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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/34914?offset=380</link>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25302/ra-bioinformatics-at-jamia-hamdard</guid>
  <pubDate>Sat, 28 Nov 2015 03:37:36 -0600</pubDate>
  <link></link>
  <title><![CDATA[RA Bioinformatics at Jamia Hamdard]]></title>
  <description><![CDATA[
<p>Research Associate, Bioinformatics Facility<br />Jamia Hamdard - New Delhi, Delhi<br />Research Associate, Bioinformatics Facility, Jamia Hamdard.<br />Emoluments: Rs. 22,000 + HRA 30%<br />Qualification: PhD or equivalent or having 3 years of research, teaching and design and development experience after M. Pharm./M.VSc./M.E./M.Tech. PhD in life sciences and related areas with experience in Bioinformatics may apply. Company Info.<br />Jamia Hamdard</p>

<p>Jamia Hamdard New Delhi - 110062 Additional Information States &amp; U.T State &amp; Union Territories Delhi How To Apply Apply Details<br />Last date of application: December 5, 2015 Web/Notification URL http://www.jamiahamdard.ac.in/</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/26335/ra-at-central-university-of-rajasthan</guid>
  <pubDate>Tue, 09 Feb 2016 03:53:35 -0600</pubDate>
  <link></link>
  <title><![CDATA[RA at Central University of Rajasthan]]></title>
  <description><![CDATA[
<p>Research Fellow Bioinformatics</p>

<p>Eligibility : MSc(Bio-Chemistry, Bio-Informatics, Bio-Tech)</p>

<p>Location : Ajmer</p>

<p>Last Date : 13 Feb 2016</p>

<p>Hiring Process : Face to Face Interview<br />Central University of Rajasthan</p>

<p>Research Fellow Job vacancies in Central University of Rajasthan</p>

<p>Project Title : “Development of natural product derived febrifugine ananlogues as a novel therapeutics against visceral leishmaniasis”</p>

<p>No. of Post : 01</p>

<p>Qualification : Master of Biochemistry, Biotechnology, Bioinformatics and related biological sciences with minimum 55%, Age limit as per government rule.</p>

<p>Desirable Experience : Candidates with experience in cell culture, Chemoinformatics, and Parasitology will be preferred.    </p>

<p>Fellowship : Rs. 25,000/- p.m. consolidated for NET qualified (14,000/- p.m. consolidated for Non-NET)<br />How to apply</p>

<p>The candidates may apply on a plain paper, along with their curriculum vitae (including name, date of birth, academic qualification starting from 10th class, summary of research experience, email id, phone number and passport size photograph) and email to vkprajapati@curaj.ac.in or post the hard copy to the Dr. Vijay Kumar Prajapati PI, DST-SERB Project (YSS/2015/000716), Department of Biochemistry, School of Life Sciences, Central University of Rajasthan, Bandarsindri, Dist- Ajmer, Rajasthan, 305 817 on or before 13th February 2016.</p>

<p>More at http://www.curaj.ac.in/Default.aspx?PageId=241</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28546/ra-bioinformatics-at-national-bureau-of-fish-genetic-resources</guid>
  <pubDate>Mon, 25 Jul 2016 03:14:06 -0500</pubDate>
  <link></link>
  <title><![CDATA[RA Bioinformatics at  National Bureau of Fish Genetic Resources]]></title>
  <description><![CDATA[
<p>F.No. 1(16)/2016-Admn. (DBT-BBSRC Project)<br />Research Associate /JRF Biotechnology Job vacancies in National Bureau of Fish Genetic Resources on contract basis</p>

<p>Research Associate /01 Post</p>

<p>Essential: Ph.D. in Bioinformatics or 03 years research experience after Post Graduation in Bioinformatics with at least one research paper in Science Citation Indexed (SCI) journals.</p>

<p>Desirable:  The candidate should have at least 1st Division during Graduation and Post Graduation.  Experience in assembly/ analysis/ annotation of genomic/transcriptomic data generated on next generation sequencing platforms and working knowledge on different genomic softwares.  Publications in Relevant Field.</p>

<p>Pay Scale : Rs. 36,000/- +20% HRA </p>

<p>Age: 40 years for male and 45 years for female candidates, as on the date of interview</p>

<p>Junior Research Fellow/ 01 </p>

<p>Essential: Master Degree in Biotechnology/Life Science with Specialization in Molecular Biology with NET qualification. </p>

<p>Desirable:  Research Experience in Molecular Biology. 1st Division during Graduation as well as Post Graduation. Publications in Relevant Field.</p>

<p>Pay Scale: Rs. 25,000/-+ 20% HRA for 1st and 2nd year and Rs. 28,000/-+ 20% HRA for 3rd year</p>

<p>Age: 35 years for male and 40 years for female candidates, as on the date of interview.<br />How to apply<br />A walk-in-interview will be held on 26.07.2016 at 10:00 hrs. at ICAR-National Bureau of Fish Genetic Resources, Lucknow.</p>

