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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/30831?offset=170</link>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29915/professor-all-levels-in-bioinformatics-and-computational-biology</guid>
  <pubDate>Tue, 22 Nov 2016 05:43:38 -0600</pubDate>
  <link></link>
  <title><![CDATA[Professor (all levels) in Bioinformatics and Computational Biology]]></title>
  <description><![CDATA[
<p>King Abdullah University of Science and Technology (KAUST) (kaust.edu.sa) is seeking a highly motivated and skilled faculty member for the Bioinformatics track whose research focuses on development of methods and tools for Bioinformatics and Computational Biology.<br />KAUST is an international, graduate-level research university dedicated to advancing science and technology through interdisciplinary research, education, and innovation. Located on the shores of the Red Sea in Saudi Arabia, KAUST offers superb research facilities, generous assured research funding, and internationally competitive salaries, attracting top international faculty, scientists, engineers, and students to conduct fundamental and goal-oriented research to address the world’s pressing scientific and technological challenges in the areas of food, water, energy, and the environment.<br />The successful applicant is expected to develop world-leading research in domain of bioinformatics/computational biology with focus on development of novel computational approaches for efficient and accurate methods of analyzing biological phenomena at molecular level. The faculty member will be part of the Computational Bioscience Research Center (CBRC) within the Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division. The position will remain open until filled.<br /> <br />Requirements:<br /> <br />PhD or equivalent in a Computer Science, Mathematics or Engineering discipline. Candidates should be well-established within the research field relevant to the position grade. They should demonstrate original research and experience at the highest international level.<br /> <br />Responsibilities and tasks:<br /> <br />Research competence in the following areas is preferred:<br />Analysis of next generation sequencing (NGS) and other ‘omics’ data (e.g. CAGE, ChIP-Seq, DHS, RNA-Seq, Ribo-Seq, proteomic, metabolic and NMR spectra, etc.).<br />Signaling, regulatory and metabolic pathways analysis.<br />Development of tools (web-based and standalone) suited for efficient computational biology/bioinformatics.<br /> <br /> <br />Visit cemse.kaust.edu.sa to apply.</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30002/excavator2tool</guid>
	<pubDate>Wed, 30 Nov 2016 04:09:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30002/excavator2tool</link>
	<title><![CDATA[EXCAVATOR2tool]]></title>
	<description><![CDATA[<p><span>EXCAVATOR2 is a collection of bash, R and Fortran scripts and codes that analyses Whole Exome Sequencing (WES) data to identify CNVs. EXCAVATOR2 enhances the identification of all genomic CNVs, both overlapping and non-overlapping targeted exons by integrating the analysis of In-targets and Off- targets reads. Specifically, it improves the precision of calling CNVs overlapping targeted exons from WES data and enlarges the spectrum of detectable CNVs to off-target events.</span><br><span>EXCAVATOR2 can be effectively employed for the identification of CNVs in small as well as large-scale re-sequencing population and cancer studies. Lastly, it&rsquo;s of particular interest that all WES experiments can be re-analysed using our method with the beneficial effect to identify novelCNVs in extra-exonic regions by having the full-genome CN profile.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/excavator2tool/" rel="nofollow">https://sourceforge.net/projects/excavator2tool/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/30198/faculty-at-indian-institute-of-science-education-and-research-berhampur</guid>
  <pubDate>Mon, 19 Dec 2016 03:34:26 -0600</pubDate>
  <link></link>
  <title><![CDATA[Faculty at Indian Institute of Science Education and Research Berhampur]]></title>
  <description><![CDATA[
<p>Advt. No: IISERBPR/DoFA/2016/2</p>

<p>Advertisement for Faculty Positions</p>

<p>The IISER Berhampur, an Institute of national importance, established through an act of Parliament is an autonomous organization under the Ministry of HRD, Govt. of India, to promote quality education and cutting edge research in basic sciences and to provide a platform for the faculty to engage in high quality education, at undergraduate and postgraduate levels. The Institute invites applications for faculty positions at the level of Assistant Professor (C) /Assistant Professor in the following disciplines:</p>

