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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/18738?offset=220</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41604/synteny-and-rearrangement-identifier-syri</guid>
	<pubDate>Tue, 05 May 2020 10:37:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41604/synteny-and-rearrangement-identifier-syri</link>
	<title><![CDATA[Synteny and Rearrangement Identifier (SyRI)]]></title>
	<description><![CDATA[<p>SyRI is a comprehensive tool for predicting genomic differences between related genomes using whole-genome assemblies (WGA). The assemblies are aligned using whole-genome alignment tools, and these alignments are then used as input to SyRI. SyRI identifies syntenic path (longest set of co-linear regions), structural rearrangements (inversions, translocations, and duplications), local variations (SNPs, indels, CNVs etc) within syntenic and structural rearrangements, and un-aligned regions.</p><p>Address of the bookmark: <a href="https://schneebergerlab.github.io/syri/" rel="nofollow">https://schneebergerlab.github.io/syri/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42470/the-new-corona-variant-has-23-mutations-in-all-which-is-unusually-huge</guid>
	<pubDate>Wed, 23 Dec 2020 03:50:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42470/the-new-corona-variant-has-23-mutations-in-all-which-is-unusually-huge</link>
	<title><![CDATA[The new corona variant has 23 mutations in all, which is unusually huge !]]></title>
	<description><![CDATA[<p>The new SARS-CoV-2 version, B.1.1.7, which was first seen in the third week of September in Kent and Greater London, has since spread to other locations in the UK. According to the COVID-19 Genomics UK Consortium (COG-UK Consortium) that analysed the genome data of the virus and identified the variant, the new variant has been spreading "rapidly" over the last four weeks and has now been detected in other locations in the UK, suggesting further spread of the variant in the region.</p><p><span>According to a<span>&nbsp;</span></span><a href="https://virological.org/t/preliminary-genomic-characterisation-of-an-emergent-sars-cov-2-lineage-in-the-uk-defined-by-a-novel-set-of-spike-mutations/563"><strong><span>preliminary report</span></strong></a><span><span>&nbsp;</span>posted on December 19 by the COG-UK Consortium scientists, as of December 15, 1,623 variant genomes have been sequenced. In a<span>&nbsp;</span></span><a href="https://twitter.com/TheCGPS/status/1340749351803629569"><strong><span>December 21 tweet</span></strong></a><span>, COG-UK Consortium said that it added 2,963 more genome sequences of SARS-CoV-2, of which 942 (32%) belong to the new variant. The Consortium<span>&nbsp;</span></span><a href="https://twitter.com/CovidGenomicsUK/status/1341073233420955654"><strong><span>intends to sequence</span></strong></a><span><span>&nbsp;</span>20,000 more SARS-CoV-2 genomes in the next two weeks to further ascertain the spread of the variant.</span></p><p><span>There is no clear proof, at least not yet, that it does cause severe pandemic. But there is a justification for seriously taking the possibility. Another coronavirus lineage in South Africa has acquired one specific mutation that is also present in B.1.1.7. This variant is increasingly spreading across South Africa's coastal regions. And doctors have observed in preliminary research that individuals infected with this variant bear a higher viral load-a higher concentration of the virus in their upper respiratory tract. In many viral diseases, this is associated with more severe symptoms.</span></p><p>&nbsp;</p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/42903/katherine-belov-lab</guid>
  <pubDate>Sun, 21 Feb 2021 22:59:35 -0600</pubDate>
  <link></link>
  <title><![CDATA[Katherine Belov Lab]]></title>
  <description><![CDATA[
<p>Evolution of the adaptive immune system Marsupial and monotreme immune genes MHC Diversity and Conservation Marsupial and monotreme genomics Comparative Genomics Genetics of Tasmanian Devil facial tumour disease</p>

<p>More at https://www.sydney.edu.au/science/about/our-people/academic-staff/kathy-belov.html</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/43418/caceres-lab</guid>
  <pubDate>Sat, 02 Oct 2021 00:20:42 -0500</pubDate>
  <link></link>
  <title><![CDATA[Cáceres Lab]]></title>
  <description><![CDATA[
<p>Lab are included within the Genomics, Bioinformatics and Evolution group of the UAB, and collaborate closely with other researchers in the Barcelona area, such as Xavier Estivill of the Centre for Genomic Regulation (CRG), Juan R González of the Centre for Research in Environmental Epidemiology (CREAL), and Tomàs Marqués-Bonet of the Institute of Evolutionary Biology (IBE), as well as with other international groups and projects.</p>

<p>https://grupsderecerca.uab.cat/cacereslab/</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/44395/genomics-india-conference-2024</guid>
  <pubDate>Fri, 27 Oct 2023 05:48:11 -0500</pubDate>
  <link></link>
  <title><![CDATA[Genomics India Conference 2024 !]]></title>
  <description><![CDATA[
<p>Genomics India Conference is back and this time we are coming to Shiv<br />Nadar Intitution of Eminenece, Delhi NCR. GIC 2024 will be held from 1st<br />to 3rd of February 2024 and we are happy to send you an early invitation<br />for India's premier genomics conference.</p>

