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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/32483?offset=1000</link>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45115/postdoctoral-fellow-in-genomics-and-comparative-genomics</guid>
  <pubDate>Thu, 09 Apr 2026 02:12:32 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Fellow in Genomics and Comparative Genomics]]></title>
  <description><![CDATA[
<p>Environnement de travail (Work environment):<br />The successful candidate will join a dynamic research group working<br />on the ecology and evolution of host'parasite'environment<br />interactions in non-model organisms, particularly snail vectors and<br />its trematode parasites. She/He will conduct genomic analyses aimed at<br />understanding host'parasite coevolution and the genetic architecture<br />of resistance in the invasive snail Pseudosuccinea columella to the<br />zoonotic parasite Fasciola hepatica. This thematic line is embedded<br />within the regional scientific project InvaSnail financed by the<br />ExposUM initiative from the Montpellier. The position is based in<br />Montpellier, a vibrant scientific hub in Southern France internationally<br />recognized for excellence in ecology and evolutionary biology. The IHPE<br />laboratory provides a collaborative research environment with access<br />to high-performance computing facilities, sequencing platforms, and<br />strong interdisciplinary interactions across research institutions in<br />the Montpellier area. University</p>

<p>Main mission:</p>

<p>Develop and implement strategies for whole-genome sequencing of non-model<br />species<br />Generate high-quality de novo genome assemblies using short- and long-read<br />sequencing technologies<br />Perform genome annotation and structural/functional characterization<br />Conduct comparative genomic analyses across related species or populations<br />Design and implement genome-wide association studies (GWAS) to identify<br />loci associated with phenotypic or adaptive traits<br />Integrate genomic, phenotypic, and environmental datasets<br />Contribute to the development of reproducible bioinformatics pipelines</p>

<p>ActivitÃ©s (Activities):</p>

<p>Lead the genomic component of the research project<br />High-molecular-weight DNA extraction optimization<br />Long-read genome assembly (PacBio HiFi / ONT)<br />Genome polishing and quality assessment (BUSCO, QUAST)<br />Structural and functional annotation<br />Variant discovery (SNPs, indels, SVs)<br />Population genomic analyses (FST, demographic inference)<br />Mixed-model GWAS accounting for structure<br />Workflow development (Snakemake/Nextflow)<br />HPC-based pipeline implementation<br />Publish results in peer-reviewed journals<br />Present findings at international conferences<br />Collaborate with experimental and computational team members<br />Contribute to project development<br />Mentor graduate students when appropriate</p>

<p>More at https://evol.mcmaster.ca/brian/evoldir/PostDocs//MontpellierU.ComparativeGenomics</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/1469/prime-minister%E2%80%99s-100k-genome-project</guid>
	<pubDate>Thu, 08 Aug 2013 09:40:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/1469/prime-minister%E2%80%99s-100k-genome-project</link>
	<title><![CDATA[Prime Minister’s 100k Genome Project]]></title>
	<description><![CDATA[<p>Genomics Ebgland is destined to sequence 100,000 patients over the next five year in England.&nbsp; A landmark project by british government.</p><p>Genomics England will play a key role in building on the UK&rsquo;s long track record as leader in medical science advances to push the boundaries by unlocking the power of DNA data. The UK will become the first ever country to introduce this technology in its mainstream health system &ndash; leading the global race for better tests, better drugs and above all better, more personalised care.</p><p>http://www.genomicsengland.co.uk/100k-genome-project/</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45226/professor-of-bioinformatics</guid>
  <pubDate>Sat, 15 Aug 2026 12:39:03 -0500</pubDate>
  <link></link>
  <title><![CDATA[Professor of Bioinformatics]]></title>
  <description><![CDATA[
<p>The Department of Statistics are seeking to recruit a Professor of Bioinformatics. The professorship will be held alongside a Fellowship at University College.</p>

<p>The Department is at the forefront of developments in machine learning, data science, and computational methods for understanding complex biological systems, integrating these approaches into both its research and teaching. This role offers significant scope to shape the future of bioinformatics and quantitative biology at Oxford and beyond.</p>

<p>You will be expected to develop and lead a world-class research programme in bioinformatics, helping to strengthen Oxford's position in areas such as statistical genomics, computational biology, machine learning for biological data, engineering biology, systems biology, and biomedical data science. We value the breadth of approaches that contribute to modern bioinformatics. Whatever your particular focus, you will understand how quantitative and computational methods can be applied to important biological and biomedical questions, and how collaboration across disciplines can generate new insights and opportunities. Alongside your own research, you will support the development of doctoral students, postdoctoral researchers, and early-career academics. You will contribute to our teaching at undergraduate and postgraduate level, delivering lectures, supervising student projects, and supporting graduate research students.</p>

