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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38489?offset=120</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34477/computational-genomics-applied-comparative-genomics</guid>
	<pubDate>Wed, 29 Nov 2017 05:11:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34477/computational-genomics-applied-comparative-genomics</link>
	<title><![CDATA[Computational Genomics: Applied Comparative Genomics]]></title>
	<description><![CDATA[<p><span>The primary goal of the course is for students to be grounded in theory and leave the course empowered to conduct independent genomic analyses.</span><span>&nbsp;We will study the leading computational and quantitative approaches for comparing and analyzing genomes starting from raw sequencing data. The course will focus on human genomics and human medical applications, but the techniques will be broadly applicable across the tree of life. The topics will include genome assembly &amp; comparative genomics, variant identification &amp; analysis, gene expression &amp; regulation, personal genome analysis, and cancer genomics. The grading will be based on assignments, a midterm exam, class presentations, and a significant class project. There are no formal course prerequisites, although the course will require familiarity with UNIX scripting and/or programming to complete the assignments and course project.</span></p><p>Address of the bookmark: <a href="https://github.com/schatzlab/appliedgenomics" rel="nofollow">https://github.com/schatzlab/appliedgenomics</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43040/coronavir-computational-resources-on-novel-coronavirus-sars-cov-2-or-covid-19</guid>
	<pubDate>Tue, 27 Apr 2021 01:58:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43040/coronavir-computational-resources-on-novel-coronavirus-sars-cov-2-or-covid-19</link>
	<title><![CDATA[CoronaVIR: Computational Resources on Novel Coronavirus (SARS-CoV-2 or COVID-19)]]></title>
	<description><![CDATA[<div>
<p style="text-align: justify;">Aim of this web site is to facilitate the scientific community to fight against severe pandemic disease COVID-19 caused by SARS-CoV-2. Here, We have collected and organized information related to novel strain of coronavirus, i.e. SARS-CoV-2.and its resulting disease COVID-19 from the literature and other resources from the Internet. We are providing links to appropriate literature. Moreover, we are Bioinformatics Group, based on our knowledge and expertise, we are also proposing potential diagnostics primers, peptide and RNA based vaccine candidates and potential drug molecules. These are predicted candidates, need to be validated by experimental Researchers, who have appropriate infrastructure. It is an integrated multi-omics repository dedicated to current genomic, proteomic, diagnostic and therapeutic knowledge about coronaviruses particularly the recent strain, i.e. SARS-CoV-2 or 2019-nCoV. This web resource will be helpful for the researchers engaged in the development of therapies and drugs for the COVID-19. The information is collected from various available resources.<br><strong>Cite:&nbsp;</strong><a href="https://www.liebertpub.com/doi/10.1089/mab.2020.0035">Patiyal, Sumeet, et al. &ldquo;A Web-based Platform on COVID-19 to Maintain Predicted Diagnostic, Drug<br>and Vaccine Candidates.&rdquo; Monoclon Antib Immunodiagn Immunother. doi.org/10.1089/mab.2020.0035</a></p>
<div>
<p>&nbsp;</p>
</div>
</div><p>Address of the bookmark: <a href="https://webs.iiitd.edu.in/raghava/coronavir/" rel="nofollow">https://webs.iiitd.edu.in/raghava/coronavir/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39372/irnad-a-computational-tool-for-identifying-d-modification-sites-in-rna-sequence</guid>
	<pubDate>Thu, 16 May 2019 00:20:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39372/irnad-a-computational-tool-for-identifying-d-modification-sites-in-rna-sequence</link>
	<title><![CDATA[iRNAD: a computational tool for identifying D modification sites in RNA sequence]]></title>
	<description><![CDATA[<p><span>iRNAD, for identifying D modification sites in RNA sequence. In this predictor, the RNA samples derived from five species were encoded by nucleotide chemical property and nucleotide density. Support vector machine was utilized to perform the classification.&nbsp;</span></p>
<p><span><a href="http://lin-group.cn/server/iRNAD/">http://lin-group.cn/server/iRNAD/</a></span></p><p>Address of the bookmark: <a href="http://lin-group.cn/server/iRNAD/" rel="nofollow">http://lin-group.cn/server/iRNAD/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36616/srbreak-a-read-depth-and-split-read-framework-to-identify-breakpoints-of-different-events-inside-simple-copy-number-variable-regions</guid>
	<pubDate>Tue, 15 May 2018 04:42:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36616/srbreak-a-read-depth-and-split-read-framework-to-identify-breakpoints-of-different-events-inside-simple-copy-number-variable-regions</link>
	<title><![CDATA[SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions]]></title>
	<description><![CDATA[SRBreak is a read-depth and split-read package written in R for identifying copy-number variants in next-generation sequencing datasets.

