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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/30459?offset=510</link>
	<atom:link href="https://bioinformaticsonline.com/related/30459?offset=510" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/7567/asst-professor-jaipur-national-university</guid>
  <pubDate>Fri, 27 Dec 2013 19:54:40 -0600</pubDate>
  <link></link>
  <title><![CDATA[Asst. Professor @ JAIPUR NATIONAL UNIVERSITY]]></title>
  <description><![CDATA[
<p>JAIPUR NATIONAL UNIVERSITY</p>

<p>Established by Government of Rajasthan</p>

<p>Approved by UGC under Sec 2(f) of UGC Act 1956</p>

<p>ADVERTISEMENT FOR FACULTY POSITION AT JAIPUR NATIONAL UNIVERSITY,JAIPUR</p>

<p>Jaipur National University, Jaipur is a premier centre of learning, providing various integrated and interdisciplinary programmes of study and research in the country. With the opening of the School of Distance Education &amp; Learning, JNU has taken education to the doorsteps of those aspirants who, for some reason, could not be a part of regular stream of education. In this era of competition &amp; ambition for excellence, it has become imperative to have quality education &amp; an alert mind coupled with the right attitude to carry onself, and for this, JNU happens to be the most sought after destination.</p>

<p>School Of Life Sciences: Bioinformatics, Chemistry</p>

<p>Total no of Post: 04</p>

<p>Education:</p>

<p>PG – M.Sc /M.Tech Bioinformatics</p>

<p>PG – M.Sc /M.Tech Chemistry</p>

<p>Experience:</p>

<p>Candidate with 1-2 years of teaching experience in college/ University will be preffered. Freshers may also apply.</p>

