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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29912?offset=490</link>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25301/jrf-bioinformatics-at-cuk</guid>
  <pubDate>Sat, 28 Nov 2015 03:26:21 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics at CUK]]></title>
  <description><![CDATA[
<p>JRF job opportunity in Central University of Kerala (CUK) on temporary basis </p>

<p>Project Title : "Targeting TAL effector mediated susceptibility for durable and broad-spectrum resistance to bacterial blight in Rice"</p>

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

<p>Qualification : MSc in any subject under Life Science or Bioinformatics/ B.Tech in Bioinformatics + 1 yr experience </p>

<p>Stipend : Rs. 14,000/-</p>

<p>How to apply</p>

<p>Interested candidates are requested to send their applications explaining their interest in the position with an updated CV to Dr. Ginny Antony, Assistant Professor, Department of Plant Science, School of Biological Sciences, Central University of Kerala, Padannakkad, Kasaragod, Kerala - 671 314 email: ginnycuk2013@gmail.com on or before 20th December, 2015.</p>

<p>More at http://cukerala.ac.in/index.php?option=com_content&amp;view=article&amp;id=1022:applications-invited-for-the-post-of-jrf-department-of-plant-science&amp;catid=106&amp;Itemid=593&amp;lang=en</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42130/shaman-a-user-friendly-website-for-metataxonomic-analysis-from-raw-reads-to-statistical-analysis</guid>
	<pubDate>Mon, 17 Aug 2020 05:21:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42130/shaman-a-user-friendly-website-for-metataxonomic-analysis-from-raw-reads-to-statistical-analysis</link>
	<title><![CDATA[SHAMAN: a user-friendly website for metataxonomic analysis from raw reads to statistical analysis]]></title>
	<description><![CDATA[<p><span>SHAMAN is a shiny application for differential analysis of metagenomic data (16S, 18S, 23S, 28S, ITS and WGS) including bioinformatics treatment of raw reads for targeted metagenomics, statistical analysis and results visualization with a large variety of plots (barplot, boxplot, heatmap, &hellip;).</span><br><span>The bioinformatics treatment is based on Vsearch [</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/27781170">Rognes 2016</a><span>] which showed to be both accurate and fast [</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/26664811">Wescott 2015</a><span>].The statistical analysis is based on DESeq2 R package [</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/20979621">Anders and Huber 2010</a><span>] which robustly identifies the differential abundant features as suggested in [</span><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974642/">McMurdie and Holmes 2014</a><span>] and [</span><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727335/">Jonsson2016</a><span>]. SHAMAN robustly identifies the differential abundant genera with the Generalized Linear Model implemented in DESeq2 [</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/25516281">Love 2014</a><span>].</span><br><span>SHAMAN is compatible with standard formats for metagenomic analysis (.csv, .tsv, .biom) and figures can be downloaded in several formats. A presentation about SHAMAN is available&nbsp;</span><a href="https://github.com/aghozlane/shaman/blob/master/www/shaman_presentation.pdf">here</a><span>&nbsp;and a poster&nbsp;</span><a href="https://github.com/aghozlane/shaman/blob/master/www/shaman_poster.pdf">here</a><span>.&nbsp;</span></p>
<p><span>More at&nbsp;<a href="https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-020-03666-4">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-020-03666-4</a></span></p><p>Address of the bookmark: <a href="https://github.com/aghozlane/shaman" rel="nofollow">https://github.com/aghozlane/shaman</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25503/assistant-professor-computational-biology-and-bioinformatics-in-navi-mumbai</guid>
  <pubDate>Fri, 04 Dec 2015 20:40:59 -0600</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor - Computational Biology and Bioinformatics in Navi Mumbai]]></title>
  <description><![CDATA[
<p>No. ACTREC / ADVT-A/2/2015 <br />Pay in Pay band and Grade Pay : PB-3 (Rs 15,600-39,100) Pay in pay band Rs 21,900+ G.P. of Rs 7,600 <br />Total emoluments = 82,000/- p.m. &amp; nbsp <br />Educational Qualification : Ph.D. or MD/Ph.D. <br />Experience : Post MD / Ph.D. Research experience of 5 years The last date of application submission is January 15th, 2016. <br />Interested candidates shall send the applications through email: office.sao(at)actrec.gov.in. <br />For More Details : www.actrec.gov.in/data%20files/Vacancies/2015/Faculty-Positions-SOE-24-11-15.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42485/fastprongs-fast-preprocessing-of-next-generation-sequencing-reads</guid>
	<pubDate>Sat, 26 Dec 2020 08:35:21 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42485/fastprongs-fast-preprocessing-of-next-generation-sequencing-reads</link>
	<title><![CDATA[FastProNGS: fast preprocessing of next-generation sequencing reads]]></title>
	<description><![CDATA[<p><span>FastProNGS to integrate the quality control process with automatic adapter removal. Parallel processing was implemented to speed up the process by allocating multiple threads. Compared with similar up-to-date preprocessing tools, FastProNGS is by far the fastest.&nbsp;</span></p><p>Address of the bookmark: <a href="https://github.com/Megagenomics/FastProNGS" rel="nofollow">https://github.com/Megagenomics/FastProNGS</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/25400/arraygen-next-generation-genome-browser-coming-soon</guid>
	<pubDate>Thu, 03 Dec 2015 05:52:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/25400/arraygen-next-generation-genome-browser-coming-soon</link>
	<title><![CDATA[ArrayGen Next Generation Genome Browser Coming Soon !!!]]></title>
	<description><![CDATA[<p>The ANG genome browser is a visualization tool, developed by ArrayGen Technologies. This is a fast and an efficient genome browser, built with Javafx and Java swing. ANG genome browser was built for latest next generation sequencing data analysis. It is platform independent and much simpler to use.</p><p>The main features are, it supports many standard file formats such as GFF, BED, GTF, FASTA, VCF, BAM and it can be integrated with other browsers or tools for analysis of genome.</p>]]></description>
	<dc:creator>ArrayGen Technologies</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44171/hairsplitter-assembling-long-reads-in-an-unknown-number-of-haplotypes</guid>
	<pubDate>Wed, 07 Dec 2022 00:13:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44171/hairsplitter-assembling-long-reads-in-an-unknown-number-of-haplotypes</link>
	<title><![CDATA[HairSplitter: assembling long reads in an unknown number of haplotypes]]></title>
	<description><![CDATA[<p>Pros and cons of HairSplitter Limitations of HairSplitter:</p>
<p>Not very fast: it re-polishes the whole assembly&nbsp;</p>
<p>Limited in the number of haplotypes</p>
<p>Strengths of HairSplitter:</p>
<p>Very modular, can be used with any assembler</p>
<p>Naive: makes no assumption on ploidy, parameter-free</p>
<p>Safe: won&rsquo;t artificially duplicate contigs</p>
<p>&nbsp;</p>
<p>HairSplitter splits collapsed assemblies from &ldquo;draft&rdquo; assemblies obtained by any means</p>
<p>HairSplitter can recover haplotypes and distinguish repeated elements</p>
<p>Only needs sequencing reads, potentially error-prone</p>
<p>HairSplitter splits collapsed assemblies from &ldquo;draft&rdquo; assemblies obtained by any means</p>
<p>HairSplitter can recover haplotypes and distinguish repeated elements</p>
<p>Only needs sequencing reads, potentially error-prone</p>
<p>Not really available yet (github.com/RolandFaure/HairSplitter)</p>
<p>https://hal.archives-ouvertes.fr/hal-03864075/file/RolandFaure_presentation_SeqBIM_2022.pdf</p><p>Address of the bookmark: <a href="https://hal.archives-ouvertes.fr/hal-03817928/document" rel="nofollow">https://hal.archives-ouvertes.fr/hal-03817928/document</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25410/srfjrf-bioinformatics-at-ciari</guid>
  <pubDate>Fri, 04 Dec 2015 00:10:09 -0600</pubDate>
  <link></link>
  <title><![CDATA[SRF/JRF Bioinformatics at CIARI]]></title>
  <description><![CDATA[
<p>Realizing the importance of Island Agriculture to meet the requirements of local population and tourists, Indian Council of Agricultural research (ICAR) established Central Island Agricultural Research Institute, Port Blair on June 23rd, 1978 by merging different regional research stations of ICAR institutes located in Islands. The ultimate aim of CIARI is the developments of island agricultural production technologies which utilizes the strengths of the island and convert the constraints in opportunities, without causing any ill effect to the fragile ecosystem of the island.The institute has made tremendous progress in the Agriculture development of the islands during the last three decades. Keeping in view the natural resources of the islands diversity, fragile ecosystem, research program would be designed to maximize the productivity without disturbing to the islands ecosystem to provide better and decent livelihood and as a source of revenue and resource generation. Research and development in Agriculture sector should cover all disciplines in order to have a balanced progress in all disciplines for the overall benefits of the farmers of these islands.</p>

