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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/3889?offset=1460</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36895/npscarf-real-time-scaffolder-using-spades-contigs-and-nanopore-sequencing-reads</guid>
	<pubDate>Mon, 11 Jun 2018 05:14:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36895/npscarf-real-time-scaffolder-using-spades-contigs-and-nanopore-sequencing-reads</link>
	<title><![CDATA[npScarf: real-time scaffolder using SPAdes contigs and Nanopore sequencing reads]]></title>
	<description><![CDATA[npScarf (jsa.np.npscarf) is a program that connect contigs from a draft genomes to generate sequences that are closer to finish. These pipelines can run on a single laptop for microbial datasets. In real-time mode, it can be integrated with simple structural analyses such as gene ordering, plasmid forming.<p>Address of the bookmark: <a href="http://japsa.readthedocs.io/en/latest/tools/jsa.np.npscarf.html" rel="nofollow">http://japsa.readthedocs.io/en/latest/tools/jsa.np.npscarf.html</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/20362/20th-international-bioinformatics-workshop-on-virus-evolution-and-molecular-epidemiology-veme</guid>
  <pubDate>Mon, 12 Jan 2015 01:39:45 -0600</pubDate>
  <link></link>
  <title><![CDATA[20th International BioInformatics Workshop on Virus Evolution and Molecular Epidemiology (VEME)]]></title>
  <description><![CDATA[
<p>20th International BioInformatics Workshop on Virus Evolution and Molecular Epidemiology (VEME)<br />9 - 14 August 2015 St. Augustine, Trinidad and Tobago </p>

<p>Organiser: Christine Carrington (University of the West Indies - UWI, St. Augustine, Trinidad and Tobago)<br />Co-organisers: Anne-Mieke Vandamme, Philippe Lemey (Katholieke Universiteit Leuven, Belgium), Marco Salemi, Mattia Prosperi (University of Florida, Gainesville, USA) and Karen E. Nelson (J. Craig Venter Institute, Rockville, USA)</p>

<p>Requests for information directly to:<br />Christine Carrington<br />Department of Preclinical Sciences<br />Faculty of Medical Sciences<br />University of the West Indies (UWI)<br />St. Augustine<br />Trinidad and Tobago<br />Telephone: +1-868-6452640 ext. 5009, +1-868-6848803<br />Fax: +1-868-6621873<br />E-mail: veme2015@sta.uwi.edu</p>

<p>Deadline for receipt of applications by local organiser: 15 March 2015<br />CALL FOR APPLICATIONS NOW OPEN<br />http://www.icgeb.org/course-application-trinidad-and-tobago-2015.html</p>