<p>1. Biological Sciences</p>

<p>2. Chemistry</p>

<p>3. Computer Sciences</p>

<p>4. Mathematics</p>

<p>5. Physics</p>

<p>Only hard copy of application in the prescribed format, via Speed Post should be sent to the Dean, Faculty Affairs, IISER Berhampur, Industrial Training Institute (ITI) Berhampur, Engineering School Road, Berhampur - 760 010, Ganjam District, Odisha, before 1700 hrs., December 30, 2016.</p>

<p>http://www.iiserbpr.ac.in</p>

<p>More Info : http://www.iiserbpr.ac.in/vacancies/Advertisement%20for%20Faculty%20Positions%20at%20IISER%20Berhampur.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30076/sga-string-graph-assembler</guid>
	<pubDate>Thu, 08 Dec 2016 05:08:59 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30076/sga-string-graph-assembler</link>
	<title><![CDATA[SGA: String Graph Assembler]]></title>
	<description><![CDATA[<p><span>SGA is a de novo genome assembler based on the concept of string graphs. The major goal of SGA is to be very memory efficient, which is achieved by using a compressed representation of DNA sequence reads.</span></p>
<p><span>More at</span></p>
<p><span>https://github.com/jts/sga</span></p>
<p>SGA dependencies:<br> -google sparse hash library (http://code.google.com/p/google-sparsehash/)<br> -the bamtools library (https://github.com/pezmaster31/bamtools)<br> -zlib (http://www.zlib.net/)<br> -(optional but suggested) the jemalloc memory allocator (http://www.canonware.com/jemalloc/download.html)</p><p>Address of the bookmark: <a href="https://github.com/jts/sga" rel="nofollow">https://github.com/jts/sga</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30093/velvet-tutorial</guid>
	<pubDate>Fri, 09 Dec 2016 04:19:07 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30093/velvet-tutorial</link>
	<title><![CDATA[Velvet tutorial]]></title>
	<description><![CDATA[<p><span>The objective of this activity is to help you understand how to run&nbsp;</span><a href="http://evomics.org/resources/software/genomics-software/assembly/velvet/" title="Velvet">Velvet</a><span>&nbsp;in general, how to accurately estimate the insert size of a paired-end library through the use of&nbsp;</span><a href="http://evomics.org/resources/software/genomics-software/assembly/bowtie/" title="Bowtie">Bowtie</a><span>, the primary parameters of velvet, and the process involved in producing a&nbsp;</span><em>de novo</em><span>&nbsp;assembly from Illumina reads.</span></p>
<p>http://evomics.org/learning/assembly-and-alignment/velvet/</p><p>Address of the bookmark: <a href="http://evomics.org/learning/assembly-and-alignment/velvet/" rel="nofollow">http://evomics.org/learning/assembly-and-alignment/velvet/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30124/understanding-greedy-algorithms</guid>
	<pubDate>Mon, 12 Dec 2016 04:37:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30124/understanding-greedy-algorithms</link>
	<title><![CDATA[Understanding Greedy Algorithms]]></title>
	<description><![CDATA[<p>Learning greedy algo for biologist.&nbsp;</p>
<p>https://www.topcoder.com/community/data-science/data-science-tutorials/greedy-is-good/</p>
<p>This webpage is also useful for the same:</p>
<p>http://learninglover.com/examples.php?id=59</p>
<p>http://www.cs.rpi.edu/~magdon/ps/conference/super_biokdd.pdf</p>
<p>https://ocw.mit.edu/courses/biology/7-91j-foundations-of-computational-and-systems-biology-spring-2014/lecture-slides/MIT7_91JS14_Lecture6.pdf</p>
<p>http://schatzlab.cshl.edu/teaching/AssemblyClass/01.%20Assembly%20Intro.pdf</p>
<p>http://lsl.sinica.edu.tw/Services/Class/files/20150612449.pdf</p>
<p>http://www.cs.jhu.edu/~langmea/resources/lecture_notes/assembly_scs.pdf</p>
<p>https://www2.eecs.berkeley.edu/Pubs/TechRpts/2016/EECS-2016-43.pdf</p><p>Address of the bookmark: <a href="https://www.topcoder.com/community/data-science/data-science-tutorials/greedy-is-good/" rel="nofollow">https://www.topcoder.com/community/data-science/data-science-tutorials/greedy-is-good/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30149/mypro-a-seamless-pipeline-for-automated-prokaryotic-genome-assembly-and-annotation</guid>
