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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/30973?offset=1570</link>
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	<description><![CDATA[]]></description>
	
	
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28819/research-project-at-iit-madras</guid>
  <pubDate>Wed, 17 Aug 2016 03:26:06 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Project at IIT, Madras]]></title>
  <description><![CDATA[
<p>Two project positions are available to work on (i) molecular modeling and molecular dynamics simulations and (ii) development of bioinformatics databases and tools at Protein Bioinformatics Lab, Department of Biotechnology, IIT Madras.</p>

<p>Duration : Initially for a period of one year. Extendable based on the performance.</p>

<p>Qualification: (i) MSc in Bioinformatics, Biotechnology, Physics, Biophysics, Biochemistry,Computer Science with NET (UGC/CSIR/GATE/BINC/INSPIRE etc) qualification. (OR) (ii) M. Tech in Bioinformatics, Biotechnology</p>

<p>Additional qualification: Programming skills</p>

<p>Candidates who fulfill the requirements of IIT have the possibility to register for PhD.</p>

<p>Fellowship: Rs.25,000 and HRA.</p>

<p>Applicants are encouraged to send the CV to the coordinator by postal mail and e-mail. The deadline to receive the applications is 31st August 2016. The project coordinator has the discretion to restrict the number of candidates to be called for interview to a reasonable limit on the basis of qualifications and experience higher than the minimum prescribed in the announcement.</p>

<p>Project Co-ordinator:</p>

<p>Dr. M. Michael Gromiha <br />Department of Biotechnology <br />Indian Institute of Technology Madras <br />Chennai 600036 <br />Email: gromiha@iitm.ac.in</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</guid>
	<pubDate>Wed, 03 Jun 2020 08:00:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</link>
	<title><![CDATA[ShinyGO v0.61: Gene Ontology Enrichment Analysis + more]]></title>
	<description><![CDATA[<p>2/3/2020: Now published by&nbsp;<a href="https://doi.org/10.1093/bioinformatics/btz931" target="_blank">Bioinformatics.</a></p>
<p>11/3/2019: V 0.61, Improve graphical visualization (thanks to reviewers). Interactive networks and much more.</p>
<p>5/20/2019: V.0.60, Annotation database updated to Ensembl 96. New bacterial and fungal genomes based on STRING-db! Just paste your gene list to get enriched GO terms and othe pathways for over 315 plant and animal species, based on annotation from Ensembl (Release 96), Ensembl plants (R. 43) and Ensembl Metazoa (R. 43). An additional 2031 genomes (including bacteria and fungi) are annotated based on STRING-db (v.10). In addition, it also produces KEGG pathway diagrams with your genes highlighted, hierarchical clustering trees and networks summarizing overlapping terms/pathways, protein-protein interaction networks, gene characterristics plots, and enriched promoter motifs.&nbsp;</p><p>Address of the bookmark: <a href="http://bioinformatics.sdstate.edu/go/" rel="nofollow">http://bioinformatics.sdstate.edu/go/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28829/jrf-bioinformatics-at-manit-india</guid>
  <pubDate>Thu, 18 Aug 2016 02:48:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics at MANIT, India]]></title>
  <description><![CDATA[
<p>Advt. No.: Maths./577/2016 Date: 12/08/2016<br />JRF Bioinformatics Job Position in Maulana Azad National Institute of Technology (MANIT) purely temporary basis<br />Project Title : “Computational Approach to Study Complex Biological Network of Diseases using Molecular Data”<br />Essential Qualifications &amp; experience: M.Tech in Bioinformatics/ Computational System biology/Computer Science or M.Sc. in Bio informatics/Biotechnology/Mathematics/Statistics from recognized University/ Institute. Preference will be given to GATE/NET qualified candidates.<br />No. of Post : 01<br />Fellowship: INR 12000<br /> <br />How to apply<br />The duly completed application on prescribed format along with copies of supporting documents must reach to: office of the Dr. Usha Chouhan, Principal Investigator, Department of Mathematics, Bioinformatics &amp; Computer Applications, Maulana Azad National Institute of Technology, Bhopal-462003 on or before 31/08/2016. A soft copy of the application should also be sent to ycchouhan@gmail.com  email address of Principal Investigator.</p>

