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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27076?offset=940</link>
	<atom:link href="https://bioinformaticsonline.com/related/27076?offset=940" rel="self" type="application/rss+xml" />
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/30654/source-code-and-pseudo-code</guid>
	<pubDate>Mon, 23 Jan 2017 10:17:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/30654/source-code-and-pseudo-code</link>
	<title><![CDATA[Source Code and Pseudo Code !!]]></title>
	<description><![CDATA[<p>An <span style="text-decoration: underline;">algorithm</span> is a procedure for solving a problem in terms of the actions to be executed and the order in which those actions are to be executed. An algorithm is merely the sequence of steps taken to solve a problem. The steps are normally "sequence," "selection, " "iteration," and a case-type statement.</p><p>In C, "sequence statements" are imperatives. The "selection" is the "if then else" statement, and the iteration is satisfied by a number of statements, such as the "while," " do," and the "for," while the case-type statement is satisfied by the "switch" statement.</p><hr><p><span style="text-decoration: underline;">Pseudocode</span> is an artificial and informal language that helps programmers develop algorithms. Pseudocode is a "text-based" detail (algorithmic) design tool.</p><p>The rules of Pseudocode are reasonably straightforward. All statements showing "dependency" are to be indented. These include while, do, for, if, switch. Examples below will illustrate this notion.</p><p><strong> GUIDE TO PSEUDOCODE LEVEL OF DETAIL: Given record/file descriptions, pseudocode should be created in sufficient detail so as to directly support the programming effort. It is the purpose of pseudocode to elaborate on the algorithmic detail and not just cite an abstraction. </strong></p><hr><p>Examples:</p><p>1.</p><pre>If student's grade is greater than or equal to 60
    Print "passed"
else
    Print "failed"  
endif
</pre><hr><p>2.</p><pre>  
Set total to zero
Set grade counter to one
While grade counter is less than or equal to ten
    Input the next grade
    Add the grade into the total
endwhile 
Set the class average to the total divided by ten
Print the class average.
</pre><hr><p>3.</p><pre>Initialize total to zero
Initialize counter to zero
Input the first grade
while the user has not as yet entered the sentinel
   add this grade into the running total 
   add one to the grade counter  
   input the next grade (possibly the sentinel)
endwhile

if the counter is not equal to zero
   set the average to the total divided by the counter
   print the average  
else
   print 'no grades were entered' 
endif 
</pre><hr><p>4.</p><pre>initialize passes to zero
initialize failures to zero
initialize student to one
while student counter is less than or equal to ten
    input the next exam result  
    if the student passed</pre><p>add one to passes else add one to failures add one to student counter endif endwhile print the number of passes print the number of failures if eight or more students passed print "raise tuition" endif</p><hr><h3><strong>5.</strong></h3><pre>Larger example:  

