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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/26535?offset=1090</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/5191/programming-language-to-build-synthetic-dna</guid>
	<pubDate>Mon, 30 Sep 2013 16:37:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/5191/programming-language-to-build-synthetic-dna</link>
	<title><![CDATA[Programming language to build synthetic DNA]]></title>
	<description><![CDATA[<p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;">A team led by <a href="http://homes.cs.washington.edu/~seelig/index.html">Georg Seelig</a>&nbsp;(<a href="http://homes.cs.washington.edu/~seelig/index.html">http://homes.cs.washington.edu/~seelig/index.html</a>) at&nbsp;University of Washington has developed a programming language for chemistry that it hopes will streamline efforts to design a network that can guide the behavior of chemical-reaction mixtures in the same way that embedded electronic controllers guide cars, robots and other devices. In medicine, such networks could serve as &ldquo;smart&rdquo; drug deliverers or disease detectors at the cellular level.</p><p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;">Reference &amp; More @</p><p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;"><a href="http://www.nature.com/nnano/journal/vaop/ncurrent/full/nnano.2013.189.html">http://www.nature.com/nnano/journal/vaop/ncurrent/full/nnano.2013.189.html</a></p><p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;"><a href="http://www.washington.edu/news/2013/09/30/uw-engineers-invent-programming-language-to-build-synthetic-dna/">http://www.washington.edu/news/2013/09/30/uw-engineers-invent-programming-language-to-build-synthetic-dna/</a></p><p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;">Image source:&nbsp;washington.edu</p><p style="color: #333333; font-size: 13px; font-style: normal; font-weight: normal; text-align: start;"><img src="http://www.washington.edu/news/files/2013/09/Programmable-chemistry-2.jpg" alt="image" style="border: 0px; border: 0px;"></p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/22938/research-assistant-in-computational-biology</guid>
  <pubDate>Wed, 24 Jun 2015 07:55:16 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research assistant in computational biology]]></title>
  <description><![CDATA[
<p>http://www.au.dk/en/about/vacant-positions/scientific-positions/stillinger/Vacancy/show/743161/5283/</p>

<p>Qualifications:<br />MSc degree in computer science, engineering, genetics or similar field with a strong emphasis on computational methods.</p>

