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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/41459?offset=620</link>
	<atom:link href="https://bioinformaticsonline.com/related/41459?offset=620" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43101/luigi-a-python-package-that-helps-you-build-complex-pipelines-of-batch-jobs</guid>
	<pubDate>Thu, 24 Jun 2021 05:43:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43101/luigi-a-python-package-that-helps-you-build-complex-pipelines-of-batch-jobs</link>
	<title><![CDATA[Luigi: a Python package that helps you build complex pipelines of batch jobs.]]></title>
	<description><![CDATA[<p>Luigi is a Python (3.6, 3.7, 3.8, 3.9 tested) package that helps you build complex pipelines of batch jobs. It handles dependency resolution, workflow management, visualization, handling failures, command line integration, and much more.</p>
<p>Run <code>pip install luigi</code> to install the latest stable version from <a href="https://pypi.python.org/pypi/luigi">PyPI</a>. <a href="https://luigi.readthedocs.io/en/stable/">Documentation for the latest release</a> is hosted on readthedocs.</p>
<p>Run <code>pip install luigi[toml]</code> to install Luigi with <a href="https://luigi.readthedocs.io/en/stable/configuration.html">TOML-based configs</a> support.</p><p>Address of the bookmark: <a href="https://github.com/spotify/luigi" rel="nofollow">https://github.com/spotify/luigi</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36502/creating-conda-environment-for-python27</guid>
	<pubDate>Mon, 07 May 2018 08:56:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36502/creating-conda-environment-for-python27</link>
	<title><![CDATA[Creating conda environment for python2.7]]></title>
	<description><![CDATA[<p>TIP: By default, environments are installed into the&nbsp;<code><span>envs</span></code>&nbsp;directory in your conda directory. Run&nbsp;<code><span>conda</span>&nbsp;<span>create</span>&nbsp;<span>--help</span></code>&nbsp;for information on specifying a different path.</p><p>Use the Terminal or an Anaconda Prompt for the following steps.</p><ol>
<li>
<p>To create an environment:</p>
<div>
<div>
<pre><span></span><span>conda</span> <span>create</span> <span>--</span><span>name</span> <span>myenv</span>
</pre>
</div>
</div>
<p>NOTE: Replace&nbsp;<code><span>myenv</span></code>&nbsp;with the environment name.</p>
</li>
<li>
<p>When conda asks you to proceed, type&nbsp;<code><span>y</span></code>:</p>
<div>
<div>
<pre><span></span>proceed ([y]/n)?
</pre>
</div>
</div>
</li>
</ol><p>This creates the myenv environment in&nbsp;<code><span>/envs/</span></code>. This environment uses the same version of Python that you are currently using, because you did not specify a version.</p><p>To create an environment with a specific version of Python:</p><div><div><pre><span></span>conda create -n myenv <span>python</span><span>=</span><span>3</span>.4
</pre></div></div><p>To create an environment with a specific package:</p><div><div><pre><span></span>conda create -n myenv scipy
</pre></div></div><p>OR:</p><div><div><pre><span></span>conda create -n myenv python
conda install -n myenv scipy
</pre></div></div><p>To create an environment with a specific version of a package:</p><div><div><pre><span></span>conda create -n myenv <span>scipy</span><span>=</span><span>0</span>.15.0
</pre></div></div><p>OR:</p><div><div><pre><span></span>conda create -n myenv python
conda install -n myenv <span>scipy</span><span>=</span><span>0</span>.15.0
</pre></div></div><p>To create an environment with a specific version of Python and multiple packages:</p><div><div><pre><span></span>conda create -n myenv <span>python</span><span>=</span><span>3</span>.4 <span>scipy</span><span>=</span><span>0</span>.15.0 astroid babel
</pre></div></div><p>TIP: Install all the programs that you want in this environment at the same time. Installing 1 program at a time can lead to dependency conflicts.</p><p>To automatically install pip or another program every time a new environment is created, add the default programs to the&nbsp;<a href="https://conda.io/docs/user-guide/configuration/use-condarc.html#config-add-default-pkgs">create_default_packages</a>&nbsp;section of your&nbsp;<code><span>.condarc</span></code>&nbsp;configuration file. The default packages are installed every time you create a new environment. If you do not want the default packages installed in a particular environment, use the&nbsp;<code><span>--no-default-packages</span></code>&nbsp;flag:</p><div><div><pre><span></span>conda create --no-default-packages -n myenv python
</pre></div></div><p>TIP: You can add much more to the&nbsp;<code><span>conda</span>&nbsp;<span>create</span></code>&nbsp;command. For details, run&nbsp;<code><span>conda</span>&nbsp;<span>create</span>&nbsp;<span>--help</span></code>.