<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/26363?offset=1060</link>
	<atom:link href="https://bioinformaticsonline.com/related/26363?offset=1060" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28802/research-associate-bioinformatics-recruitment-in-icgeb-new-delhi</guid>
  <pubDate>Tue, 16 Aug 2016 03:38:05 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Associate Bioinformatics recruitment in ICGEB, New Delhi]]></title>
  <description><![CDATA[
<p>Research Associate Bioinformatics recruitment in ICGEB, New Delhi </p>

<p>Project :“Genetic Transformation and Development of Elite Transgenic Maize (Zea mays L.) for Biotic and Abiotic Stresses Tolerance”.</p>

<p>Qualification: Ph.D. degree in:Biotechnology/Bioinformatics/Biochemistry/Plant Molecular Biology/Plant Physiology/Botany or any related area with evidence of prior experience in maize transformation.</p>

<p>Additional experience in plant transformation of any cereal crop would be preferable.</p>

<p>The appointment would initially be for one year.</p>

<p>How to apply<br />Interested applicants should send their detailed CV including brief synopsis regarding the previous research experience (along withcontact email address by email) to: Dr. Tanushri Kaul (tanushri@icgeb.res.in). Group Leader, Nutritional Improvement of Crops Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi-110 067.</p>

<p>Closing date for applications: 22 August 2016.</p>

<p>More at http://www.icgeb.org/vacancies.html</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28851/senior-manager-bioinformatics-operations-at-rgcb-india</guid>
  <pubDate>Fri, 19 Aug 2016 04:37:17 -0500</pubDate>
  <link></link>
  <title><![CDATA[Senior Manager (Bioinformatics Operations) at RGCB, India]]></title>
  <description><![CDATA[
<p>Senior Manager (Bioinformatics Operations) <br />Rajiv Gandhi Centre for Biotechnology (RGCB) - Thiruvananthapuram, Kerala <br />₹15,600 - ₹39,100 a month<br />Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications for the following positions from Indian citizens with prescribed qualifications </p>

<p>Senior Manager (Bioinformatics Operations) <br />No. of posts: 01 (General) <br />Pay Scale: PB-3 15600-39100 + Grade Pay Rs.6600/- <br />Min. Qualification: PhD in Bioinformatics, , Life Sciences or Computer Science applied to biological questions. <br />A Min. 5 years of experience <br />Age limit: 40 years as on August 01, 2016</p>

<p>More at http://www.rgcb.res.in/positions.php</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28889/project-scientist-at-national-agri-food-biotechnology-institute-nabi</guid>
  <pubDate>Thu, 25 Aug 2016 05:49:36 -0500</pubDate>
  <link></link>
  <title><![CDATA[Project Scientist at National Agri-Food Biotechnology Institute (NABI)]]></title>
  <description><![CDATA[
<p>Advt. No. NABI/8(18)/2012-PME-3<br />Project Scientist recruitment in National Agri-Food Biotechnology Institute (NABI)<br />Project Title : “Transfer and Evaluation of Indian Banana with Pro-Vitamin A (PVA) Constructs”<br />Essential qualifications:  Ph.D. thesis submitted/awarded in any branch of life/plant sciences. Desirable qualification: a) Excellent academic record with research experience in area relevant to plant metabolic engineering, molecular biology and bioinformatics supported with high quality publications. b) Knowledge and experience of Chromatography and Mass Spectrometry based technological analysis of samples. c) Knowledge and experience of in-silico analysis such as trascriptomics, proteomics and genomics. c) Relevant research publications in reputed international journals with high impact factors.<br />No. of Post : 01<br />Age: 35 years<br />Emoluments:  Rs.40,000/- per month.<br />How to apply<br />Walk-In-Interview on 29/08/2016 at National Agri-Food Biotechnology Institute, C-127, Industrial Area, Phase VIII, S.A.S. Nagar, Mohali-160 071 Email: siddharth@nabi.res.in</p>