<p>Deadline<br />01.08.2015</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34386/slidesort-bpr</guid>
	<pubDate>Mon, 20 Nov 2017 09:19:52 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34386/slidesort-bpr</link>
	<title><![CDATA[SLIDESORT-BPR]]></title>
	<description><![CDATA[<p>Chromosomal rearrangement events are caused by abnormal breaking and rejoining of DNA molecules. They are responsible for many of the cancer related diseases. Detecting the DNA breaking and repairing mechanism, therefore, may offer vital clues about the pathologic causes and diagnostic/therapeutic target of these diseases. But this effort also poses considerable challenges, because the structural variations and the genomes are different from one person to another. Intermediate comparison via reference genome could lead to the loss information. Unlike the current methods which make use the reference genome, we developed a method to detect the breakpoint reads directly from observing the differences between two (or more) NGS short reads samples. Slidesort-BPR is a command line tool implemented in C++.</p><p>Address of the bookmark: <a href="https://github.com/ewijaya/slidesort-bpr" rel="nofollow">https://github.com/ewijaya/slidesort-bpr</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/38293/tree-illustrating-the-lack-of-interchromosomal-rearrangement-of-the-microchromosomes</guid>
	<pubDate>Mon, 26 Nov 2018 04:20:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/38293/tree-illustrating-the-lack-of-interchromosomal-rearrangement-of-the-microchromosomes</link>
	<title><![CDATA[Tree illustrating the lack of interchromosomal rearrangement of the microchromosomes.]]></title>
	<description><![CDATA[<p><span>Tree illustrating the lack of interchromosomal rearrangement of the microchromosomes. No interchromosomal microchromosome fusions from the avian ancestor unless otherwise stated (macrochromosomal fusions not listed). The overall pattern of microchromosome stability and rearrangement across the species is illustrated</span></p><p><span><span>Jarvis et al. (2014)</span></span></p><p><span><span>Reference&nbsp;https://link.springer.com/article/10.1007/s00412-018-0685-6</span></span></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/12883/breaking-chromosomes-to-study-cancer</guid>
	<pubDate>Fri, 18 Jul 2014 05:42:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/12883/breaking-chromosomes-to-study-cancer</link>
	<title><![CDATA[Breaking chromosomes to study cancer !!!]]></title>
	<description><![CDATA[<p>Chromosomes are present in every cell of our body and they contain the information the body needs to develop and function properly. This information is carried in genes that are arranged along the chromosomes. There are usually 46 chromosomes in every cell. These chromosomes come in pairs, one from our mother and one from our father. The chromosomes can be sorted into 23 pairs by looking at them down a microscope.</p><p>Most people who have a balanced translocation have the right amount of chromosome material but it has been rearranged in some way. This may happen if two chromosomes swap pieces (a reciprocal translocation). In other cases two whole chromosomes may become stuck together (a Robertsonian translocation). This page describes what happens when someone has a reciprocal translocation. <br /><br />Reciprocal chromosomal translocations occur following double-strand breaks (DSBs) in DNA when a section of one chromosome is exchanged with that of another, non-homologous chromosome. These exchanges may produce a dysfunctional fusion gene that disrupts cell growth and survival pathways, such as the translocations seen in leukemia and childhood sarcomas. <br /><br />Chromosomal translocations have been well studied in cancer cell lines which are associated with two types of cancer, acute myeloid leukemia and Ewing's sarcoma, but determining how they contribute to cancer development is complicated by additional mutations and altered gene expression profiles in these cultured cells. Now, Juan Carlos Ramirez, head of the Viral Vector Facility at the Fundacion Centro Nacional de Investigaciones Cardiovasculares (CNIC) and his colleagues Raul Torres at CNIC and Sandra Rodriguez-Peralez at the Spanish National Cancer Center (CNIO) in Madrid, Spain have used a new genome editing tool, CRISPR-Cas9, to induce chromosomal translocations for the first time in a human cell line and in primary cells. The study's authors conclude by stating that the use of this technology will allow for the clarification of how and why chromosomal translocation occurs, which without doubt will allow new anti-cancer therapeutic strategies to be tackled.</p><p>Using RNA-Guided Endonuclease (RGEN) technology or CRISPR/Cas9 genome engineering technology, CNIO and CNIC researchers have shown that it is possible to obtain such chromosomal translocations. The CRISPR-Cas9 system is extremely simple to introduce a cut at the desired locus, easier to design, and cheaper than many other systems. Using the CRISPR-Cas9 system, Ramirez and his colleagues reproduced the translocations observed in Ewing&rsquo;s Sarcoma (ES) and Acute Myeloid Leukemia (AML) patient cell lines in HEK293 cells and also generated the ES translocation in human mesenchymal stem cells and the AML translocation in umbilical cord blood cells.</p><p>By focusing on chromosomal translocation without the confounding characteristics of established cell lines, these new cells lines should help answer the fundamental question of what causes a cell to become cancerous. Ramirez and his team now look forward to modeling other chromosome translocations in a variety of cell types.</p><p>Reference:</p><p>http://en.wikipedia.org/wiki/Chromosomal_translocation</p><p>http://www.nature.com/ncomms/2014/140603/ncomms4964/abs/ncomms4964.html<br /><br /></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17504/postdoc-scientist-bioinformatics-at-ccmb</guid>
  <pubDate>Fri, 26 Sep 2014 19:58:41 -0500</pubDate>
  <link></link>
  <title><![CDATA[PostDoc Scientist Bioinformatics at CCMB]]></title>
  <description><![CDATA[
<p>1. Project Assistant/Junior Research Fellow/ Project Fellow [PA_JRF_PF]</p>

<p>a) M.Sc/or equivalent in biological sciences/related areas [Position Code: PA_JRF_PF_a]<br />b) B.E/B.Tech/ M.Sc in biotechnology/bioinformatics/computer science/Chemistry/Physics or MCA [Position Code: PA_JRF_PF_b]<br />c) M.Sc/or equivalent in wildlife sciences/ecology/environmental sciences or MBBS/BVSc/MVSc. [Position Code: PA_JRF_PF_c]</p>

