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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/33741?offset=900</link>
	<atom:link href="https://bioinformaticsonline.com/related/33741?offset=900" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44914/predicting-pathogen-virulence-using-bioinformatics-tools</guid>
	<pubDate>Tue, 04 Nov 2025 07:55:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44914/predicting-pathogen-virulence-using-bioinformatics-tools</link>
	<title><![CDATA[Predicting Pathogen Virulence Using Bioinformatics Tools]]></title>
	<description><![CDATA[<p>In the genomic era, the ability to predict the virulence potential of pathogens has become an indispensable part of infectious disease research. With the exponential growth of microbial genome data, bioinformatics tools now enable scientists to identify virulence factors, model pathogen behavior, and even forecast outbreak risks &mdash; all from sequence data.</p><p>In an age where pathogens continue to evolve and cross boundaries, understanding <strong>what makes them virulent</strong>&mdash;that is, capable of causing disease&mdash;has become a critical focus in modern microbiology and genomics. <strong>Virulence prediction</strong> bridges computational biology, genomics, and machine learning to forecast the pathogenic potential of microbes before they strike.</p><h3>What Is Virulence?</h3><p><em>Virulence</em> refers to the degree of damage a pathogen can inflict on its host. It is determined by a combination of genetic factors&mdash;called <strong>virulence factors (VFs)</strong>&mdash;that allow the organism to attach, invade, evade, and harm the host. These include genes coding for toxins, secretion systems, adhesins, and enzymes that disrupt host defenses.</p><p>Understanding virulence factors not only helps in deciphering the mechanisms of infection but also provides early warning signs for emerging threats.</p><h3>Why Predict Virulence?</h3><p>Traditional virulence studies relied heavily on experimental infection models, which, although accurate, are <strong>time-consuming, expensive, and ethically constrained</strong>.<br /> Today, the availability of whole-genome sequences and large-scale pathogen databases has paved the way for <strong>in silico virulence prediction</strong>&mdash;a computational approach that can screen thousands of genomes within hours.</p><p>This approach enables researchers to:</p><ul>
<li>
<p>Rapidly identify potential <strong>high-risk strains</strong>.</p>
</li>
<li>
<p>Prioritize pathogens for <strong>containment, surveillance, or further study</strong>.</p>
</li>
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<p>Guide <strong>vaccine development</strong> and <strong>drug target discovery</strong>.</p>
</li>
<li>
<p>Support <strong>One Health frameworks</strong>, linking animal, human, and environmental health data.</p>
</li>
</ul><h3>How Is Virulence Predicted?</h3><p>Virulence prediction combines <strong>bioinformatics pipelines</strong> with <strong>machine learning</strong> and <strong>comparative genomics</strong>. The process generally involves:</p><ol>
<li>
<p><strong>Genome Annotation:</strong> Identifying genes and coding sequences in microbial genomes.</p>
</li>
<li>
<p><strong>Feature Extraction:</strong> Comparing sequences with curated databases like <strong>VFDB (Virulence Factor Database)</strong>, <strong>PATRIC</strong>, or <strong>Victors</strong>.</p>
</li>
<li>
<p><strong>Pattern Recognition:</strong> Using algorithms (e.g., Random Forest, SVM, or deep learning models) to classify genes or strains as virulent or non-virulent based on sequence patterns, motifs, and protein domains.</p>
</li>
<li>
<p><strong>Scoring and Visualization:</strong> Assigning a virulence score or confidence level and visualizing it through heatmaps or genome maps.</p>
</li>
</ol><h3>Tools and Resources for Virulence Prediction</h3><p>A number of tools and databases make virulence prediction accessible to the scientific community:</p><ul>
<li>
<p><strong>VFanalyzer</strong> &ndash; For identifying virulence genes based on VFDB.</p>
</li>
<li>
<p><strong>PathoFact</strong> &ndash; Predicts virulence, antimicrobial resistance (AMR), and toxin genes from metagenomic data.</p>
</li>
<li>
<p><strong>Pangenome-based models</strong> &ndash; Identify virulence-associated gene clusters across strains.</p>
</li>
<li>
<p><strong>Machine learning models</strong> &ndash; Use features like GC content, codon usage bias, or protein domains to predict pathogenicity.</p>
</li>
</ul><p>Emerging tools now integrate <strong>multi-omic data</strong>&mdash;including transcriptomics, proteomics, and metabolomics&mdash;to understand virulence in a systems biology framework.</p><h3>Applications in the Real World</h3><p>Virulence prediction has major implications across public health and research sectors:</p><ul>
<li>
<p><strong>Epidemic preparedness:</strong> Early identification of virulent strains in outbreak samples.</p>
</li>
<li>
<p><strong>AMR surveillance:</strong> Linking virulence profiles with antibiotic resistance determinants.</p>
</li>
<li>
<p><strong>Environmental monitoring:</strong> Predicting pathogenic potential of soil or waterborne microbes.</p>
</li>
<li>
<p><strong>Clinical diagnostics:</strong> Supporting personalized treatment through pathogen profiling.</p>
</li>
</ul><p>For instance, integrating virulence prediction pipelines into <strong>national surveillance networks</strong> could enable faster risk assessment and response to infectious outbreaks.</p><h3>The Road Ahead</h3><p>As machine learning and genomics advance, virulence prediction will evolve from simple gene-based detection to <strong>dynamic, context-aware models</strong> that account for host&ndash;pathogen interactions, environmental signals, and evolutionary adaptation.</p><p>Future tools may predict <strong>not just if a strain is virulent</strong>, but <strong>under what conditions</strong> it expresses that virulence&mdash;bridging the gap between genotype and phenotype.</p><h3>In Summary</h3><p>Virulence prediction is redefining how we understand and anticipate infectious diseases. By coupling <strong>genomic insights</strong> with <strong>computational intelligence</strong>, researchers can identify potential threats earlier, design smarter interventions, and ultimately, strengthen our preparedness against emerging pathogens.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/5946/bioinformatics-tata-memorial-centre-navi-mumbai</guid>
  <pubDate>Mon, 28 Oct 2013 10:40:25 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics @ TATA MEMORIAL CENTRE, NAVI MUMBAI]]></title>
  <description><![CDATA[
<p>TATA MEMORIAL CENTRE<br />ADVANCED CENTRE FOR TREATMENT, RESEARCH AND EDUCATION IN CANCER<br />KHARGHAR, NAVI MUMBAI – 410210</p>

