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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/13226?offset=660</link>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/26567/ra-at-university-of-pune</guid>
  <pubDate>Mon, 07 Mar 2016 03:48:33 -0600</pubDate>
  <link></link>
  <title><![CDATA[RA at University of Pune]]></title>
  <description><![CDATA[
<p>Research Associate Job vacancies in University of Pune on temporary basis</p>

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

<p>Department : Science and Technology</p>

<p>Qualifications : Ph.D. with specialization in Bioinformatics/Machine Learning/ Mathematical Biology/ Computational Biology/ Systems Biology with a minimum of 55% marks in M. Sc. (50% for candidates belongs to reserved category) or equivalent grade.  Candidates who have submitted their Ph.D. thesis and are waiting for award of Ph.D. are also eligible. OR M. Sc. Bioinformatics with two years of research experience in the areas mentioned above, a minimum of 55% marks in M.Sc. (50% for candidates belongs to reserved categories) or equivalent grade and at least one publication in Science Citation Index (SCI) journal. Preference will be given to B.I.N.C. /J.R.F. /N.E.T. /S.E.T. qualified candidates.  </p>

<p>Emoluments : Rs. 20,000/- (Including H.R.A.) per month.<br />How to apply</p>

<p>The complete application along with necessary documents and certificates should reach to 'The Director, Bioinformatics Centre, Savitribai Phule Pune University (Formerly University of Pune), Caneshkhind Road. Pune - 411 007 on or before 21st March, 2016 within official hours except Sundays (i.e. 10.20 am to 06.00 pm).</p>

<p>More at http://collegecirculars.unipune.ac.in/sites/documents/Job%20Openings/Forms/AllItems.aspx</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/26336/project-fellow-bioinformatics-at-central-university-of-himachal-pradesh</guid>
  <pubDate>Tue, 09 Feb 2016 03:58:00 -0600</pubDate>
  <link></link>
  <title><![CDATA[Project Fellow Bioinformatics at Central University of Himachal Pradesh]]></title>
  <description><![CDATA[
<p>Project Fellow Bioinformatics</p>

<p>Eligibility : MSc(Bio-Chemistry, Bio-Informatics)</p>

<p>Location : Kulu</p>

<p>Last Date : 07 Mar 2016</p>

<p>Hiring Process : Face to Face Interview<br />Central University of Himachal Pradesh</p>

<p>Project Fellow Bioinformatics Job in Central University of Himachal Pradesh</p>

<p>Project (MRP) entitled: “A project proposal on targeting novel prokaryotic ubiquitin like post-translational modification pathway for therapeutic interventions against Mycobacterium tuberculosis” (No. MRP-MAJOR-MICR-2013-26840)</p>

<p>Essential Qualification: 1. Master degree in Bioinformatics/Biochemistry/Biotechnology/Environmental Science/Microbiology or any branch of Life Sciences with a minimum of 55% marks for general category (50% in case of SC/ST/PH) 2. UGC/CSIR NET, GATE qualified candidates will be given preference. Desirable Qualification: Experience in basic Bioinformatics and Molecular Biology techniques.</p>

<p>Age: Below 40 years as on 01/10/2015.</p>

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

<p>Salary: NET/GATE qualified candidate: Rs. 16,000/-p.m. for initial two years and Rs. 18,000/- p.m. for the third year. Non-NET/GATE candidates: Rs. 14,000/-p.m. for initial two years and Rs. 16,000/-p.m. for the third year.</p>

<p>Mode of Selection: The selection shall be made on the basis of merit. The eligible candidates are required to appear for interview before the duly constituted Selection Committee for the purpose. The scheduled date, time and venue for the interview shall be intimated to the eligible candidates through phone/ e-mail.<br />How to apply</p>

