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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38447?</link>
	<atom:link href="https://bioinformaticsonline.com/related/38447?" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38449/koala-keggs-internal-annotation-tool-for-k-number-assignment-of-kegg-genes-using-ssearch-computation</guid>
	<pubDate>Wed, 12 Dec 2018 09:16:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38449/koala-keggs-internal-annotation-tool-for-k-number-assignment-of-kegg-genes-using-ssearch-computation</link>
	<title><![CDATA[KOALA: KEGG&#039;s internal annotation tool for K number assignment of KEGG GENES using SSEARCH computation]]></title>
	<description><![CDATA[<p>KOALA (KEGG Orthology And Links Annotation) is KEGG's internal annotation tool for&nbsp;<a href="https://www.kegg.jp/kegg/ko.html">K number</a>&nbsp;assignment of KEGG GENES using SSEARCH computation. BlastKOALA and GhostKOALA assign K numbers to the user's sequence data by&nbsp;<a href="http://www.ncbi.nlm.nih.gov/blast/">BLAST</a>&nbsp;and&nbsp;<a href="http://www.bi.cs.titech.ac.jp/ghostx/">GHOSTX</a>&nbsp;searches, respectively, against a nonredundant set of KEGG GENES. Annotate Sequence in KEGG Mapper and Pathogen Checker in KEGG Pathogen are special interfaces to the BlastKOALA server and can be executed in an interactive mode. &nbsp;&nbsp; See&nbsp;<a href="https://www.kegg.jp/blastkoala/help_blastkoala.html" target="_blastkoala">Step-by-step Instructions</a>.</p>
<div>Reference: Kanehisa, M., Sato, Y., and Morishima, K. (2016) BlastKOALA and GhostKOALA: KEGG tools for functional characterization of genome and metagenome sequences. J. Mol. Biol. 428, 726-731. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/26585406">pubmed</a>] [<a href="https://doi.org/10.1016/j.jmb.2015.11.006">pdf</a>]</div><p>Address of the bookmark: <a href="https://www.kegg.jp/blastkoala/" rel="nofollow">https://www.kegg.jp/blastkoala/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/2778/mom-knows-best</guid>
	<pubDate>Thu, 22 Aug 2013 13:30:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/2778/mom-knows-best</link>
	<title><![CDATA[Mom Knows Best]]></title>
	<description><![CDATA[<p>We always get instructions to wash our hands, sterilize kitchen stuff and bla bla. However, recent findings suggest something else. Perhaps we can't survive, or will face lots of problems if bacteria&rsquo;s colonies are absent in mother womb. Please find the detail sources of microbial transmission in humans from mother to child in recently published PLOS paper.</p><p><a href="http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001631">http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001631</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28164/greengenes-database</guid>
	<pubDate>Wed, 29 Jun 2016 10:03:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28164/greengenes-database</link>
	<title><![CDATA[Greengenes database]]></title>
	<description><![CDATA[<p>The greengenes web application provides access to the 2011 version of the greengenes 16S rRNA gene sequence alignment for browsing, blasting, probing, and downloading. The data and tools presented by greengenes can assist the researcher in choosing phylogenetically specific probes, interpreting microarray results, and aligning/annotating novel sequences. If you are an ARB user, you can use greengenes to keep your own local database current.</p><p>Address of the bookmark: <a href="http://greengenes.lbl.gov/cgi-bin/nph-index.cgi" rel="nofollow">http://greengenes.lbl.gov/cgi-bin/nph-index.cgi</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36997/cgview-circular-genome-viewer</guid>
	<pubDate>Wed, 20 Jun 2018 10:15:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36997/cgview-circular-genome-viewer</link>
	<title><![CDATA[CGView - Circular Genome Viewer]]></title>
	<description><![CDATA[CGView is a Java package for generating high quality, zoomable maps of circular genomes. Its primary purpose is to serve as a component of sequence annotation pipelines, as a means of generating visual output suitable for the web. Feature information and rendering options are supplied to the program using an XML file, a tab delimited file, or an NCBI ptt file. CGView converts the input into a graphical map (PNG, JPG, or Scalable Vector Graphics format), complete with labels, a title, legends, and footnotes. In addition to the default full view map, the program can generate a series of hyperlinked maps showing expanded views. The linked maps can be explored using any web browser, allowing rapid genome browsing, and facilitating data sharing. The feature labels in maps can be hyperlinked to external resources, allowing CGView maps to be integrated with existing web site content or databases. For examples of the various output types, see the CGView gallery.