<p>(Candidates with result awaited are NOT eligible to apply)</p>

<p>Upper Age limit 28years</p>

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

<p>2. Post Doctoral Fellow/Research Associate in multiple research areas [PDF_RA]</p>

<p>Ph.D. (submitted/awarded) in any branch of biological Sciences. Candidates with Ph.D. in other sciences are also encouraged to apply.</p>

<p>Experience in molecular biology, biochemistry, structural biology, cell biology, infectious disease, conservation genetics, veterinary science, reproductive biology, and molecular diagnostics is desired but not mandatory.</p>

<p>[Position Code: PDF_RA]</p>

<p>UpperAge limit 35years</p>

<p>Rs. 22000- 26000 (as sanctioned by the funding agency)</p>

<p>3. Post Doctoral Scientist Fellow [PDSF]</p>

<p>Ph.D in any of the following areas: bioinformatics, next generation sequencing, high throughput data analysis, proteomics, bio-statistics, computer science, information technology, computer hardware and networking/clustering, parallel processing.<br />[Position Code: PDSF]</p>

<p>Upper Age limit 40 years</p>

<p>Rs. 40000 consolidated (as sanctioned by the funding agency)</p>

<p>Download Application: Last date for apply online: 09th Oct 2014</p>

<p>Advertisement: www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>

<p>Apply online http://www.ccmb.res.in/positions/temp_notif/online_form.html</p>

<p>More at http://www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/17652/arraygen-bioinformatics-genomics-group</guid>
  <pubDate>Sun, 28 Sep 2014 14:09:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[ArrayGen Bioinformatics Genomics Group]]></title>
  <description><![CDATA[
<p>ArrayGen is a global bioinformatics company which is a one stop solution for microarray designing and genomics data analysis. Our novel Array Design Approach Strategy (ADAS) aims to condense the time lag between demands of scientific community and manufacture industry, thereby expediting research processes.</p>

<p>ArrayGen specializes in Genomics data analysis and research, as we believe in the level of precision, predictability, benchmark-ability, and data analysis capability of genomics data over other forms of biological data. ArrayGen constantly strives to develop new solutions, and plug the existing gaps in the technological advancement of the field.</p>

<p>More http://www.arraygen.com/</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17873/postdoc-position-in-protein-annotation-and-machine-learning-paris-france</guid>
  <pubDate>Sat, 04 Oct 2014 08:10:45 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoc position in protein annotation and machine learning - Paris, France]]></title>
  <description><![CDATA[
<p>We are interested in finding an excellent postdoc with interests in protein functional annotation, machine learning and computer grids. The position is open for 3.5 years at the Université Pierre et Marie Curie, in the heart of Paris.</p>

<p>Research topic: Protein function annotation, multiple probabilistic models, domain architecture, machine learning, combinatorial optimization, computer grid.</p>

<p>This project is run on the Laboratoire de Biologie Computationnelle et Quantitative UMR7238 CNRS-UPMC – Analytical Genomics team, headed by A.Carbone. It is co-advised with Pierre-Henri Wuillemin, Laboratoire d’Informatique de Paris 6 – Equipe DECISION.</p>

<p>The postdoc will be payed under a contract of Ingénieur de Recherche lasting 3.5 years and it is available from September 1st, 2014.</p>

<p>Group Web Page: http://www.lcqb.upmc.fr/AnalGenom/home.html</p>

<p>Ref. E-Mail: Alessandra Carbone alessandra.carbone@lip6.fr</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/18819/jrfsrf-at-jawaharlal-nehru-institute-ofadvanced-studies-jnias-hyderabad</guid>
  <pubDate>Fri, 31 Oct 2014 08:48:23 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF/SRF at Jawaharlal Nehru Institute ofAdvanced Studies (JNIAS), Hyderabad]]></title>
  <description><![CDATA[
<p>Applications for Academic Projects in Biotechnology, Bioinformatics, Environmental Sciences and Computer Science &amp; Engineering</p>

