Design -- plus science, business, global issues, the arts and much more.
Find closed captions and translated subtitles in many languages at http://www.ted.com/translate

Follow TED news on Twitter: http://www.twitter.com/tednews
Like TED on Facebook: https://www.facebook.com/TED

Subscribe to our channel: http://www.youtube.com/user/TEDtalksDirector]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44173/mpxv-bookmarks</guid>
	<pubDate>Mon, 19 Dec 2022 01:58:20 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44173/mpxv-bookmarks</link>
	<title><![CDATA[MPXV Bookmarks]]></title>
	<description><![CDATA[<p>MPVX infection across the globe</p>
<p><a href="https://www.google.com/url?q=https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html&amp;sa=D&amp;source=docs&amp;ust=1671439883060005&amp;usg=AOvVaw39WwSqp2A5TD8KjRvaaxzW" target="_blank">https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html</a></p><p>Address of the bookmark: <a href="https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html" rel="nofollow">https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34477/computational-genomics-applied-comparative-genomics</guid>
	<pubDate>Wed, 29 Nov 2017 05:11:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34477/computational-genomics-applied-comparative-genomics</link>
	<title><![CDATA[Computational Genomics: Applied Comparative Genomics]]></title>
	<description><![CDATA[<p><span>The primary goal of the course is for students to be grounded in theory and leave the course empowered to conduct independent genomic analyses.</span><span>&nbsp;We will study the leading computational and quantitative approaches for comparing and analyzing genomes starting from raw sequencing data. The course will focus on human genomics and human medical applications, but the techniques will be broadly applicable across the tree of life. The topics will include genome assembly &amp; comparative genomics, variant identification &amp; analysis, gene expression &amp; regulation, personal genome analysis, and cancer genomics. The grading will be based on assignments, a midterm exam, class presentations, and a significant class project. There are no formal course prerequisites, although the course will require familiarity with UNIX scripting and/or programming to complete the assignments and course project.</span></p><p>Address of the bookmark: <a href="https://github.com/schatzlab/appliedgenomics" rel="nofollow">https://github.com/schatzlab/appliedgenomics</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41493/coronavirus-resources</guid>
	<pubDate>Wed, 25 Mar 2020 17:11:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41493/coronavirus-resources</link>
	<title><![CDATA[Coronavirus Resources !]]></title>
	<description><![CDATA[<p><span>2019nCoVR features comprehensive integration of genomic and proteomic sequences as well as their metadata information from the GISAID, NCBI, NMDC and CNCB/NGDC. It also incorporates a wide range of relevant information including scientific literatures, news, and popular articles for science dissemination, and provides visualization functionalities for genome variation analysis results based on all collected 2019-nCoV strains.</span></p>
<p><span>Annotation</span></p>
<p><span><a href="https://bigd.big.ac.cn/ncov/variation/annotation">https://bigd.big.ac.cn/ncov/variation/annotation</a></span></p>
<p><span>Genome wharehouse&nbsp;</span></p>
<p><span><a href="https://bigd.big.ac.cn/gwh/browse/index">https://bigd.big.ac.cn/gwh/browse/index</a></span></p>
<p>Released Genome</p>
<p><a href="https://bigd.big.ac.cn/ncov/release_genome">https://bigd.big.ac.cn/ncov/release_genome</a></p>
<p>Download data&nbsp;</p>
<p><a href="ftp://download.big.ac.cn/Genome/Viruses/Coronaviridae/">ftp://download.big.ac.cn/Genome/Viruses/Coronaviridae/</a></p>
<p>Raw data</p>
<p><a href="https://bigd.big.ac.cn/gsa/browse/run/?tag=Coronaviridae">https://bigd.big.ac.cn/gsa/browse/run/?tag=Coronaviridae</a></p><p>Address of the bookmark: <a href="https://bigd.big.ac.cn/ncov/about" rel="nofollow">https://bigd.big.ac.cn/ncov/about</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/42707/bioinformatics-in-africa-part-1</guid>
	<pubDate>Sun, 31 Jan 2021 09:04:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/42707/bioinformatics-in-africa-part-1</link>
	<title><![CDATA[Bioinformatics in Africa:- Part 1]]></title>
	<description><![CDATA[<p>The Institut Pasteur de C&ocirc;te d&rsquo;Ivoire was created by the N&deg;72&shy;511 law of July 27th, 1972 under the Presidency of his Excellency Felix Houphou&euml;t Boigny and Professor Jacques Monod, then Leading of&nbsp;the&nbsp;Pasteur&nbsp;institute&nbsp;of&nbsp;Paris.</p><p>The&nbsp;objectives&nbsp;of&nbsp;the&nbsp;Bioinformatics&nbsp;pole&nbsp;are:</p><p>&bull; Encourage the access to innovations in research and the best exploitation of research data management.</p><p>&bull; Develop&nbsp;the&nbsp;critical&nbsp;spirit&nbsp;of&nbsp;the&nbsp;researchers&nbsp;around&nbsp;their&nbsp;axis&nbsp;of&nbsp;research.</p><p>&bull; Bring an active help to the improvement of the public health while having for constant worries&nbsp;to&nbsp;feed&nbsp;it&nbsp;by&nbsp;research&nbsp;and&nbsp;the&nbsp;innovation.&nbsp;</p><p>&bull; Start&nbsp;training&nbsp;researchers&nbsp;to&nbsp;use&nbsp;bioinformatics&nbsp;as&nbsp;an&nbsp;indispensable&nbsp;tool&nbsp;to&nbsp;research.</p><p>&bull; Encourage interdisciplinary creating a network of scientific information available to the researchers&nbsp;of&nbsp;the&nbsp;institute&nbsp;and&nbsp;partners</p><p>Long&shy;term&nbsp;training&nbsp;activities:</p><p>&bull; To&nbsp;integrate&nbsp;the&nbsp;bioinformatics&nbsp;in&nbsp;the&nbsp;training&nbsp;programs&nbsp;of&nbsp;academic&nbsp;scientists.</p><p>&bull; Development&nbsp;of&nbsp;West&nbsp;Africa&nbsp;Centre&nbsp;training&nbsp;in&nbsp;bioinformatics&nbsp;and&nbsp;genome&nbsp;data&nbsp;analysis.</p><p>Short&shy;term&nbsp;training&nbsp;activities:</p><p>The IPCI will organize in the month of May 2007 a yearly regional course of initiation and using genome data analysis with the participation of the Centre Biotechnologique de Sfax, Tunisia (Pr Ahmed&nbsp;Reba&iuml;,&nbsp;Department&nbsp;of&nbsp;bioinformatics).</p><p>More at&nbsp;https://www.pasteur.ci/</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4100/should-you-get-sequenced-not-all-bad-genes-predict-disease</guid>
	<pubDate>Thu, 29 Aug 2013 15:10:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4100/should-you-get-sequenced-not-all-bad-genes-predict-disease</link>
	<title><![CDATA[Should you get sequenced? Not all bad genes predict disease]]></title>
	<description><![CDATA[<p><span>&ldquo;What we really don&rsquo;t know yet is whether the predictive aspects of the genome are going to turn out to be beneficial or potentially harmful&rdquo;</span></p>
<p><span><span>&ldquo;As we roll out genomic medicine we are fighting against this society-wide misconception that having the bad gene means you&rsquo;re going to get the disease. That&rsquo;s only true in a very few cases.&rdquo;</span></span></p>
<p><span><span><strong>Source</strong>:Today Health</span></span></p><p>Address of the bookmark: <a href="http://www.today.com/health/should-you-get-sequenced-not-all-bad-genes-predict-disease-8C11017154" rel="nofollow">http://www.today.com/health/should-you-get-sequenced-not-all-bad-genes-predict-disease-8C11017154</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/4961/genetics-epigenetics-and-disease</guid>
	<pubDate>Fri, 27 Sep 2013 11:32:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/4961/genetics-epigenetics-and-disease</link>
	<title><![CDATA[Genetics, epigenetics and disease]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/SHpfkNRscOc" frameborder="0" allowfullscreen></iframe>Royal Society GlaxoSmithKline Prize Lecture given by Professor Adrian Bird CBE FMedSci FRS on Tuesday 22 January 2013.