<p>Compensation: Compensation will not be a problem for the right candidate</p>

<p>HOW TO APPLY:</p>

<p>SEND THE UPDATED RESUME THROUGH MAIL OR POST AT</p>

<p>dsbhatia5@yahoo.com</p>

<p>contact no: 7568246839</p>

<p>Website: http://www.jnujaipur.ac.in</p>

<p>Please mail your resume to Prof.D.S.Bhatia</p>

<p>Email Address: dsbhatia5@yahoo.com</p>

<p>Ph:, +917568246839</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44616/basics-of-blast-programs</guid>
	<pubDate>Fri, 26 Jul 2024 06:04:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44616/basics-of-blast-programs</link>
	<title><![CDATA[Basics of BLAST Programs !]]></title>
	<description><![CDATA[<p>The Basic Local Alignment Search Tool (BLAST) is a powerful bioinformatics program used to compare an input sequence (such as DNA, RNA, or protein sequences) against a database of sequences to find regions of similarity. Developed by the National Center for Biotechnology Information (NCBI), BLAST is widely used for identifying species, finding functional and evolutionary relationships between sequences, and predicting the function of novel sequences.</p><p>Key Features of BLAST:<br />1. Sequence Comparison: BLAST searches for local alignments between the query sequence and sequences in a database. It identifies regions of similarity, which can help infer functional and evolutionary relationships.</p><p>2. Speed and Efficiency: BLAST uses heuristic algorithms, making it faster than exhaustive search methods, suitable for large-scale database searches.</p><p>3. Versatility: There are several versions of BLAST for different types of sequence comparisons:<br /> - blastn: Compares a nucleotide query sequence against a nucleotide sequence database.<br /> - blastp: Compares a protein query sequence against a protein sequence database.<br /> - blastx: Compares a nucleotide query sequence translated in all reading frames against a protein sequence database.<br /> - tblastn: Compares a protein query sequence against a nucleotide sequence database translated in all reading frames.<br /> - tblastx: Compares the six-frame translations of a nucleotide query sequence against the six-frame translations of a nucleotide sequence database.</p><p>4. Scoring and E-value: BLAST results are scored based on the quality and length of the alignments. The E-value (expect value) indicates the number of alignments one can expect to find by chance, with lower E-values representing more significant matches.</p><p>5. Output Formats: BLAST provides results in various formats, including plain text, HTML, XML, and JSON, making it adaptable for different types of analyses and integrations with other tools.</p><p>Applications of BLAST:<br />- Genomic Research: Identifying genes, understanding genetic diversity, and mapping genome sequences.<br />- Protein Function Prediction: Inferring the function of unknown proteins by comparing them to known protein sequences.<br />- Evolutionary Studies: Exploring evolutionary relationships between organisms by comparing their genetic material.<br />- Medical Research: Identifying pathogens, understanding disease mechanisms, and developing treatments by comparing sequences of interest.</p><p>Overall, BLAST is an essential tool in bioinformatics, offering a reliable and efficient way to analyze and interpret biological sequence data.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/7986/list-of-bioinformatics-open-source-projectssoftware</guid>
	<pubDate>Tue, 21 Jan 2014 14:28:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/7986/list-of-bioinformatics-open-source-projectssoftware</link>
	<title><![CDATA[List of bioinformatics open source projects/software.]]></title>
	<description><![CDATA[<p>Open source software is software that can be freely used, changed, and shared (in modified or unmodified form) by anyone. Open source software is made by many people, and distributed under licenses that comply with the Open Source Definition.The Open Source Initiative (OSI) is a global non-profit that supports and promotes the open source movement. Followings are the OS bioinformatics projects/software :</p><p><strong>.NET Bio</strong></p><p>http://blogs.msdn.com/b/msr_er/archive/2011/10/18/microsoft-biology-foundation-evolves-into-new-toolkit-net-bio.aspx</p><p>A language-neutral bioinformatics toolkit built using the Microsoft 4.0 .NET Framework to help developers, researchers, and scientists.