<p>No. ACTREC/Advt./ 72 /2013</p>

<p>WALK IN INTERVIEW</p>

<p>1. JRF*<br />Genome-wide RNAi screen with human pooled tyrosine kinase shRNA libraries in head and neck squamous call carcinoma (HNSCC) cell lines<br />DBT A/C No. 3071, Dr. Amit Dutt</p>

<p>2. JRF<br />IRB Project ACTREC Funds<br />Dr. Amit Dutt</p>

<p>3. RA<br />Defining the cancer genome of Head and Neck Squamous Cell Carcinoma (HNSCC) with SNP arrays and next generation sequencing technology<br />A/C No. 2895, Dr. Amit Dutt</p>

<p>Duration of the Project: One year from the date of appointment, or as and when project terminates.</p>

<p>Consolidated Salary: RA : Rs. 40,000/- p.m.<br />JRF* (DBT): Rs. 20,800/- p.m.<br />JRF: Rs. 16,000/- p.m.<br />Date &amp; Time: 6th November, 2013, at 10.00 a.m.</p>

<p>Venue: Conference Room</p>

<p>Minimum Qualifications and Experience:</p>

<p>RA: The ideal applicant should have a PhD in a relevant field. He/she should have a strong computational biology background, with demonstrated experience in coding using Perl, Python, Java or C++. He/she should be familiar with working in unix enviromnent, devising computational algorithms for data analysis, statistical data analysis in R and matlab and database programming using MySQL. Hands on experience in analyzing high throughput data would be an added advantage.</p>