Adrian Bird CBE FMedSci FRS is the Buchanan Chair of Genetics at the University of Edinburgh.

The human genome sequence has been available for more than a decade, but its significance is still not fully understood. While most human genes have been identified, there is much to learn about the DNA signals that control them. This lecture described an unusually short DNA sequence, just two base pairs long, CG, which occurs in several chemically different forms. Defects in signalling by CG are implicated in disease. For example, the autism spectrum disorder Rett syndrome is caused by loss of a protein that reads methylated CG and affects the activity of genes.

The Royal Society GlaxoSmithKline Prize Lecture is awarded for original contributions to medical and veterinary sciences published within ten years from the date of the award.]]></description>
	
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/861/fiona-brinkman-laboratory</guid>
  <pubDate>Sun, 14 Jul 2013 12:46:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Fiona Brinkman Laboratory]]></title>
  <description><![CDATA[
<p>Infectious disease control needs to be made more “sustainable”. We need to reduce selective pressure on pathogens to evolve antibiotic resistance. We need to control infectious disease outbreaks and associated immune disorders with a better understanding of the genetic,  environmental and social factors that impact disease spread and severity.</p>

<p>Research Area</p>

<p>Investigating the role in disease of both the microbe and its host (i.e immune system failure), using genomics and systems biology-based approaches<br />Using genomics and network analysis to characterize disease outbreaks and their environmental/social/genetic causes, and<br />Identifying new anti-infective and immune modulating therapies/biomarkers.</p>

<p>Link @ http://www.brinkman.mbb.sfu.ca/</p>
]]></description>
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