Note: SBReak was designed to work for multiple samples. It can work for &gt;= 2 samples, but we suggest that users should use &gt;= 5 samples as in the work tested in our paper.<p>Address of the bookmark: <a href="https://github.com/hoangtn/SRBreak" rel="nofollow">https://github.com/hoangtn/SRBreak</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35148/mojolicious-a-next-generation-web-framework-for-the-perl-programming-language</guid>
	<pubDate>Fri, 12 Jan 2018 16:48:10 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35148/mojolicious-a-next-generation-web-framework-for-the-perl-programming-language</link>
	<title><![CDATA[mojolicious: a next generation web framework for the Perl programming language.]]></title>
	<description><![CDATA[<p><span>Back in the early days of the web, many people learned Perl because of a wonderful Perl library called&nbsp;</span><a href="https://metacpan.org/module/CGI" target="_blank">CGI</a><span>. It was simple enough to get started without knowing much about the language and powerful enough to keep you going, learning by doing was much fun. While most of the techniques used are outdated now, the idea behind it is not. Mojolicious is a new endeavor to implement this idea using bleeding edge technologies.</span></p>
<h2>Features</h2>
<ul>
<li>An amazing&nbsp;<strong>real-time web framework</strong>, allowing you to easily grow single file prototypes into well-structured MVC web applications.
<ul>
<li>Powerful out of the box with RESTful routes, plugins, commands, Perl-ish templates, content negotiation, session management, form validation, testing framework, static file server, CGI/<a href="http://plackperl.org/" target="_blank">PSGI</a>&nbsp;detection, first class Unicode support and much more for you to discover.</li>
</ul>
</li>
<li>A powerful&nbsp;<strong>web development toolkit</strong>, that you can use for all kinds of applications, independently of the web framework.
<ul>
<li>Full stack HTTP and WebSocket client/server implementation with IPv6, TLS, SNI, IDNA, HTTP/SOCKS5 proxy, UNIX domain socket, Comet (long polling), Promises/A+, keep-alive, connection pooling, timeout, cookie, multipart and gzip compression support.</li>
<li>Built-in non-blocking I/O web server, supporting multiple event loops as well as optional pre-forking and hot deployment, perfect for building highly scalable web services.</li>
<li>JSON and HTML/XML parser with CSS selector support.</li>
</ul>
</li>
<li>Very clean, portable and object-oriented pure-Perl API with no hidden magic and no requirements besides Perl 5.24.0 (versions as old as 5.10.1 can be used too, but may require additional CPAN modules to be installed)</li>
<li>Fresh code based upon years of experience developing&nbsp;<a href="http://catalystframework.org/" target="_blank">Catalyst</a>, free and open source.</li>
<li>Hundreds of 3rd party&nbsp;<a href="https://metacpan.org/requires/distribution/Mojolicious">extensions</a>&nbsp;and high quality spin-off projects like the&nbsp;<a href="https://metacpan.org/pod/Minion">Minion</a>&nbsp;job queue.</li>
</ul>
<p>http://mojolicious.org/</p><p>Address of the bookmark: <a href="http://mojolicious.org/" rel="nofollow">http://mojolicious.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38829/nquire-a-statistical-framework-for-ploidy-estimation-using-ngs-short-read-data</guid>
	<pubDate>Thu, 31 Jan 2019 05:12:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38829/nquire-a-statistical-framework-for-ploidy-estimation-using-ngs-short-read-data</link>
	<title><![CDATA[nQuire: A statistical framework for ploidy estimation using NGS short-read data]]></title>
	<description><![CDATA[<p>nQuire implements a set of commands to estimate ploidy level of individuals from species, where recent polyploidization occurred and intraspecific ploidy variation is observed. Specifically, nQuire uses next-generation sequencing data to distinguish between diploids, triploids and tetraploids, on the basis of frequency distributions at variant sites where only two bases are segregating.</p>
<p>For more background see also the publication at&nbsp;<a href="https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-018-2128-z">BMC Bioinformatics</a>.</p>
<p>https://github.com/clwgg/nQuire</p><p>Address of the bookmark: <a href="https://github.com/clwgg/nQuire" rel="nofollow">https://github.com/clwgg/nQuire</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44481/unialigner-a-parameter-free-framework-for-fast-sequence-alignment</guid>
	<pubDate>Fri, 08 Mar 2024 23:36:12 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44481/unialigner-a-parameter-free-framework-for-fast-sequence-alignment</link>
	<title><![CDATA[UniAligner: a parameter-free framework for fast sequence alignment]]></title>
	<description><![CDATA[<p>UniAligner (formerly, TandemAligner) is the first parameter-free algorithm for sequence alignment that introduces a sequence-dependent alignment scoring that automatically changes for any pair of compared sequences. Classical alignment approaches, such as the Smith-Waterman algorithm, that work well for most sequences, fail to construct biologically adequate alignments of extra-long tandem repeats (ETRs), such as human centromeres and immunoglobulin loci. This limitation was overlooked in the previous studies since the sequences of the centromeres and other ETRs across multiple genomes only became available recently.</p>
<p>More at https://www.nature.com/articles/s41592-023-01970-4</p><p>Address of the bookmark: <a href="https://github.com/seryrzu/unialigner" rel="nofollow">https://github.com/seryrzu/unialigner</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/5898/an-entire-genome-written-in-lab</guid>
	<pubDate>Fri, 25 Oct 2013 09:43:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/5898/an-entire-genome-written-in-lab</link>
	<title><![CDATA[An entire genome written in lab]]></title>
	<description><![CDATA[<p>This is the first time ever the genetic code has been fundamentally changed. The breakthrough is a huge step forward in synthetic biology and opens up the possibility of turning re-coded bacteria into biofactories, capable of producing potent new forms of protein that could fight disease or generate sustainable materials.</p><p>More @ <a href="http://news.yale.edu/2013/10/17/researchers-rewrite-entire-genome-and-add-healthy-twist">http://news.yale.edu/2013/10/17/researchers-rewrite-entire-genome-and-add-healthy-twist</a></p><p>News Reference:&nbsp;Yale news</p><p><img src="http://images.sciencedaily.com/2011/07/110714142130-large.jpg" alt="image" width="800" height="530" style="border: 0px; border: 0px;"></p><p>Image Source: Sciencedaily.</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/9602/msc-or-mscphd-combined-or-phd-positions-in-hanyank-university-seoul-korea</guid>
  <pubDate>Thu, 03 Apr 2014 17:20:30 -0500</pubDate>
  <link></link>
  <title><![CDATA[MSc, or MSc/PhD (combined) or PhD positions in HanYank University Seoul Korea]]></title>
  <description><![CDATA[
<p>MSc, or MSc/PhD (combined) or PhD positions available for HYU September 2014 intake with full scholarship:</p>