<p>JRF* (DBT project): M.Sc. in Life Sciences or M.Tech in Biotechnology with good academic record (Minimum of 60% aggregate). Valid UGC-CSIR/DBT/ICMR JRF qualification and laboratory experience in molecular biology. Previous experience in molecular biology and animal tissue culture with high throughput platforms and ability to work with a large team would be desirable.</p>

<p>JRF (ACTREC project): M.Sc. in Life Sciences or M.Tech in Biotechnology with good academic record (Minimum of 60% aggregate). Minimum 2 yrs experience in molecular biology and animal tissue culture with high throughput platforms and ability to work with a large team is essential.</p>

<p>*M.Sc. degree obtained after a one year course will not be considered.</p>

<p>Candidates fulfilling above requirements should send their application by e-mail to<br />‘careers.duttlab@gmail.com. in the format given below so as to reach on or before<br />4th November, 2013.</p>

<p>Advertisement:</p>

<p>http://www.actrec.gov.in/data%20files/2013/AD-RA-JR-TECHN-6-NOV.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2631/what-junk-dna-it%E2%80%99s-an-operating-system</guid>
	<pubDate>Mon, 19 Aug 2013 15:24:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2631/what-junk-dna-it%E2%80%99s-an-operating-system</link>
	<title><![CDATA[What Junk DNA? It’s an Operating System]]></title>
	<description><![CDATA[<p>The report adds to growing experimental support for the idea that all that extra stuff in the human genes, once referred to as &ldquo;junk DNA,&rdquo; is more than functionless, space-filling material that happens to make up nearly 98% of the genome. The paper adds to a growing body of knowledge establishing a considerable role for this material in the regulation of gene expression and its potential role in human disease.</p><p>Address of the bookmark: <a href="http://www.genengnews.com/keywordsandtools/print/3/32115/" rel="nofollow">http://www.genengnews.com/keywordsandtools/print/3/32115/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6012/project-junior-research-fellow-ccmb</guid>
  <pubDate>Fri, 01 Nov 2013 10:38:22 -0500</pubDate>
  <link></link>
  <title><![CDATA[Project Junior Research Fellow @ CCMB]]></title>
  <description><![CDATA[
<p>Temporary Project positions available purely on temporary basis - Oct/2013</p>

<p>1. Project Junior Research Fellow / Project Assistant</p>

<p>Last Date: 11th Nov 2013</p>

<p>Qualification B.Tech (Comp. Sci.), B.Tech/M.Tech (Bioinformatics), MCA,  M.Sc. (Mathematics/Statistics)</p>

<p>Desirable Qualifications: Programming in FORTRAN/ C /PERL, Web application technologies</p>

<p>Upper Age limit 28</p>

<p>Rs.12000 / Rs.16000 (as sanctioned by the funding agency)</p>

<p>General terms and conditions:</p>

<p>    Positions are purely temporary and co-terminus with the project.</p>

<p>    HRDG (CSIR) prevailing guidelines are applicable these positions.</p>

<p>    All categories of applicants are required to submit online application.</p>

<p>    Enhancement of stipend to Project JRF to Project SRF will be with the due recommendation of Principal Investigator and approval of the Director on the evaluation of the 3 member Standing Committee consisting of Chairperson at the level of Chief Scientist, Coordinator of the JRFs/RAs/PDFs and the Principal Investigator of the Project.</p>

<p>    The age relaxation as per HRDG (CSIR) norms: SC/ST/OBC/Women/Physically Handicapped persons – five years.</p>

<p>    The Stipend normally be fixed at Rs.22000/- for Research Associates/Post Doc. Fellows. However, a selected RA/PDF may be placed in the higher start of stipend if there is ample justification and such recommendation is made by the Selection Committee. Based on the recommendation with justification by the PI and approval of the Director, person getting stipend at lower rate may be elevated to higher rate subject to availability of the funds in the project.</p>