<p>http://rega.kuleuven.be/cev/veme-workshop/2015</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37498/nextsv-a-meta-caller-for-structural-variants-from-low-coverage-long-read-sequencing-data</guid>
	<pubDate>Mon, 06 Aug 2018 17:24:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37498/nextsv-a-meta-caller-for-structural-variants-from-low-coverage-long-read-sequencing-data</link>
	<title><![CDATA[NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data]]></title>
	<description><![CDATA[<p>NextSV, a meta SV caller and a computational pipeline to perform SV calling from low coverage long-read sequencing data. NextSV integrates three aligners and three SV callers and generates two integrated call sets (sensitive/stringent) for different analysis purpose. The output of NextSV is in ANNOVAR-compatible bed format. Users can easily perform downstream annotation using ANNOVAR and disease gene discovery using Phenolyzer.</p>
<p>&nbsp;</p>
<h2>&nbsp;</h2><p>Address of the bookmark: <a href="https://github.com/Nextomics/NextSV" rel="nofollow">https://github.com/Nextomics/NextSV</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/20437/wuxi-has-acquired-nextcode-health</guid>
	<pubDate>Mon, 19 Jan 2015 08:17:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/20437/wuxi-has-acquired-nextcode-health</link>
	<title><![CDATA[WuXi has acquired NextCODE Health]]></title>
	<description><![CDATA[<p>Shanghai, China-headquartered pharmatech company WuXi (NYSE: WX) has acquired NextCODE Health, a genomic analysis and bioinformatics company based in the USA.<br /><br />The acquisition was made for $65 million in cash, and WuXi plans to merge its genome center with NextCODE Health to form a new company, WuXi NextCODE Genomics. The business will be headquartered in Shanghai and have operations in Cambridge, Massachusetts, and Reykjavik, Iceland.<br /><br />With the huge unmet medical needs in diseases with a genetic component and the rapid advances in genomics and bioinformatics, now is the right time for WuXi to make a strategic investment in this field, and NextCODE is the right partner. This new venture of WuXi NextCODE Genomics will create important new genomic and bioinformatic products and services to help make personalized treatment and medicine a reality.&nbsp; It will also enable doctors to provide better treatments to patients.<br /><br /></p>]]></description>
	<dc:creator>Pranjali Yadav</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37602/indexcov-fast-coverage-quality-control-for-whole-genome-sequencing</guid>
	<pubDate>Wed, 29 Aug 2018 09:20:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37602/indexcov-fast-coverage-quality-control-for-whole-genome-sequencing</link>
	<title><![CDATA[Indexcov: fast coverage quality control for whole-genome sequencing]]></title>
	<description><![CDATA[<p><em>indexcov</em><span>, an efficient estimator of whole-genome sequencing coverage to rapidly identify samples with aberrant coverage profiles, reveal large-scale chromosomal anomalies, recognize potential batch effects, and infer the sex of a sample.&nbsp;</span><em>Indexcov</em><span>&nbsp;is available at&nbsp;</span><a href="https://github.com/brentp/goleft" target="_blank">https://github.com/brentp/goleft</a><span>&nbsp;under the MIT license.</span></p><p>Address of the bookmark: <a href="https://github.com/brentp/goleft" rel="nofollow">https://github.com/brentp/goleft</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/21200/ra-bioinformatics-at-ciba</guid>
  <pubDate>Fri, 13 Feb 2015 11:23:18 -0600</pubDate>
  <link></link>
  <title><![CDATA[RA Bioinformatics at CIBA]]></title>
  <description><![CDATA[
<p>Recruitment The following posts are to be filled purely on temporary basis under CIBA Component of “Centre for Agricultural Bioinformatics (CABin)” project at this Institute.</p>

<p>Posts Research Associate</p>

<p>Date &amp; Time of Interview 18th Feb 2015 at 10.00 a.m.</p>

<p>Project Name “Centre for Agricultural Bioinformatics (CABin)”</p>

<p>Duration 12th Plan (2012-2017) / co-terminus with the project 12th Plan (2012-2017) / co-terminus with the project</p>

<p>Essential Qualification Ph.d / M.Sc./ M.Phil (Bioinformatics) With 1st division or 60% marks or equivalent overall grade point average with at least two years of research experience in the relevant subject.</p>

<p>Technician</p>

<p>B.Tech. or Master degree in computer science/Computer Engineering /MCA or equivalent. Desirable qualification: Experience in Java/ C++/ PHP/ PERL/ Python etc. based application development using Linux, Apache and MySQL/Oracle.</p>

<p>Emoluments Rs.24000/- p.m. + 30% HRA for Ph.D holders / Rs.23000/- p.m. + 30% HRA for Master Degree holders A consolidated pay Rs.25000/- per month.</p>

<p>Age Limit Maximum 40 years for men and 45 years for women as on date of interview.</p>

<p>Age limits are relaxable for SC / ST / OBC candidates as per rules.</p>

<p>Maximum 40 years for men and 45 years for women as on date of interview.</p>

<p>Age limits are relaxable for SC / ST / OBC candidates as per rules.</p>

<p>Eligible Candidates may send their Curriculum Vitae along with the contact numbers to ashok@ciba.res.in on or before 13-02-2015.</p>

