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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/41991?offset=520</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/17924/software-developed-in-pevsner-lab</guid>
	<pubDate>Mon, 06 Oct 2014 12:41:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/17924/software-developed-in-pevsner-lab</link>
	<title><![CDATA[Software developed in pevsner lab]]></title>
	<description><![CDATA[<div>
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<p><a href="http://pevsnerlab.kennedykrieger.org/dragon.htm">DRAGON</a>: Database Referencing of Array Genes Online</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/96">SNOMAD</a>: Standardization and Normalization of Microarray Data</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/70">SNPduo</a>: SNP Analysis Between Two Individuals</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/71">SNPtrio</a>: Analyzing and Visualizing and Inheritance Patterns in Trios</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/64">SNPscan</a>: Data Analysis and Visualization of SNP Data</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/64">pediSNP</a>: Analyze SNP Data From a Pedigree of Two Generations</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/73">kcoeff</a>: Calculate Cotterman Coefficients of SNP Genotype Data</p>
<p><a href="http://pevsnerlab.kennedykrieger.org/php/node/113">triPOD:</a> Detects chromosomal abnormalities in parent-child trio-based microarray data</p>
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</div><p>Address of the bookmark: <a href="http://pevsnerlab.kennedykrieger.org/php/?q=software" rel="nofollow">http://pevsnerlab.kennedykrieger.org/php/?q=software</a></p>]]></description>
	<dc:creator>Robert M Willioms</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44902/hite-a-fast-and-accurate-dynamic-boundary-adjustment-approach-for-full-length-transposable-elements-detection-and-annotation-in-genome-assemblies</guid>
	<pubDate>Sat, 20 Sep 2025 09:34:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44902/hite-a-fast-and-accurate-dynamic-boundary-adjustment-approach-for-full-length-transposable-elements-detection-and-annotation-in-genome-assemblies</link>
	<title><![CDATA[HiTE: a fast and accurate dynamic boundary adjustment approach for full-length Transposable Elements detection and annotation in Genome Assemblies]]></title>
	<description><![CDATA[<p dir="auto"><code>HiTE</code>&nbsp;is a Python software that uses a dynamic boundary adjustment approach to detect and annotate full-length Transposable Elements in Genome Assemblies. In comparison to other tools, HiTE demonstrates superior performance in detecting a greater number of full-length TEs.</p>
<div dir="auto">
<h2 dir="auto">panHiTE</h2>
<a href="https://github.com/CSU-KangHu/HiTE#panhite"></a></div>
<p dir="auto">We have developed panHiTE, a comprehensive and accurate pipeline for TE detection in large-scale population genomes. It has been successfully applied to hundreds of plant population genomes, demonstrating its effectiveness and scalability.</p>
<p dir="auto">For detailed instructions, please refer to the&nbsp;<a href="https://github.com/CSU-KangHu/HiTE/wiki/panHiTE-tutorial">panHiTE tutorial</a>.</p><p>Address of the bookmark: <a href="https://github.com/CSU-KangHu/HiTE" rel="nofollow">https://github.com/CSU-KangHu/HiTE</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/22318/research-fellows-at-csir-institute-of-himalayan-bioresource-technology-palampur-himachal-pradesh</guid>
  <pubDate>Tue, 19 May 2015 07:17:32 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Fellows at  CSIR - Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh]]></title>
  <description><![CDATA[
<p>CSIR - Institute of Himalayan Bioresource Technology 2 vacancies of Project Fellow</p>

<p>Name of the Post: Project Fellow</p>

<p>No. of the Post: 02 Two</p>

<p>Salary: Rs. 12000/- per month or Rs. 14000/- per month</p>

<p>Age Limit: Max. 28 years as on 10.06.2015 and relaxation as per rules</p>

<p>Required Job Profile:</p>

<p>Candidate must possess first class B.Tech. in bioinformatics or computational biology OR M.Sc. in bioinformatics or computational biology with fifty five percent marks OR M.Tech. in bioinformatics or computational biology with fifty five percent marks.</p>

<p>How to apply:</p>

<p>Eligible and interested candidates should need to appear for walk-in interview on 10.06.2015 at 9:00 am at the above mentioned address.</p>

