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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27696?offset=1310</link>
	<atom:link href="https://bioinformaticsonline.com/related/27696?offset=1310" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/9868/raghavas-group</guid>
  <pubDate>Tue, 15 Apr 2014 23:59:48 -0500</pubDate>
  <link></link>
  <title><![CDATA[Raghava's Group]]></title>
  <description><![CDATA[
<p>Raghava's group is known for developing open source software or web servers. Group have developed large number of web-based services.</p>

<p>Find more at http://www.imtech.res.in/raghava/</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/10127/assistant-professor-at-sardar-patel-university</guid>
  <pubDate>Mon, 21 Apr 2014 21:03:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor at SARDAR PATEL UNIVERSITY]]></title>
  <description><![CDATA[
<p>SARDAR PATEL UNIVERSITY<br />Centre for Interdisciplinary Studies in Science and Technology</p>

<p>No.: SPU/CISST/Advt./2014-15/519</p>

<p>ADVERTISEMENT for Teaching Positions (Contractual)</p>

<p>Applications for the following Contractual Teaching Position are invited for Centre for Interdisciplinary Studies in Science and Technology (CISST), Sardar Patel University:</p>

<p>2. Assistant Professor (ONE) (Contractual)</p>

<p>For the subject of Bioinformatics</p>

<p>Qualifications:</p>

<p>(I) Good academic record as defined by the concerned university with at least 55 % marks (or an equivalent grade in a point scale wherever grading system is followed) at the Master’s level</p>

<p>(II) Ph.D. degree in the concerned subject or in a relevant interdisciplinary subject<br />from an Indian University or NET/SLET clearance Contractual appointment carries a total Fixed Emoluments of Rs. 30,000/- p.m without any assurance of permanent Positions and related benefits.</p>

<p>An Application Form in prescribed Performa, available on University Website: www.spuvvn.edu should be filled in completely in Twelve Copies with self attested copies of certificates of qualifications and experience. Only one copy of each mark sheet be attached with the first copy of the application form. All 12 (Twelve) Application forms should be sent to Registrar’s office along with Demand Draft of Application form fee of Rs. 250/- (Non-refundable) in favour of “REGISTRAR, SARDAR PATEL UNIVERSITY, VALLABH VIDYANAGAR”. The S.C. and S.T. category candidates need not to pay Application fee.</p>

<p>Applicants who are in service should apply through their present employers. Candidates called for interview shall be required to attend at their own cost.</p>

<p>In absence of suitable candidate, the University may relax the eligibility criteria, for conditional appointment.</p>

<p>The last date of receipt of application by the University is 30th April, 2014</p>