NOTE:  NEVER ANY DATA DECLARATIONS IN PSEUDOCODE

Print out appropriate heading and make it pretty
While not EOF do:
     Scan over blanks and white space until a char is found 
	(get first character on the line)
     set can't-be-ascending-flag to 0
     set consec cntr to 1
     set ascending cntr to 1
     putchar first char of string to screen
     set read character to hold character
     While next character read != blanks and white space
          putchar out on screen
          if new char = hold char + 1
               add 1 to consec cntr
               set hold char = new char
               continue
          endif
          if new char &gt;= hold char 
               if consec cntr &lt; 3 
                    set consec cntr to 1
               endif
               set hold char = new char
               continue
          endif
          if new char &lt; hold char
               if consec cntr &lt; 3
                    set consec cntr to 1
               endif
               set hold char = new char
               set can't be ascending flag to 1
               continue
           endif
     end while
     if consec cntr &gt;= 3 
          printf (Appropriate message 1 and skip a line)
          add 1 to consec total
     endif
     if  can't be ascending flag = 0
          printf (Appropriate message 2 and skip a line)
          add 1 to ascending total
     else
          printf (Sorry message and skip a line)
          add 1 to sorry total
     endif
end While
Print out totals:  Number of consecs, ascendings, and sorries.
Stop
</pre><p>Some Keywords That Should be Used And Additional Points</p><p>For looping and selection, The keywords that are to be used include Do While...EndDo; Do Until...Enddo; While .... Endwhile is acceptable. Also, Loop .... endloop is also VERY good and is language independent. Case...EndCase; If...Endif; Call ... with (parameters); Call; Return ....; Return; When;</p><p>Always use scope terminators for loops and iteration.</p><p>As verbs, use the words Generate, Compute, Process, etc. Words such as set, reset, increment, compute, calculate, add, sum, multiply, ... print, display, input, output, edit, test , etc. with careful indentation tend to foster desirable pseudocode. Also, using words such as Set and Initialize, when assigning values to variables is also desirable.</p><p>More on Formatting and Conventions in Pseudocoding</p><ul>
<li>INDENTATION in pseudocode should be identical to its implementation in a programming language. Try to indent at least four spaces.</li>
<li>As noted above, the pseudocode entries are to be cryptic, AND SHOULD NOT BE PROSE. NO SENTENCES.</li>
<li>No flower boxes (discussed ahead) in your pseudocode.</li>
<li>Do not include data declarations in your pseudocode.</li>
<li>But do cite variables that are initialized as part of their declarations. E.g. "initialize count to zero" is a good entry.<hr>Function Calls, Function Documentation, and Pseudocode</li>
<li>Calls to Functions should appear as:
<ul>     </ul>
</li>
<li>Returns in functions should appear as:
<ul> </ul>
</li>
<li>Function headers should appear as:
<ul>     </ul>
</li>
<li>Note that in C, arguments and parameters such as "fieldn" could be written: "pointer to fieldn ...."</li>
<li>Functions called with addresses should be written as:
<ul>         </ul>
</li>
<li>Function headers containing pointers should be indicated as:
<ul>        </ul>
</li>
<li>Returns in functions where a pointer is returned:
<ul>   </ul>
</li>
<li>It would not hurt the appearance of your pseudocode to draw a line or make your function header line "bold" in your pseudocode. Try to set off your functions.</li>
<li>Try to use scope terminators in your pseudocode and source code too. It really hels the readability of the text.<hr>Source Code</li>
<li>EVERY function should have a flowerbox PRECEDING IT. This flower box is to include the functions name, the main purpose of the function, parameters it is expecting (number and type), and the type of the data it returns. All of these listed items are to be on separate lines with spaces in between each explanatory item.</li>
<li>FORMAT of flowerbox should be
<p>&nbsp;</p>
<pre>	 ********************************************************
	 Function:   ( cryptic text describing single function
		     ....... (indented like this) 	
		     .......
	 Calls:      Start listing functions "this" function calls
		     Show these functions:  one per line, indented

	 Called by:  List of functions that calls "this" function
		     Show these functions:  one per line, indented.

	 Input Parameters:  list, if appropriate; else None
	 
	 Returns:    List, if appropriate.
	 ****************************************************************
</pre>
</li>
<li>INDENTATION is critically important in Source Code. Follow standard examples given in class. If in doubt, ASK. Always indent statements within IFs, FOR loops, WILLE loops, SWITCH statements, etc. a consistent number of spaces, such as four. Alternatively, use the tab key. One or two spaces is insufficient.</li>
<li>Use scope terminators at the end of if statements, for statements, while statements, and at the end of functions. It will make your program much more readable.
<p><strong> SPELLING ERRORS ARE NOT ACCEPTABLE </strong></p>
</li>
</ul>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31064/cgaln</guid>
	<pubDate>Wed, 22 Feb 2017 05:14:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31064/cgaln</link>
	<title><![CDATA[Cgaln]]></title>
	<description><![CDATA[<p>Cgaln (Coarse grained alignment) is a program designed to align a pair of whole genomic sequences of not only bacteria but also entire chromosomes of vertebrates on a nominal desktop computer. Cgaln performs an alignment job in two steps, at the block level and then at the nucleotide level. The former "coarse-grained" alignment can explore genomic rearrangements and reduce the regions to be analyzed in the next step. The latter is devoted to detailed alignment within the limited regions found in the first stage. The output of Cgaln is 'glocal' in the sense that rearrangements are taken into consideration while each alignable region is extended as long as possible. Thus, Cgaln is not only fast and memory-efficient, but also can filter noisy outputs without missing the most important homologous segment pairs.</p>
<p>http://www.iam.u-tokyo.ac.jp/chromosomeinformatics/rnakato/cgaln/</p><p>Address of the bookmark: <a href="http://www.iam.u-tokyo.ac.jp/chromosomeinformatics/rnakato/cgaln/" rel="nofollow">http://www.iam.u-tokyo.ac.jp/chromosomeinformatics/rnakato/cgaln/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/30747/11th-international-joint-conference-on-biomedical-engineering-systems-and-technologies</guid>
  <pubDate>Wed, 01 Feb 2017 17:39:27 -0600</pubDate>
  <link></link>
  <title><![CDATA[11th International Joint Conference on Biomedical Engineering Systems and Technologies]]></title>
  <description><![CDATA[
<p>BIOSTEC, the 11th International Joint Conference on Biomedical Engineering Systems and Technologies.<br /> Registration to BIOINFORMATICS allows free access to all other BIOSTEC conferences. </p>