<p>More at http://www.web.manit.ac.in/Year%202016/JRF/walk%20in.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44188/understanding-go-analysis</guid>
	<pubDate>Wed, 08 Feb 2023 04:22:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44188/understanding-go-analysis</link>
	<title><![CDATA[Understanding GO analysis]]></title>
	<description><![CDATA[<p>The confusion about gene ontology and gene ontology analysis can start right from the term itself. There are actually two different entities that are commonly referred to as gene ontology or &ldquo;GO&rdquo;:</p>
<ol>
<li>the&nbsp;<span>ontology itself</span>, which is a set of terms with their precise definitions and defined relationships between them, and</li>
<li>the&nbsp;<span>associations between gene products and GO terms</span>, which are used to capture the existing knowledge about what each gene is known to do.</li>
</ol>
<p>But the term gene ontology, or GO, is commonly used to refer to both, which is sometimes a source of potential confusion. In order to avoid this, here we will use the term &ldquo;GO ontology&rdquo; to describe the set of terms and their hierarchical structure and &ldquo;GO annotations&rdquo; to describe the set of associations between genes and GO terms.</p>
<p>There are 3 types of terms, or domains if you wish, in the gene ontology:</p>
<ul>
<li>Biological Processes (BP)</li>
<li>Molecular Functions (MF)</li>
<li>Cellular Components (CC)</li>
</ul><p>Address of the bookmark: <a href="https://advaitabio.com/faq-items/understanding-gene-ontology/" rel="nofollow">https://advaitabio.com/faq-items/understanding-gene-ontology/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28926/scientist-at-advanced-centre-for-treatment-research-and-education-in-cancer-navi-mumbai-maharashtra</guid>
  <pubDate>Tue, 30 Aug 2016 04:16:15 -0500</pubDate>
  <link></link>
  <title><![CDATA[Scientist at Advanced Centre for Treatment, Research and Education in Cancer - Navi Mumbai, Maharashtra]]></title>
  <description><![CDATA[
<p>Scientist <br />Advanced Centre for Treatment, Research and Education in Cancer - Navi Mumbai, Maharashtra<br />Scientist (One position) <br />Project: Bioinformatics centre DBT- Sub-DIC at ACTREC <br />Funding agency: DBT Grant No.232 </p>

<p>Duration of the Project: Six Months from the date of appointment can be extended further for six months <br />Essential Qualification and Experience: 1st Class Masters Degree in Bioinformatics or Life Sciences equivalent degree from a recognized University with 4 years R&amp;D experience in Bioinformatics or relevant subjects from recognized institutes. <br />OR <br />Ph.D. degree in Bioinformatics or Life Sciences from recognized University. <br />M.Sc. degree obtained after a one year course will not be considered. <br />Experience: Research/teaching experience in Bioinformatics or relevant subjects form recognized Institute(s). </p>

<p>More at http://www.actrec.gov.in/data%20files/Vacancies/2016/AV-scin-stud-trainee-6-Sept-16.docx</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44620/diy-transcriptomics</guid>
	<pubDate>Wed, 31 Jul 2024 01:19:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44620/diy-transcriptomics</link>
	<title><![CDATA[DIY Transcriptomics]]></title>
	<description><![CDATA[<p><span>A semester-long course covering best practices for the analysis of high-throughput sequencing data from gene expression (RNA-seq) studies, with a primary focus on empowering students to be independent in the use of lightweight and open-source software using the R programming language and the Bioconductor suite of packages. This course follows a hybrid format in which online lectures are paired with in-person labs where students participate in hands-on, live coding exercises using real &lsquo;omic datasets. The course is focused on datasets and topics central to infectious disease research, immunology, and One-Health, but the concepts and approaches covered are applicable to any genomic study.</span></p>
<p>https://diytranscriptomics.com</p><p>Address of the bookmark: <a href="https://diytranscriptomics.com" rel="nofollow">https://diytranscriptomics.com</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29262/bioinformatics-jobs-at-chittaranjan-national-cancer-institute</guid>
  <pubDate>Thu, 29 Sep 2016 09:36:33 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics jobs at Chittaranjan National Cancer Institute]]></title>
  <description><![CDATA[
<p>Chittaranjan National Cancer Institute Advertisement No.497/2016 Invites Applications For Senior Scientific Officer, Gr. II </p>

