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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/41863?offset=30</link>
	<atom:link href="https://bioinformaticsonline.com/related/41863?offset=30" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35108/mobyle-a-new-full-web-bioinformatics-framework</guid>
	<pubDate>Sun, 07 Jan 2018 19:33:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35108/mobyle-a-new-full-web-bioinformatics-framework</link>
	<title><![CDATA[Mobyle: a new full web bioinformatics framework]]></title>
	<description><![CDATA[<p><span>Mobyle, to provide a flexible and usable Web environment for defining and running bioinformatics analyses. It embeds simple yet powerful data management features that allow the user to reproduce analyses and to combine tools using a hierarchical typing system. Mobyle offers invocation of services distributed over remote Mobyle servers, thus enabling a federated network of curated bioinformatics portals without the user having to learn complex concepts or to install sophisticated software.</span></p><p>Address of the bookmark: <a href="https://academic.oup.com/bioinformatics/article/25/22/3005/179064" rel="nofollow">https://academic.oup.com/bioinformatics/article/25/22/3005/179064</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37800/heatmapper-web-enabled-heat-mapping-for-all</guid>
	<pubDate>Mon, 01 Oct 2018 08:34:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37800/heatmapper-web-enabled-heat-mapping-for-all</link>
	<title><![CDATA[Heatmapper: web-enabled heat mapping for all]]></title>
	<description><![CDATA[<p><span>Heatmapper is a freely available web server that allows users to interactively visualize their data in the form of heat maps through an easy-to-use graphical interface. Heatmapper is a versatile tool that allows users to easily create a wide variety of heat maps for many different data types and applications. Heatmapper allows users to generate, cluster and visualize: </span></p>
<p><span>1)&nbsp;</span><span>expression-based heat maps</span><span>&nbsp;from transcriptomic, proteomic and metabolomic experiments; 2)&nbsp;</span><span>pairwise distance maps</span><span>; </span></p>
<p><span>3)&nbsp;</span><span>correlation maps</span><span>; </span></p>
<p><span>4)&nbsp;</span><span>image overlay heat maps</span><span>; </span></p>
<p><span>5)&nbsp;</span><span>latitude and longitude heat maps</span><span>&nbsp;and </span></p>
<p><span>6)&nbsp;</span><span>geopolitical (choropleth) heat maps</span><span>. </span></p>
<p><span>Heatmapper offers a number of simple and intuitive customization options for easy adjustments to each heat map&rsquo;s appearance and plotting parameters. Heatmapper also allows users to interactively explore their numeric data values by hovering their cursor over each heat map, or by using a searchable/sortable data table view.</span></p>
<p><span>Ref&nbsp;https://www.ncbi.nlm.nih.gov/pubmed/27190236</span></p><p>Address of the bookmark: <a href="http://www2.heatmapper.ca/" rel="nofollow">http://www2.heatmapper.ca/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40221/dash-a-web-application-framework-that-provides-pure-python-abstraction-around-html-css-and-javascript</guid>
	<pubDate>Tue, 05 Nov 2019 06:39:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40221/dash-a-web-application-framework-that-provides-pure-python-abstraction-around-html-css-and-javascript</link>
	<title><![CDATA[Dash: a web application framework that provides pure Python abstraction around HTML, CSS, and JavaScript.]]></title>
	<description><![CDATA[<p style="margin-top: 0px; margin-bottom: 0.75rem;">Dash is a web application framework that provides pure Python abstraction around HTML, CSS, and JavaScript.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">Dash Bio is a suite of bioinformatics components that make it simpler to analyze and visualize bioinformatics data and interact with them in a Dash application.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">The source can be found on GitHub at<span>&nbsp;</span><a href="https://github.com/plotly/dash-bio">plotly/dash-bio</a>.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">These docs are using Dash Bio version 0.1.4.</p><p>Address of the bookmark: <a href="https://dash.plot.ly/dash-bio" rel="nofollow">https://dash.plot.ly/dash-bio</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44885/firecrawl-the-web-data-api-for-ai-turn-entire-websites-into-llm-ready-markdown-or-structured-data</guid>
