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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28439?offset=380</link>
	<atom:link href="https://bioinformaticsonline.com/related/28439?offset=380" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</guid>
	<pubDate>Thu, 23 Jun 2016 07:26:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</link>
	<title><![CDATA[WgSim]]></title>
	<description><![CDATA[<p>Reads simulator</p>
<p>Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simulate diploid genomes with SNPs and insertion/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution sequencing errors. It does not generate INDEL sequencing errors, but this can be partly compensated by simulating INDEL polymorphisms.<br><br>Wgsim outputs the simulated polymorphisms, and writes the true read coordinates as well as the number of polymorphisms and sequencing errors in read names. One can evaluate the accuracy of a mapper or a SNP caller with wgsim_eval.pl that comes with the package.<br><br></p><p>Address of the bookmark: <a href="https://github.com/lh3/wgsim" rel="nofollow">https://github.com/lh3/wgsim</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28117/quin%E2%80%99s-web-server</guid>
	<pubDate>Mon, 27 Jun 2016 10:44:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28117/quin%E2%80%99s-web-server</link>
	<title><![CDATA[QuIN’s web server]]></title>
	<description><![CDATA[<p><span>Recent studies of the human genome have indicated that regulatory elements (e.g. promoters and enhancers) at distal genomic locations can interact with each other via chromatin folding and affect gene expression levels. Genomic technologies for mapping interactions between DNA regions, e.g., ChIA-PET and HiC, can generate genome-wide maps of interactions between regulatory elements. These interaction datasets are important resources to infer distal gene targets of non-coding regulatory elements and to facilitate prioritization of critical loci for important cellular functions. With the increasing diversity and complexity of genomic information and public ontologies, making sense of these datasets demands integrative and easy-to-use software tools. Moreover, network representation of chromatin interaction maps enables effective data visualization, integration, and mining. Currently, there is no software that can take full advantage of network theory approaches for the analysis of chromatin interaction datasets. To fill this gap, we developed a web-based application, QuIN, which enables: 1) building and visualizing chromatin interaction networks, 2) annotating networks with user-provided private and publicly available functional genomics and interaction datasets, 3) querying network components based on gene name or chromosome location, and 4) utilizing network based measures to identify and prioritize critical regulatory targets and their direct and indirect interactions.&nbsp;</span></p>
<p><strong>AVAILABILITY:</strong><span>&nbsp;QuIN&rsquo;s web server is available at&nbsp;</span><a href="http://quin.jax.org/">http://quin.jax.org</a><span>&nbsp;QuIN is developed in Java and JavaScript, utilizing an Apache Tomcat web server and MySQL database and the source code is available under the GPLV3 license available on GitHub:</span><a href="https://github.com/UcarLab/QuIN/">https://github.com/UcarLab/QuIN/</a><span>.</span></p><p>Address of the bookmark: <a href="http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004809" rel="nofollow">http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004809</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</guid>
	<pubDate>Fri, 01 Jul 2016 12:09:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</link>
	<title><![CDATA[Genome Workbench 2.10.7]]></title>
	<description><![CDATA[<p>Genome Workbench 2.10.7 is here! New features include added support for local custom BLAST databases and improvements to Tree View.</p><p>For the full list of features, improvements and fixes, see the release notes:<a href="https://ncbi.nlm.nih.gov/tools/gbench/releasenotes" target="_blank">https://ncbi.nlm.nih.gov/tools/gbench/releasenotes</a></p><p>New Features</p><ul>
<li>BLAST Tool: added support for local custom BLAST databases</li>
<li>Graphical Sequence View: added log scaling option for graph tracks</li>
<li>Generic Table View:&nbsp;<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial17">new tutorial</a>&nbsp;added</li>
</ul><p>Bug Fixes and Improvements</p><ul>
<li>Project Tree View: Genomic Collections/Assemblies now show accessions, not just names</li>
<li>Tree View: layout updated to better accommodate nodes of different sizes</li>
<li>Table Import Dialog (MacOS): fixed issue with table visibility</li>
<li>Fixed bug where different molecules IDs in GenBank could resolve to the same sequence</li>
<li>Graphical Sequence View: fixed issue where sequence track was not shown for some sequences</li>
<li>Graphical Sequence View: fixed protein coloration methods</li>
<li>Graphical Sequence View: improved rendering of Markers to better indicate boundaries and produce higher quality PDF images</li>
<li>Create Gene Model tool: fixed scenario when gene model tool failed with local sequences</li>
<li>Search View: ORF Finder &ndash; fixed incorrect protein lengths</li>
<li>Fixed bug with not opening project file (.gbp) on a click</li>
<li>Fixed issues in GVF import</li>
<li>Fixed BLAST Search tool against NCBI databases not working</li>
<li>Fixed tblastn (protein BLAST) not working in standalone mode</li>
<li>Fixed GTF export failure</li>
</ul>]]></description>
	<dc:creator>Gudiya Pal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28290/bioinformatics-tools-and-software</guid>
	<pubDate>Tue, 05 Jul 2016 10:02:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28290/bioinformatics-tools-and-software</link>
	<title><![CDATA[Bioinformatics tools and software]]></title>
	<description><![CDATA[<p><a href="http://drive5.com/usearch">USEARCH &gt;</a><br><span>Extreme high-throughput sequence analysis. Orders of magnitude faster than BLAST.</span>&nbsp;<a href="http://drive5.com/muscle">MUSCLE &gt;</a><br><span>Multiple sequence alignment. Faster and more accurate than CLUSTALW.</span></p>
<p>&nbsp;<a href="http://drive5.com/uparse">UPARSE &gt;</a><br><span>OTU clustering for 16S and other marker genes. Highly accurate OTU sequences and improved diversity measures.</span>&nbsp;<a href="http://drive5.com/uchime">UCHIME &gt;</a><br><span>Chimeric sequence detection.</span>&nbsp;<a href="http://drive5.com/piler">PILER &gt;</a><br><span>De novo genome repeat finder.</span>&nbsp;<a href="http://drive5.com/pilercr">PILER-CR &gt;</a><br><span>Detection of CRISPR repeats in bacterial genomes.</span>&nbsp;<a href="http://drive5.com/qscore">QSCORE &gt;</a><br><span>Compare two multiple alignments for benchmarking.</span>&nbsp;<a href="http://drive5.com/pals">PALS &gt;</a><br><span>Whole-genome alignment.</span>&nbsp;<a href="http://drive5.com/muscle/prefab.htm">PREFAB &gt;</a><br><span>Protein Reference Alignment Database.</span>&nbsp;<a href="http://drive5.com/bench">MSA benchmark collection &gt;</a><br><span>Selected multiple alignment benchmarks in a standardized FASTA format.</span></p><p>Address of the bookmark: <a href="http://drive5.com/software.html" rel="nofollow">http://drive5.com/software.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28425/advertisement-for-junior-research-fellowjrf-at-school-of-computational-and-integrative-sciences-jawaharlal-nehru-university</guid>
  <pubDate>Thu, 14 Jul 2016 07:24:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[Advertisement for Junior Research Fellow(JRF)  at School of Computational and Integrative Sciences  Jawaharlal Nehru University]]></title>
  <description><![CDATA[
<p>Advertisement for Junior Research Fellow(JRF) - (1)</p>