<p>http://www.academia.edu/6564970/MSc_PhD_position_announcement_at_our_Graduate_School</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/10124/jrf-at-bose-institute-kolkata</guid>
  <pubDate>Mon, 21 Apr 2014 19:41:14 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF at Bose Institute, Kolkata]]></title>
  <description><![CDATA[
<p>ADVT. No. S/BIC/01/2014-15</p>

<p>Bose Institute, Kolkata, invites applications from Indian Citizens for ONE (01) temporary position of Junior Research Fellow in the DBT sponsored project entitled, “Centre of Excellance (CoE) in Bioinformatics at Bose Institute”, running under Prof. Pinakpani Chakrabarti, Project Co-ordinatior, Bioinformatics Centre. The project is tenable upto 31.03.2017, but duration of the fellowship is one year only. The JRF will work with one of the faculty members of the center based on his / her motivation in any specific area on Bioinformatics.</p>

<p>Essential Qualification: 1st class M.Sc. / M.Tech degree in any stream of Chemical/ Biological Sciences with CSIR-UGC-NET-JRF / ICMR-JRF / DBT-JRF or CSIR-UGCNET- LS / GATE qualification.</p>

<p>Desirable qualification:</p>

<p>(i) Specialized knowledge in Organic / Physical chemistry.<br />(ii) Any exposure to research involving the small molecules (like drug) and / or protein structure determination or prediction.<br />(iii) Basic knowledge in computer programming, e.g. using FORTRAN, C, shell, perl etc.<br />(iv) Hands-on-experience on any of the following software : CHARMM/AMBER/NAMD/GROMACS,Gaussian/Gamess, Haddock/Autodock, Schrodinger etc. (or any other software serving similar purposes in molecular modeling)</p>

<p>Fellowship :</p>

<p>(i) Rs. 16,000/- p.m., plus admissible HRA &amp; Medical Benefit for M.Sc. with CSIRUGC NET-JRF/ICMR-JRF/DBT-JRF or M.Tech. with CSIR-UGC NETJRF/<br />ICMR-JRF/DBT-JRF/CSIR-UGC NET-LS/GATE<br />(ii) Rs. 12,000/- p.m., plus admissible HRA &amp; Medical Benefit for M.Sc. with CSIRUGC NET-LS/GATE</p>

<p>Age : Below 28 years as on the day on which the application is made (relaxable in case of SC/ST/OBC/WOMEN candidates only as per rule).</p>

<p>Interested and eligible candidates should apply on plain paper duly signed by them clearly mentioning the area of interest in research, possession of any desirable qualification (s) as mentioned above and quoting Advertisement No. on the envelop as well as application with complete Bio-data giving e-mail ID, Phone No. and details of qualification i.e. examination passed, year, division, percentage of marks, from Secondary onwards with attested copies of testimonials, addressed to the Registrar, Bose Institute, P-1/12, CIT Scheme VII-M, Kankurgachi, Kolkata-700054 on or before April 25, 2014.</p>

<p>The shortlisted candidates will be called for an interview. Applicants are advised to check our website for future updates.</p>

<p>Advertisement: www.boseinst.ernet.in/ADVT/14/p_2.pdf</p>
]]></description>
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