</p><p>➜ redundans git:(master) ✗ conda create --name py27 python=2.7<br />Solving environment: done</p><p><br />==&gt; WARNING: A newer version of conda exists. &lt;==<br /> current version: 4.5.0<br /> latest version: 4.5.2</p><p>Please update conda by running</p><p>$ conda update -n base conda</p><p>&nbsp;</p><p>## Package Plan ##</p><p>environment location: /home/urbe/anaconda3/envs/py27</p><p>added / updated specs: <br /> - python=2.7</p><p><br />The following packages will be downloaded:</p><p>package | build<br /> ---------------------------|-----------------<br /> wheel-0.31.0 | py27_0 61 KB<br /> python-2.7.15 | h1571d57_0 12.1 MB<br /> certifi-2018.4.16 | py27_0 142 KB<br /> sqlite-3.23.1 | he433501_0 1.5 MB<br /> setuptools-39.1.0 | py27_0 582 KB<br /> openssl-1.0.2o | h20670df_0 3.4 MB<br /> pip-10.0.1 | py27_0 1.7 MB<br /> ca-certificates-2018.03.07 | 0 124 KB<br /> ------------------------------------------------------------<br /> Total: 19.6 MB</p><p>The following NEW packages will be INSTALLED:</p><p>ca-certificates: 2018.03.07-0 <br /> certifi: 2018.4.16-py27_0 <br /> libedit: 3.1-heed3624_0 <br /> libffi: 3.2.1-hd88cf55_4 <br /> libgcc-ng: 7.2.0-hdf63c60_3 <br /> libstdcxx-ng: 7.2.0-hdf63c60_3 <br /> ncurses: 6.0-h9df7e31_2 <br /> openssl: 1.0.2o-h20670df_0<br /> pip: 10.0.1-py27_0 <br /> python: 2.7.15-h1571d57_0<br /> readline: 7.0-ha6073c6_4 <br /> setuptools: 39.1.0-py27_0 <br /> sqlite: 3.23.1-he433501_0<br /> tk: 8.6.7-hc745277_3 <br /> wheel: 0.31.0-py27_0 <br /> zlib: 1.2.11-ha838bed_2</p><p>Proceed ([y]/n)? y</p><p><br />Downloading and Extracting Packages<br />wheel 0.31.0: #################################################################################################################################################################################################### | 100% <br />python 2.7.15: ################################################################################################################################################################################################### | 100% <br />certifi 2018.4.16: ############################################################################################################################################################################################### | 100% <br />sqlite 3.23.1: ################################################################################################################################################################################################### | 100% <br />setuptools 39.1.0: ############################################################################################################################################################################################### | 100% <br />openssl 1.0.2o: ################################################################################################################################################################################################## | 100% <br />pip 10.0.1: ###################################################################################################################################################################################################### | 100% <br />ca-certificates 2018.03.07: ###################################################################################################################################################################################### | 100% <br />Preparing transaction: done<br />Verifying transaction: done<br />Executing transaction: done<br />#<br /># To activate this environment, use:<br /># &gt; source activate py27<br />#<br /># To deactivate an active environment, use:<br /># &gt; source deactivate<br />#</p><p>➜ redundans git:(master) ✗ source activate py27</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44179/python-mini-projects</guid>
	<pubDate>Mon, 16 Jan 2023 02:14:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44179/python-mini-projects</link>
	<title><![CDATA[Python Mini Projects !]]></title>
	<description><![CDATA[<p><span>There is a directory for each chapter of the book. Each directory contains a&nbsp;</span><code>test.py</code><span>&nbsp;program you can use with&nbsp;</span><code>pytest</code><span>&nbsp;to check that you have written the program correctly. I have included a short README to describe each exercise. If you have problems writing code (or if you would like to support this project!), the book contains details about the skills you need.</span></p>
<p>https://github.com/kyclark/tiny_python_projects</p><p>Address of the bookmark: <a href="https://github.com/kyclark/tiny_python_projects" rel="nofollow">https://github.com/kyclark/tiny_python_projects</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30168/gene-synteny-database</guid>
	<pubDate>Fri, 16 Dec 2016 11:09:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30168/gene-synteny-database</link>
	<title><![CDATA[Gene Synteny Database]]></title>
	<description><![CDATA[<p>Comparative genomics remains a pivotal strategy to study the evolution of gene organization, and this primacy is reinforced by the growing number of full genome sequences available in public repositories. Despite this growth, bioinformatic tools available to visualize and compare genomes and to infer evolutionary events remain restricted to two or three genomes at a time, thus limiting the breadth and the nature of the question that can be investigated. Here we present Genomicus, a new synteny browser that can represent and compare unlimited numbers of genomes in a broad phylogenetic view. In addition, Genomicus includes reconstructed ancestral gene organization, thus greatly facilitating the interpretation of the data.</p>
<p><strong>Availability:</strong>&nbsp;Genomicus is freely available for online use at&nbsp;<a href="http://www.dyogen.ens.fr/genomicus" target="pmc_ext">http://www.dyogen.ens.fr/genomicus</a>&nbsp;while data can be downloaded at&nbsp;<a href="ftp://ftp.biologie.ens.fr/pub/dyogen/genomicus" target="pmc_ext">ftp://ftp.biologie.ens.fr/pub/dyogen/genomicus</a></p>
<p><strong>Contact:</strong>&nbsp;<a href="mailto:dev@null">rf.sne.eigoloib@crh</a></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853686/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853686/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41694/mercator-multiple-whole-genome-orthology-map-construction</guid>