</p><p><strong>AMPHORA</strong> ("AutoMated Phylogenomic infeRence Application")</p><p>http://wolbachia.biology.virginia.edu/WuLab/Software.html</p><p><a href="http://en.wikipedia.org/wiki/Metagenomics" title="Metagenomics">Metagenomics</a> analysis software</p><p><strong>Anduril</strong></p><p>http://www.anduril.org/anduril/site/</p><p>Component-based <a href="http://en.wikipedia.org/wiki/Workflow" title="Workflow">workflow</a> framework for data analysis</p><p>Armadillo workflow platform</p><p>Tool for designing and executing phylogenetic workflows</p><p><strong>AutoDock</strong></p><p>http://autodock.scripps.edu/</p><p>suite of automated docking tools</p><p><strong>Biochemical Algorithms Library (BALL)</strong></p><p>http://www.ball-project.org/</p><p>C++ library and framework for molecular modeling and visualization designed for rapid prototyping</p><p><strong>Bio4j</strong></p><p>http://bio4j.com/</p><p>Bio4j is a <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">bioinformatics</a> platform and <a href="http://en.wikipedia.org/wiki/Chart" title="Chart">graph</a> based <a href="http://en.wikipedia.org/wiki/Database" title="Database">database</a> built around most data available in <a href="http://en.wikipedia.org/wiki/UniProt" title="UniProt">UniProt</a> KB(<a href="http://en.wikipedia.org/wiki/Swiss-Prot" title="Swiss-Prot">Swiss-Prot</a> + <a href="http://en.wikipedia.org/wiki/TrEMBL" title="TrEMBL">TrEMBL</a>), <a href="http://en.wikipedia.org/wiki/Gene_Ontology" title="Gene Ontology">Gene Ontology</a> (GO), <a href="http://en.wikipedia.org/w/index.php?title=UniRef&amp;action=edit&amp;redlink=1" title="UniRef (page does not exist)">UniRef</a> (50,90,100), <a href="http://en.wikipedia.org/wiki/RefSeq" title="RefSeq">RefSeq</a>, <a href="http://en.wikipedia.org/wiki/National_Center_for_Biotechnology_Information" title="National Center for Biotechnology Information">NCBI</a> taxonomy, and Expasy Enzyme DB</p><p><strong>Bioclipse</strong></p><p>www.bioclipse.net</p><p>Visual platform for <a href="http://en.wikipedia.org/wiki/Cheminformatics" title="Cheminformatics">chemo</a>- and <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">bioinformatics</a> based on the <a href="http://en.wikipedia.org/wiki/Eclipse_%28software%29" title="Eclipse (software)">Eclipse</a> Rich Client Platform (RCP).</p><p><strong>Bioconductor</strong></p><p>http://www.bioconductor.org/</p><p><a href="http://en.wikipedia.org/wiki/R_%28programming_language%29" title="R (programming language)">R (programming language)</a> language toolkit</p><p><strong>Bioinformatics Learning Tutorial (BLT)</strong></p><p>http://sourceforge.net/projects/biotutorial/</p><p>Educational <a href="http://en.wikipedia.org/wiki/Interactive_tutorials" title="Interactive tutorials">interactive tutorials</a> and 3D animations for Replication, Transcription, and Translation</p><p><strong>BioHaskell</strong></p><p>http://biohaskell.org/</p><p><a href="http://en.wikipedia.org/wiki/Haskell_%28programming_language%29" title="Haskell (programming language)">Haskell (programming language)</a></p><p><strong>BioJava</strong></p><p>http://biojava.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Java_%28programming_language%29" title="Java (programming language)">Java (programming language)</a></p><p><strong>BioMOBY</strong></p><p>http://biomoby.org/</p><p>registry of <a href="http://en.wikipedia.org/wiki/Web_services" title="Web services">web services</a></p><p><strong>BioPerl</strong></p><p>http://www.bioperl.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Perl" title="Perl">Perl</a> language toolkit</p><p><strong>BioPHP</strong></p><p>http://www.biophp.org/</p><p><a href="http://en.wikipedia.org/wiki/PHP" title="PHP">PHP</a> language toolkit</p><p><strong>Biopython</strong></p><p>http://biopython.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Python_%28programming_language%29" title="Python (programming language)">Python</a> language toolkit</p><p><strong>BioRails</strong></p><p>https://github.com/biorails</p><p>a <a href="http://en.wikipedia.org/wiki/Data_management_system" title="Data management system">data management system</a> designed to support researchers in <a href="http://en.wikipedia.org/wiki/Drug_discovery" title="Drug discovery">drug discovery</a></p><p><strong>BioRuby</strong></p><p>http://bioruby.org/</p><p><a href="http://en.wikipedia.org/wiki/Ruby_%28programming_language%29" title="Ruby (programming language)">Ruby</a> language toolkit</p><p><strong>BioSmalltalk</strong></p><p>https://code.google.com/p/biosmalltalk/</p><p><a href="http://en.wikipedia.org/wiki/Smalltalk_%28programming_language%29" title="Smalltalk (programming language)">Smalltalk</a> language toolkit</p><p><strong>BioUno</strong></p><p>http://www.biouno.org/</p><p><a href="http://en.wikipedia.org/w/index.php?title=BioUno&amp;action=edit&amp;redlink=1" title="BioUno (page does not exist)">BioUno</a> is a project that applies <a href="http://en.wikipedia.org/wiki/Continuous_Integration" title="Continuous Integration">Continuous Integration</a> tools and techniques in <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">Bioinformatics</a>. It uses <a href="http://en.wikipedia.org/wiki/Jenkins_%28software%29" title="Jenkins (software)">Jenkins</a> and its plug-in API to create <a href="http://en.wikipedia.org/wiki/Bioinformatics_workflow_management_system" title="Bioinformatics workflow management system">biology workflows</a> and manage <a href="http://en.wikipedia.org/wiki/Computer_clusters" title="Computer clusters">computer clusters</a>.