<p>Advertisement: www.spuvvn.edu/careers/CISST%20Advt.%20April%202014.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/38886/evaluation-of-genome-assembly-software-based-on-long-reads</guid>
	<pubDate>Fri, 01 Feb 2019 11:55:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/38886/evaluation-of-genome-assembly-software-based-on-long-reads</link>
	<title><![CDATA[Evaluation of genome assembly software based on long reads]]></title>
	<description><![CDATA[<p>TGS technologies have been used to produce highly accurate de novo assemblies of hundreds of microbial genomes and highly contiguous reconstructions of many dozens of plant and animal genomes, enabling new insights into evolution and sequence diversity. They have also been applied to resequencing analyses, to create detailed maps of structural variations in many species. Also, these new technologies have been used to fill in many of the gaps in the human reference genome.</p><p>In this report, we compare and evaluate several genome assembly software based on TSG technology. The experimentation has been performed on 4 reference genomes and the results evaluated with the QUAST software. The 11 software that have been evaluated are: Celera Assembler , Falcon , Miniasm, Newbler , SGA Assembler, Smartdenovo, Abruijn, Ra, DBG2OLC, Spades and Cerulean. The first 8 software use only long reads, while the 3 last software can merge long and short reads</p>]]></description>
	<dc:creator>BioStar</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/38886" length="382699" type="application/pdf" />
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/10394/bioinformatics-protocols</guid>
	<pubDate>Mon, 05 May 2014 10:21:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/10394/bioinformatics-protocols</link>
	<title><![CDATA[Bioinformatics Protocols]]></title>
	<description><![CDATA[<h2><span> RNA Seq </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1KbTiBHtvHLfPRZ39AY3uriazrINA8TJzgjjwn1zPP7Y">RNA-Seq tutorial</a> based on <a href="http://www.nature.com/protocolexchange/protocols/2327">Trapnell et al. (2012)</a> <em>Nature Protocols</em></li>
</ul>
<dl><dd>In this tutorial we cover the concepts of <a href="http://en.wikipedia.org/wiki/RNA-Seq">RNA-Seq</a> differential gene expression (DGE) analysis using a very small synthetic dataset from a well studied organism.</dd></dl>
<p><strong> Advanced Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1fQ1XfeOKhezJUDTzMXtZVY20c3RGoHe-HLvFOGzqU4s/pub">RNA-Seq (Advanced) Tutorial</a></li>
</ul>
<dl><dd>In this tutorial we compare the performance of three statistically-based differential expression tools:</dd><dd>* CuffDiff</dd><dd>* EdgeR</dd><dd>* DESeq2</dd></dl>
<p><strong> Advanced Command Line Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1ayJXtgBP1OXtnV7o7lq4QHKMNk5SdPHFq4hGkqndBtI/pub">Graphical Output with CummeRbund</a> introduces some basic commands using the cummeRbund package of the R programming language</li>
</ul>
<dl><dd>You will need to install R, RStudio and cummeRbund on your PC (explained in the Tutorial). You will learn how to produce graphical output from RNA-Seq analysis previously done using a Cuffdiff analysis.</dd></dl>
<h2><span> Variant Detection </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1ZRzrjjOCvtAu3m-IKL-rbJ1f4On60dDL_IEwG7oejdI">Variant Detection tutorial</a></li>
</ul>
<dl><dd>In this tutorial we cover the concepts of detecting small variants (SNVs and indels) in human genomic DNA using a small set of reads from chromosome 22.</dd></dl>
<p><strong>Advanced Galaxy Tutorial</strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1CuKkKylVDb03tnN7RSWl5EUzleetn0ctjmvaidPKLxM">Variant Detection (Advanced) Tutorial</a></li>
</ul>
<dl><dd>In this tutorial we compare the performance of three statistically-based variant detection tools:</dd><dd>* SAMtools: Mpileup</dd><dd>* GATK: Unified Genotyper</dd><dd>* FreeBayes</dd><dd>Each of these tools takes as its input a BAM file of aligned reads and generates a list of likely variants in VCF format</dd></dl>
<p><strong>Pipelines</strong> are for those who are comfortable with using the UNIX command line; and often allow more control over branching and iteration logic.</p>
<ul>
<li><a href="https://github.com/claresloggett/variant_calling_pipeline">WGS/exome GATK-based variant calling pipeline</a></li>
</ul>
<dl><dd>This is a basic variant-calling and annotation pipeline developed at the Victorian Life Sciences Computation Initiative (VLSCI), University of Melbourne. It is based around BWA, GATK and ENSEMBL and was originally designed for human (or similar) data. The master branch is configured for WGS data; there is an exome branch configured for variant calling in exome data.</dd><dd>To run the pipeline you will need Rubra: <a href="https://github.com/bjpop/rubra">https://github.com/bjpop/rubra</a>. Rubra uses the python Ruffus library: <a href="http://www.ruffus.org.uk/">http://www.ruffus.org.uk/</a>.</dd></dl>
