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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/4357?offset=10</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/33917/webinar-on-leukocyte-immunobiology-helps-us-predict-post-operative-risk-using-pre-operative-markers-on-9-aug-8-am-pst</guid>
	<pubDate>Tue, 18 Jul 2017 08:21:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/33917/webinar-on-leukocyte-immunobiology-helps-us-predict-post-operative-risk-using-pre-operative-markers-on-9-aug-8-am-pst</link>
	<title><![CDATA[Webinar on Leukocyte immunobiology helps us predict post-operative risk using pre-operative markers on 9 Aug, 8 am PST]]></title>
	<description><![CDATA[<h2><strong><a href="http://www.strand-ngs.com/webinar_registration#registration-form">Free Live Webinar on Leukocyte immunobiology helps us predict post-operative risk using pre-operative markers on 9 Aug, 8 am PST</a></strong></h2><h2 id="Next-gen-seq"><em><a href="http://www.strand-ngs.com/webinar_registration">Speaker:</a></em></h2><p><strong>Mario Deng</strong><span>&nbsp;MD FACC FESC</span><br /><span>Professor of Medicine</span><br /><span>Advanced Heart Failure/Mechanical</span><br /><span>Support/Heart Transplant</span><br /><span>David Geffen School of&nbsp;</span><br /><span>Medicine at UCLA</span><br /><span>Ronald Reagan UCLA Medical Center</span></p><h2><em><a href="http://www.strand-ngs.com/webinar_registration">Abstract:</a></em></h2><div id="more-webinar"><p>Strand NGS supports a comprehensive and flexible RNA-Seq data analysis workflow consisting of Alignment, Quality Assessment, Filters, and a range of analysis and visualization options that help in studying a variety of samples and answering long-standing biological questions.</p></div><div><p>In this webinar, Dr. Deng will discuss the analysis of transcriptome, flow cytometry and cytokine data from pre-operative blood samples of advanced heart failure patients undergoing Mechanical Circulatory Support (MCS) surgery. He will discuss in detail the identification of prominent clinical variables, a set of transcriptome biomarkers, and their role in the context of systems biology. Finally, the application of Class Prediction algorithms in Strand NGS for identification of high-risk patients will be illustrated.</p><p>This immunobiology based study highlights the potential of machine learning techniques in clinical risk prediction and patient management, and from a clinician&rsquo; s perspective, the utility of biomarker discovery studies in helping patients make more informed decisions as a step towards personalized precision medicine.</p><p><em><a href="http://www.strand-ngs.com/webinar_registration#registration-form">Register here</a></em></p></div>]]></description>
	<dc:creator>Yeshodari</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/5621/genome2014</guid>
  <pubDate>Tue, 15 Oct 2013 12:47:32 -0500</pubDate>
  <link></link>
  <title><![CDATA[Genome2014]]></title>
  <description><![CDATA[
<p>Genomics has profoundly changed our way of conducting research in microbiology. The power of high–throughput DNA sequencing technologies, in particular the recent development of next generation sequencing allows researchers now to address an increasingly diverse range of biological problems. The scale and efficiency of sequence-based analyses that can now be achieved is providing unprecedented progress in diverse areas that range from the analyses of genomes to related disciplines such as transcriptional profiling - or protein - nucleic acid interaction studies: Population and metagenomics studies can now be conducted in an unprecedented large scale, regulatory processes can be studied genome-wide under hundreds of different conditions. The genome wide study of the interaction of DNA or RNA with proteins brings completely new insight into regulatory processes and even single cell analyses become now possible. The many diverse applications of next–generation sequencing and the importance of the insights that are being gained through these methods are very exiting and challenging. It is the perfect time to come together and exchange new knowledge and technologies in this area.<br /> <br />Thus the conference on "Microbiology after the genomics revolution - Genomes 2014" will be an appropriate and timely occasion to offer an outstanding discussion forum for the best international researchers in all fields of cutting edge microbiology research to discuss newly discovered aspects of microbiology.</p>

<p>More @ http://www.genomes-2014.org/</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/841/research-fellow</guid>
  <pubDate>Sat, 13 Jul 2013 11:23:20 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Fellow]]></title>
  <description><![CDATA[
<p>UNIVERSITY OF CALCUTTA</p>

<p>A walk-in-interview will be held on 15.7.2013 at 12 noon in the Department of Biophysics, Molecular Biology and Bioinformatics, 92 A.P.C Road, Kolkata-700 009 to select one trainee research fellow and two students under DIC. The positions are purely temporary and would be for a period of six months from the date of joining which may be extended by another six months subject to successful performance.</p>

<p>Qualification:</p>

<p>For the Trainee Research Fellow: Should have a master degree in Bioinformatics or allied subjects and should have biological database development experience. Must have at least one publication.</p>