<p>Position I</p>

<p>Job Title : Junior Research Fellow</p>

<p>No. of Posts : One</p>

<p>Project : Establishment of sub distributed information centre</p>

<p>Qualification : M.Sc in Basic Science with NET or B.Sc in professional course with NET or M.Sc in professional course</p>

<p>Desired Experience : Experience in Bioinformatics and molecular biology</p>

<p>Payscale : Rs. 25000 per month</p>

<p>Age Limit : Upto 35 for men and 40 for women with 5 years relaxation to SC/ST and 3 years relaxation for OBC.</p>

<p>Position II</p>

<p>Job Title : Traineeship</p>

<p>No. of Posts : One</p>

<p>Project : Establishment of sub distributed information centre</p>

<p>Qualification : B.Sc Bioinformatics /Biotechnology / Life Science / Computer Science</p>

<p>Desired Experience : Experience in Bioinformatics and molecular biology</p>

<p>Payscale : Rs. 8000 per month</p>

<p>Age Limit : Upto 35 for men and 40 for women with 5 years relaxation to SC/ST and 3 years relaxation for OBC.</p>

<p>Position III</p>

<p>Job Title : Studentship</p>

<p>No. of Posts : Two</p>

<p>Project : Establishment of sub distributed information centre</p>

<p>Qualification : B.Sc Bioinformatics /Biotechnology / Life Science / Computer Science</p>