<p>    Recruitment will be based on initial screening based on qualifications and experience criteria and also based on suitability of the candidates to the nature of research project. This screening will be followed by written test followed / interview. After completing this process, candidates will be shortlisted and appointed in specific project subjects as and when appropriate positions become available. The pool of selected candidates will be valid for six months.</p>

<p>    Remunerations indicate are maximum admissible and will depend upon the availability of funds and subject to conditions applicable to projects from different funding agencies at the time of recruitment.</p>

<p>Apply : http://www.ccmb.res.in/positions/projects/temp_positions.php</p>

<p>Form download : http://www.ccmb.res.in/positions/projects/oct-2013/pdf_download.php</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6559/ai-cadd-project-kerela-university</guid>
  <pubDate>Tue, 19 Nov 2013 17:48:15 -0600</pubDate>
  <link></link>
  <title><![CDATA[Ai-CADD Project @ Kerela University]]></title>
  <description><![CDATA[
<p>Applications are invited for the following Positions in the AiCADD project funded by MHRD Govt of India</p>

<p>Last Date for Submitting Application: 25th November 2013</p>

<p>1. Senior Scientist: (01 position)<br />Pay Scale: Rs.40, 000/-<br />Qualifications:  PhD/ Post Doctoral with Experience in CADD</p>

<p>2. Junior Scientist (10 positions)<br />Pay Scale: Rs. 22,000/-<br />Qualifications: MPhil / Masters Degree in Bioinformatics / Computational Biology / CADD / Ayurveda</p>

<p>3. Technical Assistant (01+01 positions)<br />Pay Scale: Rs.12,000/-<br />Qualifications: 1. BSc Computer Science/ MCA<br />Qualifications: 2. MSc Biotechnology / MSc Microbiology </p>

<p>4. Programmer (01 position)<br />Pay Scale: Rs.20,000/-<br />Qualifications: MSc Computer Science/ MCA / B Tech (Experience in MATLAB, C, C++) Industrial experience is desirable</p>

<p>5. Teaching Assistant (03 positions)<br />Pay Scale: Rs.10,000/-<br />Qualifications: MSc in Bioinformatics </p>

<p>6. Administration Assistant (02 positions)<br />Pay Scale: Rs.8,000/-<br />Qualifications: Degree + PGDCA</p>

<p>The Selection process comprises of written test and interview. Positions are purely temporary (initially for the period of one year) and co-terminus with the project. For more details mail to: cbi.uok [at] gmail.com</p>

<p>More detail @ https://sites.google.com/site/centreforbioinformatics/announcements/applicationsinvitedforapplicationforai-caddproject</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6577/scientist-b-vector-control-research-centre</guid>
  <pubDate>Tue, 19 Nov 2013 21:19:15 -0600</pubDate>
  <link></link>
  <title><![CDATA[Scientist-B @ VECTOR CONTROL RESEARCH CENTRE]]></title>
  <description><![CDATA[
<p>VECTOR CONTROL RESEARCH CENTRE<br />(Indian Council of Medical Research)<br />Indira Nagar Medical Complex<br />Puducherry-605006</p>

<p>WALK-IN-INTERVIEW</p>

<p>The following vacancies shall be filled purely on adhoc basis under Non-Institutional adhoc project “Bioinformatics in ICMR Institutes” funded by Indian Council of Medical Research at Vector Control Research Centre, Puducherry, to be renewed annually and filled through Walk-in-Interview as indicated below. Candidates who wish to appear for the Walk-in-Interview can download the application format given in the website of Vector Control Research Centre (www.vcrc.res.in). Duly filled in application along with attested copies of certificate should be submitted at time of interview.</p>

<p>Date &amp; Time : 05.12.2013 at 9.00 AM – Scientist-C (Non-Medical)</p>

<p>05.12.2013 at 1.30 PM – Scientist-B (Non-Medical)<br />06.12.2013 at 9.00 AM – Technical Assistant (Research Assistant)<br />06.12.2013 at 1.30 PM – Multi Tasking Staff (General)</p>