<p>Refer to http://www.ihbt.res.in/recruit/AdvtNo7_2015.pdf</p>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/8798/list-of-gene-ontology-software-and-tools</guid>
	<pubDate>Sun, 09 Mar 2014 14:48:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/8798/list-of-gene-ontology-software-and-tools</link>
	<title><![CDATA[List of gene ontology software and tools]]></title>
	<description><![CDATA[<p>The Gene Ontology (GO) is a set of associations from biological phrases to specific genes that are either chosen by trained curators or generated automatically. GO is designed to rigorously encapsulate the known relationships between biological terms and and all genes that are instances of these terms. These Gene Ontology has become an extremely useful tool for the analysis of genomic data and structuring of biological knowledge. Several excellent software tools for navigating the gene ontology have been developed.</p><p><img src="http://ohnosequences.com/images/GoSlimBlog.svg" alt="image" width="500" height="380" style="border: 0px; border: 0px;"></p><p>The GO provides core biological knowledge representation for modern biologists, whether computationally or experimentally based. GO resources include biomedical ontologies that cover molecular domains of all life forms as well as extensive compilations of gene product annotations to these ontologies that provide largely species-neutral, comprehensive statements about what gene products do. Although extensively used in data analysis workflows, and widely incorporated into numerous data analysis platforms and applications, the general user of GO resources often misses fundamental distinctions about GO structures, GO annotations, and what can and can not be extrapolated from GO resources. Here are ten quick tips for using the Gene Ontology.</p><p>Read "Ten Quick Tips for Using the Gene Ontology" at http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1003343</p><p>Following are the most commonly used old and new GO term enrichment determination tools. These tools are recommended to people working in a wet-lab.</p><p><strong>CLASSIFI (Department of Pathology, UT Southwestern Medical Center)</strong></p><p>CLASSIFI (Cluster Assignment for Biological Inference) is a data-mining tool that can be used to identify significant co-clustering of genes with similar functional properties (e.g. cellular response to DNA damage). Briefly, CLASSIFI uses the Gene OntologyTM (GO) gene annotation scheme to define the functional properties of all genes/probes in a microarray data set, and then applies a cumulative hypergeometric distribution analysis to determine if any statistically significant gene ontology co-clustering has occurred.</p><p><a href="http://pathcuric1.swmed.edu/pathdb/classifi.html">http://pathcuric1.swmed.edu/pathdb/classifi.html</a></p><p><strong>EasyGO (China Agricultural University)</strong></p><p>EasyGO is designed to automate enrichment job for experimental biologists to identify enriched Gene Ontology (GO) terms in a list of microarray probe sets or gene identifiers (with expression information for PAGE analysis). Also EasyGO is also a GO annotation database, especially focus on agronomical species, supporting 30 species. It is user friendly, with advanced result browsing format and in-time update.</p><p><a href="http://bioinformatics.cau.edu.cn/neweasygo/">http://bioinformatics.cau.edu.cn/neweasygo/</a></p><p><a href="http://bioinformatics.cau.edu.cn/easygo/">http://bioinformatics.cau.edu.cn/easygo/</a></p><p><strong>g:GOSt (Institute of Computer Science, University of Tartu)</strong></p><p>g:GOSt retrieves most significant Gene Ontology (GO) terms, KEGG and REACTOME pathways, and TRANSFAC motifs to a user-specified group of genes, proteins or microarray probes. g:GOSt also allows analysis of ranked or ordered lists of genes, visual browsing of GO graph structure, interactive visualisation of retrieved results, and many other features. Multiple testing corrections are applied to extract only statistically important results.</p><p><a href="http://biit.cs.ut.ee/gprofiler/">http://biit.cs.ut.ee/gprofiler/</a></p><p><strong>DAVID</strong> : Gene Functional Classification (Laboratory of Immunopathogenesis and Bioinformatics, NIAID)</p><p>The Functional Classification Tool provides a rapid means to organize large lists of genes into functionally related groups to help unravel the biological content captured by high throughput technologies.