<p>For the Students: Should have a master degree in Bioinformatics or allied subjects and should be proficient in C-programming language. Must be familiar with techniques of Developmental Biology.</p>

<p>The Trainee Research Fellow would be paid a consolidated sum of Rs 10000/- per month and the students would be paid a sum amount Rs. 7000/- per month during the tenure of the project.</p>

<p>Advertisement:<br />www.caluniv.ac.in/News%20&amp;%20Announcement/trainee_rf_DIC.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/5812/animated-3d-cells-in-the-body</guid>
	<pubDate>Mon, 21 Oct 2013 06:28:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/5812/animated-3d-cells-in-the-body</link>
	<title><![CDATA[animated 3d cells in the body]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/UVtRGNElnkk" frameborder="0" allowfullscreen></iframe><p>cutting edge medical animation of cells</p>]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/12944/orione-%E2%80%93-a-web-based-framework-for-ngs-analysis-in-microbiology</guid>
	<pubDate>Wed, 23 Jul 2014 06:43:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/12944/orione-%E2%80%93-a-web-based-framework-for-ngs-analysis-in-microbiology</link>
	<title><![CDATA[Orione – a web-based framework for NGS analysis in microbiology]]></title>
	<description><![CDATA[<p>End-to-end NGS microbiology data analysis requires a diversity of tools covering bacterial resequencing, de novo assembly, scaffolding, bacterial RNA-Seq, gene annotation and metagenomics. However, the construction of computational pipelines that use different software packages is difficult due to a lack of interoperability, reproducibility, and transparency. To overcome these limitations researchers at <a href="http://www.crs4.it/" target="_blank">CRS4</a>, Italy have developed Orione, a Galaxy-based framework consisting of publicly available research software and specifically designed pipelines to build complex, reproducible workflows for NGS microbiology data analysis. Enabling microbiology researchers to conduct their own custom analysis and data manipulation without software installation or programming, Orione provides new opportunities for data-intensive computational analyses in microbiology and metagenomics.</p>
<p>Reference</p>
<p>Cuccuru G1, Orsini M, Pinna A, Sbardellati A, Soranzo N, Travaglione A, Uva P, Zanetti G, Fotia G. (2014)<strong> Orione, a web-based framework for NGS analysis in microbiology.</strong> <em>Bioinformatics</em> [Epub ahead of print]. [<a href="http://bioinformatics.oxfordjournals.org/content/early/2014/03/10/bioinformatics.btu135.long" target="_blank">article</a>]</p><p>Address of the bookmark: <a href="http://orione.crs4.it/" rel="nofollow">http://orione.crs4.it/</a></p>]]></description>
	<dc:creator>Martin Jones</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45314/nf-coremag-v5-advancing-genome-resolved-metagenomics</guid>
	<pubDate>Sat, 12 Sep 2026 20:27:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45314/nf-coremag-v5-advancing-genome-resolved-metagenomics</link>
	<title><![CDATA[nf-core/mag v5: Advancing Genome-Resolved Metagenomics]]></title>
	<description><![CDATA[<p>Metagenomics is rapidly moving beyond short-read sequencing. With the increasing adoption of long-read technologies, researchers can generate more contiguous assemblies&mdash;but converting these reads into reliable metagenome-assembled genomes (MAGs) remains computationally challenging.</p><p>nf-core/mag v5 (https://github.com/nf-core/mag) addresses this challenge by extending its reproducible Nextflow-based workflow for modern genome-resolved metagenomics.</p><p>A key addition is support for long-read-only metagenomic assembly and bin refinement, enabling long-read data to be processed through an integrated workflow. The release also introduces five additional binning tools, providing complementary strategies for recovering genomes from complex microbial communities.</p><p>The workflow has also expanded beyond conventional bacterial and archaeal MAGs, with improved classification of viruses and eukaryotes, together with enhanced genome-quality assessment.</p><p>Conceptually, the workflow brings together:</p><p>Reads &rarr; QC &rarr; Assembly &rarr; Binning &rarr; Bin refinement &rarr; Taxonomic classification &rarr; MAG quality assessment</p><p>The real strength of nf-core/mag is not any single algorithm, but the integration and reproducibility of multiple tools within a standardized workflow. This is particularly important for large-scale metagenomic studies where software versions, parameters, databases and computational environments can strongly influence results.</p><p>After seven years of development involving multiple curator teams and the wider nf-core community, v5 demonstrates how community-driven workflow development can keep metagenomic analysis aligned with rapidly evolving sequencing technologies.</p><p>The future of genome-resolved metagenomics is not simply longer reads&mdash;it is better integration of assembly, binning, refinement and quality control within reproducible computational workflows.</p><p>Read the full paper in Bioinformatics https://academic.oup.com/bioinformatics/article/42/9/btag628/8770536?</p>]]></description>
	<dc:creator>LEGE</dc:creator>
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