<p>We are looking for someone who combines scholarly distinction with a collaborative and ambitious approach to research. You will be a researcher with an international reputation in bioinformatics, with a strong record of producing influential research at the interface of statistics, computational biology, genomics, and data science, and of securing research funding. Your work should advance the field, whether through methodological innovation, biological discovery, or the development of new approaches to understanding complex biological and biomedical data. You will bring experience of shaping research strategy, building productive collaborations, and exercising academic leadership. Above all, we wish to appoint someone who shares our values of intellectual curiosity, academic excellence, scholarly integrity, and a commitment to fostering a positive, supportive, and inclusive environment for all.</p>

<p>If you would like to discuss this post, please contact the Head of the Department of Statistics, Professor Frank Windmeijer, frank.windmeijer@stats.ox.ac.uk, or for information about University College please contact the Senior Tutor, Dr Andrew Bell, andrew.bell@univ.ox.ac.uk. All enquiries will be treated in strict confidence and will not form part of the selection decision.</p>

<p>The closing date for applications is 12:00 noon UK time on Monday 21 September 2026. Interviews are expected to be held in November 2026.</p>

<p>Apply here https://my.corehr.com/pls/uoxrecruit/erq_jobspec_version_4.display_form</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/1491/2013-nextgen-genomics-bioinformatics-technologies-ngbt-conference-new-delhi-india</guid>
  <pubDate>Thu, 08 Aug 2013 16:21:16 -0500</pubDate>
  <link></link>
  <title><![CDATA[2013 NextGen Genomics &amp; Bioinformatics Technologies (NGBT) Conference, New Delhi, INDIA]]></title>
  <description><![CDATA[
<p>2013 NextGen Genomics &amp; Bioinformatics Technologies (NGBT) Conference</p>

<p>SciGenom Research Foundation (SGRF) and Institute of Genomics and Integrative Biology (IGIB) are pleased to host the Next-Generation Sequencing and Bioinformatics for Genomics &amp; Healthcare conference.</p>

<p>In the ten years since the first human reference genome was completed for US$3 billion the sequencing technologies have radically changed leading to great reduction in sequencing cost. Today a human genome can be sequenced for under US$ 5000 in less than two weeks. It is expected that by the end of 2015 the cost of sequencing a human genome will drop to below thousand dollars. The next generation sequencing technologies over the past five years have enabled a large number of genomic studies that impact human health and disease. Also, this has made possible the growth of microbial, animal and plant genomics studies. While the data production has increased at a rapid pace challenges remain in analyzing and understanding the data. The conference will cover the next generation sequencing (NGS) technologies, bioinformatics for NGS and applications of NGS in many areas including personalized medicine.</p>

<p>For more info : http://www.scigenomconferences.com/2013/default.php</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/45337/yeaman-lab</guid>
  <pubDate>Wed, 16 Sep 2026 04:01:26 -0500</pubDate>
  <link></link>
  <title><![CDATA[Yeaman Lab]]></title>
  <description><![CDATA[
<p>The natural world is a diverse place. To contend with highly variable environments, organisms have evolved a wide range of traits and behaviours as adaptations to their environment. From armour plating in stickleback to trade-offs between growth rate and cold tolerance in lodgepole pine, organisms have found many different genetic solutions to the challenge of existing in their environment. In my lab, we study a range of questions asking how such complex adaptations evolve: <br />How is the genetic basis of local adaptation shaped by the interplay between natural selection and dispersal?<br />Does the architecture of genome evolve to facilitate further adaptation?<br />How can we use genomic technologies and bioinformatics to study adaptation?<br />How do organisms adapt to rapidly changing environments?</p>

<p>To attempt to answer these questions about the basics of how evolution works, we use a combination of computational biology, analytical theory, comparative genomics.</p>

<p>More at https://yeamanlab.weebly.com</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/1720/postdoctoral-associate-bioinformatics-at-duke-university-medical-center</guid>
  <pubDate>Sat, 10 Aug 2013 18:38:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Associate - Bioinformatics  at Duke University Medical Center]]></title>
  <description><![CDATA[
<p>The Department of Biostatistics and Bioinformatics at Duke University Medical Center is seeking a Postdoctoral Associate for a one year appointment to work on several high-dimensional research projects. The specific goals of the project are to identify genes or molecular markers that are predictive of clinical outcomes in renal and prostate cancer.</p>

<p>Candidates must have: a PhD degree in statistics, biostatistics or bioinformatics, extensive experience in analyzing high-dimensional data (microarray, SNP, CNVs) and of validation approaches. In addition, experience in penalized regression methods, data base manipulation; and strong programming skills in order to conduct Monte Carlo studies and applications (R). Candidate must have excellent communication skills (verbal, written and presentation), a strong proficiency in Linux system.</p>