<p>Applications are invited for a post in DST, India funded Project entitled: "Positive and negative impacts of macromolecular crowding agents during target site location by DNA binding proteins – origin of optimal search at physiological ionic concentration (Reference Number: ECR/2016/000188) ''. The selected candidate will be appointed purely on temporary basis, initially for two years as a JRF that may be extended to one year of SRF based on the performance.</p>

<p>Position: Junior Research Fellow (1)</p>

<p>Qualifications &amp; Experience: Candidate must have a consistently good academic record with at least 60% marks in all throughout and must have qualified NET/GATE.</p>

<p>Desirable: Basic knowledge in the field of biophysics, molecular simulations and computational biology are desirable.</p>

<p>Salary: Consolidated Rs. 25,000 per month.</p>

<p>Tenure: The project duration is for three years and the selected candidate would be appointed after an interview. Appointment will be purely on temporary basis as stipulated by the existing rules of the University.</p>

<p>Interested candidates need to send an application to the address mentioned below mentioning the name of the project and post applied for (on the cover of the envelope).</p>

<p>The applications along with CV should be mailed at the address given below. Name, address, contact number and e. mail address of two referees must be enclosed with the application. The last date for the application is July 31st 2016.</p>

<p>Dr. Arnab Bhattacharjee (Principal Investigator) <br />Assistant Professor <br />School of Computational and Integrative Sciences <br />Jawaharlal Nehru University <br />New Delhi-110067 <br />E-mail: arnab@jnu.ac.in</p>

<p>Note: 1. Only shortlisted candidates will be communicated to appear in the interview at SCIS, JNU and no other communications in this regard will be entertained.</p>