	<pubDate>Thu, 28 Aug 2025 02:34:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44885/firecrawl-the-web-data-api-for-ai-turn-entire-websites-into-llm-ready-markdown-or-structured-data</link>
	<title><![CDATA[Firecrawl: The Web Data API for AI - Turn entire websites into LLM-ready markdown or structured data]]></title>
	<description><![CDATA[<p dir="auto"><a href="https://firecrawl.dev/?ref=github">Firecrawl</a>&nbsp;is an API service that takes a URL, crawls it, and converts it into clean markdown or structured data. We crawl all accessible subpages and give you clean data for each. No sitemap required. Check out our&nbsp;<a href="https://docs.firecrawl.dev/">documentation</a>.</p>
<p dir="auto"><em>Pst. hey, you, join our stargazers :)</em></p>
<p><em>&nbsp;</em></p>
<p><a href="https://github.com/firecrawl/firecrawl"></a></p><p>Address of the bookmark: <a href="https://github.com/firecrawl/firecrawl" rel="nofollow">https://github.com/firecrawl/firecrawl</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34814/bioinformatics-web-application-development-with-perl</guid>
	<pubDate>Tue, 26 Dec 2017 18:14:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34814/bioinformatics-web-application-development-with-perl</link>
	<title><![CDATA[Bioinformatics Web Application Development with Perl]]></title>
	<description><![CDATA[<div><p>Perl's second wave of adoption came from the growth of the world wide web. Dynamic web pages&mdash;the precursor to modern web applications&mdash;were easy to create with Perl and CGI. Thanks to Perl's ubiquity as a language for system administrators and its power to manipulate text, it was the default choice for web programming. Its presence everywhere made it popular and, in some ways, the duct tape of the Internet.</p><h4>Web Application Development</h4><p>The old days of CGI programs and the simple development style that represented seem clunky. Web pages have become web applications. Development has moved from generating static HTML to both client and server side programming, with rich client interfaces and powerful backends.</p><p>Perl is still well suited for developing modern web apps. The language grows more powerful and easier to use every year, the available libraries are wonderful and keep getting better, and the inventions and discoveries available in modern Perl are unsurpassed.</p><p>In particular, a modern Perl developer can do amazing things with modern Perl tools. If you still think of Perl web development as a&nbsp;<em>cgi-bin</em>&nbsp;directory full of messy scripts that spew warnings to STDERR, you're a decade out of date. Better yet, you can replace that mess piecemeal, thanks to the new tools and techniques of modern Perl. See, for example, the ever-growing list of technologies&nbsp;<a href="http://www.builtinperl.com/">Built in Perl</a>.</p><h4>Modern Perl Web Frameworks</h4><p>While the old wave of web development may have made the CGI.pm module central, modern Perl web programming follows a stricter separation of business logic, URL and request routing, and output. The days of slinging a string here, an array there, a Perl hash yonder, declaring every variable at the top of the program, and maybe making a subroutine are gone. The Perl world has seen the value of abstraction and ways to mechanize away boilerplate. Perl has dozens of frameworks and toolkits designed to make web development and deployment simpler.</p><p>Any of a dozen of these frameworks will help you do great things, but three in particular stand out. You can build web sites and web applications of tremendous value with all three. These are neither the only good possibilities (think of POE or Jifty or Continuity or...) nor the only mechanisms for web programming with Perl (see Mechanize or LWP or Mojo::UserAgent for more). Yet if you want three good options to choose between, start here.</p><h4>Catalyst</h4><p>The&nbsp;<a href="http://catalystframework.org/">Catalyst</a>&nbsp;framework is a flexible and powerful system for building small to large web apps. It uses the&nbsp;<a href="http://moose.perl.org/">Moose</a>&nbsp;object system to provide great APIs for extension and further development. It's the most mature of the modern top Perl web frameworks, yet it retains its flexibility and vibrancy. In particular, its plugin and extension ecosystem allows it to evolve to provide new and essential features.</p><p>Catalyst has embraced the Plack/PSGI standard for Perl web deployment and recent versions are exploring high-scalability, event-based request handling models.