<p>GIC2024 focuses on "Advances In Genomics From AI-ML To Targeted<br />Therapies". GIC2024 encourages researchers to present original<br />contributions for poster presentations.</p>

<p>Note: Early bird registration closes on 1st December 2023.</p>

<p>Kindly, register at GIC 2024 Earlybird registartion</p>

<p>https://genomicsindia.co.in/</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/44650/manthey-research-group-%E2%80%93-evolutionary-genomics</guid>
  <pubDate>Thu, 22 Aug 2024 06:25:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[Manthey Research Group – Evolutionary Genomics]]></title>
  <description><![CDATA[
<p>We focus on fundamental questions in genomics, ecology, and evolution. Our methods include fieldwork and labwork, but most of our time is spent analyzing genomics data using computational biology approaches.</p>

<p>Ant / bacteria co-evolution, landscape genomics, and population genomics<br />Vertebrate and/or invertebrate genome evolution</p>

<p>If you might be interested in joining our research group, send an email with your intent and why this group would potentially be a good fit for your future goals along with a CV / Resume to jdmanthey (at) gmail (dot) com</p>

<p>More at https://mantheylab.org/</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/1906</guid>
	<pubDate>Sun, 11 Aug 2013 11:13:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/1906</link>
	<title><![CDATA[Compressive Genomics]]></title>
	<description><![CDATA[<p>The key to finding a solution is to notice that most&nbsp;<a href="http://www.i-programmer.info/news/181-algorithms/4537-a-new-dna-sequence-search-compressive-genomics.html">genomic</a>sequences differ by very little. It may well be that the number of complete genome sequences being stored is increasing rapidly, but the actual amount of new data is very small. In other words, a single DNA sequence isn't particularly compressible but a set of sequences shares so much in common that the redundancy can be used to store them in a much smaller storage space. (Source:e-article from&nbsp;Alex Armstrong)</p><p><a href="http://www.i-programmer.info/news/181-algorithms/4537-a-new-dna-sequence-search-compressive-genomics.html">http://www.i-programmer.info/news/181-algorithms/4537-a-new-dna-sequence-search-compressive-genomics.html</a></p><p><a href="http://en.wikipedia.org/wiki/Compression_of_Genomic_Re-Sequencing_Data">http://en.wikipedia.org/wiki/Compression_of_Genomic_Re-Sequencing_Data</a></p><p><a href="http://www.nature.com/nbt/journal/v30/n7/full/nbt.2241.html">http://www.nature.com/nbt/journal/v30/n7/full/nbt.2241.html</a></p><p><a href="http://bioinformatics.oxfordjournals.org/content/29/13/i283.full">http://bioinformatics.oxfordjournals.org/content/29/13/i283.full</a></p><p><a href="http://groups.csail.mit.edu/cb/cast/">http://groups.csail.mit.edu/cb/cast/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4197/bioinformatics-course-and-lectures</guid>
	<pubDate>Tue, 03 Sep 2013 16:41:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4197/bioinformatics-course-and-lectures</link>
	<title><![CDATA[Bioinformatics course and lectures]]></title>
	<description><![CDATA[<p><a href="http://openwetware.org/wiki/User:Jarle_Pahr/Bioinformatics">http://openwetware.org/wiki/User:Jarle_Pahr/Bioinformatics</a></p><p>Address of the bookmark: <a href="http://gtpb.igc.gulbenkian.pt/bicourses/index.html" rel="nofollow">http://gtpb.igc.gulbenkian.pt/bicourses/index.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>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6132/computational-methods-for-the-analysis-of-the-diversity-and-dynamics-of-genomes</guid>
  <pubDate>Sat, 09 Nov 2013 20:19:02 -0600</pubDate>
  <link></link>
  <title><![CDATA[Computational Methods for the Analysis of the Diversity and Dynamics of Genomes]]></title>
  <description><![CDATA[
<p>The German-Canadian international research training group</p>

<p>"Computational Methods for the Analysis of the Diversity and Dynamics of Genomes"</p>

<p>has currently open positions for graduate students, to study at Simon Fraser University (Vancouver, Canada) and <br />Bielefeld University (Germany), starting in the fall 2014.</p>

<p>This international graduate program is a close cooperation of:</p>

<p>Bielefeld University, Germany: Graduate progam "DiDy"<br />Simon Fraser University (SFU), Vancouver, Canada: Graduate program "MADD-Gen"</p>

<p>The available positions include six PhD positions at Bielefeld University, as well as PhD and MSc positions at SFU.</p>

<p>Application deadline: December 31st, 2013<br />Webpage: http://wiki.techfak.uni-bielefeld.de/didy/Announcement</p>
]]></description>
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