</p><p><strong>caCORE</strong></p><p>&nbsp;</p><p>ontologic representation environment</p><p><strong>caArray</strong></p><p>https://cabig-stage.nci.nih.gov/community/tools/caArray</p><p>ontologic representation environment</p><p><strong>EMBOSS</strong></p><p>http://emboss.sourceforge.net/</p><p>Suite of packages for sequencing, searching, etc.</p><p><strong>Gaggle</strong></p><p>https://www.gaggle.net/</p><p>A framework for interoperability between systems biology software</p><p><strong>Galaxy</strong></p><p>http://galaxyproject.org/</p><p><a href="http://en.wikipedia.org/wiki/Scientific_workflow_system" title="Scientific workflow system">Scientific workflow</a> and <a href="http://en.wikipedia.org/wiki/Data_integration" title="Data integration">data integration</a> system</p><p><strong>GenePattern</strong></p><p>http://www.broadinstitute.org/cancer/software/genepattern/</p><p><a href="http://en.wikipedia.org/wiki/Scientific_workflow_system" title="Scientific workflow system">Scientific workflow system</a> that provides access to more than 150 genomic analysis tools</p><p><strong>GeWorkbench</strong></p><p>http://wiki.c2b2.columbia.edu/workbench/index.php/Home</p><p>Genomic <a href="http://en.wikipedia.org/wiki/Data_integration" title="Data integration">data integration</a> platform</p><p><strong>GMOD</strong></p><p>http://www.gmod.org/wiki/Main_Page</p><p>Toolkit for addressing many common challenges at biological databases.</p><p><strong>GeneProf</strong></p><p>http://www.geneprof.org/GeneProf/</p><p>A web-based, bioinformatics software suite for the analysis of functional genomics experiments, e.g. RNA-seq or ChIP-seq.</p><p><strong>GeneTalk</strong></p><p>http://www.gene-talk.de/</p><p>Tool for filtering sequence variants in <a href="http://en.wikipedia.org/wiki/Variant_Call_Format" title="Variant Call Format">VCF</a> files. Network for scientists and clinicians for expertise and knowledge exchange. Database of annotations aboute sequence variants with clinically relevant information.</p><p><strong>GenGIS</strong></p><p>http://kiwi.cs.dal.ca/GenGIS/Main_Page</p><p>Application that allows users to combine digital map data with information about biological sequences collected from the environment.</p><p><strong>GenomeSpace</strong></p><p>http://www.genomespace.org/</p><p>Centralized web application that provides data format transformations and facilitates connections with other bioinformatics tools</p><p><strong>GENtle</strong></p><p>http://directory.fsf.org/wiki/GENtle</p><p>An equivalent to the proprietary <a href="http://en.wikipedia.org/wiki/Vector_NTI" title="Vector NTI">Vector NTI</a>, a tool to analyze and edit <a href="http://en.wikipedia.org/wiki/DNA" title="DNA">DNA</a> sequence files</p><p><strong>Integrated Genome Browser</strong></p><p>http://bioviz.org/igb/</p><p><a href="http://en.wikipedia.org/wiki/Java_%28software_platform%29" title="Java (software platform)">Java</a>-based desktop <a href="http://en.wikipedia.org/wiki/Genome_browser" title="Genome browser">genome browser</a></p><p><strong>Integrative Genomics Viewer (IGV)</strong></p><p>http://www.broadinstitute.org/igv/</p><p>High-performance desktop tool for interactive visual exploration of diverse genomic data</p><p><strong>IntAct</strong></p><p>http://www.ebi.ac.uk/intact/</p><p>molecular interaction database</p><p><strong>InterMine</strong></p><p>http://intermine.github.io/intermine.org/</p><p>Extensive data warehouse system for the analysis and integration of biological datasets</p><p><strong>Java Treeview</strong></p><p>http://jtreeview.sourceforge.net/</p><p>microarray data viewer</p><p><strong>LabKey Server</strong></p><p>http://labkey.com/</p><p>platform for integrating, analyzing and sharing data</p><p><strong>OpenClinica</strong></p><p>https://www.openclinica.com/</p><p>software for capturing and managing data in clinical trials</p><p><a href="http://www.biomedcentral.com/1471-2164/13/512">PromKappa</a></p><p>http://xbioinformatics.wordpress.com/tag/promkappa/</p><p>PromKappa (Promoter analysis by Kappa) software program used for promoter pattern generation and promoter analysis.</p><p><strong>MeV: Multi-Experiment Viewer</strong></p><p>http://www.tm4.org/mev.html</p><p>a desktop application for the analysis, visualization and data-mining of large-scale genomic data</p><p><strong>PathVisio</strong></p><p>http://www.pathvisio.org/</p><p>a desktop software for drawing, analysis and visualization of biological pathways</p><p>REDCRAFT</p><p>software for determining tertiary protein structure given assigned Residual Dipolar Coupling data</p><p>SAM Tools</p><p>Data format (SAM) and accompanying tool suite, for storing large nucleotide sequence alignments</p><p><a href="http://en.wikipedia.org/wiki/Staden_Package" title="Staden Package">Staden Package</a></p><p>Sequence assembly, editing and analysis, primarily consisting of gap4, gap5 and spin.