<p>Note: Experience in the following field required: Molecular cancer cytogenetic and genetic toxicology Molecular drug Designing and targeted therapy Cancer genomics, proteomics, bioinformatics and next generation sequencing Therapeutic stem cell research and gene therapy Molecular cancer immunology and immunotherapy Molecular epidemiology Tumor endocrinology Translation research Ultra structural/tissue engg/development biology research Virus and cancer Molecular pathology No. of Posts: 11 (Eleven), (SC-1, OBC-3, UR-7) </p>

<p>Location: Kolkata (Calcutta) Salary: Rs.15600-39100 + Grade, Pay Rs.5400/- </p>

<p>For details kindly refer to the Employment News dated 24-30 September, 2016 and in the Institute’s Website: http://www.cnci.org.in </p>

<p>Last date for receipt of applications is 30 days from the date of notification in the Employment News. Director Chittaranjan National Cancer Institute 378, S.P. </p>

<p>Institute’s Website: http://www.cnci.org.in</p>
]]></description>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44900/pegas-a-comprehensive-bioinformatic-solution-for-pathogenic-bacterial-genomic-analysis</guid>
	<pubDate>Mon, 01 Sep 2025 01:18:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44900/pegas-a-comprehensive-bioinformatic-solution-for-pathogenic-bacterial-genomic-analysis</link>
	<title><![CDATA[PeGAS: A Comprehensive Bioinformatic Solution for Pathogenic Bacterial Genomic Analysis]]></title>
	<description><![CDATA[<p><span>This is PeGAS, a powerful bioinformatic tool designed for the seamless quality control, assembly, and annotation of Illumina paired-end reads specific to pathogenic bacteria. This tool integrates state-of-the-art open-source software to provide a streamlined and efficient workflow, ensuring accurate insights into the genomic makeup of pathogenic microbial strains.</span></p>
<p><span><img src="https://github.com/liviurotiul/PeGAS/raw/main/Features.png" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/liviurotiul/PeGAS" rel="nofollow">https://github.com/liviurotiul/PeGAS</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34463/single-cell-rnaseq-data-analysis-tutorial</guid>
	<pubDate>Mon, 27 Nov 2017 16:24:29 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34463/single-cell-rnaseq-data-analysis-tutorial</link>
	<title><![CDATA[Single Cell RNAseq data analysis tutorial !!]]></title>
	<description><![CDATA[<ul>
<li>A major breakthrough (replaced microarrays) in the late 00&rsquo;s and has been widely used since</li>
<li>Measures the&nbsp;average expression level&nbsp;for each gene across a large population of input cells</li>
<li>Useful for comparative transcriptomics, e.g.&nbsp;samples of the same tissue from different species</li>
<li>Useful for quantifying expression signatures from ensembles, e.g.&nbsp;in disease studies</li>
<li>Insufficient&nbsp;for studying heterogeneous systems, e.g.&nbsp;early development studies, complex tissues (brain)</li>
<li>Does&nbsp;not&nbsp;provide insights into the stochastic nature of gene expression</li>
</ul><p>Following are the useful links:</p><p><a href="http://hemberg-lab.github.io/scRNA.seq.course/scRNA-seq-course.pdf" target="_blank">Single Cell RNAseq data analysis Tutorial</a></p><p><a href="https://f1000research.com/articles/5-2122/v2" target="_blank">A step-by-step workflow for low-level analysis of single-cell RNA-seq data</a></p><p><a href="https://www.bioconductor.org/help/workflows/simpleSingleCell/" target="_blank">A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor</a></p><p>SCell: single-cell RNA-seq analysis software</p><p><a href="https://github.com/diazlab/SCell">https://github.com/diazlab/SCell</a></p><p>Beta-Poisson model for single-cell RNA-seq data analyses</p><p><a href="https://github.com/nghiavtr/BPSC">https://github.com/nghiavtr/BPSC</a></p><p>Sincera: A Computational Pipeline for Single Cell RNA-Seq Profiling Analysis</p><p><a href="https://research.cchmc.org/pbge/sincera.html">https://research.cchmc.org/pbge/sincera.html</a></p><p>SC3 &ndash; consensus clustering of single-cell RNA-Seq data</p><p><a