<p>Last date for the receipt of applications is 07.03.2016. </p>

<p>More at http://www.cuhimachal.ac.in/news_all.aspx</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26378/centurion</guid>
	<pubDate>Fri, 12 Feb 2016 04:45:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26378/centurion</link>
	<title><![CDATA[Centurion]]></title>
	<description><![CDATA[<p>Although centromeres are essential for life and are the subject of extensive research, centromere locations in yeast genomes are difficult to infer, and in most species they are still unknown. Recently, the chromatin conformation assay Hi-C has been re-purposed for diverse applications, including de novo genome assembly, deconvolution of metagenomic samples, and inference of centromere locations. We describe a method, Centurion, that jointly infers the locations of all centromeres in a single yeast genome by exploiting the centromeres&rsquo; tendency to cluster in 3D space. We first demonstrate the accuracy of Centurion in identifying known centromere locations from high coverage Hi-C data of budding yeast and a human malaria parasite. We then use two metagenomic samples with relatively low coverage Hi-C data to infer centromere locations for each chromosome in 14 different yeast species. For yeasts with large centromeres (e.g., S. pombe) Centurion predicts the exact centromere locations. For seven yeasts with point centromeres, Centurion predicts most of the centromeres at an average of 5~kb distance from their known locations. Finally, we predict centromere coordinates for six yeast species that currently lack centromere annotations. These results suggest that Centurion can be used for centromere identification for a large number of yeast species, even with a limited amount of Hi-C sequencing.</p>
<p>Paper:http://www.ncbi.nlm.nih.gov/pubmed/25940625</p>
<p>More at http://cbio.ensmp.fr/centurion/</p><p>Address of the bookmark: <a href="http://cbio.ensmp.fr/centurion/" rel="nofollow">http://cbio.ensmp.fr/centurion/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26409/ucsc-genome-browser-and-blat-software</guid>
	<pubDate>Thu, 18 Feb 2016 03:18:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26409/ucsc-genome-browser-and-blat-software</link>
	<title><![CDATA[UCSC Genome Browser and Blat software !]]></title>
	<description><![CDATA[<p>This directory contains Genome Browser and Blat application binaries built for standalone <br>command-line use on various supported Linux and UNIX platforms. To determine which set of binaries <br>to download, type "uname -a" on the command line to display your machine type. In most cases the <br>usage statement for the application can be viewed by running the binary with no arguments. <br><br>The UCSC Genome Browser and Blat software are free for academic, nonprofit, and personal use. A <br>license is required for commercial download and installation of these binaries, with the exception <br>of items built from the following source code directories, which are freely available for all uses:<br><br>&nbsp;- kent/src/utils (includes big* tools)<br>&nbsp;- kent/src/lib<br>&nbsp;- kent/src/hg/autoSql<br>&nbsp;- kent/src/hg/autoXml<br><br>For information about commercial licensing of the Genome Browser software, see <br>http://genome.ucsc.edu/license/. The Blat and In-Silico PCR software may be commercially<br>licensed through Kent Informatics (http://www.kentinformatics.com).</p>
<p>More at http://hgdownload.cse.ucsc.edu/admin/exe/</p><p>Address of the bookmark: <a href="http://hgdownload.cse.ucsc.edu/admin/exe/" rel="nofollow">http://hgdownload.cse.ucsc.edu/admin/exe/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/26456/the-mills-lab</guid>
  <pubDate>Wed, 24 Feb 2016 16:18:38 -0600</pubDate>
  <link></link>
  <title><![CDATA[The Mills lab]]></title>
  <description><![CDATA[
<p>The laboratory is focused on the discovery and analysis of structural variation (SVs) from genomic sequence data. As part of the 1000 Genomes Project and other endeavors, we have helped produce initial fine-scale maps using a variety of SV discovery approaches including: (i) paired-end mapping (or read pair analysis) based on abnormally mapped pairs of clone ends; (ii) read-depth analysis, which detects deletions and duplications through analysis of the read depth-of-coverage; (iii) split read analysis, which detects SVs by evaluating gapped sequence alignments; and (iv) sequence assembly, which enables the discovery of novel (non-reference) sequence insertions.</p>