<p>About JNIAS<br />Jawaharlal Nehru Institute of Advanced Studies (JNIAS), Hyderabad has been established by Dr. D. Swaminadhan Research Foundation (DSRF), Hyderabad as a Research and Educational Institution with a view to contribute in developing advanced technologies and build „core competence‟ in specific areas. The activities of JNIAS involves: Education, Research Training and Innovations in the fields of Sciences, Technologies, Humanities and Social Sciences. It aims to blossom into an Advanced Institute of education and research with a reservoir of expertise and experience in the relevant fields and the necessary capability to harness multi-disciplinary research and studies. JNIAS has been recognized as an Advanced Research Institute by Jawaharlal Nehru Technological University Hyderabad (JNTUH), Hyderabad and Jawaharlal Nehru Technological University Anantapur (JNTUA), for offering Ph.D., P.G M.Phil, P.G Diploma and Training Programmes in Sciences and Engineering &amp; Technology.</p>

<p>Jawaharlal Nehru Architecture and Fine Arts University (JNAFAU) Hyderabad also recognized JNIAS for offering UG, PG degree in Architecture.</p>

<p>Projects &amp; Facilities</p>

<p>JNIAS offers wide range of projects:</p>

<p>Biotechnology area:</p>

<p>Molecular Biology<br />Microbiology<br />Nanotechnology<br />Bioinformatics (Schrodinger Software)<br />In Silico studies &amp; Drug Designing<br />Sequence analysis<br />Protein structure function studies</p>

<p>Registration<br />Tuition Fees: Interested students need to pay the following tuition fees:<br />1. Six Month’s Project: Rs. 20,000/-<br />2. Four Month’s Project: Rs. 15,000/-<br />3. Three Month’s Project: Rs. 10,000/-<br />4. One Month - Hands on Training : Rs. 8,000/-</p>

<p>For enquires call:<br />91-7893203414 (Biotechnology), 91-9949582263 (Environmental Sciences) 91-8977369305 (Computer Science)</p>

<p>Interested student may download the application from the website (www.jnias.in) and send the hard copy of the completed application forms and Curriculum Vitae along with the Demand Draft drawn on any nationalized Banks in favor of “The Registrar, JNIAS, Secunderabad”. Application forms can be sent through email to academicprojects@jnias.in</p>

<p>Address<br />Jawaharlal Nehru Institute of Advanced Studies (JNIAS)<br />6th Floor, Buddha Bhavan, M.G Road,<br />Secunderabad - 500 003<br />Andhra Pradesh, India<br />Tele/Fax: 040- 27541551; 27541553<br />Mobile: 08885541554<br />Web site: www.jnias.in</p>

<p>Brochure : https://drive.google.com/file/d/0B3zPwhgA-u-nU0dyMFd2OWcxNUpSTWNYc0xDSGs5UDI4UDNB/view?usp=sharing</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/18866/celebrating-crystallography-an-animated-adventure</guid>
	<pubDate>Fri, 31 Oct 2014 15:59:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/18866/celebrating-crystallography-an-animated-adventure</link>
	<title><![CDATA[Celebrating Crystallography - An animated adventure]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/uqQlwYv8VQI" frameborder="0" allowfullscreen></iframe>NEW: Now with French or Spanish subtitles (click on the 'Captions' icon to select). Plus... Watch the French language version here: https://www.youtube.com/watch?v=PvLu7BOsJhM

X-ray crystallography is arguably one of the greatest innovations of the twentieth century, but not that many people know what it is or how it came about.

Join us on an animated journey through the 100 year history of crystallography -- from the pioneering work of William and Lawrence Bragg in 1913 to the surface of Mars!

Narrated by structural biologist Stephen Curry and produced by animation company 12foot6, the film explores the extraordinary history of crystallography. To date 28 Nobel Prizes have been awarded to projects related to the field and X-ray crystallography remains the foremost technique in determining the structures of a huge range of complex molecules.

This film was produced in celebration of the Bragg Centenary and was funded by STFC.

Watch more science videos on the amazing Ri Channel: http://richannel.org

Watch more animations from 12foot6: http://12foot6.com/

The Ri is on Twitter: http://twitter.com/ri_science
and Facebook: http://www.facebook.com/royalinstitution
Subscribe for the latest science videos: http://richannel.org/newsletter]]></description>
	
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