<p>More at http://www.nbfgr.res.in/Recruitments.aspx</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/30331/16th-congress-of-the-european-society-for-evolutionary-biology-eseb</guid>
  <pubDate>Thu, 22 Dec 2016 08:08:37 -0600</pubDate>
  <link></link>
  <title><![CDATA[16th Congress of the European Society for Evolutionary Biology (ESEB)]]></title>
  <description><![CDATA[
<p>Abstract submissions for our upcoming symposium on the Genomics of Adaptation that will take place as part of the 16th Congress of the European Society for Evolutionary Biology (ESEB). The conference will take place from August 20th - August 25th, 2017 in Groningen, the Netherlands. </p>

<p>SYMPOSIUM DESCRIPTION: Genomics of Adaptation [S16] Model organisms for life-history research are mainly studied in the lab where functional genetics is assessable. In general, however, knowledge about their eco-evolutionary dynamics, such as biotic interactions, is rare. By contrast, in organisms for which the ecology and adaptation strategies in the field are well known, we typically lack the appropriate genetic tools to investigate functionality. Advances in genomics and statistics as well as investments in evolutionary model organisms are now providing access to putatively adaptive genome-wide variation within species from across the tree of life. In this symposium, we focus on integrating life-history biology, genetics and evolutionary ecology in the genomics era. </p>

<p>We wish to (1) highlight the role of genetic architecture of complex traits, such as adaptations to biotic interactions or life-history traits; (2) contrast this to morphological traits which are generally thought to have a less complex genetic architecture; and (3) discuss the opportunities and drawbacks of specific model systems. </p>

<p>INVITED SPEAKERS: Josephine Pemberton, University of Cambridge (http://bit.ly/2hJWytJ ) Peter Tiffin, University of Minnesota (http://bit.ly/2hK7HuS ) </p>

<p>ABSTRACT SUBMISSION The deadline for abstract submission is January 10, 2017. For more information and to submit abstracts online, please visit: http://bit.ly/2fBXlvN We look forward to an exciting symposium and seeing you all in Groningen! Sincerely, Ben Blackman, UC Berkeley Maaike de Jong, University of Bristol Bart Pannebakker, Wageningen University Noah Whiteman, UC Berkeley Jelle Zandveld, Wageningen University</p>
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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/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</guid>
	<pubDate>Tue, 03 Sep 2013 18:00:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</link>
	<title><![CDATA[Latest paper on comparison of mapping tools]]></title>
	<description><![CDATA[<p>A. Hatem, D. Bozdag, A. E. Toland, U. V. Catalyurek "Benchmarking short sequence mapping tools" BMC Bioinformatics, 14(1):184, 2013.</p>
<p>http://bmi.osu.edu/hpc/software/benchmark/</p>
<p><a href="http://bmi.osu.edu/hpc/software/pmap/pmap.html">http://bmi.osu.edu/hpc/software/pmap/pmap.html</a></p>
<p>Other similiar papers:</p>
<p><a href="http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022">http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022</a></p>
<p><a href="http://bioinformatics.oxfordjournals.org/content/28/24/3169">http://bioinformatics.oxfordjournals.org/content/28/24/3169</a></p>
<p>Some new Mapping tool links:<a href="http://bmi.osu.edu/hpc/software/benchmark/"></a></p>
<p><strong>GSNAP</strong></p>
<p><a href="http://research-pub.gene.com/gmap/"></a><a href="http://research-pub.gene.com/gmap/">http://research-pub.gene.com/gmap/</a></p>
<p><strong>RMAP</strong></p>
<p><a href="http://rulai.cshl.edu/rmap/"></a><a href="http://rulai.cshl.edu/rmap/">http://rulai.cshl.edu/rmap/</a></p>
<p><strong>mrsFAST</strong></p>
<p><a href="http://mrsfast.sourceforge.net/Home"></a><a href="http://mrsfast.sourceforge.net/Home">http://mrsfast.sourceforge.net/Home</a></p>
<p><a href="http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/">http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/</a></p>
<p><strong>BFAST</strong></p>
<p><a href="http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page">http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page</a></p>
<p><strong>SHRiMP (for&nbsp;AB SOLiD color-space reads)</strong></p>
<p><a href="http://compbio.cs.toronto.edu/shrimp/">http://compbio.cs.toronto.edu/shrimp/</a></p>
<p><strong>RazerA 3</strong></p>
<p><a href="http://www.seqan.de/projects/razers/">http://www.seqan.de/projects/razers/</a></p><p>Address of the bookmark: <a href="http://www.biomedcentral.com/1471-2105/14/184" rel="nofollow">http://www.biomedcentral.com/1471-2105/14/184</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10093/bio-rad-acquires-gnubio</guid>
	<pubDate>Sat, 19 Apr 2014 10:36:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10093/bio-rad-acquires-gnubio</link>
	<title><![CDATA[Bio-Rad Acquires GnuBIO]]></title>
	<description><![CDATA[<p>http://www.businesswire.com/news/home/20140411005331/en/Bio-Rad-Acquires-GnuBIO-Developer-Droplet-Based-DNA-Sequencing#.U1KXnPm1b8o</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10246/deadly-human-pathogen-cryptococcus-sequenced</guid>
	<pubDate>Fri, 25 Apr 2014 11:02:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10246/deadly-human-pathogen-cryptococcus-sequenced</link>
	<title><![CDATA[Deadly Human Pathogen Cryptococcus  Sequenced]]></title>
	<description><![CDATA[<p><span>"Now, researchers have sequenced the entire genome and all the RNA products of the most important pathogenic lineage of Cryptococcus neoformans, a strain called H99. The results, which appear in&nbsp;</span><em>PLOS Genetics</em><span>, also describe a number of genetic changes that can occur after laboratory handling of H99 that make it more susceptible to stress, hamper its ability to sexually reproduce and render it less virulent."</span></p><p><span><strong>Source</strong>:</span></p><p><span>http://www.biosciencetechnology.com/news/2014/04/deadly-human-pathogen-cryptococcus-fully-sequenced</span></p><p><span><strong>Paper</strong>:</span></p><p><span>http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1004292</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/11249/how-to-sequence-the-human-genome-mark-j-kiel</guid>
	<pubDate>Fri, 30 May 2014 13:24:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/11249/how-to-sequence-the-human-genome-mark-j-kiel</link>
	<title><![CDATA[How to sequence the human genome - Mark J. Kiel]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/MvuYATh7Y74" frameborder="0" allowfullscreen></iframe>View full lesson: http://ed.ted.com/lessons/how-to-sequence-the-human-genome-mark-j-kiel