<p>This position is available immediately and will be filled as soon as possible. Appointment could be extended beyond the first year based on additional funding.</p>

<p>For more information about the Department of Biostatistics and Bioinformatics, please visit our website: http://www.biostat.duke.edu.</p>

<p>For more info: http://biostat.duke.edu/sites/biostat.duke.edu/files/Halabi%20-%20Postdoc%20Job%20Posting%202013%20updated.pdf</p>

<p>Duke University is an Equal Opportunity/Affirmative Action Employer.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/fun/view/4196/chemical-elements-of-bioinformatics</guid>
	<pubDate>Tue, 03 Sep 2013 16:35:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/fun/view/4196/chemical-elements-of-bioinformatics</link>
	<title><![CDATA[Chemical Elements of Bioinformatics]]></title>
	<description><![CDATA[<p>You must be familiar with periodic table and colour pattern, but this time you are going to amaze by new elements table by Eagle genomics. Just check it out and have fun :)</p><p><a href="http://elements.eaglegenomics.com/">http://elements.eaglegenomics.com/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/2021</guid>
	<pubDate>Mon, 12 Aug 2013 09:27:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/2021</link>
	<title><![CDATA[What are the difference between BioRuby and BioGem?]]></title>
	<description><![CDATA[<p>I came across two diferent but matching term BioRuby and BioGem. What are the difference between these two term? If both are using same Ruby language for development then why did they develope two different biological packages.</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/3889/bioinformatics-and-sequencing-courses-and-workshops</guid>
	<pubDate>Sat, 24 Aug 2013 16:41:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/3889/bioinformatics-and-sequencing-courses-and-workshops</link>
	<title><![CDATA[Bioinformatics and Sequencing Courses and Workshops]]></title>
	<description><![CDATA[<p>Swiss Institute of Bioinformatics (SIB) organises lots of bioinformatics courses covering wide range of topics:</p><p><a href="http://www.isb-sib.ch/education/training-courses.html">http://www.isb-sib.ch/education/training-courses.html</a></p><p>Canadian bioinformatics also organises various bioinformatics and sequencing courses:</p><p><a href="http://bioinformatics.ca/workshops">http://bioinformatics.ca/workshops</a></p><p>In addition to above two, EMBI&nbsp;Europe, EMBO Europe, Cold Spring Harbour USA, Wellcome Trust UK and NOVA&nbsp;Europe&nbsp;also organise bioinformatics and sequencing courses annually:</p><p><a href="http://www.embl.de/training/events/index.php?p_outstation=ALL">http://www.embl.de/training/events/index.php?p_outstation=ALL</a></p><p><a href="http://www.embo.org/funding-awards/courses-workshops">http://www.embo.org/funding-awards/courses-workshops</a></p><p><a href="http://meetings.cshl.edu/courses.html">http://meetings.cshl.edu/courses.html</a></p><p><a href="http://www.wellcome.ac.uk/Education-resources/Courses-and-conferences/Advanced-Courses-and-Scientific-Conferences/Advanced-Courses/index.htm">http://www.wellcome.ac.uk/Education-resources/Courses-and-conferences/Advanced-Courses-and-Scientific-Conferences/Advanced-Courses/index.htm</a></p><p><a href="http://www.nova-university.org/pagetop.cfm?MenySidorTop_id=2&amp;open=7">http://www.nova-university.org/pagetop.cfm?MenySidorTop_id=2&amp;open=7</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/4090/computational-biology-in-the-21st-century-making-sense-out-of-massive-data</guid>
	<pubDate>Thu, 29 Aug 2013 08:32:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/4090/computational-biology-in-the-21st-century-making-sense-out-of-massive-data</link>
	<title><![CDATA[Computational Biology in the 21st Century: Making Sense out of Massive Data]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/I99UiA_vaJQ" frameborder="0" allowfullscreen></iframe>Computational Biology in the 21st Century: Making Sense out of Massive Data    
    
Air date:  Wednesday, February 01, 2012, 3:00:00 PM
Category:  Wednesday Afternoon Lectures  
 
Description:  The last two decades have seen an exponential increase in genomic and biomedical data, which will soon outstrip advances in computing power to perform current methods of analysis. Extracting new science from these massive datasets will require not only faster computers; it will require smarter algorithms. We show how ideas from cutting-edge algorithms, including spectral graph theory and modern data structures, can be used to attack challenges in sequencing, medical genomics and biological networks. 

The NIH Wednesday Afternoon Lecture Series includes weekly scientific talks by some of the top researchers in the biomedical sciences worldwide. 

Author:  Dr. Bonnie Berger  
Runtime:  00:58:06  
Permanent link:  http://videocast.nih.gov/launch.asp?17563]]></description>
	
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