<p>Upcoming Deadlines<br />Regular Paper Submission: July 31, 2017 <br />Regular Paper Authors Notification: October 16, 2017 <br />Regular Paper Camera Ready and Registration: October 30, 2017 </p>

<p>The purpose of the International Conference on Bioinformatics Models, Methods and Algorithms is to bring together researchers and practitioners interested in the application of computational systems, algorithmic concepts and information technologies to address challenging problems in Biomedical research with a particular focus on the emerging problems in Bioinformatics and computational biology. There is a tremendous need to explore how mathematical, statistical and computational models can be used to better understand biological processes and systems, while developing new methodologies and tools to analysis the massive currently-available biological data. Areas of interest to this community include systems biology, sequence analysis, biostatistics, image analysis, network and graph models, scientific data management and data mining, machine learning, pattern recognition, computational evolutionary biology, computational genomics and proteomics, and related areas.</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/30874/important-journals-blogs-and-forums-for-bioinformaticians</guid>
	<pubDate>Wed, 08 Feb 2017 09:15:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/30874/important-journals-blogs-and-forums-for-bioinformaticians</link>
	<title><![CDATA[Important Journals, Blogs and Forums for Bioinformaticians]]></title>
	<description><![CDATA[<p><em>Journals</em>. Most journals have RSS feeds for their current updates.</p><ul>
<li><a href="http://bioinformatics.oxfordjournals.org/rss/" target="_blank">Bioinformatics - RSS feed of current and advance online publications</a></li>
<li><a href="http://genome.cshlp.org/rss/" target="_blank">Genome Research - current &amp; advance</a></li>
<li><a href="http://genomebiology.com/" target="_blank">Genome Biology - editors picks, latest, most viewed, most forwarded</a>. (Hit the RSS icon under each tab).</li>
<li><a href="http://www.plosgenetics.org/static/rssFeeds.action" target="_blank">PLoS Genetics - new articles</a></li>
<li><a href="http://www.ploscompbiol.org/static/rssFeeds.action" target="_blank">PLoS Computational Biology - new articles</a></li>
<li><a href="http://www.nature.com/ng/newsfeeds.html" target="_blank">Nature Genetics - current TOC and AOP</a></li>
<li><a href="http://www.nature.com/nrg/info/newsfeeds.html" target="_blank">Nature Reviews Genetics - current TOC and AOP</a></li>
</ul><ul>
<li><a href="https://academic.oup.com/bioinformatics" target="_blank">Bioinformatics</a></li>
<li><a href="https://bmcbioinformatics.biomedcentral.com/" target="_blank">BMC Bioinformatics</a></li>
<li><a href="https://academic.oup.com/bib" target="_blank">Briefings in Bioinformatics</a></li>
<li><a href="http://genomebiology.biomedcentral.com/" target="_blank">Genome Biology</a></li>
<li><a href="http://genome.cshlp.org/rss/" target="_blank">Genome Research: current and AOP</a></li>
<li><a href="http://microbiomejournal.biomedcentral.com/" target="_blank">Microbiome</a></li>
<li><a href="http://www.nature.com/ng/newsfeeds.html" target="_blank">Nature Genetics, current &amp; AOP</a></li>
<li><a href="http://www.nature.com/nrg/info/newsfeeds.html" target="_blank">Nature Reviews Genetics, current &amp; AOP</a></li>
<li><a href="https://academic.oup.com/nar" target="_blank">Nucleic Acids Research</a></li>
<li><a href="http://journals.plos.org/ploscompbiol/s/help-using-this-site#loc-article-feeds" target="_blank">PLOS Computational Biology</a></li>
<li><a href="http://journals.plos.org/plosgenetics/s/help-using-this-site#loc-article-feeds" target="_blank">PLOS Genetics</a></li>
</ul><p><em>Blogs</em><span>. Some of these blogs are very relevant to bioinfo jobs. Others are more personal interest.</span></p><ul>
<li><a href="http://blog.openhelix.eu/" target="_blank">The OpenHelix Blog</a></li>
<li><a href="http://www.ensembl.info/" target="_blank">Ensembl blog</a></li>