<p>2. No TA/DA will be paid for appearing in interview.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28554/megan6</guid>
	<pubDate>Mon, 25 Jul 2016 05:45:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28554/megan6</link>
	<title><![CDATA[MEGAN6]]></title>
	<description><![CDATA[<p>Microbiome analysis using a single application</p>
<p>MEGAN6 is a comprehensive toolbox for interactively analyzing microbiome data. All the interactive tools you need in one application.</p>
<ul>
<li>Taxonomic analysis using the NCBI taxonomy or a customized taxonomy such as SILVA</li>
<li>Functional analysis using InterPro2GO, SEED, eggNOG or KEGG</li>
<li>Bar charts, word clouds, Voronoi tree maps and many other charts</li>
<li>PCoA, clustering and networks</li>
<li>Supports metadata</li>
<li>MEGAN parses many different types of input</li>
</ul>
<p>Why use MEGAN6?</p>
<div>&nbsp;The software is:</div>
<div><ol>
<li>Easy to use. MEGAN6 is a single application and all features are available through menus, toolbars and graphics. No scripting skills required.</li>
<li>Powerful. MEGAN6 allows you to work with hundreds of samples containing&nbsp;hundreds of millions of sequencing reads. Blast-like analysis can be performed using DIAMOND.</li>
<li>Comprehensive. MEGAN6 offers a large range of analysis tools, and is under active development.</li>
</ol></div><p>Address of the bookmark: <a href="https://ab.inf.uni-tuebingen.de/software/megan6" rel="nofollow">https://ab.inf.uni-tuebingen.de/software/megan6</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28577/research-associate-computer-sciences-recruitment-in-national-bureau-of-plant-genetic-resources</guid>
  <pubDate>Thu, 28 Jul 2016 04:39:13 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Associate (Computer Sciences) recruitment in National Bureau of Plant Genetic Resources]]></title>
  <description><![CDATA[
<p>Research Associate (Computer Sciences) recruitment in National Bureau of Plant Genetic Resources</p>

<p>Project: Indo-UK Centre for improvement of Nitrogen use efficiency in wheat Dr. Soma S. Marla, Pr. Scientist (Bioinformatics), Division of Genomic Resources, ICAR, NBPGR, ND.</p>

<p>Qualification: Ph.D. Degree in Computer Sciences/Bioinformatics OR 1. First class Master’s degree in any discipline of Plant Sciences with specialization in Computer Sciences/ Bioinformatics having 1st division or 60% marks or equivalent overall grade point average with at least two years of research experience as evidenced from Fellowship/ Associate ship. 2. NET qualification is essential for the candidates with 3+2 years B.Sc.+ M.Sc. Desirable: Demonstrated experience &amp; skills in database design, management, UNIX OS, in NGS data analysis. Experience substantiated by publications of high quality will be preferred.</p>

<p>No.of Post: 1</p>

<p>Pay Scale: Rs. 40,000 (Ph.D)/ Rs + 30 % HRA; Rs.38,000 ( Masters Degree 0 + 30 % HRA).</p>

<p>Age Limit : below 40 years for RA position<br />How to apply<br />Applicants for RA post should send their complete CV (Advance copy of the application may be sent by email to :soma.marla@icar.gov.in or ssmarl@yahoo.com, should enclose the copy of the research publications; one page summary of their achievement relevant to the post applied for; and should enclose two reference letters (one must be from the person with whom worked latest). Shortlisted candidate will be intimated for interview by email.</p>

<p>The candidates who wish to attend the walk-in interview are requested to bring with them five copies of the CV (one copy with photograph) as per the format given below. Also, the candidates should bring the original documents such as degree certificates, marks sheets, publications, thesis, experience certificate etc. for verification. </p>

<p>Date of Interview: 17.8.2016.</p>

<p>More at http://www.nbpgr.ernet.in/Downloadfile.aspx?EntryId=7133</p>
]]></description>
</item>

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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28618/jrf-bioinformatics-at-dpu-india</guid>
  <pubDate>Fri, 05 Aug 2016 03:06:26 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics at DPU, India]]></title>
  <description><![CDATA[
<p>Advertisement for position of “JRF (Junior Research Fellow)” on DST research project “Molecular modeling and docking studies on Deguelin and its derivatives with cell cycle arrest, apoptosis and anti-angiogenesis pathway proteins in cancer cell signaling pathway”</p>

<p>Applications are invited on plain paper from eligible candidates along with biodata and copies of certificates in support of age, qualification and experience for the following position:</p>

<p>Particulars Description</p>

<p>1. Position &amp; No. JRF (Junior Research Fellow) 01</p>

<p>2. Title of the Project Molecular modeling and docking studies on Deguelin and its derivatives with cell cycle arrest, apoptosis and anti-angiogenesis pathway proteins in cancer cell signaling pathway</p>

<p>3. Tenure 3 years</p>

<p>4. Investigator Dr. K. V.Swamy</p>

<p>5. Institute Dr. D. Y. Patil Biotechnology and Bioinformatics Institute, Tathawade, Pune 411033.</p>