<p>Candidates selected after initial screening will be called for interview.</p>

<p>Advertisement: www.ciba.res.in/attachments/jobs/CABin-3006.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37749/d2tools-the-toolbox-for-counting-the-frequency-of-k-tuple-from-sequencing-datasets-and-calculate-the-dissimilarity</guid>
	<pubDate>Thu, 20 Sep 2018 08:38:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37749/d2tools-the-toolbox-for-counting-the-frequency-of-k-tuple-from-sequencing-datasets-and-calculate-the-dissimilarity</link>
	<title><![CDATA[d2Tools: The toolbox for counting the frequency of k-tuple from sequencing datasets and calculate the dissimilarity]]></title>
	<description><![CDATA[<p><code>d2Tools</code>&nbsp;are the toolbox for counting the frequency of K-tuple from sequencing datasets and then calculating the pairwise dissimilarity matrix between samples with the&nbsp;<strong>d2-style</strong>(d2/d2<code>*</code>/d2S representing d2/d2Star/d2shepp, respectively) measures. Hao, Dai, Eucliean, Mahattan, and Chebyshev distance measures are also included in d2Tools.</p>
<p>Manual at&nbsp;https://code.google.com/archive/p/d2-tools/wikis/d2ToolMannual.wiki</p><p>Address of the bookmark: <a href="https://code.google.com/archive/p/d2-tools/" rel="nofollow">https://code.google.com/archive/p/d2-tools/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/20677/postdoctoral-researcher-at-department-of-biotechnology-catholic-university-of-daegu-kyungsan-kyungbuk-south-korea</guid>
  <pubDate>Thu, 29 Jan 2015 12:11:16 -0600</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Researcher at Department of Biotechnology, Catholic University of Daegu, Kyungsan, Kyungbuk, South Korea.]]></title>
  <description><![CDATA[
<p>Applications are invited from Indian nationals for a Post Doctoral position at Molecular Medical Laboratory, Department of Biotechnology, Catholic University of Daegu, Kyungsan, Kyungbuk, South Korea.</p>

<p>Qualification required: PhD in Life Sciences/ Molecular Biology/ Bioinformatics or related discipline.</p>

<p>Desirable Qualification:</p>

<p>1. Candidates having experience in molecular biology techniques and must be well versed with bioinformatics tool or expert in relevant fields will be preferred.<br />2. The candidate should have good communication skill, knowledge about designing experiments and analyzing data.<br />3. Sense of initiative, autonomy, organization and thoroughness, good relation qualities.<br />Remuneration: 2000USD per month.</p>

<p>Last date of submitting the complete applications furnishing Bio-data is 10th February, 2015.</p>

<p>Interested candidates should send their resume including all personal as well as academic details to the principal investigator Prof Seung-Won Park (email:microsw@cu.ac.kr)</p>

<p>The shortlisted candidates will be intimated within February 2015.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38205/sim3c-read-pair-simulation-of-3c-based-sequencing-methodologies-hic-meta3c-dnase-hic</guid>
	<pubDate>Tue, 13 Nov 2018 07:25:38 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38205/sim3c-read-pair-simulation-of-3c-based-sequencing-methodologies-hic-meta3c-dnase-hic</link>
	<title><![CDATA[sim3C: Read-pair simulation of 3C-based sequencing methodologies (HiC, Meta3C, DNase-HiC)]]></title>
	<description><![CDATA[<p><strong>Required python modules</strong></p>
<ul>
<li>biopython</li>
<li>intervaltree</li>
<li>numpy</li>
<li>scipy</li>
<li>tqdm</li>
<li>PyYAML</li>
</ul><p>Address of the bookmark: <a href="https://github.com/cerebis/sim3C" rel="nofollow">https://github.com/cerebis/sim3C</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/22438/research-associate-nbfgr-lucknow-uttar-pradesh</guid>
  <pubDate>Thu, 28 May 2015 19:37:22 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Associate NBFGR - Lucknow, Uttar Pradesh]]></title>
  <description><![CDATA[
<p>NBFGR, Lucknow is recruiting Bioinformatics experts for the post of Research Associate</p>

<p>Name of Position : Research Associate<br />No of Post : One<br />Desired candidate Profile : Candidate should be PhD in Bioinformatics or equivalent or Post-Graduation Bioinformatics with 1st division or 60% marks. Preference will be given to candidates having experience in server management<br />Remuneration : Rs 24000/- pm + HRA for PhD holders<br />Age requirement- 40 years (5 years relaxation for SC/ST/women candidates and 3 years for OBC candidates) as on date of interview.</p>

<p>How to apply- Interested candidates can walk -in-interview on 30.05.2015 at 10:00 hrs at National Bureau of Fish Genetic Resources, Lucknow.</p>

<p>Ref- http://www.nbfgr.res.in/PDF/News%20&amp;%20Events/Walk%20in%20interview%20on%2030.05.2015.pdf</p>
]]></description>
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