<li><a href="http://wiki.g2.bx.psu.edu/News" target="_blank">Galaxy News</a></li>
<li><a href="http://bcbio.wordpress.com/" target="_blank">Blue Collar Bioinformatics</a></li>
<li><a href="http://www.homolog.us/blogs/" target="_blank">Homologus</a></li>
<li><a href="http://blog.goldenhelix.com/" target="_blank">Golden Helix - our 2 SNPs</a></li>
<li><a href="http://genomicslawreport.com/" target="_blank">Genomics Law Report</a></li>
<li><a href="http://www.r-bloggers.com/" target="_blank">R-bloggers</a>&nbsp;(aggregates feeds from &gt;350 blogs about R)</li>
<li><a href="http://genomesunzipped.org/" target="_blank">Genomes Unzipped</a></li>
<li><a href="http://compgen.blogspot.com/" target="_blank">Jason Moore's Epistasis Blog</a></li>
<li><a href="http://spittoon.23andme.com/" target="_blank">23andMe - the Spitoon</a></li>
</ul><ul>
<li><a href="http://varianceexplained.org/" target="_blank">Variance Explained</a>: David Robinson&rsquo;s blog (Data Scientist at Stack Overflow, works in R and Python).</li>
<li><a href="https://globalbiodefense.com/" target="_blank">Global Biodefense</a>: News on pathogens, outbreaks, and preparedness, with periodic posts on genomics and bioinformatics-related developments and funding opportunities.</li>
<li><a href="https://flxlexblog.wordpress.com/" target="_blank">In between lines of code</a>: Lex Nederbragt&rsquo;s blog on biology, sequencing, bioinformatics, &hellip;</li>
<li><a href="http://simplystatistics.org/" target="_blank">Simply Statistics</a>: A statistics blog by Rafa Irizarry, Roger Peng, and Jeff Leek.</li>
<li><a href="https://liorpachter.wordpress.com/" target="_blank">Bits of DNA</a>: Reviews and commentary on computational biology by Lior Pachter (fair warning: dialogue here can get a bit heated!).</li>
<li><a href="http://bcb.io/articles/" target="_blank">Blue Collar Bioinformatics</a>: articles related tool validation and the open source bioinformatics community.</li>
<li><a href="https://microbiomedigest.com/" target="_blank">Microbiome Digest &ndash; Bik&rsquo;s Picks</a>: A daily digest of scientific microbiome papers, by Elisabeth Bik, Science Editor at uBiome.</li>
<li><a href="http://ivory.idyll.org/blog/" target="_blank">Living in an Ivory Basement</a>: Titus Brown&rsquo;s blog on metagenomics, open science, testing, reproducibility, and programming.</li>
<li><a href="http://enseqlopedia.com/" target="_blank">Enseqlopedia</a>: James Hadfield&rsquo;s blog on all things NGS.</li>
<li><a href="http://www.epistasisblog.org/" target="_blank">Epistasis Blog</a>: Jason Moore&rsquo;s computational biology blog.</li>
<li><a href="https://blog.rstudio.org/" target="_blank">RStudio Blog</a>: announcements about new RStudio functionality, updates about the&nbsp;<a href="http://tidyverse.org/" target="_blank">tidyverse</a>, and more.</li>
<li><a href="http://nextgenseek.com/" target="_blank">nextgenseek.com</a>: Next-Gen Sequencing Blog covering new developments in NGS data &amp; analysis.</li>
<li><a href="http://www.rna-seqblog.com/" target="_blank">RNA-Seq Blog</a>: Transcriptome Research &amp; Industry News.</li>
<li><a href="http://www.theallium.com/" target="_blank">The Allium</a>: We all need a little humor in our lives. Like&nbsp;<em>The Onion</em>, but for science.</li>
</ul><p><em>Forums.</em></p><ul>
<li><a href="http://seqanswers.com/forums/forumdisplay.php?f=18" target="_blank">Seqanswers - bioinformatics forum</a></li>
<li><a href="http://seqanswers.com/forums/forumdisplay.php?f=26" target="_blank">Seqanswers - RNA-Seq forum</a></li>
<li><a href="http://www.biostars.org/rss/" target="_blank">BioStar</a></li>
<li><a href="http://bioinformaticsonline.com/">BOL</a></li>
</ul>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/30928/jrf-bioinformatics-job-vacancies-in-tezpur-university</guid>
  <pubDate>Tue, 14 Feb 2017 16:40:26 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics job vacancies in Tezpur University]]></title>
  <description><![CDATA[
<p>Memo No. DoRD/CSE/SSS/20-295/112-A Date: 01/02/2017</p>