<p>More at http://www.nabi.res.in/Vacancies/NABI/ResearchFellowships/JRFSRFRA/2016/NABI8(18)2012-PME-3/Advt.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</guid>
	<pubDate>Mon, 29 Aug 2016 04:08:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</link>
	<title><![CDATA[Useful Bioinformatics Tools]]></title>
	<description><![CDATA[<p>Collections of few handy tools for bioinformatician</p>
<p>http://molbiol-tools.ca/Convert.htm</p><p>Address of the bookmark: <a href="http://molbiol-tools.ca/Convert.htm" rel="nofollow">http://molbiol-tools.ca/Convert.htm</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29123/artemis-comparison-tool-act</guid>
	<pubDate>Wed, 07 Sep 2016 03:54:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29123/artemis-comparison-tool-act</link>
	<title><![CDATA[Artemis Comparison Tool (ACT)]]></title>
	<description><![CDATA[<p><span>ACT is a Java application for displaying pairwise comparisons between two or more DNA sequences. It can be used to identify and analyse regions of similarity and difference between genomes and to explore conservation of synteny, in the context of the entire sequences and their annotation.&nbsp;It can read complete EMBL,&nbsp;GENBANK and GFF entries or sequences in FASTA or raw format.&nbsp;</span></p><p>Address of the bookmark: <a href="http://www.sanger.ac.uk/science/tools/artemis-comparison-tool-act" rel="nofollow">http://www.sanger.ac.uk/science/tools/artemis-comparison-tool-act</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29016/traineeshipstudentship-conducts-university-of-delhi-gargi-college</guid>
  <pubDate>Mon, 05 Sep 2016 03:45:58 -0500</pubDate>
  <link></link>
  <title><![CDATA[Traineeship/Studentship conducts University of Delhi (Gargi College)]]></title>
  <description><![CDATA[
<p>Traineeship/Studentship cunducts University of Delhi (Gargi College) on purely temporary for a period of six months.<br />Traineeship — 01 (one post)<br />Essential Qualification: Post Graduate degree in Bioinformatics or any other branch of Life Sciences preferably with dissertation in Bioinformatics. Desirable Qualification: Prior knowledge of programming languages such as C, VB, SQL etc. and software/database development<br />Studentship- 01 (one post)<br />Essential Qualifications: Final year Post Graduate students pursuing a degree in Bioinformatics or any branch of Life Science with knowledge of bioinformatics<br />Salary: Rs.8000/- p.m.<br />How to apply<br />Interested candidates are required to appear for the walk in interview on 14th. September, 2016 at 9.30 AM in Principal's Office, Gargi College, Sirifort Road, N. Delhi-110049</p>