<p>Desired Experience : Experience in Bioinformatics and molecular biology</p>

<p>Payscale : Rs. 8000 per month</p>

<p>Age Limit : Upto 35 for men and 40 for women with 5 years relaxation to SC/ST and 3 years relaxation for OBC.</p>

<p>How to Apply : Candidates who meet the requirements can attend the walk in interview at CIARI,Port Blair on 09.12.2015 10.30AM.</p>

<p>http://icar-ciari.res.in/employment/9-12-15.pdf</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35055/jabba-hybrid-error-correction-for-long-sequencing-reads</guid>
	<pubDate>Fri, 05 Jan 2018 03:58:14 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35055/jabba-hybrid-error-correction-for-long-sequencing-reads</link>
	<title><![CDATA[Jabba: Hybrid Error Correction for Long Sequencing Reads]]></title>
	<description><![CDATA[<p>Jabba is a hybrid error correction tool to correct third generation (PacBio / ONT) sequencing data, using second generation (Illumina) data.</p>
<p>Input</p>
<p>Jabba takes as input a concatenated de Bruijn graph and a set of sequences:</p>
<p>the de Bruijn graph should appear in fasta format with 1 entry per node, the meta information should be in the format:<br>&gt;NODE <br>the set of sequences should be in fasta or fastq format. These sequences will be corrected (e.g. PacBio reads). The corrections will be written to a file Jabba fasta.<br>The output is a file in fasta format with corrections of the long reads, and additionally a file in the input format containing uncorrected reads.</p>
<p>https://github.com/biointec/jabba/wiki</p>
<p>https://almob.biomedcentral.com/articles/10.1186/s13015-016-0075-7</p><p>Address of the bookmark: <a href="https://github.com/biointec/jabba" rel="nofollow">https://github.com/biointec/jabba</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25674/post-doc-position-at-labgem-evry-france</guid>
  <pubDate>Fri, 11 Dec 2015 06:24:00 -0600</pubDate>
  <link></link>
  <title><![CDATA[Post-doc position at LABGeM - Evry, France]]></title>
  <description><![CDATA[
<p>The LABGeM team (CEA/Genoscope, CNRS UMR 8030, France, Dir. Claudine Médigue) is developing integrated approaches which combines bioinformatics methods based (i) on genomic and metabolic contexts, (ii) on an orignal metabolic network representation and (iii) on a structural classification of active sites for the discovery of new metabolic enzymatic activities.</p>

<p>We are hiring a post-doctoral fellow for the development of innovative bioinformatics methods to explore metabolic networks and enzyme families. These methods will be based on protein family analysis and graph approaches combining genomic and metabolic contexts.</p>

<p>For more details, please see this link : http://goo.gl/tHQOqk</p>

<p>Qualifications:<br />PhD degree in bioinformatics or computational biology<br />- Previous experience in network or protein family analysis<br />- Programming skills (C/C++, Python, Java) and in common biostatistical analyses<br />- Team player, innovative and creative thinking, good oral and written communication skills</p>

<p>24 months, Post Doctoral position<br />Start: from March 2016<br />Place: CEA, Genoscope UMR8030, LABGeM (Laboratory of Bioinformatics Analyses for Genomics and Metabolism), Evry, France<br />Contact: David Vallenet, vallenet@genoscope.cns.fr<br />Publications: https://scholar.google.com/citations?user=rJNPLSAAAAAJ<br />Remuneration per month: from 2,850 €</p>

<p>Interested candidates should send their CV, statement of research interests, and contact information of at least 2 references to David Vallenet (vallenet@genoscope.cns.fr).</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40940/consed-a-finishing-package-bam-file-viewer-assembly-editor-autofinish-autoreport-autoedit-and-align-reads-to-reference-sequence</guid>
	<pubDate>Fri, 07 Feb 2020 07:16:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40940/consed-a-finishing-package-bam-file-viewer-assembly-editor-autofinish-autoreport-autoedit-and-align-reads-to-reference-sequence</link>
	<title><![CDATA[Consed--A Finishing Package (BAM File Viewer, Assembly Editor, Autofinish, Autoreport, Autoedit, and Align Reads To Reference Sequence)]]></title>
	<description><![CDATA[<ul>
<li>Supports Illumina, 454, other Next-Gen and Sanger Reads and allows mixtures of these read types</li>
<li>Consed includes BamScape which can view bam files with unlimited numbers of reads. BamScape can bring up consed to edit reads and the reference sequence in targeted regions.</li>
<li>Consed is compatible with Newbler, Cross_match, Phrap, MIRA, Velvet and PCAP output.</li>
<li>Quickly takes the user to each variant site for viewing (also available as an automated report)</li>
<li>Overview of assembly can help detect and fix misassemblies</li>
<li>Editing time reduced by the program's ability to pin-point problem areas</li>
<li>Editing is guided by error probabilities</li>
</ul><p>Address of the bookmark: <a href="http://www.phrap.org/consed/consed.html" rel="nofollow">http://www.phrap.org/consed/consed.html</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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