</p><h4>Dancer</h4><p>The&nbsp;<a href="http://perldancer.org/">Dancer</a>&nbsp;framework is deliberately minimal in syntax and scope, but it also has a vibrant plugin ecosystem. Dancer particularly excels for smaller sites and applications, though good programmers can build larger things with it.</p><p>The first version of Dancer was easy to use. Dancer 2 continues that ease while improving the internals and robustness of applications.</p><h4>Mojolicious</h4><p>The&nbsp;<a href="http://mojolicio.us/">Mojolicious</a>&nbsp;(Mojo) framework has a real-time design based on high performance event handling. Its focus is solving new and interesting problems in simple and effective ways, and the project has produced a lot of new code that does old things in better ways.</p><p>In particular, Mojolicious goes to great lengths to support new web standards, such as CSS 3, web sockets, and HTTP 2.</p><p>Where Catalyst embraces the CPAN fully, Mojolicious by design provides most of what an average app might need in a single download. It's still fully compatible with the CPAN, but the intention is to provide good working defaults in a package that's easy to start with. Mojo's fans are quick to praise it as fun to develop.</p><p>A modern Perl web developer should be familiar with at least one of these frameworks.</p><h4>Modern Perl Storage Mechanisms</h4><p>Perl's venerable&nbsp;<a href="http://search.cpan.org/perldoc?DBI">DBI</a>&nbsp;module has been the focal point of database access since its invention. Its design allows it to provide the same interface to huge relational databases and flat files alike through its DBD extension mechanism. Yet the DBI by itself isn't the be-all, end-all of data storage and access in Perl.</p><h4>DBIx::Class</h4><p><a href="http://search.cpan.org/perldoc?DBIx::Class">DBIx::Class</a>&nbsp;sits on top of DBI to provide an API to your database based on the concept of queries and results. This is often sufficient to remove all but the most complicated of SQL from your code, leaving you to manipulate your business models instead of the small details of how a relational database works. The power and maintainability you receive is well the small cost of the learning curve.</p><p>Even better, DBIC can manage (and even generate) your database schema for you.</p><p>Recent versions of DBIC have demonstrated that a well-written ORM can perform much better than even clever hand-written code. Because it builds on the Perl DBI, it scales everywhere from SQLite to PostgreSQL, MySQL, Oracle, and more.</p><h3>Rose::DB</h3><p>The lesser-known but no less powerful&nbsp;<a href="http://search.cpan.org/perldoc?Rose::DB::Object">Rose::DB::Object</a>&nbsp;builds on&nbsp;<a href="http://search.cpan.org/perldoc?Rose::DB">Rose::DB</a>&nbsp;to provide an object-relational mapper for Perl. While its high level features most directly compare to those of DBIx::Class, it's often measurably faster.</p><h4>NoSQL on the CPAN</h4><p>Of course the&nbsp;<a href="http://search.cpan.org/">CPAN</a>&nbsp;has modules for almost any NoSQL database or job queue or persistence mechanism you could name, and several you have never heard of. Everything you need is a quick CPAN or cpanm away!</p><h4>Modern Perl Deployment Strategies</h4><p>In the early days of the web, deploying a Perl web application meant putting one or more&nbsp;<em>.cgi</em>&nbsp;or&nbsp;<em>.pl</em>&nbsp;files in a special directory and hoping that your system administrator had everything configured correctly. The execution model was often slow and cumbersome, and accessing shared resources such as databases was often tricky.</p><p>Modern Perl has better choices. While deployment strategies are the source of many arguments, the return on your investment from learning the modern way is impressive.</p><h4>Plack/PSGI</h4><p>The PSGI specification (as exemplified by&nbsp;<a href="http://plackperl.org/">Plack</a>) describes a strategy for building Perl web apps independent of server and with the possibility to share custom processing behaviors.</p><p>In other words, it's a standard for writing Perl apps to take advantage of the huge ecosystem of Perl development available on the CPAN without tying yourself to a server like Apache, Apache 2, nginx, or anything else.