<p>More at http://www.du.ac.in/du/index.php?mact=News,cntnt01,detail,0&amp;cntnt01articleid=12859&amp;cntnt01returnid=83</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29112/sybil</guid>
	<pubDate>Wed, 07 Sep 2016 03:20:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29112/sybil</link>
	<title><![CDATA[Sybil]]></title>
	<description><![CDATA[<p><span>The Sybil software package provides a primarily web-based front-end to comparative genome datasets warehoused in a chado relational database. It was developed by the bioinformatics department at The Institute for Genomic Research (</span><a href="http://www.tigr.org/">TIGR</a><span>) and development continues at the J. Craig Venter Institute (</span><a href="http://jcvi.org/">JCVI</a><span>) and the Institute for Genome Sciences (</span><a href="http://igs.umaryland.edu/">IGS</a><span>) at the University of Maryland: Baltimore. Sybil has been used at TIGR/JCVI, IGS, NYU, New York Medical College, Novartis Vaccines and University of Maryland: College Park to support a number of research projects that involve comparative genome analysis. The following sections provide some high-level technical details about the overall architecture and external dependencies of the Sybil package.</span></p><p>Address of the bookmark: <a href="http://sybil.sourceforge.net/" rel="nofollow">http://sybil.sourceforge.net/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29210/cgview-circular-genome-viewer</guid>
	<pubDate>Mon, 19 Sep 2016 07:52:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29210/cgview-circular-genome-viewer</link>
	<title><![CDATA[CGView - Circular Genome Viewer]]></title>
	<description><![CDATA[<p>GView is a Java package used to display and navigate bacterial genomes. GView is useful for producing high-quality genome maps for use in publications and websites, or as a visualization tool in a sequence annotation pipeline. Users can interact with the genome using a powerful pan-and-zoom interface, or GView can write static images of a genome to a file. GView can draw a genome using either circular or linear layouts. For examples of some of the images GView can produce, see the <a href="https://www.gview.ca/bin/view/GView/ImageGallery">Image Gallery</a>. GView is a re-write of <a href="http://wishart.biology.ualberta.ca/cgview/" target="_top">CGView</a>, a circular genome viewer written by Paul Stothard. The goal of GView is to provide greater user interaction, and more flexibility in how the genome map is rendered. To aid with easily configuring the display of a genome, a style editor has been included to provide an intuitive, user-friendly graphical user interface for customizing genome maps. Styling attributes such as colours or fonts for the various map elements can be adjusted in real time. Customized styles can be saved for later use or for application to other genome maps using GView's <a href="https://www.gview.ca/bin/view/GViewDocumentation/GViewGSS">custom file format</a>.</p><p>Address of the bookmark: <a href="http://wishart.biology.ualberta.ca/cgview/" rel="nofollow">http://wishart.biology.ualberta.ca/cgview/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29270/blast-ring-image-generator-brig</guid>
	<pubDate>Fri, 30 Sep 2016 09:18:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29270/blast-ring-image-generator-brig</link>
	<title><![CDATA[BLAST Ring Image Generator (BRIG)]]></title>
	<description><![CDATA[<p>BRIG is a free cross-platform (Windows/Mac/Unix) application that can display circular comparisons between a large number of genomes, with a focus on handling genome assembly data. The application is available at: <a href="http://sourceforge.net/projects/brig">http://sourceforge.net/projects/brig</a></p>
<p>If you have any questions or comments, post them on <a href="http://sourceforge.net/tracker/?group_id=328245">one of the trackers</a> on BRIG&rsquo;s SourceForge page: <a href="http://sourceforge.net/tracker/?group_id=328245">http://sourceforge.net/tracker/?group_id=328245</a>.</p>
<p>Features:</p>
<ul>
<li>Images show similarity between a central reference sequence and other sequences as concentric rings.</li>
<li>BRIG will perform all BLAST comparisons and file parsing automatically via a simple GUI.</li>
<li>Contig boundaries and read coverage can be displayed for draft genomes; customized graphs and annotations can be displayed.</li>
<li>Using a user-defined set of genes as input, BRIG can display gene presence, absence, truncation or sequence variation in a set of complete genomes, draft genomes or even raw, unassembled sequence data.</li>
<li>BRIG also accepts SAM-formatted read-mapping files enabling genomic regions present in unassembled sequence data from multiple samples to be compared simultaneously</li>
</ul><p>Address of the bookmark: <a href="http://brig.sourceforge.net/" rel="nofollow">http://brig.sourceforge.net/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29280/nemo-%E2%80%93-a-stochastic-individual-base-genetically-explicit-simulation-platform</guid>
	<pubDate>Sat, 01 Oct 2016 14:45:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29280/nemo-%E2%80%93-a-stochastic-individual-base-genetically-explicit-simulation-platform</link>
	<title><![CDATA[Nemo – A stochastic, individual-base, genetically explicit simulation platform]]></title>
	<description><![CDATA[<ul>
<li>
<p>A&nbsp;<strong>recombination map</strong>&nbsp;has been added for all multi-locus traits. The map positions (chromosomal) for neutral markers (e.g. SNPs) and loci under selection (QTLs, deleterious mutations, DMIs) can now be specified explicitly, or set at random. The map can hold an unlimited number of loci of different types jointly, at any recombination scale (cM or lower). The effects of linkage can thus be finely explored.</p>
</li>
<li>
<p>A new trait coding for (Bateson-)<strong>Dobzhansky-Muller incompatibility loci</strong>. Multiple haploid or diploid pairs of incompatible loci can be spread throughout the genome and affect individual fitness.</p>
</li>
<li>
<p><strong>Multi-type selection</strong>:&nbsp;<a href="http://nemo2.sourceforge.net/classIndividual.html" title="This class contains traits along with other individual information (sex, pedigree, etc. ).">Individual</a>&nbsp;fitness can be jointly determined by different types of loci under selectinon, such as QTLs coding for quantitative traits under spatially variable selection, universally deleterious mutations, and Dobzhansky-Muller incompatibility loci.</p>
</li>
<li>
<p><strong>An unlimited number of quantitative traits</strong>&nbsp;under different forms of selection can be modelled, based on universally pleiotropic loci with several bi- or multi-allelic models.</p>
</li>
<li>
<p><strong>Spatial and temporal variation of selection</strong>&nbsp;on quantitative traits is possible, modelling shifts of environmental conditions over time.</p>
</li>
<li>
<p>The dispersal matrix describing the movement of individuals among sub-populations can be replaced by a connectivity matrix and a reduced dispersal matrix describing migration only among the connected sub-populations. This offers a substantial gain in computing time and system memory when simulating very large grids.</p>
</li>
<li>
<p>Input parameters' arguments may be specified in separate files. This is particularly convenient when specifying large matrices.</p>
</li>
<li>
<p>Many adjustments have been made for refined control of the input of parameters and data output. See updates in the manual.</p>
</li>
</ul><p>Address of the bookmark: <a href="http://nemo2.sourceforge.net/index.html" rel="nofollow">http://nemo2.sourceforge.net/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

</channel>
</rss>