</p><p><a href="http://en.wikipedia.org/wiki/STAMP" title="STAMP">STAMP</a></p><p>Software package for analyzing metagenomic profiles that promotes &lsquo;best practices&rsquo; in choosing appropriate statistical techniques and reporting results.</p><p><a href="http://supfam.org/supraHex">supraHex</a></p><p>An open-source R/Bioconductor package for omics data analysis using a supra-hexagonal map</p><p><a href="http://en.wikipedia.org/wiki/Taverna_workbench" title="Taverna workbench">Taverna workbench</a></p><p>Tool for designing and executing workflows</p><p>TGAC Browser</p><p>Genome Browser, visualisation solutions for big data in the genomic era</p><p>T-REX WebServer</p><p>Bioinformatics and phylogenetics webserver (NJ, PhyML, RAxML, MAFFT, MUSCLE, Newick viewer, <a href="http://en.wikipedia.org/wiki/Horizontal_gene_transfer" title="Horizontal gene transfer">Horizontal gene transfer</a> detection, Reticulograms, Substitution models)</p><p><a href="http://en.wikipedia.org/wiki/UGENE" title="UGENE">UGENE</a></p><p>integrated bioinformatics tools</p><p>Visomics</p><p>bioinformatics tools for omics data</p><p>Genome Analysis Toolkit 1.0 (GATK 1.0)</p><p>a software package to analyse next-generation resequencing data</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33693/circleator</guid>
	<pubDate>Sun, 25 Jun 2017 18:04:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33693/circleator</link>
	<title><![CDATA[Circleator]]></title>
	<description><![CDATA[<p>The Charm City Circleator--or Circleator for short--is a Perl-based visualization tool developed at the&nbsp;<a href="http://igs.umaryland.edu/">Institute for Genome Sciences</a>&nbsp;in the University of Maryland's School of Medicine. Circleator produces circular plots of genome-associated data, like this one:</p>
<p><a href="https://camo.githubusercontent.com/0b414f050a7dcb672386932ee0cd83e5f42d2271/687474703a2f2f6a6f6e617468616e63726162747265652e6769746875622e696f2f436972636c6561746f722f696d616765732f43503030323732352d322d3432302e706e673f7261773d74727565" target="_blank"><img src="https://camo.githubusercontent.com/0b414f050a7dcb672386932ee0cd83e5f42d2271/687474703a2f2f6a6f6e617468616e63726162747265652e6769746875622e696f2f436972636c6561746f722f696d616765732f43503030323732352d322d3432302e706e673f7261773d74727565" alt="Sample Circleator image" title="Sample Circleator Image" style="border: 0px;"></a></p>
<p>Common uses of the tool include:</p>
<ul>
<li>Displaying the sequence and/or genes in a&nbsp;<a href="http://www.ncbi.nlm.nih.gov/genbank/">GenBank</a>&nbsp;flat file.</li>
<li>Highlighting differences and/or similarities in gene content between related organisms.</li>
<li>Comparing SNPs and indels between closely-related strains or serovars.</li>
<li>Comparing gene expression values across multiple samples or timepoints.</li>
<li>Visualizing coverage plots of RNA-Seq read alignments.</li>
</ul>
<h3><a href="https://github.com/jonathancrabtree/Circleator#key-features"></a>Key Features</h3>
<p>Circleator...</p>
<ul>
<li>Builds on&nbsp;<a href="http://www.bioperl.org/">BioPerl</a>&nbsp;and the input file formats that it supports, including:
<ul>
<li><a href="http://www.ncbi.nlm.nih.gov/genbank/">GenBank</a>&nbsp;flat files, GFF, FASTA</li>
</ul>
</li>
<li>Accepts a number of other commonly-used datatypes and file formats:
<ul>
<li><a href="http://bsr.igs.umaryland.edu/">BSR</a>&nbsp;and&nbsp;<a href="http://tandem.bu.edu/trf/trf.html">TRF</a>&nbsp;output,&nbsp;<a href="http://samtools.sourceforge.net/">SAM/BAM</a>&nbsp;files,&nbsp;<a href="http://vcftools.sourceforge.net/">VCF</a>-encoded SNPs, tab-delimited files</li>
</ul>
</li>
<li>Outputs publication-ready figures in the&nbsp;<a href="http://www.w3.org/Graphics/SVG/">SVG</a>&nbsp;(Scalable Vector Graphics) format.</li>
<li>Requires only a single configuration file whose layout mirrors that of the figure itself.
<ul>
<li>Predefined configuration files and "track" types are supplied for common datasets.</li>
<li>Advanced features allow limited analyses to be performed as a figure is drawn.</li>
</ul>
</li>
<li>Includes an extensive set of regression tests.</li>
<li>Offers a prototype web-based GUI (under the "Ringmaster" project.)</li>
</ul>
<p>https://github.com/jonathancrabtree/Circleator</p><p>Address of the bookmark: <a href="https://github.com/jonathancrabtree/Circleator" rel="nofollow">https://github.com/jonathancrabtree/Circleator</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/8174/the-2014-cemm-phd-program</guid>
  <pubDate>Wed, 05 Feb 2014 06:03:15 -0600</pubDate>
  <link></link>
  <title><![CDATA[The 2014 CeMM PhD Program]]></title>
  <description><![CDATA[
<p>For our next PhD Program starting in October 2014 we are looking for exceptionally motivated PhD candidates with a keen interest in genomics and medicine and a strong interest to work in teams.</p>

