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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27261?offset=240</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</guid>
	<pubDate>Mon, 29 Aug 2016 04:08:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</link>
	<title><![CDATA[Useful Bioinformatics Tools]]></title>
	<description><![CDATA[<p>Collections of few handy tools for bioinformatician</p>
<p>http://molbiol-tools.ca/Convert.htm</p><p>Address of the bookmark: <a href="http://molbiol-tools.ca/Convert.htm" rel="nofollow">http://molbiol-tools.ca/Convert.htm</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29123/artemis-comparison-tool-act</guid>
	<pubDate>Wed, 07 Sep 2016 03:54:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29123/artemis-comparison-tool-act</link>
	<title><![CDATA[Artemis Comparison Tool (ACT)]]></title>
	<description><![CDATA[<p><span>ACT is a Java application for displaying pairwise comparisons between two or more DNA sequences. It can be used to identify and analyse regions of similarity and difference between genomes and to explore conservation of synteny, in the context of the entire sequences and their annotation.&nbsp;It can read complete EMBL,&nbsp;GENBANK and GFF entries or sequences in FASTA or raw format.&nbsp;</span></p><p>Address of the bookmark: <a href="http://www.sanger.ac.uk/science/tools/artemis-comparison-tool-act" rel="nofollow">http://www.sanger.ac.uk/science/tools/artemis-comparison-tool-act</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29008/circos-visualize</guid>
	<pubDate>Fri, 02 Sep 2016 08:29:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29008/circos-visualize</link>
	<title><![CDATA[CIRCOS Visualize !!]]></title>
	<description><![CDATA[<p>Before uploading a data file, check the&nbsp;<a href="http://mkweb.bcgsc.ca/tableviewer/samples">samples gallery</a>&nbsp;to make sure that your data format is compatible.</p>
<ul>
<li>Your file must be&nbsp;<strong>plain text</strong>.</li>
<li>Your data values must be&nbsp;<strong>non-negative integers</strong>.</li>
<li>Data must be space-separated (<strong>one or more</strong>&nbsp;tab or space, which will be collapsed).</li>
<li>No two rows or columns may have the same name.</li>
<li>Column and row names must&nbsp;<strong>begin with a letter</strong>&nbsp;(e.g. 'A', 'A0', 'A-0') and can only contain letters, numbers and _. No punctuation!</li>
<li>Maximum row + column total is 150 &mdash; if exceeded, rows and columns are limited to 75.</li>
<li>If you are using order, size and color rows/columns in combination they must appear in that order.</li>
</ul>
<p>Need help? Post questions to the&nbsp;<a href="https://groups.google.com/forum/#!forum/circos-data-visualization">Circos Google Group</a>.</p>
<p>http://mkweb.bcgsc.ca/tableviewer/visualize/</p><p>Address of the bookmark: <a href="http://mkweb.bcgsc.ca/tableviewer/visualize/" rel="nofollow">http://mkweb.bcgsc.ca/tableviewer/visualize/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/29110/structural-variants-ppt</guid>
	<pubDate>Wed, 07 Sep 2016 03:16:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/29110/structural-variants-ppt</link>
	<title><![CDATA[Structural variants PPT]]></title>
	<description><![CDATA[<p>1000 Genomes data tutorial at ASHG</p><p>Structural variants presentation by</p><p>Jan Korbel</p><p>European Molecular Biology Laboratory (EMBL) Heidelberg Genome Biology Research Unit</p><p>Reference:&nbsp;</p><p>https://www.genome.gov/pages/research/der/1000genomesprojecttutorials/structuralvariants-jankorbel.pdf</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/29110" length="1090837" type="application/pdf" />
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29144/fermi</guid>
	<pubDate>Fri, 09 Sep 2016 05:37:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29144/fermi</link>
	<title><![CDATA[FERMI]]></title>
	<description><![CDATA[<p><span>Fermi is a de novo assembler with a particular focus on assembling Illumina&nbsp;</span><span>short sequence reads from a mammal-sized genome. In addition to the role of a&nbsp;</span><span>typical assembler, fermi also aims to preserve heterozygotes which are often&nbsp;</span><span>collapsed by other assemblers. Its ultimate goal is to find a minimal set of</span><br><span>unitigs to represent all the information in raw reads.</span><br><br><span>Fermi follows the overlap-layout-consensus paradigm and uses the FM-DNA-index&nbsp;</span><span>(FMD-index) as the key data structure. It is inspired by the string graph&nbsp;</span><span>assembler (Simpson and Durbin, 2010 and 2012) and has a similar workflow.