</p><p>Any good modern Perl web framework (including those listed here) supports PSGI. Several deployment mechanisms exist to meet various business needs which also support PSGI. In particular, you can deploy the same application with a local testing server on your own machine as you can to your production server or servers without changing your application at all.</p><h4>mod_perl</h4><p>The older but still viable mod_perl Apache httpd module embeds Perl into the web server. This was the first widespread persistence mechanism for Perl web applications themselves and it's still popular to this day, though PSGI compliance is often the choice for new development. (PSGI handlers to use mod_perl as the backend are available.)</p><p>Modern Perl developers should familiarize themselves with PSGI and the wealth of available Plack middleware.</p><h4>Perl Web Development</h4><p>Of course no discussion of Perl web development would be complete without mentioning the strength of the CPAN. Almost any project will benefit from the wealth of freely available libraries built to solve real problems. These distributions run the gamut from full-blown web frameworks and content management systems to APIs for web services, development tools, testing systems, and interfaces to document formats and external resources.</p><p>For example, if you need to write a web service which accepts JSON data and produces Excel spreadsheets, you can glue together a few CPAN distributions and get the job done early. If you need to consume XML from a remote service and emit a PDF, you're in luck.</p><p>Perl's prowess as a general purpose programming language as well as its flexibility and power in managing text and gluing systems together make it a wonderful fit for web development. The community's adoption of modern Perl standards such as PSGI and Plack only enhance your power.</p><p>Web application development in Perl is still viable, and modern Perl tools and techniques and libraries make it more powerful and pleasant than ever.</p></div>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41571/wego-simple-but-useful-tool-for-visualizing-comparing-and-plotting-go-gene-ontology-annotation-results</guid>
	<pubDate>Sun, 12 Apr 2020 10:02:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41571/wego-simple-but-useful-tool-for-visualizing-comparing-and-plotting-go-gene-ontology-annotation-results</link>
	<title><![CDATA[WEGO : simple but useful tool for visualizing, comparing and plotting GO (Gene Ontology) annotation results]]></title>
	<description><![CDATA[<p><span>WEGO (Web Gene Ontology Annotation Plot) is a simple but useful tool for visualizing, comparing and plotting GO (Gene Ontology) annotation results. As the GO vocabulary became more and more popular, WEGO was widely adopted and used in many researches. Therefore we have updated WEGO 2.0 in 2018. Here are some changes we&rsquo;ve made:</span><br><span>1. The limit of input file numbers was cancelled. Now the users could upload as many files as they want with one operation.</span><br><span>2. We have added the reference data of 9 species for users selection.</span><br><span>3. Besides the traditional WEGO histogram, WEGO 2.0 outputs an additional type of bar graph showing GO terms with significant gene number differences.</span></p><p>Address of the bookmark: <a href="http://wego.genomics.org.cn/" rel="nofollow">http://wego.genomics.org.cn/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44914/predicting-pathogen-virulence-using-bioinformatics-tools</guid>
	<pubDate>Tue, 04 Nov 2025 07:55:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44914/predicting-pathogen-virulence-using-bioinformatics-tools</link>
	<title><![CDATA[Predicting Pathogen Virulence Using Bioinformatics Tools]]></title>
	<description><![CDATA[<p>In the genomic era, the ability to predict the virulence potential of pathogens has become an indispensable part of infectious disease research. With the exponential growth of microbial genome data, bioinformatics tools now enable scientists to identify virulence factors, model pathogen behavior, and even forecast outbreak risks &mdash; all from sequence data.</p><p>In an age where pathogens continue to evolve and cross boundaries, understanding <strong>what makes them virulent</strong>&mdash;that is, capable of causing disease&mdash;has become a critical focus in modern microbiology and genomics. <strong>Virulence prediction</strong> bridges computational biology, genomics, and machine learning to forecast the pathogenic potential of microbes before they strike.</p><h3>What Is Virulence?