	<pubDate>Tue, 19 May 2020 16:46:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41694/mercator-multiple-whole-genome-orthology-map-construction</link>
	<title><![CDATA[Mercator: Multiple Whole-Genome Orthology Map Construction]]></title>
	<description><![CDATA[<p><span>Whole-genome homology maps attempt to identify the evolutionary relationships between and within multiple genomes. The term "syntenic" is often used to describe regions of multiple genomes that are believed to have evolved from the same region in an ancestral genome. However, it has been pointed out that this use of the term is incorrect (</span><a href="https://www.biostat.wisc.edu/~cdewey/mercator/#refSynteny">Passarge et al. 1999</a><span>) and thus we will use the terms "homologous", "orthologous", and "paralogous" instead. Ideally, given K genomes, we would like to identify all orthologous genomic regions as well as paralogous regions within each genome and hypothetical ancestral genome. Maps listing these relationships are extremely valuable to researchers performing comparative analyses of genomic sequence. Here we present our initial work in the form a program called&nbsp;</span><em>Mercator</em><span>&nbsp;that constructs orthology maps between multiple whole genomes.</span></p><p>Address of the bookmark: <a href="https://www.biostat.wisc.edu/~cdewey/mercator/" rel="nofollow">https://www.biostat.wisc.edu/~cdewey/mercator/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</guid>
	<pubDate>Mon, 17 Feb 2020 05:38:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</link>
	<title><![CDATA[Chromonomer: a tool set for repairing and enhancing assembled genomes through integration of genetic maps and conserved synteny]]></title>
	<description><![CDATA[<p>Chromonomer is a program designed to integrate a genome assembly with a genetic map. Chromonomer tries very hard to identify and remove markers that are out of order in the genetic map, when considered against their local assembly order; and to identify scaffolds that have been incorrectly assembled according to the genetic map, and split those scaffolds.</p><p>Address of the bookmark: <a href="http://catchenlab.life.illinois.edu/chromonomer/" rel="nofollow">http://catchenlab.life.illinois.edu/chromonomer/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</guid>
	<pubDate>Mon, 06 May 2024 06:21:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</link>
	<title><![CDATA[Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes]]></title>
	<description><![CDATA[<p><span>Genomic regulatory blocks are chromosomal regions spanned by long clusters of highly conserved noncoding elements devoted to long-range regulation of developmental genes, often immobilizing other, unrelated genes into long-lasting syntenic arrangements. Synorth&nbsp;</span><a href="http://synorth.genereg.net/" target="_blank">http://synorth.genereg.net/</a><span>&nbsp;is a web resource for exploring and categorizing the syntenic relationships in genomic regulatory blocks across multiple genomes, tracing their evolutionary fate after teleost whole genome duplication at the level of genomic regulatory block loci, individual genes, and their phylogenetic context.</span></p>
<p><span>More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745767/</span></p><p>Address of the bookmark: <a href="http://synorth.genereg.net/" rel="nofollow">http://synorth.genereg.net/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<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/bookmarks/view/26380/hicdat</guid>
	<pubDate>Fri, 12 Feb 2016 05:23:44 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26380/hicdat</link>
	<title><![CDATA[HiCdat]]></title>
	<description><![CDATA[<p>HiCdat: a fast and easy-to-use Hi-C data analysis tool</p>
<p>HiCdat is easy-to-use and provides solutions starting from aligned reads up to in-depth analyses. Importantly, HiCdat is focussed on the analysis of larger structural features of chromosomes, their correlation to genomic and epigenomic features, and on comparative studies. It uses simple input and output formats and can therefore easily be integrated into existing workflows or combined with alternative tools.</p>
<p>More at http://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-015-0678-x</p><p>Address of the bookmark: <a href="https://github.com/MWSchmid/HiCdat" rel="nofollow">https://github.com/MWSchmid/HiCdat</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39453/fuma-gwas-functional-mapping-and-annotation-of-genome-wide-association-studies</guid>
	<pubDate>Sat, 01 Jun 2019 03:11:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39453/fuma-gwas-functional-mapping-and-annotation-of-genome-wide-association-studies</link>
	<title><![CDATA[FUMA GWAS: Functional Mapping and Annotation of Genome-Wide Association Studies]]></title>
	<description><![CDATA[<p><span>FUMA is a platform that can be used to annotate, prioritize, visualize and interpret GWAS results.&nbsp;</span><br><span>The&nbsp;</span><a href="https://fuma.ctglab.nl/snp2gene">SNP2GENE</a><span>&nbsp;function takes GWAS summary statistics as an input, and provides extensive functional annotation for all SNPs in genomic areas identified by lead SNPs.&nbsp;</span><br><span>The&nbsp;</span><a href="https://fuma.ctglab.nl/gene2func">GENE2FUNC</a><span>&nbsp;function takes a list of gene IDs (as identified by SNP2GENE or as provided manually) and annotates genes in biological context&nbsp;</span></p><p>Address of the bookmark: <a href="https://fuma.ctglab.nl/" rel="nofollow">https://fuma.ctglab.nl/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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