<p>Project Title : Integrating genome scale metabolic analysis of model plant pathogen Ralstonia solanacearum with RNAseq and fluxomics</p>

<p>Essential qualification : M.Tech. in CSE/IT (With specialization in Computational Biology/Bioinformatics) or M.Sc. in Bioinformatics/Biosciences/Molecular Biology Biotechnology preferably with NET/GATE/BET. Candidates should have minimum 55 % mark both in 10th and 10+2 Science examinations and mathematics at 10+2 Science. Desirable: Preference will be given to the candidates having experience in computational analysis of genome sequences or similar projects.</p>

<p>No. of Post : 01</p>

<p>Remuneration : Rs. 25,000/- for the 1st two years and Rs. 28,000/- for the 3rd year for SRF and applicable to the candidate having post graduate degree in Basic Science with NET/GATE/BET qualification or post graduate degree in professional course. Rs. 12,000/- for the 1st two years and Rs. 14,000/- for the 3 rd year for SRF, </p>

<p>Age : 28 years</p>

<p>Duration : Three (03) years or till completion of the project or until further order, whichever is earlier.</p>

<p>Hiring Process : Walk - In<br />Job Role: Research/JRF/SRF</p>

<p>Walk-in-interview will be held on 17th February, 2017, 11.15 a.m. at the office of the Head, Department of Computer Science and Engineering, Tezpur University.</p>

<p>Interested candidates may appear before the interview board with original documents from 10th standard onwards and photocopies of mark sheets, certificates, testimonials, caste certificate (if applicable), experience certificate certificates of NET/GATE/BET or similar examination qualifications, any other testimonials and a copy of recent curriculum vitae (CV) on the day of interview.</p>

<p>More at http://www.tezu.ernet.in/ProjectWalkin/Advt-DoRD-CSE-SSS-20-295-112-A.pdf</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/32227/postdoctoral-research-position-in-bioinformatics-in-milan</guid>
  <pubDate>Thu, 20 Apr 2017 12:53:12 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Research Position in Bioinformatics in Milan]]></title>
  <description><![CDATA[
<p>The lab of Immunobiology of Neurological Disorders has a main interest in the biological processes associated with multiple sclerosis, an inflammatory disorder of the central nervous system. The projects of interest for this application involve research on translational bioinformatics in complex human neurological disorders.</p>