</h3><p><em>Virulence</em> refers to the degree of damage a pathogen can inflict on its host. It is determined by a combination of genetic factors&mdash;called <strong>virulence factors (VFs)</strong>&mdash;that allow the organism to attach, invade, evade, and harm the host. These include genes coding for toxins, secretion systems, adhesins, and enzymes that disrupt host defenses.</p><p>Understanding virulence factors not only helps in deciphering the mechanisms of infection but also provides early warning signs for emerging threats.</p><h3>Why Predict Virulence?</h3><p>Traditional virulence studies relied heavily on experimental infection models, which, although accurate, are <strong>time-consuming, expensive, and ethically constrained</strong>.<br /> Today, the availability of whole-genome sequences and large-scale pathogen databases has paved the way for <strong>in silico virulence prediction</strong>&mdash;a computational approach that can screen thousands of genomes within hours.</p><p>This approach enables researchers to:</p><ul>
<li>
<p>Rapidly identify potential <strong>high-risk strains</strong>.</p>
</li>
<li>
<p>Prioritize pathogens for <strong>containment, surveillance, or further study</strong>.</p>
</li>
<li>
<p>Guide <strong>vaccine development</strong> and <strong>drug target discovery</strong>.</p>
</li>
<li>
<p>Support <strong>One Health frameworks</strong>, linking animal, human, and environmental health data.</p>
</li>
</ul><h3>How Is Virulence Predicted?</h3><p>Virulence prediction combines <strong>bioinformatics pipelines</strong> with <strong>machine learning</strong> and <strong>comparative genomics</strong>. The process generally involves:</p><ol>
<li>
<p><strong>Genome Annotation:</strong> Identifying genes and coding sequences in microbial genomes.</p>
</li>
<li>
<p><strong>Feature Extraction:</strong> Comparing sequences with curated databases like <strong>VFDB (Virulence Factor Database)</strong>, <strong>PATRIC</strong>, or <strong>Victors</strong>.</p>
</li>
<li>
<p><strong>Pattern Recognition:</strong> Using algorithms (e.g., Random Forest, SVM, or deep learning models) to classify genes or strains as virulent or non-virulent based on sequence patterns, motifs, and protein domains.</p>
</li>
<li>
<p><strong>Scoring and Visualization:</strong> Assigning a virulence score or confidence level and visualizing it through heatmaps or genome maps.</p>
</li>
</ol><h3>Tools and Resources for Virulence Prediction</h3><p>A number of tools and databases make virulence prediction accessible to the scientific community:</p><ul>
<li>
<p><strong>VFanalyzer</strong> &ndash; For identifying virulence genes based on VFDB.</p>
</li>
<li>
<p><strong>PathoFact</strong> &ndash; Predicts virulence, antimicrobial resistance (AMR), and toxin genes from metagenomic data.</p>
</li>
<li>
<p><strong>Pangenome-based models</strong> &ndash; Identify virulence-associated gene clusters across strains.</p>
</li>
<li>
<p><strong>Machine learning models</strong> &ndash; Use features like GC content, codon usage bias, or protein domains to predict pathogenicity.</p>
</li>
</ul><p>Emerging tools now integrate <strong>multi-omic data</strong>&mdash;including transcriptomics, proteomics, and metabolomics&mdash;to understand virulence in a systems biology framework.</p><h3>Applications in the Real World</h3><p>Virulence prediction has major implications across public health and research sectors:</p><ul>
<li>
<p><strong>Epidemic preparedness:</strong> Early identification of virulent strains in outbreak samples.</p>
</li>
<li>
<p><strong>AMR surveillance:</strong> Linking virulence profiles with antibiotic resistance determinants.</p>
</li>
<li>
<p><strong>Environmental monitoring:</strong> Predicting pathogenic potential of soil or waterborne microbes.</p>
</li>
<li>
<p><strong>Clinical diagnostics:</strong> Supporting personalized treatment through pathogen profiling.</p>
</li>
</ul><p>For instance, integrating virulence prediction pipelines into <strong>national surveillance networks</strong> could enable faster risk assessment and response to infectious outbreaks.</p><h3>The Road Ahead</h3><p>As machine learning and genomics advance, virulence prediction will evolve from simple gene-based detection to <strong>dynamic, context-aware models</strong> that account for host&ndash;pathogen interactions, environmental signals, and evolutionary adaptation.</p><p>Future tools may predict <strong>not just if a strain is virulent</strong>, but <strong>under what conditions</strong> it expresses that virulence&mdash;bridging the gap between genotype and phenotype.</p><h3>In Summary</h3><p>Virulence prediction is redefining how we understand and anticipate infectious diseases. By coupling <strong>genomic insights</strong> with <strong>computational intelligence</strong>, researchers can identify potential threats earlier, design smarter interventions, and ultimately, strengthen our preparedness against emerging pathogens.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/11798/phd-scholarship-denmark</guid>