<p>5. Qualifications/Eligibility</p>

<p>Essential: NET (National Eligibility Test) qualified M. Sc Bioinformatics/ M. Tech Bioinformatics/M. Sc Biotechnology/M. Tech Biotechnology or Graduate degree in Professional course with NET qualification or Post graduation degree in professional course</p>

<p>The following examinations conducted by various Central Government Departments/Agencies are considered as National Eligibility Test (NET).</p>

<p>1. CSIR-UGC-LS <br />2. GATE (Graduate Aptitude Test in Engineering) <br />3. JAM (Joint Admission Test) <br />4. GPAT (Graduate Pharmacy Aptitude Test) <br />5. BET(Biotechnology Eligibility Test) <br />6. BINC(Bioinformatics National Consortium) <br />7. JEST( Joint Entrance Screening Test) <br />8. JGEEBILS(Joint Graduate Entrance Examination for Biology &amp; Interdisciplinary Life Sciences) <br />9. NBHM Ph.D scholarship Screening Test <br />10. ICMR- JRF Entrance Examination <br />11. AICE (ICAR-All India competitive Examination ) <br />(For all above examinations valid score considered at the time of interview)</p>

<p>Desirable: Knowledge and skills in Bioinformatics tools/ softwares</p>

<p>6. Monthly Emoluments Rs.25,000/ (As per DST-SERB rules)</p>

<p>7. Last date for submission of prescribed application 20/08/2016</p>

<p>Kindly send your applications to “Dr. K. V. Swamy, Asst.Professor, Dr. D. Y. Patil Biotechnology &amp; Bioinformatics Institute, Survey No. 87/88, Mumbai-Pune Express Way, Tathawade, Pune - 411033, Maharashtra, India”. Highlight the envelope with “Application for post of JRF (Junior Research Fellow)”.</p>

<p>Note: No TA/DA will be paid for attending the interview.</p>

<p>Advertisement: http://careers.dpu.edu.in/Biotech.aspx</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/42490/bioinformatics-scientist-%E2%80%93-icmr-computational-genomics-centre</guid>
  <pubDate>Sat, 26 Dec 2020 10:18:29 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics Scientist – ICMR Computational Genomics Centre]]></title>
  <description><![CDATA[
<p>ICMR invites online applications, from Indian Citizens, up to 8th January 2020 till 5:30 PM to fill up the following post to be filled purely on a temporary basis under “ICMR Computational Genomics Centre” under Dr. Harpreet Singh, Head, Division of Biomedical Informatics (BMI), ICMR HQRS, New Delhi 110029.<br />The Terms &amp; Conditions for the post are as follows:</p>

<p>a) Scientist-B – UR (2 posts-Bioinformatics) on consolidated salary of Rs.48,000/- pm + HRA</p>

<p>b) Scientist C – UR (1 post -Bioinformatics) on consolidated salary of Rs. 51,000 pm+ HRA</p>

<p>c) Scientist B- UR (2 post-Statistics) on a consolidated salary of Rs.48,000/- pm +HRA</p>

<p>d) Computer Programmer 1 post UR &amp; 1 post SC on a consolidated salary of Rs. 32,500/- pm</p>

<p>e) Research Assistant -UR 1 post on a consolidated salary of Rs. 31,000/- pm</p>

<p>More at https://projectjobs.icmr.org.in/sccbioinformatics/uploads/recruitment/Adv_BMI_24122020.pdf</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29235/valet</guid>
	<pubDate>Thu, 22 Sep 2016 04:27:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29235/valet</link>
	<title><![CDATA[valet]]></title>
	<description><![CDATA[<div>
<div>
<div>VALET is a pipeline for performing&nbsp;<em>de novo</em>&nbsp;validation of metagenomic assemblies. VALET checks a number of properties that should hold true for a correct assembly (e.g., mate-pairs are aligned at the correct distance from each other in the assembly, the depth of coverage is fairly uniform along contigs, etc.). The violations of these invariants are reported allowing one to pinpoint areas that were potentially mis-assembled, or to compare the quality of different assemblies. For comparing multiple assemblies of the same data-sets, VALET also reports an overall estimate of the likelihood a particular assembly is correct.</div>
</div>
</div>
<div>
<div>Home Page:&nbsp;</div>
<div>
<div><a href="https://github.com/jgluck/VALET">VALET code repository</a></div>
</div>
</div><p>Address of the bookmark: <a href="https://www.cbcb.umd.edu/software/valet" rel="nofollow">https://www.cbcb.umd.edu/software/valet</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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