<p>Place : Vector Control Research Centre, Puducherry</p>

<p>Project entitled : Biomedical Informatics Centres of ICMR</p>

<p>1. Scientist - C (Non-Medical) Number of post – ONE</p>

<p>Essential qualification</p>

<p>B.E./ B. Tech. Degree in Bioinformatics/ Computational Biology from a recognized University with 6 years experience in the relevant field  OR</p>

<p>First class Master’s Degree and Ph.D. Degree in Bioinformatics/ Computational Biology from a recognized University OR</p>

<p>First class Master’s Degree in Bioinformatics/ Computational Biology from a recognized University with 4 years R &amp; D experience in the related subjects as mentioned above OR</p>

<p>Second class Master’s Degree + Ph.D. in Bioinformatics/ Computational Biology from a recognized University with 4 years research experience in bio-medical subjects</p>

<p>Age: Not exceeding 40 years Consolidated Salary – Rs.39,960/- p.m. + HRA as<br />admissible </p>

<p>Desirable qualification (i) Post-doctorate in Bioinformatics/ Computational Biology or M.E. / M. Tech. Degree in Bioinformatics/ Computational Biology from a recognized University for candidates with First Class relevant degree.</p>

<p>(ii) Additional post-doctoral research / teaching experience in Bioinformatics/Computational Biology in recognized Institute(s).</p>

<p>(iii) Knowledge of computer applications or data management</p>

<p>Job requirements i) To apply Bioinformatics / Computational Biology tools in understanding interactions between vectors and parasites/ pathogens and target based development of drug / insecticides.</p>

<p>ii) To assist the investigators to carry out genomic studies on parasites/pathogens/vectors of vector borne diseases</p>

<p>Advertisement: http://vcrc.res.in/Adv_Bio13.pdf</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/6835/roslin-bioinformatics-group</guid>
  <pubDate>Mon, 25 Nov 2013 23:55:25 -0600</pubDate>
  <link></link>
  <title><![CDATA[Roslin Bioinformatics Group]]></title>
  <description><![CDATA[
<p>Roslin Bioinformatics Group</p>

<p>The Law group provides internal Institute-specific development, training and support roles for data manipulation, sequence analysis and any other aspect of the analysis of biological data using computer systems. Additionally we provide databases and applications supporting the international animal science community, particularly tools and resources for genome mapping.</p>

<p>Head: Andy Law. Members: John Bowman (animal facility database applications), Zen Lu (bioinformatics support), Trevor Paterson (software development)</p>