<p>You have a  PhD in Computational Science, Bioinformatics,  or equivalent, and expertise in analysis and modeling of human RNA-seq data, statistics, data mining and machine learning. Excellent communication skills in English (written and oral) is a must. Flexibility and willingness to work across multiple projects and technologies in a rapidly evolving scientific context is required.<br />Salary will depend on qualification and experience. Starting date: immediate.</p>

<p>Interested candidates should send to farina.cinthia@hsr.it:</p>

<p>1. CV (please show evidences of relevant titles, projects, courses, references, etc.)           <br />2. One page with a list of research topics (i.e. ongoing projects)     <br />3. earliest availability</p>

<p>4. 2-3 contact names</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/31258/bioinformatics-walk-in-interview-at-tezpur-university</guid>
  <pubDate>Thu, 02 Mar 2017 04:24:46 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics walk-in-interview at Tezpur University]]></title>
  <description><![CDATA[
<p>A walk-in-interview will be held on 09 March, 2017, 11.15 a.m. at the office of the Head, Department of Computer Science and Engineering, Tezpur University for one (01) temporary position of Junior Research Fellow (JRF) in the DBT, Govt. of India sponsored project entitled “Integrating genome scale metabolic analysis of model plant pathogen Ralstonia solanacearum with RNAseq and fluxomics” under Dr. Siddhartha Sankar Satapathy (ssankar@tezu.ernet.in), Associate Professor, Department of Computer Science and Engineering, Tezpur University.<br /> <br />Interested candidates may appear before the interview board with original documents from 10th standard onwards and photocopies of mark sheets, certificates, testimonials, caste certificate (if applicable), experience certificate certificates of NET/GATE/BET or similar examination qualifications, any other testimonials and a copy of recent curriculum vitae (CV) on the day of interview.<br /> <br />Essential qualification: M.Tech. in CSE/IT (With specialization in Computational Biology/Bioinformatics) or M.Sc. in Bioinformatics/Biosciences/Molecular Biology Biotechnology preferably with NET/GATE/BET.<br /> <br />Candidates should have minimum 55 % mark both in 10th and 10+2 Science examinations and mathematics at 10+2 Science.<br /> <br />Desirable: Preference will be given to the candidates having experience in computational analysis of genome sequences or similar projects.<br /> <br />Remuneration: Rs. 25,000/- (Rupees twenty five thousand) only + HRA as admissible per month for the 1st two years and Rs. 28,000/- (Rupees twenty eight thousand) only + HRA as admissible per month for the 3rd year for SRF and applicable to the candidate having post graduate degree in Basic Science with NET/GATE/BET qualification or post graduate degree in professional course. Rs. 12,000/- (Rupees twelve thousand) only + HRA as admissible per month for the 1st two years and Rs. 14,000/- (Rupees fourteen thousand) only + HRA as admissible per month for the 3 rd year for SRF, for the candidate without NET/GATE/BET qualification. HRA will not be provided if campus accommodation is availed.<br /> <br />Age: Candidate shall not be more than 28 years of age on the date of interview. Upper age limit may be relaxed up to 5 years in the case of candidate belonging to SC/ST/ OBC/Women/Differently abled.<br /> <br />Duration: Three (03) years or till completion of the project or until further order, whichever is earlier.<br /> <br />N.B. No TA/DA will be paid to the candidates for attending the interview. For further details please contact: Dr. S. S. Satapathy Associate Professor Department of Computer Science and Engineering Tezpur University, Napaam-784028 Email: ssankar@tezu.ernet.in Contact no.: +91-9435979648<br /> <br />More Info:  www.tezu.ernet.in/ProjectWalkin/Advt-DoRD-CSE-SSS-20-295-188-A.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31881/gbtools-interactive-visualization-of-metagenome-bins-in-r</guid>
	<pubDate>Sun, 26 Mar 2017 15:41:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31881/gbtools-interactive-visualization-of-metagenome-bins-in-r</link>
	<title><![CDATA[gbtools: Interactive Visualization of Metagenome Bins in R]]></title>