<p>The 2014 CeMM PhD Program will focus on two thematic areas: INFECTION and CANCER, that are built on the pillars of epigenetics, bioinformatics and systems biology, chemical biology and the mechanism of action of drugs, high-throughput genetics, genomics and proteomics, and molecular and cell biology.</p>

<p>The choice of this strategic focus rests on the synergies between immunology, infection and cancer in pathophysiological and technological terms. It furthermore reflects the strength of the current CeMM faculty, itself built around the historical and contemporary expertise in immunology and cancer of the Medical University of Vienna.</p>

<p>As a CeMM PhD student you will get the chance to work at the cutting edge of interdisciplinary molecular medicine research and be trained by the entire CeMM and associated faculty to become one of the scientists shaping the future of molecular medicine.<br />Requirements</p>

<p>To be eligible to enroll in the CeMM PhD Program all candidates are required to have a bachelor’s or master’s degree in medicine, biology, chemistry, bioinformatics, mathematics or any scientific/technical, subject-relevant degree. Candidates do not need to have completed their degree at the time of application, however they must have obtained their final degree certificate by mid-September. The working language at CeMM is English, so excellent written and oral communication skills in English are required.<br />Timeline</p>

<p>    Applications open on 20th January and close on 20th March 2014.<br />    Two references are required to be submitted through the online system by 31st March 2014.<br />    All complete candidate applications are reviewed by the CeMM Faculty in early April.<br />    Selected candidates are invited to a Skype panel interview in late April.<br />    Shortlisted candidates are then invited to Vienna in May for a full interview process, including an opportunity to introduce yourself through a presentation and interview rounds, meet research group members, and attend an informal dinner to get to know the Faculty members and learn more about their research.<br />    Positions are offered by CeMM Faculty in June.<br />    Start of PhD Program: 1st October 2014 .</p>