<p>http://millslab.org/research.html</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26573/efficient-genome-searching-with-biostrings-and-the-bsgenome-data-package</guid>
	<pubDate>Mon, 07 Mar 2016 05:18:06 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26573/efficient-genome-searching-with-biostrings-and-the-bsgenome-data-package</link>
	<title><![CDATA[Efficient genome searching with Biostrings and the BSgenome data package]]></title>
	<description><![CDATA[<p>Address of the bookmark: <a href="https://www.bioconductor.org/packages/3.3/bioc/vignettes/BSgenome/inst/doc/GenomeSearching.pdf" rel="nofollow">https://www.bioconductor.org/packages/3.3/bioc/vignettes/BSgenome/inst/doc/GenomeSearching.pdf</a></p>]]></description>
	<dc:creator>Aasha</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26906/paired-end-assembler-for-dna-sequences</guid>
	<pubDate>Wed, 06 Apr 2016 05:25:34 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26906/paired-end-assembler-for-dna-sequences</link>
	<title><![CDATA[PAired-eND Assembler for DNA sequences]]></title>
	<description><![CDATA[<p>PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence.</p>
<p>&nbsp;</p>
<p>More at https://github.com/neufeld/pandaseq</p><p>Address of the bookmark: <a href="https://github.com/neufeld/pandaseq" rel="nofollow">https://github.com/neufeld/pandaseq</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26919/pear-a-fast-and-accurate-illumina-paired-end-read-merger</guid>
	<pubDate>Wed, 06 Apr 2016 13:27:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26919/pear-a-fast-and-accurate-illumina-paired-end-read-merger</link>
	<title><![CDATA[PEAR: a fast and accurate Illumina Paired-End reAd mergeR]]></title>
	<description><![CDATA[<p><strong>PEAR</strong>&nbsp;is an ultrafast, memory-efficient and highly accurate pair-end read merger. It is fully parallelized and can run with as low as just a few kilobytes of memory.</p>
<p>PEAR evaluates all possible paired-end read overlaps and without requiring the target fragment size as input. In addition, it implements a statistical test for minimizing false-positive results. Together with a highly optimized implementation, it can merge millions of paired end reads within a couple of minutes on a standard desktop computer.</p>
<p>More at&nbsp;http://www.exelixis-lab.org/web/software/pear</p>
<p>Paper:&nbsp;http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933873/</p><p>Address of the bookmark: <a href="http://www.exelixis-lab.org/web/software/pear" rel="nofollow">http://www.exelixis-lab.org/web/software/pear</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26968/scalce</guid>
	<pubDate>Fri, 15 Apr 2016 05:09:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26968/scalce</link>
	<title><![CDATA[SCALCE]]></title>
	<description><![CDATA[<p><span>SCALCE (</span><code>/skeɪlz/</code><span>, a.k.a. boosting&nbsp;</span><span style="text-decoration: underline;">S</span><span>equence&nbsp;</span><span style="text-decoration: underline;">C</span><span>ompression&nbsp;</span><span style="text-decoration: underline;">A</span><span>lgorithms using&nbsp;</span><span style="text-decoration: underline;">L</span><span>ocally&nbsp;</span><span style="text-decoration: underline;">C</span><span>onsistent</span><span style="text-decoration: underline;">E</span><span>ncoding) is a tool for compressing FASTQ files. It is designed specifically for the Illumina-generated FASTQ files, but supports any valid FASTQ with consistent read lengths.&nbsp;</span></p>
<p><span>More at&nbsp;http://sfu-compbio.github.io/scalce/</span></p><p>Address of the bookmark: <a href="http://sfu-compbio.github.io/scalce/" rel="nofollow">http://sfu-compbio.github.io/scalce/</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27035/spades</guid>
	<pubDate>Tue, 19 Apr 2016 08:37:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27035/spades</link>
	<title><![CDATA[SPAdes]]></title>
	<description><![CDATA[<p>SPAdes &ndash; St. Petersburg genome assembler &ndash; is intended for both standard isolates and single-cell MDA bacteria assemblies. This manual will help you to install and run SPAdes. SPAdes version 3.7.1 was released under GPLv2 on March 8, 2016 and can be downloaded from <a href="http://bioinf.spbau.ru/en/spades" target="_blank">http://bioinf.spbau.ru/en/spades</a>.</p>
<p>Manual at http://spades.bioinf.spbau.ru/release3.7.1/manual.html</p><p>Address of the bookmark: <a href="http://bioinf.spbau.ru/spades" rel="nofollow">http://bioinf.spbau.ru/spades</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>

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