	<description><![CDATA[<p><span>We have developed gbtools, a software package that allows users to visualize metagenomic assemblies by plotting coverage (sequencing depth) and GC values of contigs, and also to annotate the plots with taxonomic information. Different sets of annotations, including taxonomic assignments from conserved marker genes or SSU rRNA genes, can be imported simultaneously; users can choose which annotations to plot. Bins can be manually defined from plots, or be imported from third-party binning tools and overlaid onto plots, such that results from different methods can be compared side-by-side. gbtools reports summary statistics of bins including marker gene completeness, and allows the user to add or subtract bins with each other.&nbsp;</span></p>
<p><span>Tool at&nbsp;https://github.com/kbseah/genome-bin-tools</span></p><p>Address of the bookmark: <a href="http://journal.frontiersin.org/article/10.3389/fmicb.2015.01451/full" rel="nofollow">http://journal.frontiersin.org/article/10.3389/fmicb.2015.01451/full</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32048/json</guid>
	<pubDate>Tue, 04 Apr 2017 08:02:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32048/json</link>
	<title><![CDATA[JSON]]></title>
	<description><![CDATA[<p><strong>JSON</strong>&nbsp;(JavaScript Object Notation) is a lightweight data-interchange format. It is easy for humans to read and write. It is easy for machines to parse and generate. It is based on a subset of the&nbsp;<a href="http://javascript.crockford.com/">JavaScript Programming Language</a>,&nbsp;<a href="http://www.ecma-international.org/publications/files/ecma-st/ECMA-262.pdf">Standard ECMA-262 3rd Edition - December 1999</a>. JSON is a text format that is completely language independent but uses conventions that are familiar to programmers of the C-family of languages, including C, C++, C#, Java, JavaScript, Perl, Python, and many others. These properties make JSON an ideal data-interchange language.</p>
<p>JSON is built on two structures:</p>
<ul>
<li>A collection of name/value pairs. In various languages, this is realized as an&nbsp;<em>object</em>, record, struct, dictionary, hash table, keyed list, or associative array.</li>
<li>An ordered list of values. In most languages, this is realized as an&nbsp;<em>array</em>, vector, list, or sequence.</li>
</ul>
<p>These are universal data structures. Virtually all modern programming languages support them in one form or another. It makes sense that a data format that is interchangeable with programming languages also be based on these structures.</p><p>Address of the bookmark: <a href="http://json.org/" rel="nofollow">http://json.org/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32152/upsetr-shiny-app</guid>
	<pubDate>Fri, 14 Apr 2017 06:19:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32152/upsetr-shiny-app</link>
	<title><![CDATA[UpSetR Shiny App!]]></title>
	<description><![CDATA[<p>UpSetR generates static&nbsp;<a href="http://vcg.github.io/upset/?dataset=0&amp;duration=1000&amp;orderBy=subsetSize&amp;grouping=groupByIntersectionSize&amp;selection=">UpSet plots</a>. The UpSet technique visualizes set intersections in a matrix layout and introduces aggregates based on groupings and queries. The matrix layout enables the effective representation of associated data, such as the number of elements in the aggregates and intersections, as well as additional summary statistics derived from subset or element attributes.</p>
<h4>To begin, input your data using one of the three input styles.</h4>
<ol>
<li>"File" takes a correctly formatted.csv file.</li>
<li>"List" takes up to 6 different lists that contain unique elements, similar to that used in the web applications BioVenn&nbsp;<a href="http://www.biomedcentral.com/content/pdf/1471-2164-9-488.pdf">(Hulsen et al., 2008)</a>&nbsp;and jvenn&nbsp;<a href="http://www.biomedcentral.com/content/pdf/1471-2105-15-293.pdf">(Bardou et al., 2014)</a></li>
<li>"Expression" takes the input used by the venneuler R package&nbsp;<a href="https://cran.r-project.org/web/packages/venneuler/venneuler.pdf">(Wilkinson, 2015)</a></li>
</ol><p>Address of the bookmark: <a href="https://gehlenborglab.shinyapps.io/upsetr/" rel="nofollow">https://gehlenborglab.shinyapps.io/upsetr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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