</p><p><a href="http://david.abcc.ncifcrf.gov/gene2gene.jsp">http://david.abcc.ncifcrf.gov/gene2gene.jsp</a></p><p><a href="http://david.abcc.ncifcrf.gov/">http://david.abcc.ncifcrf.gov/</a></p><p>API <a href="https://github.com/chrisamiller/davidapi">https://github.com/chrisamiller/davidapi</a></p><p><strong>GOEAST</strong> (Institute of Genetics and Developmental Biology, Chinese Academy of Sciences)</p><p>GOEAST is web based software toolkit providing easy to use, visualizable, comprehensive and unbiased Gene Ontology (GO) analysis for high-throughput experimental results, especially for results from microarray hybridization experiments. The main function of GOEAST is to identify significantly enriched GO terms among give lists of genes using accurate statistical methods.</p><p><a href="http://omicslab.genetics.ac.cn/GOEAST/">http://omicslab.genetics.ac.cn/GOEAST/</a></p><p><strong>GOstat</strong> (Walter and Eliza Hall Institute of Medical Research)</p><p>Find statistically overrepresented GO terms within a group of genes</p><p><a href="http://gostat.wehi.edu.au/">http://gostat.wehi.edu.au/</a></p><p><strong>GOrilla</strong> (Technion - Laboratory of Computational Biology , Israel Institute of Technology)</p><p>GOrilla is a tool for identifying and visualizing enriched GO terms in ranked lists of genes.<br /> It uses two approaches, first by searching for enriched GO terms that appear densely at the top of a ranked list of genes&nbsp; or by searching for enriched GO terms in a target list of genes compared to a background list of genes.</p><p><a href="http://cbl-gorilla.cs.technion.ac.il/">GOrilla</a> makes nice pictures !!!!</p><p><a href="http://cbl-gorilla.cs.technion.ac.il/">http://cbl-gorilla.cs.technion.ac.il/</a></p><p><strong>Gene Ontology for Functional Analysis (GOFFA)</strong></p><p>GOFFA is a tool developed for ArrayTrack&trade; that takes a list of genes and identifies terms in Gene Ontology (GO) disclaimer icon associated with those genes.</p><p>It provides several tools to view/access the GO term hierarchy, full listing of GO terms annotated with the genes associated with a given term with statically useful report.</p><p><a href="http://www.fda.gov/ScienceResearch/BioinformaticsTools/ucm233315.htm">http://www.fda.gov/ScienceResearch/BioinformaticsTools/ucm233315.htm</a></p><p><strong>GOAT</strong> (The University of Manchester)</p><p>The aim of the GOAT project is to create an application that will guide users, especially biomedical researchers, in the annotation of gene products with terms from the <a href="http://www.geneontology.org">Gene Ontology</a>.</p><p><a href="http://goat.man.ac.uk/">http://goat.man.ac.uk/</a></p><p>Script <a href="https://github.com/tanghaibao/goatools/">https://github.com/tanghaibao/goatools/</a></p><p><strong>REVIGO</strong> ( Rudjer Boskovic Institute, Croatia)</p><p>REViGO is a web server that can take long lists of Gene Ontology terms and summarize them by removing redundant GO terms. The remaining terms can be visualized in semantic similarity-based scatterplots, interactive graphs, or tag clouds.</p><p><a href="http://revigo.irb.hr/">http://revigo.irb.hr/</a></p><p><strong>QuickGo</strong> (EMBL-EBI Institute)</p><p>It uses extensive computational filters to allow the generation of specific subsets of GO annotations, mapped to sequence identifiers of your choice. Then GO slims are used which is collective list of GO full set of terms available from the Gene Ontology project.</p><p><a href="http://www.ebi.ac.uk/QuickGO/">http://www.ebi.ac.uk/QuickGO/</a></p><p><strong>GOLEM</strong></p><p>An interactive graph-based gene-ontology navigation and analysis tool. GOLEM is a userful tool which allows the viewer to navigate and explore a local portion of the <a href="http://www.geneontology.org/">Gene Ontology</a> (GO) hierarchy.</p><p><a href="http://reducio.princeton.edu/GOLEM/">http://reducio.princeton.edu/GOLEM/</a></p><p><strong>BGI Web Gene Ontology (WEGO)</strong> Annotation Plot (Beijing Genomics Institute)</p><p>WEGO () is a useful tool for plotting GO annotation results. It has been widely used in many important biological research projects, such as the rice genome project [<a href="http://wego.genomics.org.cn/pubs/rice_indica.pdf">Yu, J. et al. Science 296, 79-92 (2002);</a> <a href="http://wego.genomics.org.cn/pubs/rice_finish.pdf">Yu, J. et al. PLoS Biol 3, e38 (2005)</a>] and the silkworm genome project [<a href="http://wego.genomics.org.cn/pubs/combine_silkworm.pdf">Xia, Q. et al. Science 306, 1937-40 (2004)</a>]. It has become one of the daily tools for downstream gene annotation analysis, especially when performing comparative genomics tasks. WEGO along with two other tools, namely <a href="http://wego.genomics.org.cn/cgi-bin/wego/External2GO.pl">External to GO Query</a> and <a href="http://wego.genomics.org.cn/cgi-bin/wego/GOArchive.pl">GO Archive Query</a>, are freely available for all users. Any suggestions are welcome at <a href="mailto:%20wego@genomics.org.cn">wego@genomics.org.cn</a>. Here is a sample output generated by WEGO</p><p><a href="http://wego.genomics.org.cn/cgi-bin/wego/index.pl">http://wego.genomics.org.cn/cgi-bin/wego/index.pl</a></p><p><strong>GeneGO MetaCore</strong> (MIT)</p><p>GeneGo is a leading provider of data mining &amp; analysis solutions in systems biology. MetaCore, GeneGo's flapship product, is an integrated software suite for functional analysis of experimental data. MetaCore is based on a curated database of human protein-protein, protein-DNA interactions, transcription factors, signaling and metabolic pathways, disease and toxicity, and the effects of bioactive molecules.