</span><br><br><span>As a typical de novo assembler, fermi tends to produce contigs with slightly&nbsp;</span><span>longer N50. However, the major weakness of fermi is the high misassembly rate.&nbsp;</span><span>Although fermi provides a tool to fix misassemblies by using paired-end reads&nbsp;</span><span>to achieve an accuracy comparable to other assemblers, this is not a favorable&nbsp;</span><span>solution.</span><br><br><span>Fermi is designed to be used on a multi-core Linux machine with large shared&nbsp;</span><span>memory. The easiest way to run fermi is to use the run-fermi.pl script. It&nbsp;</span><span>generates a Makefile. The actual assembly is done by invoking make. Premature&nbsp;</span><span>assembly processes can be resumed. Here is an example:</span><br><br><span>run-fermi.pl -dAPe ./fermi -p NA12878 -t16 -f18 reads*.fq.gz &gt; NA12878.mak</span><br><span>make -f NA12878.mak -j16</span></p><p>Address of the bookmark: <a href="https://github.com/lh3/fermi" rel="nofollow">https://github.com/lh3/fermi</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29500/genomescope-open-source-web-tool-to-rapidly-estimate-the-overall-characteristics-of-a-genome-including-genome-size-heterozygosity-rate-and-repeat-content-from-unprocessed-short-reads</guid>
	<pubDate>Fri, 21 Oct 2016 05:46:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29500/genomescope-open-source-web-tool-to-rapidly-estimate-the-overall-characteristics-of-a-genome-including-genome-size-heterozygosity-rate-and-repeat-content-from-unprocessed-short-reads</link>
	<title><![CDATA[GenomeScope: open-source web tool to rapidly estimate the overall characteristics of a genome, including genome size, heterozygosity rate, and repeat content from unprocessed short reads]]></title>
	<description><![CDATA[<div>
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<div id="content-block-markup">
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<div id="abstract-1">
<p id="p-2">Summary: GenomeScope is an open-source web tool to rapidly estimate the overall characteristics of a genome, including genome size, heterozygosity rate, and repeat content from unprocessed short reads. These features are essential for studying genome evolution, and help to choose parameters for downstream analysis. We demonstrate its accuracy on 324 simulated and 16 real datasets with a wide range in genome sizes, heterozygosity levels, and error rates. Availability and Implementation: http://qb.cshl.edu/genomescope/, https://github.com/schatzlab/genomescope.git</p>
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<span></span></div>
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</div><p>Address of the bookmark: <a href="http://qb.cshl.edu/genomescope/" rel="nofollow">http://qb.cshl.edu/genomescope/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29603/statistical-for-biological-research</guid>
	<pubDate>Thu, 03 Nov 2016 04:59:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29603/statistical-for-biological-research</link>
	<title><![CDATA[Statistical for biological research]]></title>
	<description><![CDATA[<p>There is no disputing the importance of statistical analysis in biological research, but too often it is considered only after an experiment is completed, when it may be too late.</p>
<p>This collection highlights important statistical issues that biologists should be aware of and provides practical advice to help them improve the rigor of their work.</p>
<p><em>Nature Methods</em>' <strong><a href="http://www.nature.com/collections/qghhqm/pointsofsignificance">Points of Significance</a></strong> column on statistics explains many key statistical and experimental design concepts. <strong><a href="http://www.nature.com/collections/qghhqm/resources">Other resources</a></strong> include an online plotting tool and links to statistics guides from other publishers.</p><p>Address of the bookmark: <a href="http://www.nature.com/collections/qghhqm" rel="nofollow">http://www.nature.com/collections/qghhqm</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29644/junior-research-fellow-at-rajiv-gandhi-centre-for-biotechnology-thiruvananthapuram</guid>
  <pubDate>Mon, 07 Nov 2016 10:27:06 -0600</pubDate>
  <link></link>
  <title><![CDATA[Junior Research Fellow at Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram]]></title>
  <description><![CDATA[
<p>Adv. # 22/ 2016<br />Applications are invited from suitable candidates for one position of Junior Research Fellow in a DST funded bioinformatics research project entitled "Major gene influxes in microbial genome evolution" in the Laboratory of Dr. Shijulal Nelson-Sathi at Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram.</p>