<p><strong>Protocols</strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1lfDYNzHjfDA1pHTHd-0w3xHhg7L4TipT1gRfzgiV8es/pub">Familial Variant Calling</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of calling familial related mutations.</dd></dl>
<ul>
<li><a href="https://docs.google.com/document/d/1PIhm8NrFGaSK0hxpDcp8wUOz11ZkOaHIrpnJshMgDec/pub">Somatic Variant Calling</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of identifying somatic variants or mutations.</dd></dl>
<h2><span> Assembly </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1N3AB9ptISUu4zULqe1kXpVF0BDyGb5f5yzxWSJd_WNM">Genome assembly tutorial</a></li>
</ul>
<dl><dd>In this tutorial we carry out de novo assembly of a microbial genome. We have also written a <a href="https://docs.google.com/document/d/1xs-TI5MejQARqo0pcocGlymsXldwJbJII890gnmjI0o/pub">De novo Genome Assembly for Illumina Data</a> Protocol for a more generic description of the method.</dd></dl>
<p><strong> Protocol </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1xs-TI5MejQARqo0pcocGlymsXldwJbJII890gnmjI0o/pub">De novo Genome Assembly for Illumina Data</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of de novo assembly for small to medium sized genomes. Use our <a href="https://docs.google.com/document/pub?id=1N3AB9ptISUu4zULqe1kXpVF0BDyGb5f5yzxWSJd_WNM">Genome assembly tutorial</a> to learn a specific case of using Galaxy to carry out de novo assembly of a microbial genome.</dd></dl>
<h2><span> Small RNAs </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1WAObJr7M0m8U-2ku-0Y0Sdt_IHmqd1h8WaJHPhnJ1lM/pub">Quality control for small RNA</a></li>
</ul>
<dl><dd>This tutorial covers initial steps of the workflow for analysis of short RNA expression such as a quality control of the raw reads, processing of the raw reads for the subsequent analysis and initial quality assessment of the library.</dd></dl>
<h2><span> ChIP Seq </span></h2>
<p><strong> Protocol </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1UPJC8dsiDeP5R9MH9U0IvoDgPF2Q3EOstAuzS3e6WCE/pub">ChIP-Seq</a></li>
</ul>
<dl><dd>In this protocol we discuss ChIP-Seq: a method to analyze the interaction between proteins and DNA.</dd></dl>
<h2><span> Amplicons </span></h2>
<p><strong>Protocol</strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1uW7JzxG86QzS92hTyeuNsLhX_d1XFbaZPSjh7jWxcSg/pub">Amplicon Alignment</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of aligning custom amplicons using primers for high precision.</dd></dl>
<h2><span> Learn Galaxy </span></h2>
<p><a href="https://docs.google.com/document/d/1wsdJDYfjZVg2uJxm9AHi_j0mY3X1M1F4gB-elkuYL7c/pub">Introduction to Galaxy,</a> for those who are very new to Galaxy.</p>
<p><a href="https://docs.google.com/document/d/1t7vVqa3mdeZYPv5-8hiHBFBYhNiynV_3mWByno9-wUM/pub">Using Histories and Workflows,</a> for those with some Galaxy knowledge.</p>
<p>The Galaxy project website has many <a href="http://wiki.galaxyproject.org/Learn">tutorials</a> and <a href="http://wiki.galaxyproject.org/Learn/Screencasts">screencasts</a> about using Galaxy and the tools, and developing new tools.</p><p>Address of the bookmark: <a href="https://genome.edu.au/wiki/Learn" rel="nofollow">https://genome.edu.au/wiki/Learn</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39450/apollo-first-instantaneous-collaborative-genomic-annotation-editor-available-on-the-web</guid>
	<pubDate>Fri, 31 May 2019 19:55:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39450/apollo-first-instantaneous-collaborative-genomic-annotation-editor-available-on-the-web</link>
	<title><![CDATA[Apollo: First instantaneous, collaborative genomic annotation editor available on the Web]]></title>
	<description><![CDATA[<ul>
<li>Apollo is a plug-in for the&nbsp;<a href="http://jbrowse.org/">JBrowse</a>&nbsp;Genome Viewer.</li>
<li>In addition to genes and pseudogenes, users can annotate ncRNAs (snRNA, snoRNA, tRNA, rRNA), miRNAs, repeat regions, and transposable elements; each annotation type has its own configuration of the &lsquo;Information Editor&rsquo;.</li>
<li>History tracking with undo/redo functions is available.</li>
<li>Users are able to directly set an annotation to a specific state, choosing from the &lsquo;History&rsquo; display.</li>
<li>Adding and updating PubMed IDs will prompt users with a publication title to confirm their submission.</li>
<li>Gene Ontology (GO) terms are supported and GO ID auto-completion has been incorporated.</li>
<li>Users may access a &lsquo;Recent Changes&rsquo; page.</li>
<li>Help page with Apollo specific content is available.</li>
</ul><p>Address of the bookmark: <a href="http://genomearchitect.github.io/" rel="nofollow">http://genomearchitect.github.io/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/10457/assistant-professor-bio-informatics-at-health-and-family-welfare-department-medical-education-in-raipur</guid>
  <pubDate>Wed, 07 May 2014 00:08:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor (Bio-Informatics) at Health and Family Welfare Department (Medical Education) in Raipur]]></title>
  <description><![CDATA[
<p>Advertisement No.05/2014/ Exam/Dated 17/04/2014</p>