<p>More @ http://www.bioinformatics.ed.ac.uk/groups/roslin-bioinformatics-group</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/17946/7th-international-conference-on-bioinformatics-and-computational-biology-bicob</guid>
	<pubDate>Mon, 06 Oct 2014 16:19:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/17946/7th-international-conference-on-bioinformatics-and-computational-biology-bicob</link>
	<title><![CDATA[7th International Conference on Bioinformatics and Computational Biology (BICoB)]]></title>
	<description><![CDATA[<p><span>In recent years, computational biology and medical informatics have seen significant advances driven by computational techniques in bioinformatics making bioinformatics and computational biology among the most vibrant research areas. The 7th international conference on Bioinformatics and Computational Biology (BICoB-2015) provides an excellent venue for researchers and practitioners in the fields of bioinformatics and computational biology to present and publish their research results and techniques. The BICoB conference seeks original and high quality papers in the fields of bioinformatics, computational biology, systems biology, medical informatics and the related disciplines. </span><span>We also encourage work in progress and research results in the emerging and evolutionary computational areas. Computational techniques have already enabled unprecedented advances in modern biology and medicine. Work in the computational methods related to, or with application in, bioinformatics is also encouraged including: data mining, text mining, machine learning, modeling and simulation, pattern recognition, data visualization, biostatistics, .etc. The topics of interest include (and are not limited to):&nbsp;</span><br><strong><span>Genome analysis:</span></strong><span>&nbsp;Genome assembly, genome annotation, gene finding, alternative splicing, EST analysis and comparative genomics.&nbsp;</span><br><strong><span>Sequence analysis:</span></strong><span>&nbsp;Multiple sequence alignment, sequence search and clustering, function prediction, motif discovery, functional site recognition in protein, RNA and DNA sequences.&nbsp;</span><br><strong><span>Phylogenetics:</span></strong><span>&nbsp;Phylogeny estimation, models of evolution, comparative biological methods, population genetics.&nbsp;</span><br><strong><span>Structural Bioinformatics:</span></strong><span>&nbsp;Structure matching, prediction, analysis and comparison; methods and tools for docking; protein design&nbsp;</span><br><strong><span>Analysis of high-throughput biological data:</span></strong><span>&nbsp;Microarrays (nucleic acid, protein, array CGH, genome tiling, and other arrays), EST, SAGE, MPSS, proteomics, mass spectrometry.&nbsp;</span><br><strong><span>Genetics and population analysis:</span></strong><span>&nbsp;Linkage analysis, association analysis, population simulation, haplotyping, marker discovery, genotype calling.&nbsp;</span><br><strong><span>Systems biology:</span></strong><span>&nbsp;Systems approaches to molecular biology, multiscale modeling, pathways,gene networks.&nbsp;</span><br><strong><span>Computational Proteomics:&nbsp;</span></strong><span>Filtering and indexing sequence databases, Peptide quantification and identification, Genome annotations via mass spectrometry, Identification of post-translational modifications, Structural genomics via mass spectrometry, Protein-protein interactions, Computational approaches to analysis of large scale Mass spectrometry data, Exploration and visualization of proteomic data, Data models and integration for proteomics and genomics, Querying and retrieval of proteomics and genomics data etc.</span></p>
<p><span><span>Authors of selected high quality papers in BICoB-2015 will be invited to submit extended version of their papers for possible publication in bioinformatics journals (</span><a href="http://www.worldscinet.com/jbcb/" target="_blank"><strong>Journal of Bioinformatics and Computational Biology JBCB).</strong></a></span></p>
<p><span><strong>Deadlines</strong>:</span></p>
<p><span></span></p>
<p>Paper Submission Deadline October 24, 2014<br>Notification of Acceptance December 15, 2014<br>Camera-Ready Manuscript January 16, 2015</p>
<p><span></span></p><p>Address of the bookmark: <a href="http://www.cs.umb.edu/bicob/" rel="nofollow">http://www.cs.umb.edu/bicob/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/7569/phd-at-university-of-calgary</guid>
  <pubDate>Fri, 27 Dec 2013 20:24:39 -0600</pubDate>
  <link></link>
  <title><![CDATA[PhD at University of Calgary]]></title>
  <description><![CDATA[
<p>Institution/Company: <br />University of Calgary<br />Location: <br />Calgary, AB<br />Job Description: </p>

<p>Novel diagnostic platform for detection of Osteoarthritis</p>

<p>I invite applications from highly motivated individuals to join my laboratory as a PhD student in Systems Biology at the University of Calgary McCaig Institute for Bone and Joint Health. This project is aimed at characterizing the networks of physical (protein-protein) interactions underlying inflammatory processes in patients with Osteoarthritis and how this differs from patients with Rheumatoid Arthritis and normal individuals. This work will eventually lead to the development of a novel diagnostic platform for the non-invasive and accurate detection of early Osteoarthritis. The selected candidate will use state-of-the-art computational methodologies to systematically analyze proteomic data, and develop /implement new algorithms to identify protein and functional interaction networks from high throughput experimental data. The individual will also benefit by working closely with experts at the UofC and UofA through an AIHS Alberta Osteoarthritis Team Grant which includes experts from all pillars of health research. The candidate will also be supported to attend bioinformatics workshops and conferences to advance and disseminate their research.<br />Qualifications: The ideal candidate will have a Master’s degree in Computational Biology, Bioinformatics, or equivalent with strong background knowledge of the Biological Sciences, Biochemistry, and Microbiology. The individual should additionally have experience in handling high-throughput data sets as well as programming skills. The candidate will be registered as a PhD student in Dr. Krawetz’s laboratory, located in the new state-of-the-art Health Research Innovation Centre at the UofC. The individual will have strong verbal and written skills and the ability to work efficiently in a team environment.</p>