href="http://biorxiv.org/content/early/2016/09/02/036558">http://biorxiv.org/content/early/2016/09/02/036558</a></p><p>Citrus: A toolkit for single cell sequencing analysis</p><p><a href="http://biorxiv.org/content/early/2016/09/14/045070">http://biorxiv.org/content/early/2016/09/14/045070</a></p><p>Single-Cell Resolution of Temporal Gene Expression during Heart Development</p><p><a href="http://www.cell.com/developmental-cell/fulltext/S1534-5807%2816%2930682-7">http://www.cell.com/developmental-cell/fulltext/S1534-5807(16)30682-7</a></p><p>Scalable latent-factor models applied to single-cell RNA-seq data separate biological drivers from confounding effects</p><p><a href="http://biorxiv.org/content/early/2016/11/15/087775">http://biorxiv.org/content/early/2016/11/15/087775</a></p><p>Single cell transcriptomes identify human islet cell signatures and reveal cell-type-specific expression changes in type 2 diabetes</p><p><a href="http://genome.cshlp.org/content/early/2016/11/18/gr.212720.116.abstract">http://genome.cshlp.org/content/early/2016/11/18/gr.212720.116.abstract</a></p><p>SCODE: An efficient regulatory network inference algorithm from single-cell RNA-Seq during differentiation</p><p><a href="http://biorxiv.org/content/early/2016/11/21/088856">http://biorxiv.org/content/early/2016/11/21/088856</a></p><p>SCOUP is a probabilistic model to analyze single-cell expression data during differentiation</p><p><a href="https://github.com/hmatsu1226/SCOUP">https://github.com/hmatsu1226/SCOUP</a></p><p>scLVM is a modelling framework for single-cell RNA-seq data</p><p><a href="https://github.com/PMBio/scLVM">https://github.com/PMBio/scLVM</a></p><p>Selective Locally linear Inference of Cellular Expression Relationships (SLICER) algorithm for inferring cell trajectories</p><p><a href="https://github.com/jw156605/SLICER">https://github.com/jw156605/SLICER</a></p><p>SinQC: A Method and Tool to Control Single-cell RNA-seq Data Quality</p><p><a href="http://www.morgridge.net/SinQC.html">http://www.morgridge.net/SinQC.html</a></p><p>TSCAN: Pseudo-time reconstruction and evaluation in single-cell RNA-seq analysis</p><p><a href="https://github.com/zji90/TSCAN">https://github.com/zji90/TSCAN</a></p><p>Visualization and cellular hierarchy inference of single-cell data using SPADE</p><p><a href="http://www.nature.com/nprot/journal/v11/n7/full/nprot.2016.066.html">http://www.nature.com/nprot/journal/v11/n7/full/nprot.2016.066.html</a></p><p>OEFinder: Identify ordering effect genes in single cell RNA-seq data</p><p><a href="https://github.com/lengning/OEFinder">https://github.com/lengning/OEFinder</a></p>]]></description>
	<dc:creator>Robert M Willioms</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/29479/how-to-install-perl-modules-on-mac-os-x-in-easy-steps</guid>
	<pubDate>Thu, 20 Oct 2016 07:26:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/29479/how-to-install-perl-modules-on-mac-os-x-in-easy-steps</link>
	<title><![CDATA[How to install Perl modules on Mac OS X in easy steps !!]]></title>
	<description><![CDATA[<p>Today at work, I learned how to install Perl modules using&nbsp;<a href="http://en.wikipedia.org/wiki/CPAN">CPAN</a>. It&rsquo;s a lot easier than I thought.</p><p>You see, for the past couple of years, I&rsquo;ve been a bit frustrated because OS X does not come with a whole lot of Perl modules pre-installed, and for all I googled, I couldn&rsquo;t find an &ldquo;idiot&rsquo;s&rdquo; guide for moderately-savvy-but-not-expert users like myself to install modules and dependencies on demand.</p><p>The only instructions I could find point to&nbsp;<a href="http://fink.sourceforge.net/">Fink</a>, which basically installs modules in a path that isn&rsquo;t included in the Perl @INC variable, meaning you have to manually specify the full path to the modules in every script &mdash; which is not a lot of fun if you&rsquo;re developing on OS X and deploying on Red Hat, for instance.</p><p>Moreover, Fink doesn&rsquo;t seem to make every module available, and it&rsquo;s not very easy to determine which Fink package you need to install if you need a particular module.