</p><p><a href="https://portal.genego.com/">https://portal.genego.com/</a></p><p><strong>GOEx</strong> (Stony Brook University)</p><p>GOEx facilitates organism-specific studies by leveraging GO and providing a rich graphical user interface. It is a simple to use tool, specialized for biologists who wish to analyze spectral counting data from shotgun proteomics.</p><p><a href="http://pcarvalho.com/patternlab">http://pcarvalho.com/patternlab</a></p><p><strong>GOssTo</strong></p><p>GOssTo and GOssToWeb are tools to calculate the <a href="https://en.wikipedia.org/wiki/Semantic_similarity#Biomedical_Informatics">semantic similarity</a> between genes or terms in the <a href="http://www.geneontology.org/">Gene Ontology</a>.</p><p><a href="http://www.paccanarolab.org/gosstoweb/">http://www.paccanarolab.org/gosstoweb/</a></p><p><strong>GO Workbench</strong></p><p>The Gene Ontology Analysis Viewer allows direct browsing of the Gene Ontology, and also the visualization of GO Term analysis results.</p><p><a href="http://wiki.c2b2.columbia.edu/workbench/index.php/Gene_Ontology_Viewer">http://wiki.c2b2.columbia.edu/workbench/index.php/Gene_Ontology_Viewer</a></p><p>Some other useful list of GO software and tools is available at <a href="http://www.geneontology.org/GO.tools.shtml#browser">http://www.geneontology.org/GO.tools.shtml#browser</a></p><p>Yet another useful webpage with list of GO tools at <a href="http://neurolex.org/wiki/Category:Resource:Gene_Ontology_Tools">http://neurolex.org/wiki/Category:Resource:Gene_Ontology_Tools</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/18384/big-genomic-data-on-google-cloud-platform</guid>
	<pubDate>Fri, 17 Oct 2014 02:16:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/18384/big-genomic-data-on-google-cloud-platform</link>
	<title><![CDATA[Big genomic data on Google Cloud Platform]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/ExNxi_X4qug" frameborder="0" allowfullscreen></iframe>As the cost of DNA sequencing has dropped, the volume of data produced has risen into the petabytes. Google is working with the genomics community to define a standard API for working with big genomic data sets in the cloud. Building on Google Cloud Platform, we show how to store, process, explore and share genomic data using technologies like BigQuery, AppEngine MapReduce, R and more.]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41948/predict-gene-ontology-with-sequences</guid>
	<pubDate>Wed, 08 Jul 2020 04:59:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41948/predict-gene-ontology-with-sequences</link>
	<title><![CDATA[Predict Gene Ontology with sequences !]]></title>
	<description><![CDATA[<p><strong>PANNZER</strong>&nbsp;(Protein ANNotation with Z-scoRE) is a fully automated service for functional annotation of prokaryotic and eukaryotic proteins of unknown function. The tool is designed to predict the functional description (DE) and GO classes.</p>
<p>PANNZER2 processes bacterial proteomes in minutes and eukaryotic proteomes in an hour. You can use&nbsp;<a href="http://ekhidna2.biocenter.helsinki.fi/AAI/">AAI-profiler</a>&nbsp;to summarize a proteome's species neighbors and reveal taxonomic identity or contamination.</p>
<p>http://ekhidna2.biocenter.helsinki.fi/sanspanz/</p>
<p>IterPro is for the beginners</p>
<p><a href="https://www.ebi.ac.uk/interpro/">h</a><a href="https://www.ebi.ac.uk/interpro/">ttps://www.ebi.ac.uk/interpro/</a></p>
<p>You can find other comparative info at&nbsp;<a href="https://academic.oup.com/view-large/118391389">https://academic.oup.com/view-large/118391389</a></p><p>Address of the bookmark: <a href="http://ekhidna2.biocenter.helsinki.fi/sanspanz/" rel="nofollow">http://ekhidna2.biocenter.helsinki.fi/sanspanz/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/18579/cluster-innovation-center-university-of-delhi</guid>
  <pubDate>Wed, 22 Oct 2014 10:39:49 -0500</pubDate>
  <link></link>
  <title><![CDATA[CLUSTER INNOVATION CENTER @ UNIVERSITY OF DELHI]]></title>
  <description><![CDATA[
<p>Applications for Pre-selection of  candidates under ‘Institutions Mode’ for DST-ISPIRE Faculty in  Computational Biology/ Systems Biology/ Bioinformatics</p>