  <pubDate>Fri, 13 Jun 2014 13:44:07 -0500</pubDate>
  <link></link>
  <title><![CDATA[PHD SCHOLARSHIP DENMARK]]></title>
  <description><![CDATA[
<p>ne PhD position is available at the Bioinformatics Center, Department of Biology, University of Copenhagen, Denmark. The PhD position concerns protein structure prediction, and will be in the Structural Bioinformatics group of Associate professor Thomas Hamelryck. The group is an integrated part of the Bioinformatics Center, which is headed by Professor Anders Krogh, employs around sixty scientists (including PhD students) and focuses on non-coding RNA, eukaryotic gene regulation and protein structure prediction. The center provides a modern, pleasant, international working environment with excellent modern facilities, in the heart of Copenhagen.<br />The project will be supervised by Associate Professor Thomas Hamelryck.</p>

<p>The protein folding problem is of enormous practical, theoretical and medical importance - and in addition forms a fascinating intellectual challenge. The aim of this project is to develop and implement a probabilistic method to infer the structure of proteins, building on various probabilistic models of protein structure developed by the Hamelryck group. The method will also take the dynamic nature of proteins into account, and involves a close collaboration with the statistics department at the university within the interdisciplinary project "Dynamical Systems: Mathematical Modeling and Statistical Methods for the Social, Health, and Natural Sciences" (http://dsin.ku.dk/).</p>

<p>Qualifications<br />Knowledge of programming (C++) and statistics or machine learning. Knowledge of biology, physics or biophysics is a plus, but not a requirement.</p>

<p>The deadline for applications is June 15, 2014</p>

<p>More at : https://job.jobnet.dk/CV/FindJob/details.aspx/3695051%20</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36846/gblocks-eliminates-poorly-aligned-positions-and-divergent-regions-of-a-dna-or-protein-alignment</guid>
	<pubDate>Sat, 02 Jun 2018 07:36:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36846/gblocks-eliminates-poorly-aligned-positions-and-divergent-regions-of-a-dna-or-protein-alignment</link>
	<title><![CDATA[Gblocks: eliminates poorly aligned positions and divergent regions of a DNA or protein alignment]]></title>
	<description><![CDATA[<p><a href="http://molevol.cmima.csic.es/castresana/Gblocks.html">Gblocks</a><span>&nbsp;eliminates poorly aligned positions and divergent regions of a DNA or protein alignment so that it becomes more suitable for phylogenetic analysis. This server implements the most important features of the Gblocks program to make its use as simple as possible without loosing the functionality that it is necessary in most of the cases. Other options can be changed in the stand-alone program. You can see here an&nbsp;</span><a href="http://molevol.cmima.csic.es/castresana/Gblocks_server/nad3.pir-gb.htm">example output file</a><span>&nbsp;showing the blocks selected from a protein alignment. Further information can be found in the&nbsp;</span><a href="http://molevol.cmima.csic.es/castresana/Gblocks/Gblocks_documentation.html">online documentation</a><span>.&nbsp;</span></p><p>Address of the bookmark: <a href="http://molevol.cmima.csic.es/castresana/Gblocks_server.html" rel="nofollow">http://molevol.cmima.csic.es/castresana/Gblocks_server.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/38238/list-of-motif-discovery-tools</guid>
	<pubDate>Tue, 20 Nov 2018 03:54:26 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/38238/list-of-motif-discovery-tools</link>
	<title><![CDATA[List of motif discovery tools !]]></title>