<p>Contact</p>

<p>Binia Maria Günther, BEd BA<br />Human Resources Manager<br />bguenther@cemm.oeaw.ac.at</p>

<p>Catherine Lloyd, Ph.D.<br />PhD and Postdoc Program Manager<br />clloyd@cemm.oeaw.ac.at</p>

<p>More Info: www.cemm.oeaw.ac.at/phd-program/application/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34380/chsminer-a-gui-tool-to-identify-chromosomal-homologous-segments</guid>
	<pubDate>Sat, 18 Nov 2017 16:55:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34380/chsminer-a-gui-tool-to-identify-chromosomal-homologous-segments</link>
	<title><![CDATA[CHSMiner: a GUI tool to identify chromosomal homologous segments]]></title>
	<description><![CDATA[<div id="ASec1">
<h3>Background</h3>
<p>The identification of chromosomal homologous segments (CHS) within and between genomes is essential for comparative genomics. Various processes including insertion/deletion and inversion could cause the degeneration of CHSs.</p>
</div>
<div id="ASec2">
<h3>Results</h3>
<p>Here we present a Java software CHSMiner that detects CHSs based on shared gene content alone. It implements fast greedy search algorithm and rigorous statistical validation, and its friendly graphical interface allows interactive visualization of the results. We tested the software on both simulated and biological realistic data and compared its performance with similar existing software and data source.</p>
</div>
<div id="ASec3">
<h3>Conclusion</h3>
<p>CHSMiner is characterized by its integrated workflow, fast speed and convenient usage. It will be useful for both experimentalists and bioinformaticians interested in the structure and evolution of genomes.</p>
<p>&nbsp;</p>
<p>https://github.com/zhenwang100/CHSMiner</p>
</div><p>Address of the bookmark: <a href="https://almob.biomedcentral.com/articles/10.1186/1748-7188-4-2" rel="nofollow">https://almob.biomedcentral.com/articles/10.1186/1748-7188-4-2</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/8123/jrf-manit</guid>
  <pubDate>Sun, 02 Feb 2014 03:07:58 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF @ MANIT]]></title>
  <description><![CDATA[
<p>MAULANA AZAD NATIONAL INSTITUTE OF TECHNOLOGY BHOPAL</p>

<p>No. CSE/14/1038</p>

<p>Walk in Interview for the post of JRF under TEQIP-II</p>

<p>SN Department – Qualification Post Graduation – Time</p>

<p>1 Bio-Informatics &amp; Mathematics M.Tech Bio-informatics/M.Sc.* Maths  10.00 AM</p>

<p>2 Biological Sciences M.Sc.* in any branch of Biological Sciences 10.30 AM</p>

<p>3 Chemical Engineering M.Tech Chemical Engineering 11.00 AM</p>

<p>4 Chemistry M.Sc.* Chemistry 11.30 AM</p>

<p>5 Civil Engineering M.Tech Structure/GeoTech. /Water -Resources/Hydraulics/Environment/Transport 12.00 Noon</p>

<p>6 GIS M.Tech GIS/Civil 12.30 PM</p>

<p>7 Computer Science &amp; Engineering M.Tech CSE/Information Security 01.00 PM</p>

<p>8 Electrical Engineering M.Tech Electrical Derives 01.30 PM</p>

<p>9 Electronics &amp; Communication M.Tech Digital Communication 02.00 PM</p>

<p>10 MSME M.Tech Material Science/ Mechanical/Metallurgy 02.30 PM</p>

<p>11 Physics M.Sc.* Physics 03.00 PM</p>

<p>* M.Sc. with NET/GATE qualified</p>

<p>Resume along with one passport size photograph and relevant documents are required at the time of interview</p>