	<pubDate>Thu, 15 Dec 2016 05:47:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30149/mypro-a-seamless-pipeline-for-automated-prokaryotic-genome-assembly-and-annotation</link>
	<title><![CDATA[MyPro: A seamless pipeline for automated prokaryotic genome assembly and annotation]]></title>
	<description><![CDATA[<p>MyPro is an improved genomics software pipeline for prokaryotic genomes. MyPro is user-friendly and requires minimal programming skills. High-quality prokaryotic genome assembly and annotation can be obtained with ease. It performed better than de novo assemblers and contig integration software. Produces more contiguous assemblies, higher N50 values and lower number of contigs.</p>
<p>More at https://sourceforge.net/projects/sb2nhri/files/MyPro/</p><p>Address of the bookmark: <a href="http://www.sciencedirect.com/science/article/pii/S0167701215001207" rel="nofollow">http://www.sciencedirect.com/science/article/pii/S0167701215001207</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30207/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</guid>
	<pubDate>Mon, 19 Dec 2016 06:07:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30207/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</link>
	<title><![CDATA[GAM-NGS: genomic assemblies merger for next generation sequencing]]></title>
	<description><![CDATA[<p><span>GAM-NGS (Genomic Assemblies Merger for Next Generation Sequencing), whose primary goal is to merge two or more assemblies in order to enhance contiguity and correctness of both. GAM-NGS does not rely on global alignment: regions of the two assemblies representing the same genomic&nbsp;</span><em>locus</em><span>&nbsp;(called&nbsp;</span><em>blocks</em><span>) are identified through reads' alignments and stored in a&nbsp;</span><em>weighted</em><span>graph. The merging phase is carried out with the help of this weighted graph that allows an&nbsp;</span><em>optimal</em><span>&nbsp;resolution of&nbsp;</span><em>local</em><span>&nbsp;problematic regions.</span></p><p>Address of the bookmark: <a href="https://github.com/vice87/gam-ngs" rel="nofollow">https://github.com/vice87/gam-ngs</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30234/last</guid>
	<pubDate>Mon, 19 Dec 2016 14:07:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30234/last</link>
	<title><![CDATA[LAST]]></title>
	<description><![CDATA[<p>LAST can:</p>
<ul>
<li>Handle&nbsp;<strong>big</strong>&nbsp;sequence data, e.g:
<ul>
<li>Compare two vertebrate genomes</li>
<li>Align billions of DNA reads to a genome</li>
</ul>
</li>
<li>Indicate the&nbsp;<a href="http://lastweb.cbrc.jp/about.html">reliability</a>&nbsp;of each aligned column.</li>
<li>Use sequence quality data&nbsp;<a href="http://nar.oxfordjournals.org/content/38/7/e100.abstract">properly</a>.</li>
<li>Compare DNA to proteins, with frameshifts.</li>
<li>Compare PSSMs to sequences</li>
<li>Calculate the likelihood of chance similarities between random sequences.</li>
<li>Do split and spliced alignment.</li>
<li><a href="http://last.cbrc.jp/doc/last-train.html">Train</a>&nbsp;alignment parameters for unusual kinds of sequence (e.g. nanopore).</li>
</ul><p>Address of the bookmark: <a href="http://last.cbrc.jp/" rel="nofollow">http://last.cbrc.jp/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30249/genome-assembly-tutorial</guid>
	<pubDate>Tue, 20 Dec 2016 07:56:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30249/genome-assembly-tutorial</link>
	<title><![CDATA[Genome Assembly Tutorial]]></title>
	<description><![CDATA[<p><span>If genomes were completely random sequences in a statistical sense, 'overlap-consensus-layout' method would have been enough to assemble large genomes from Sanger reads. In contrast, real genomes often have long repetitive regions, and they are hard to assemble using overlap-consensus-layout approach. De Bruijn graph-based assembly approach was originally proposed to handle the assembly of repetitive regions better.</span></p>
<p><span>More at&nbsp;http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1</span></p><p>Address of the bookmark: <a href="http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1" rel="nofollow">http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>

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