	<description><![CDATA[<div><div>In genetics, a sequence motif is a nucleotide or amino-acid sequence pattern that is widespread and has, or is conjectured to have, a biological significance. For proteins, a sequence motif is distinguished from a structural motif, a motif formed by the three-dimensional arrangement of amino acids which may not be adjacent.</div><div>&nbsp;</div><div>Following are the list of tools for motif discovery:</div><div>&nbsp;</div><div><a href="http://genius.embnet.dkfz-heidelberg.de/menu/biounit/open-husar/">2Dsweep -- protein annotation by secondary structure elements</a></div><p>Perform secondary structure predictions on protein sequences.</p></div><div><div><a href="http://floresta.eead.csic.es/3dfootprint/">3D-footprint -- database of DNA-binding protein structures</a></div><p>Find binding specificity information about DNA-protein complexes.</p></div><div><div><a href="http://floresta.eead.csic.es/3dfootprint/">3D-footprint: DNA-binding protein database</a></div><p>Find information about the binding specificity of DNA-binding proteins.</p></div><div><div><a href="http://3d-partner.life.nctu.edu.tw/">3D-partner -- a web server to infer interacting partners and binding models</a></div><p>Predict interacting partners and binding models.</p></div><div><div><a href="http://motif.stanford.edu/distributions/3motif/">3MOTIF -- a protein structure visualization system for conserved sequence motifs</a></div><p>Use this web-based sequence motif visualization system to display sequence motif information in its appropriate three-dimensional (3D) context.</p></div><div><div><a href="http://bioinfo.mpiz-koeln.mpg.de/afawe/">AFAWE -- Automatic functional annotation in a distributed Web Services Environment</a></div><p>Protein function prediction and annotation in an integrated environment powered by web service.</p></div><div><div><a href="http://anchor.enzim.hu/">ANCHOR -- Prediction of Protein Binding Regions in Disordered Proteins</a></div><p>Find information about protein binding.</p></div><div><div><a href="http://annie.bii.a-star.edu.sg/annie/home.do">ANNIE -- ANNotation and Interpretation Environment for Protein Sequences</a></div><p>Use to predict function from de novo protein sequences.</p></div><div><div><a href="http://bioinformatica.isa.cnr.it/ASC/">Active Sequences Collection (ASC) database -- A new tool to assign functions to protein sequences</a></div><p>Search for short active protein sequences with demonstrated biological activities.</p></div><div><div><a href="http://blocks.fhcrc.org/">Blocks -- Ungapped segments in conserved protein sequences</a></div><p>Search for ungapped segments corresponding to the most highly conserved regions of proteins.</p></div><div><div><a href="http://cast.engr.uic.edu/">CASTp -- computed atlas of surface topography of proteins with structural and topographical mapping of functionally annotated residues</a></div><p>Identify and measure surface accessible pockets as well as interior inaccessible cavities, for proteins and other molecules.</p></div><div><div><a href="http://www.ebi.ac.uk/thornton-srv/databases/CSA">CSA -- The Catalytic Site Atlas</a></div><p>To search for catalytic residue annotation for enzymes in the Protein Data Bank.</p></div><div><div><a href="http://www.sbg.bio.ic.ac.uk/~confunc/">ConFunc -- Conserved residue Protein Function Prediction Server</a></div><p>Predict protein function using Gene Ontology.</p></div><div><div><a href="http://consurf.tau.ac.il/">ConSurf-DB -- evolutionary conservation profiles of protein structures database</a></div><p>Automatically calculate evolutionary conservation scores of key amino acid residues and map them on protein structures.</p></div><div><div><a href="http://salilab.org/DBAli/">DBAli -- A Database of Structure Alignments</a></div><p>Mine the protein structure space.</p></div><div><div><a href="http://dilimot.embl.de/">DILIMOT -- discovery of linear motifs in proteins</a></div><p>Predict short linear motifs (3-8 residues) in a set of protein sequences.</p></div><div><div><a href="http://www.ebi.ac.uk/dasty/">Dasty2 -- an Ajax protein DAS client</a></div><p>A web client for visualizing protein sequence feature information using DAS.</p></div><div><div><a href="http://genius.embnet.dkfz-heidelberg.de/menu/biounit/open-husar/">DomainSweep -- protein annotation by domain analysis</a></div><p>Identify the domain architecture within a protein sequence.</p></div><div><div><a href="http://e1ds.csbb.ntu.edu.tw/">E1DS -- catalytic site prediction based on 1D signatures of concurrent conservation</a></div><p>Predict enzyme catalytic site.</p></div><div><div><a href="http://elm.eu.org/">ELM -- Eukarotic Linear Motif Resource</a></div><p>Predict functional sites in eukaryotic proteins.