<p>No of vacancies: 01</p>

<p>Pay scale:Rs. 15600 – 39100 + 6600/-</p>

<p>Essential Academic Qualifications / Experience : Good academic record as defined by the concerned university with at least 55% marks (or an equivalent grade in a point scale wherever grading system is followed) at the Master's Degree level in a relevant subject from an Indian University, or an equivalent degree from an accredited foreign university.</p>

<p>Besides fulfilling the above qualifications, the candidate must have cleared the National Eligibility Test (NET) conducted by the UGC, CSIR or similar test accredited by the UGC like SLET/ SET.</p>

<p>Notwithstanding anything contained in sub-clauses (a) and (b) to this Clause, candidates, who are, or have been awarded a Ph.D. Degree in accordance with the University Grants Commission (Minimum Standards and Procedure for Award of Ph.D. Degree) Regulations, 2009, shall be exempted from the requirement of the minimum eligibility condition of NET/SLET/SET for recruitment and appointment of Assistant Professor or equivalent positions in Universities/Colleges/Institutions.</p>

<p>NET/SLET/SET shall also not be required for such Masters Programmes in disciplines for which NET/SLET/SET is not conducted.</p>

<p>Apply online: http://www.psc.cg.gov.in/htm/OA_ME2014.html</p>

<p>Last Date for Online Registration: 22/05/2014</p>

<p>For more details: http://www.psc.cg.gov.in/pdf/Advertisement/ADV_ME2014.pdf</p>
]]></description>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40302/simug-a-general-purpose-genome-simulator</guid>
	<pubDate>Thu, 28 Nov 2019 04:33:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40302/simug-a-general-purpose-genome-simulator</link>
	<title><![CDATA[simuG: a general-purpose genome simulator]]></title>
	<description><![CDATA[<p><span>Simulated genomes with pre-defined and random genomic variants can be very useful for benchmarking genomic and bioinformatics analyses. Here we introduce simuG, a lightweight tool for simulating the full-spectrum of genomic variants (single nucleotide polymorphisms, Insertions/Deletions, copy number variants, inversions and translocations) for any organisms (including human). The simplicity and versatility of simuG make it a unique general-purpose genome simulator for a wide-range of simulation-based applications.</span></p><p>Address of the bookmark: <a href="https://github.com/yjx1217/simuG" rel="nofollow">https://github.com/yjx1217/simuG</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/10659/gps-dna-tracking-university-of-sheffield</guid>
	<pubDate>Sat, 10 May 2014 04:33:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/10659/gps-dna-tracking-university-of-sheffield</link>
	<title><![CDATA[GPS DNA tracking - University of Sheffield]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/Aap-s1kle4Q" frameborder="0" allowfullscreen></iframe>University of Sheffield geneticist and bioinformatics expert Dr Eran Elhaik demonstrates the power of his new DNA research, which allows people to discover their genetic homeland from 1000 years ago. Find out more about our biological research here http://www.sheffield.ac.uk/aps]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41144/seqmule-automated-human-exomegenome-variants-detection</guid>
	<pubDate>Tue, 18 Feb 2020 03:22:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41144/seqmule-automated-human-exomegenome-variants-detection</link>
	<title><![CDATA[SeqMule: Automated human exome/genome variants detection]]></title>
	<description><![CDATA[<p>SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its configuration file.</p><p>Address of the bookmark: <a href="https://doc-openbio.readthedocs.io/projects/seqmule/en/latest/" rel="nofollow">https://doc-openbio.readthedocs.io/projects/seqmule/en/latest/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/12593/visiting-scientist-computational-genomics-two-positions</guid>
  <pubDate>Mon, 07 Jul 2014 22:53:41 -0500</pubDate>
  <link></link>
  <title><![CDATA[Visiting Scientist - Computational Genomics (two positions)]]></title>
  <description><![CDATA[
<p>Scientific/Managerial &amp; International Recruitment</p>