<p>Applications are invited for pre-selection  of candidates for Ministry of Science and Technology, Department of Science and Technology INSPIRE Faculty Scheme: a component of “Assured Opportunity for Research Career (AORC)” under INSPIRE in the area of computational Biology/Systems Biology/Bioinformatics.</p>

<p>Candidates having done their B.Tech/B.E.  and or M.Sc./M.Tech in Computer Science or Biotechnology and Ph.D. in Systems/ Computational Biology or Bioinformatics may apply in the following format prescribed by DST to the Director, Cluster Innovation Center, University Stadium, GC Narang Marg, University of Delhi, Delhi -11107. Detials of other qualification, age limits etc., please visit www.inspire-dst.gov.in.</p>

<p>Application on the prescribed format may be submitted by email to director@cic.du.ac.in before October 25, 2014. Selected candidates shall be called for an interview. The date, time and venue of the interview shall be informed by email/telephone. For more information about Cluster Innovation Center, please visit https://ducic.ac.in.</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33479/novelseq-novel-sequence-insertion-detection</guid>
	<pubDate>Fri, 09 Jun 2017 04:31:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33479/novelseq-novel-sequence-insertion-detection</link>
	<title><![CDATA[NovelSeq: Novel Sequence Insertion Detection]]></title>
	<description><![CDATA[<p><span>The NovelSeq framework is designed to detect novel sequence insertions using high throughput paired-end whole genome sequencing data.</span></p>
<p>http://novelseq.sourceforge.net/Home</p>
<p>Paper at&nbsp;https://www.ncbi.nlm.nih.gov/pubmed/20385726</p><p>Address of the bookmark: <a href="http://novelseq.sourceforge.net/Home" rel="nofollow">http://novelseq.sourceforge.net/Home</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/19059/ipython-interactive-notebooks</guid>
	<pubDate>Fri, 07 Nov 2014 12:07:02 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/19059/ipython-interactive-notebooks</link>
	<title><![CDATA[IPython: Interactive notebooks]]></title>
	<description><![CDATA[<p>The IPython Notebook is a web-based interactive computational environment where you can combine code execution, text, mathematics, plots and rich media into a single document.</p><p>These notebooks are normal files that can be shared with colleagues, converted to other formats such as HTML or PDF, etc. You can share any publicly available notebook by using the IPython Notebook Viewer service which will render it as a static web page. This makes it easy to give your colleagues a document they can read immediately without having to install anything.</p><p><img src="http://ipython.org/_images/9_home_fperez_prof_grants_1207-sloan-ipython_proposal_fig_ipython-notebook-specgram.png" width="985" height="916" alt="image" style="border: 0px;"><br /><br />To learn more about using the IPython Notebook, you can visit our example collection, and you can read the documentation for all the details on how to use and configure the system. The Notebook Gallery showcases many interesting notebooks covering a variety of topics, from basic programming to advanced scientific computing.</p><p>&nbsp;</p><p>More http://www.nature.com/news/interactive-notebooks-sharing-the-code-1.16261</p><p>http://ipython.org/ipython-doc/1/interactive/notebook.html</p><p>Reference http://ipython.org/notebook.html</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36893/beap-blast-extension-and-assembly-program</guid>
	<pubDate>Mon, 11 Jun 2018 04:52:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36893/beap-blast-extension-and-assembly-program</link>
	<title><![CDATA[BEAP: Blast Extension and Assembly Program]]></title>
	<description><![CDATA[The Blast Extension and Assembly Program (BEAP) is a computer program that uses a short starting DNA fragment, often a EST or partial gene segment, as "primer", to recursively blast nucleotide databases in an attempt to obtain all sequences that overlaps, directly or indirectly, with the "primer" therefore help to "extend" the length of the original sequence for constructing a "full length" sequence for functional analysis, or at least to obtain neighboring regions of the segment for SNP discovery and linkage disequilibrium analysis. The confidence of assembling the resulting sequences is achieved by using a known genome, such as human genome, as a reference.
 
https://www.animalgenome.org/tools/beap/<p>Address of the bookmark: <a href="https://www.animalgenome.org/tools/beap/" rel="nofollow">https://www.animalgenome.org/tools/beap/</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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