http://wishart.biology.ualberta.ca/cgview/gallery.html

http://stothard.afns.ualberta.ca/downloads/CCT/index.html

https://www.gview.ca/wiki/GView/WebHome

https://server.gview.ca/

http://stothard.afns.ualberta.ca/cgview_server/

Paper https://academic.oup.com/bib/advance-article/doi/10.1093/bib/bbx081/4037458<p>Address of the bookmark: <a href="http://wishart.biology.ualberta.ca/cgview/" rel="nofollow">http://wishart.biology.ualberta.ca/cgview/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44489/proksee</guid>
	<pubDate>Wed, 27 Mar 2024 11:11:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44489/proksee</link>
	<title><![CDATA[Proksee]]></title>
	<description><![CDATA[<p><span>Proksee is an expert system for genome assembly, annotation and visualization. To begin using Proksee, provide a complete genome sequence, sequencing reads or a CGView/Proksee map JSON file.</span></p>
<fieldset><legend>Please Cite the Following</legend>
<div>Grant JR, Enns E, Marinier E, Mandal A, Herman EK, Chen C, Graham M, Van Domselaar G, and Stothard P</div>
<div><a href="https://pubmed.ncbi.nlm.nih.gov/37140037/">Proksee: in-depth characterization and visualization of bacterial genomes</a></div>
<div>Nucleic Acids Research, 2023, gkad326, https://doi.org/10.1093/nar/gkad326</div>
</fieldset><p>Address of the bookmark: <a href="https://proksee.ca/" rel="nofollow">https://proksee.ca/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4184/zombies-like-bacteria</guid>
	<pubDate>Tue, 03 Sep 2013 08:44:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4184/zombies-like-bacteria</link>
	<title><![CDATA[Zombies like bacteria!!!]]></title>
	<description><![CDATA[<p>Do you believe in Zombies stories &hellip; Hmm confused? Don&rsquo;t worry there is a news for you. Scientists from the Integrated Ocean Drilling Program have announced the findings &nbsp;of the long-lived bacteria, reproducing only once every 10,000 years, which have been found in rocks 2.5km (1.5 miles) below the ocean floor that are as much as 100 million years old.</p><p><span>" the microbes exist in very low concentrations, of around 1,000 microbes in every tea spoon full of rock, compared with billions or trillions of bacteria that would typically be found in the same amount of soil at Earth's surface."</span></p><p><span>Reference:</span></p><p><span><a href="http://www.bbc.co.uk/news/science-environment-23855436">http://www.bbc.co.uk/news/science-environment-23855436</a></span></p><p>&nbsp;</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41033/clark-fast-accurate-and-versatile-sequence-classification-system</guid>
	<pubDate>Sat, 15 Feb 2020 01:49:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41033/clark-fast-accurate-and-versatile-sequence-classification-system</link>
	<title><![CDATA[CLARK: Fast, accurate and versatile sequence classification system]]></title>
	<description><![CDATA[<p><span></span><a href="http://dx.doi.org/10.1186/s12864-015-1419-2"><strong>CLARK</strong></a><span>, a method based on a supervised sequence classification using discriminative&nbsp;</span><em>k</em><span>-mers. Considering two distinct specific classification problems (see the article for details), namely (1) the taxonomic classification of metagenomic reads to known bacterial genomes, and (2) the assignment of BAC clones and transcript to chromosome arms/centromeres (in the absence of a finished assembly for the reference genome), CLARK outperforms in classification speed and precision the best state-of-the-art methods.</span></p>
<p><span><a href="http://clark.cs.ucr.edu/Spaced/">http://clark.cs.ucr.edu/Spaced/</a></span></p><p>Address of the bookmark: <a href="http://clark.cs.ucr.edu/Spaced/" rel="nofollow">http://clark.cs.ucr.edu/Spaced/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/29214/published-genescf-a-real-time-based-functional-enrichment-tool-with-support-for-multiple-organisms</guid>
	<pubDate>Mon, 19 Sep 2016 13:24:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/29214/published-genescf-a-real-time-based-functional-enrichment-tool-with-support-for-multiple-organisms</link>
	<title><![CDATA[Published: GeneSCF: a real-time based functional enrichment tool with support for multiple organisms]]></title>
	<description><![CDATA[<p><span>GeneSCF is more reliable compared to other enrichment tools because of its ability to use reference functional databases in real-time to perform enrichment analysis. It is an easy-to-integrate tool with other pipelines available for downstream analysis of high-throughput data. More importantly, GeneSCF can run multiple gene lists simultaneously on different organisms thereby saving time for the users. Since the tool is designed to be ready-to-use, there is no need for any complex compilation and installation procedures.</span></p><p><strong>Access article:</strong></p><p><span>http://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-016-1250-z</span></p>]]></description>
	<dc:creator>EagleEye</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42280/urmap-an-ultra-fast-read-mapper</guid>
	<pubDate>Thu, 29 Oct 2020 23:03:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42280/urmap-an-ultra-fast-read-mapper</link>
	<title><![CDATA[URMAP, an ultra-fast read mapper]]></title>
	<description><![CDATA[<p><span>URMAP, a new read mapping algorithm. URMAP is an order of magnitude faster than BWA with comparable accuracy on several validation tests. On a Genome in a Bottle (GIAB) variant calling test with 30&times; coverage 2&times;150 reads, URMAP achieves high accuracy (precision 0.998, sensitivity 0.982 and F-measure 0.990) with the strelka2 caller. However, GIAB reference variants are shown to be biased against repetitive regions which are difficult to map and may therefore pose an unrealistically easy challenge to read mappers and variant callers.</span></p>
<p><span>More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320720/</span></p><p>Address of the bookmark: <a href="https://github.com/rcedgar/urmap" rel="nofollow">https://github.com/rcedgar/urmap</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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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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