<p>ICRISAT seeks applications from Indian nationals Visiting Scientist-Computational Genomics (2 positions), to be part of a team of Centre of Excellence in Genomics (CEG), (www.icrisat.org/ceg) to work on legume genomics projects.  The positions will be based at ICRISAT’s Headquarters in Patancheru, Hyderabad, India.</p>

<p>ICRISAT is a non-profit, non-political organization that conducts agricultural research for development in Asia and sub-Saharan Africa with a wide array of partners throughout the world. Covering 6.5 million square kilometers of land in 55 countries, the semi-arid tropics is home to over 2 billion people, with 650 million of these are the poorest of the poor. ICRISAT and its partners help empower those living in the semi-arid tropics, especially smallholder farmers, to overcome poverty, hunger, malnutrition and a degraded environment through more efficient and profitable agriculture. ICRISAT is headquartered in Greater Hyderabad, Andhra Pradesh, India and belongs to the Consortium of Centers supported by the Consultative Group on International Agricultural Research (CGIAR).</p>

<p>The Job: Responsibilities for these positions include:</p>

<p>    Analyzing and handling large-scale next generation sequencing DNA and RNA data<br />    Data mining and development of pipelines and troubleshooting<br />    Genome diversity analysis such as SNPs, Indels, Structural Variations, population structure<br />    Genome wide association study (GWAS) related analysis- LD analysis, hapmap and trait mapping<br />    Expression analysis based on RNA-Seq data, annotation, gene ontology and metabolic pathway analysis<br />    Epigenome analysis, small RNA identification<br />    Gene family analysis, sequence level protein analysis, orthology/paralogy and molecular modelling<br />    Compiling and analysis of results, writing reports and research papers</p>

<p>The Person:  Ph.D. or MSc/MTech/PGDCA with two years research experience in Biotechnology, Computational biology, Agricultural/ Plant Biotechnology, Genetics, Molecular Biology or related discipline. Good knowledge of programming/scripting in at least two of following languages: Perl, C, C++, R, Shell Scripting and Python is plus.</p>

<p>How to apply: Please apply latest by 20 July 2014.  The application should include the name of the position applied for, a letter of motivation, a full Curriculum Vita (CV), and the names and contact information of three references that are knowledgeable of the candidate’s professional qualifications and work experience. Technical details and more information about these positions can be obtained from R.K.VARSHNEY@CGIAR.ORG. All applications will be acknowledged, however only short listed candidates will be contacted.</p>

<p>Apply here https://recruit.zoho.com/ats/Portal.na?digest=T642sgLYWZOStExJ77cPrcM*sIMGZETWw4yPxngbmHA-</p>
]]></description>
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