Your genome, every human's genome, consists of a unique DNA sequence of A's, T's, C's and G's that tell your cells how to operate. Thanks to technological advances, scientists are now able to know the sequence of letters that makes up an individual genome relatively quickly and inexpensively. Mark J. Kiel takes an in-depth look at the science behind the sequence.

Lesson by Mark J. Kiel, animation by Marc Christoforidis.]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/17843/pathway-analysis</guid>
	<pubDate>Fri, 03 Oct 2014 08:51:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/17843/pathway-analysis</link>
	<title><![CDATA[Pathway Analysis]]></title>
	<description><![CDATA[<p>Pathway Analysis is usually performed with aim to enrich the genes with their functional information and reveal the underlying biological mechanisms pursue by genes. Pathway Analysis is not only limited to what biological pathways a particular set of expressed genes follow but also to disclose the relationships between these genes. With availability of more genomics, transcriptomics and proteomics data, interactions between genes involve in multiple pathways become more clear and also relationships between the genes, their transcripts, and their gene products. However, existing tools and dbs mainly based on knowledge driven approach in which pathways will be identified by finding the correlation between the&nbsp;<span>information in one of the pathway knowledge databases (KEGG,Reactome,Panther,BioCarta, Panther,GO,NCI,WikiPathways,etc) and gene expression result for a specific conditions for instance tumor, obesity , cold resistant crops/plants, etc.</span></p><p><span><strong>Introductory Articles/ppt/sources</strong>:</span></p><p><a href="http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1002375"><span>http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1002375</span></a></p><p><a href="http://bioinformatics.mdanderson.org/MicroarrayCourse/Lectures09/Pathway%20Analysis.pdf"><span>http://bioinformatics.mdanderson.org/MicroarrayCourse/Lectures09/Pathway%20Analysis.pdf</span></a></p><p><a href="http://gettinggeneticsdone.blogspot.de/2012/03/pathway-analysis-for-high-throughput.html"><span>http://gettinggeneticsdone.blogspot.de/2012/03/pathway-analysis-for-high-throughput.html</span></a></p><p><a href="http://davetang.org/muse/tag/pathway/"><span>http://davetang.org/muse/tag/pathway/</span></a></p><p><a href="https://www.biostars.org/p/42219/"><span>https://www.biostars.org/p/42219/</span></a></p><p><a href="http://bioinformatics.ca//files/public/Pathways_2014_Module4_v2.pdf"><span>http://bioinformatics.ca//files/public/Pathways_2014_Module4_v2.pdf</span></a></p><p><a href="http://bioinformatics.ca//files/public/Pathways_2014_Module2.pdf"><span>http://bioinformatics.ca//files/public/Pathways_2014_Module2.pdf</span></a></p><p><span><strong>Impotant Database and Tools</strong>:</span></p><p>GeneMANIA, Cytoscape,&nbsp;<a href="http://www.ingenuity.com/products/ipa">IPA</a>&nbsp;and <a href="http://thomsonreuters.com/metacore/">Metacore</a> (Commerical ),&nbsp;<span>Pathway Commons, Reactome ,Panther, BioCyc, WikiPathways, Pathvisio, KEGG, NCI, Stringdb, Amigo,&nbsp;<span>WebGestalt ,<span>ConsensusPathDB ,GSEA,Blast2go</span></span></span></p><p><span><strong>Popular R based tools</strong>:</span></p><p><span>Reactome.db, ReactomePA, ClusterProfiler, Gage, SPIA, topGO, Pathview,DOSE,GOStat</span></p><p><span><strong>More</strong>:</span></p><p><a href="http://www.bioconductor.org/help/search/index.html?q=Enrichment+analysis+"><span>http://www.bioconductor.org/help/search/index.html?q=Enrichment+analysis+</span></a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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