<p>ESSENTIAL QUALIFICATIONS:<br />We are looking for a motivated candidate with keen interest in bioinformatics and microbial genome evolution. The candidate must have a Master’s Degree in Bioinformatics, Computational Biology, Computer Science, Microbiology, Biology or a related field with good academic record.</p>

<p>DESIRABLE QUALIFICATIONS<br />Hands on research experience on handling next generation sequencing data and phylogenetic reconstruction methods. Excellent programming skills (Perl/Python/Java/Php) and experience in working on Unix/Linux platform is preferred. Furthermore; good knowledge is required in statistics (R/Matlab) and the application of bioinformatics analysis tools.</p>

<p>AGE:<br />Below 28 years as on 15th November, 2016.</p>

<p>EMOLUMENTS:<br />Rs. 25,000 + 20% HRA for NET/GATE qualified and Post Graduate in Professional Degree course qualified candidates and <br />Rs. 12,000/- + 20% HRA for others.</p>

<p>DURATION:<br />Initial appointment will be given for one year and further extension will be based on the performance till termination of the project.<br />Only those fulfilling the above criteria need apply and will be called for interview. In the event of more than 10 candidates being short-listed by screening the applications, a written test will be conducted before the selection interview and only those who are successful in the written test will be interviewed. No TA/ DA will be given for appearing in the interview.</p>

<p>Suitably qualified candidates may send applications in the prescribed format (Download here) with a photograph, a copy of full resume indicating the percentage of Marks obtained and attested photocopies of credentials &amp; experience to reach the undersigned on or before 15th November, 2016. Envelopes must be superscripted with abbreviated title of the project, advertisement number and job title. Selection to the position will not entitle the candidate to any future positions at RGCB (permanent or otherwise). As with all project positions at RGCB, the position will be co terminus with end of the project.</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29658/bookmarks-biostatistics-materials-and-books</guid>
	<pubDate>Tue, 08 Nov 2016 07:42:42 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29658/bookmarks-biostatistics-materials-and-books</link>
	<title><![CDATA[Bookmarks Biostatistics materials and books]]></title>
	<description><![CDATA[<p>Biostatistics did not spring fully formed from the brow of R. A. Fisher, but evolved over many years. This process is continuing, although it may not be obvious from the outside. It has been ten years since the first edition of this book appeared (and rather longer since it was begun). Over this time, new areas of biostatistics have been developed and emphases and interpretations have changed</p>
<p>Please bookmarks your favourate biostatistics&nbsp;books in commend sectons ...</p><p>Address of the bookmark: <a href="http://www.cos.ufrj.br/~bioestatistica/livros/Introduction%20to%20Biostatistics.pdf" rel="nofollow">http://www.cos.ufrj.br/~bioestatistica/livros/Introduction%20to%20Biostatistics.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29842/research-assistant-bioinformatics-recruitment-in-national-institute-of-cancer-prevention-research-icmr-on-contract-basis</guid>
  <pubDate>Tue, 15 Nov 2016 17:15:48 -0600</pubDate>
  <link></link>
  <title><![CDATA[Research Assistant Bioinformatics recruitment in National Institute Of Cancer Prevention &amp; Research (ICMR) on Contract basis]]></title>
  <description><![CDATA[
<p>National Institute Of Cancer Prevention &amp; Research - ICMR</p>

<p>Research Assistant Bioinformatics recruitment in National Institute Of Cancer Prevention &amp; Research (ICMR) on Contract basis <br />Project entitled: “Next generation EGFR inhibitor identification using ligand based QSAR technique” </p>

<p>Essential: M.Sc. in Bioinformatics or related field. Desirable: Experience in QSAR and structure based drug designing.<br />Age: 28 years<br />No.of Post: 1</p>

<p>Pay Scale : Rs.27000</p>

<p>Application format is attached and should be sent by post to Dr. Subhash M Agarwal, Scientist D, Division of Bioinformatics, National Institute of Cancer Prevention &amp; Research (ICMR), Plot No. I-7, Sector-39, Noida 201301 (U.P).</p>

<p>More at http://www.icmr.nic.in/icmrnews/NICPR_Advertisement%20for%20RA.pdf</p>
]]></description>
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