</p><p>So, with a script that called on several apparently unavailable modules, and a deadline looming, I finally decided to suck it up and figure out how to use CPAN to install them:</p><h4>1) Make sure you have the Apple Developer Tools (XCode) installed.</h4><p>These are on one of your install discs, or available as a huge but free download from the&nbsp;<a href="https://developer.apple.com/xcode/">Apple Developer Connection</a>&nbsp;[free registration required] or the Mac App Store. I thought I had them, but apparently when we upgraded that computer to Tiger, they went missing.</p><p>If you don&rsquo;t have this stuff installed, your installation will fail with errors about unavailable commands.</p><h4>1.5) Install Command Line Tools (Recent XCode versions only)</h4><p>(Thank you to Tom Marchioro for informing me about this step.)</p><p>Older versions of XCode installed the command line tools (which are required to properly install CPAN modules) by default, but apparently newer ones do not. To check whether you have the command line tools already installed, run the following from the Terminal:</p><p><code>$ which make</code></p><p>This command checks the system for the &ldquo;<code>make</code>&rdquo; tool. If it spits out something like&nbsp;<code>/usr/bin/make</code>&nbsp;you&rsquo;re golden and can skip ahead to Step 2. If you just get a new prompt and no output, you&rsquo;ll need to install the tools:</p><ol>
<li>Launch XCode and bring up the Preferences panel.</li>
<li>Click on the Downloads tab</li>
<li>Click to install the Command Line Tools</li>
</ol><p>If you like, you can run&nbsp;<code>which make</code>&nbsp;again to confirm that everything&rsquo;s installed correctly.</p><h4>2) Configure CPAN.</h4><p><code>$ sudo perl -MCPAN -e shell</code></p><p><code>perl&gt; o conf init</code></p><p>This will prompt you for some settings. You can accept the defaults for almost everything (just hit &ldquo;return&rdquo;). The two things you must fill in are the path to&nbsp;<code>make</code>&nbsp;(which should be&nbsp;<code>/usr/bin/make</code>&nbsp;or the value returned when you run&nbsp;<code>which make</code>&nbsp;from the command line) and your choice of CPAN mirrors (which you actually choose don&rsquo;t really matter, but it won&rsquo;t let you finish until you select at least one). If you use a proxy or a very restrictive firewall, you may have to configure those settings as well.</p><p>If you skip Step 2, you may get errors about&nbsp;<code>make</code>&nbsp;being unavailable.</p><h4>3) Upgrade CPAN</h4><p><code>$ sudo perl -MCPAN -e 'install Bundle::CPAN'</code></p><p>Don&rsquo;t forget the&nbsp;<code>sudo</code>, or it&rsquo;ll fail with permissions errors, probably when doing something relatively unimportant like installing&nbsp;<code>man</code>&nbsp;files.</p><p>This will spend a long time downloading, testing, and compiling various files and dependencies. Bear with it. It will prompt you a few times about dependencies. You probably want to enter &ldquo;yes&rdquo;. I agreed to everything it asked me, and everything turned out fine. YMMV of course. If everything installs properly, it&rsquo;ll give you an &ldquo;OK&rdquo; at the end.</p><h4>4) Install your modules. For each module&hellip;.</h4><p><code>$ sudo perl -MCPAN -e 'install Bundle::Name'</code></p><p>or</p><p><code>$ sudo perl -MCPAN -e 'install Module::Name'</code></p><p>This will install the module&nbsp;<em>and</em>&nbsp;its dependencies. Nice, eh? Again, don&rsquo;t forget the&nbsp;<code>sudo</code>.</p><p>The first time you run this after upgrading CPAN, it may prompt you to configure again (see Step 2). If you accept its offer to try to configure itself automatically, it may just run through everything without a problem.</p><p>There are a couple of potential pitfalls with specific modules (such as the<code>LWP::UserAgent</code>&nbsp;/&nbsp;<code>HEAD</code>&nbsp;issue), but most have workarounds, and I haven&rsquo;t run into anything that wasn&rsquo;t easily recoverable.</p><p>And that&rsquo;s it!</p><p>Did you find this useful? Is there anything I missed?</p>]]></description>
	<dc:creator>Jit</dc:creator>
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