<p>Amount of Fellowship: Rs 18000/-month+ HRA</p>

<p>Duration: 31st Dec 2014 (End of TEQIP-II project)</p>

<p>Date of Interview: 7th  February 2014</p>

<p>Venue Institute Committee Room</p>

<p>Advertisement:</p>

<p>http://www.manit.ac.in/manitbhopal/Year2014/Recruitment/Advertisement%20JRF.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34567/jobtree-based-python-wrapper-to-run-the-genome-simulation-tool-suite-evolver</guid>
	<pubDate>Fri, 08 Dec 2017 16:26:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34567/jobtree-based-python-wrapper-to-run-the-genome-simulation-tool-suite-evolver</link>
	<title><![CDATA[jobTree based python wrapper to run the genome simulation tool suite Evolver]]></title>
	<description><![CDATA[<p><span>evolverSimControl</span><span>&nbsp;(</span><span>eSC</span><span>) can be used to simulate multi-chromosome genome evolution on an arbitrary phylogeny (</span><a href="http://evolution.genetics.washington.edu/phylip/newicktree.html">Newick format</a><span>). In addition to simply running evolver,&nbsp;</span><span>eSC</span><span>&nbsp;also automatically creates statistical summaries of the simulation as it runs including text and image files. Also included are convenience scripts to: check on a running simulation and see detailed status and logging information; extract fasta sequence files from the leaf nodes of a completed simulation; extract pairwise multiple alignment files (</span><a href="http://genome.ucsc.edu/FAQ/FAQformat.html#format5">.maf</a><span>) from leaf and branch nodes from a completed simulation and with the help of&nbsp;</span><a href="https://github.com/dentearl/mafTools/">mafJoin</a><span>, join them together into a single maf covering the entire simulation.</span></p><p>Address of the bookmark: <a href="https://github.com/dentearl/evolverSimControl" rel="nofollow">https://github.com/dentearl/evolverSimControl</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/8287/post-doc-in-computational-genetics-and-genomics-at-ceinge-biotecnologie-avanzate-naples-italy</guid>
  <pubDate>Tue, 11 Feb 2014 08:06:47 -0600</pubDate>
  <link></link>
  <title><![CDATA[Post doc in Computational Genetics and Genomics at CEINGE Biotecnologie Avanzate, Naples, Italy]]></title>
  <description><![CDATA[
<p>We are seeking one motivated scientist to analyze genomics and transcriptomics data of a large collection of neuroblastoma tumors. The successful candidate will be part of a team of researchers with extensive expertise in genome cancer study. He/she will be involved in the analysis of DNA-seq, RNA-seq, ChIP-seq data using available methods running in R and UNIX environment.</p>

<p>Qualifications</p>

<p>PhD or Post-Graduated Master degree is required. Successful candidates will have some expertise in data analysis of NGS data by using methods running in R and UNIX environment. Familiarity with genome databases and browsers is required.</p>

<p>Application</p>

<p>Candidates should send a CV and a brief personal statement focusing on their skills and interests related to the research project.</p>

<p>Contacts</p>

<p>Start date: 1° April 2014<br />Salary on grant: 25,000 euros per year.<br />Contact Person (Referent): Mario Capasso<br />Ref. Email: mario.capasso@unina.it and achille.iolascon@unina.it<br />Tel: +39 081 3737889</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35249/gpopsim-a-simulation-tool-for-whole-genome-genetic-data</guid>
	<pubDate>Wed, 17 Jan 2018 03:47:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35249/gpopsim-a-simulation-tool-for-whole-genome-genetic-data</link>
	<title><![CDATA[GPOPSIM: a simulation tool for whole-genome genetic data]]></title>
	<description><![CDATA[<p><span>GPOPSIM is a simulation tool for pedigree, phenotypes, and genomic data, with a variety of population and genome structures and trait genetic architectures. It provides flexible parameter settings for a wide discipline of users, especially can simulate multiple genetically correlated traits with desired genetic parameters and underlying genetic architectures.</span></p><p>Address of the bookmark: <a href="https://github.com/SCAU-AnimalGenetics/GPOPSIM" rel="nofollow">https://github.com/SCAU-AnimalGenetics/GPOPSIM</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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