<p>In addition to the outstanding research opportunities available in this setting, students also enjoy the many cultural and sporting amenities provided in the city of Calgary, and can take advantage of the unparalleled skiing and hiking in the Rocky Mountains that are less than an hour away.</p>

<p>Candidates must be academically competitive and will be expected to apply for external funding. The stipend is $25,000/yr. For outstanding PhD students, internal top-up award opportunities are available on a competitive basis. If interested in joining the lab, please contact Dr. Krawetz directly at rkrawetz@ucalgary.ca and provide the following information:</p>

<p>- Short cover letter explaining your interest in the lab<br />- Resume<br />- Scanned copy of transcript or listing of course grades<br />- Names and contact information for two individuals who will be willing to provide letters of reference</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/22179/marie-curie-phd-position-available-immediately</guid>
  <pubDate>Fri, 24 Apr 2015 09:23:57 -0500</pubDate>
  <link></link>
  <title><![CDATA[Marie Curie PhD position available immediately]]></title>
  <description><![CDATA[
<p>Sub-project 10: Development of bioinformatic tools for the analysis of MACE data<br />Host Organizations GenXPRO (Germany)<br />Objectives : The ESR will be in charge of standardising pipelines that will be used for RNA-seq and MACE analyses by all the participants. He will be involved in performing next generation sequencing to characterise environmental adaptation. A single pipeline to analyse listerial transcriptomic and proteomic data will be developed and implemented by each partner for the sake of uniformity of all the data produced within List_MAPS. The ESR will be involved in the interpretation of transcriptomic and proteomic data for which pathway analyses and good data visualization will be required. A cytoscape app will be developed as visualization tool.<br />Expected Results: MACE analysis pipeline. Database. Transcriptome comparisons in selected habitats. Data visualization tool.<br />Duration (months) 24<br />Contact Dr. Bjorn ROTTER: rotter@genxpro.de </p>

<p>11. Development of innovative tools for rapid phenotypic characterisation of intraspecific diversity of Listeria monocytogenes (Joint supervision PhD)<br />Host Organizations BioFilm Control (France) and GenXPRO (Germany)<br />Objectives<br /> 1. The ESR will develop an assay to test biofilm phenotype in a large array of food processing-related environmental conditions (salt, acides, disinfectants, preservatives) in BFC facilities. He will be in charge of the development and validation of an in silico virulence assay. This assay will target specific mRNAs in order to estimate the virulence potential of strains of L. monocytogenes. Transcript targets will be selected and tested by qPCR in GXP premises. In the process of validation, virulence results of several strains collected in a humanised mouse model will be compared with the in silico analysis. Once these innovative tools will be validated, intraspecific phenotypic diversity (biofilm and virulence) will be assessed on a collection of environmental and clinical isolates of L. monocytogenes. Genotypic diversity will be assessed under the supervision of GPX.<br />Expected Results : Adaptation of the BioFilm Ring test R to test food processing environmental conditions. Development of an innovative in silico virulence assay surrogate to animal models. Diversity results will inform stakeholders on the level of health hazard according to the strain. This in turn will help secure food safety all along the shelf life of foodstuff.<br />Duration (months) 36<br />Contact : Dr. Thierry BERNARDI: thbe@biofilmcontrol.com <br />Dr. Bjorn ROTTER: rotter@genxpro.de<br />ELIGIBLE CRITERIA of Marie Sklokowska Curie actions:<br />Researchers may be of any nationality<br />Candidates shall at the time of recruitment by the host organization, be in the first four years (full-time equivalent research experience) of their research careers. Full-time equivalent research experience is measured from the date when a researcher obtained the degree which would formally entitle him or her to embark on a doctorate, either in the co</p>
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