</p></div><div><div><a href="http://us.expasy.org/tools/#proteome">EXPASY Proteome Tools Collection</a></div><p>Use a collection of tools for protein analyses.</p></div><div><div><a href="http://us.expasy.org/tools/findmod/">EXPASY-Findmod</a></div><p>Predict potential protein post-translational modifications and find potential single amino acid substitutions in peptides.</p></div><div><div><a href="http://mbs.cbrc.jp/EzCatDB/">EzCatDB -- the Enzyme Catalytic-mechanism Database</a></div><p>Search for information related to the catalytic mechanisms of enzymes.</p></div><div><div><a href="http://bioinf.cs.ucl.ac.uk/ffpred/">FFPred -- feature-based function prediction</a></div><p>An integrated feature-based function prediction server for vertebrate proteomes.</p></div><div><div><a href="http://www.ebi.ac.uk/printsscan/">FingerPRINT Scan</a></div><p>Identify the closest matching PRINTS sequence motif fingerprints in a protein sequence.</p></div><div><div><a href="http://firedb.bioinfo.cnio.es/">FireDB -- a database of functionally important residues from proteins of known structure</a></div><p>Search for functional annotation of important sites in proteins with known structures.</p></div><div><div><a href="http://bioserv.rpbs.univ-paris-diderot.fr/cgi-bin/Frog2">Frog2 -- a FRee Online druG 3D conformation generator</a></div><p>Produce 3D conformations of small drug compounds.</p></div><div><div><a href="http://www.hgpd.jp/">HGPD -- Human Gene and Protein Database</a></div><p>A database presenting experiment-based results in human proteomics.</p></div><div><div><a href="http://hhsenser.tuebingen.mpg.de/">HHsenser -- exhaustive transitive profile search using HMMx96HMM comparison</a></div><p>Conduct exhaustive intermediate profile searches of a set of homologous protein sequences.</p></div><div><div><a href="http://loschmidt.chemi.muni.cz/hotspotwizard/">HotSpot Wizard -- Substrate Specificity Hot Spot Identification web server</a></div><p>Design protein mutations in site-directed mutagenesis.</p></div><div><div><a href="http://phylogenomics.berkeley.edu/intrepid/">INTREPID -- INformation-theoretic TREe traversal for Protein functional site IDentification</a></div><p>Use for protein functional site identification.</p></div><div><div><a href="http://www.cbs.dtu.dk/">Integrating protein annotation resources through the Distributed Annotation System</a></div><p>Annotate protein using this integrated annotation resource.</p></div><div><div><a href="http://www.ebi.ac.uk/InterProScan/">InterProScan -- protein domains identifier</a></div><p>Identify protein family (and DNA) domains, patterns, motifs, protein families, and functional sites.</p></div><div><div><a href="http://kfc.mitchell-lab.org/">KFC -- Knowledge-based FADE and Contacts</a></div><p>Interactive forecasting of protein interaction hot spots.</p></div><div><div><a href="http://biominer.bime.ntu.edu.tw/magiicpro/">MAGIIC-PRO -- detecting functional signatures by efficient discovery of long patterns in protein sequences</a></div><p>Discover long patterns in protein sequences.</p></div><div><div><a href="http://prodata.swmed.edu/malisam">MALISAM -- Manual ALIgnments for Structurally Analogous Motifs</a></div><p>Database containing pairs of structural analogs and their alignments.</p></div><div><div><a href="http://meme.nbcr.net/">MEME -- discovering and analyzing DNA and protein sequence motifs</a></div><p>Find sequence patterns in DNA and protein sequences.</p></div><div><div><a href="http://www.nii.res.in/modpropep.html">MODPROPEP -- a program for knowledge-based modeling of protein-peptide complexes</a></div><p>A web server for knowledge-based modeling of protein-peptide complexes, specifically peptides in complex with major histocompatibility complex (MHC) proteins and kinases.</p></div><div><div><a href="http://www.bioinfo.tsinghua.edu.cn/~tigerchen/memo.html">MeMo -- a web tool for prediction of protein methylation modifications</a></div><p>Predict protein methylation sites.</p></div><div><div><a href="http://caps.ncbs.res.in/MegaMotifbase/index.html">MegaMotifBase -- a database of structural motifs in protein families and superfamilies</a></div><p>Find structural segments or motifs for protein structures.</p></div><div><div><a href="http://mnm.engr.uconn.edu/MNM/SMSSearchServlet">Minimotif Miner -- a tool for investigating protein function</a></div><p>Find motifs in a protein sequence.</p></div><div><div><a href="http://umber.sbs.man.ac.uk/dbbrowser/motif3d/motif3d.html">Motif3D -- Relating protein sequence motifs to 3D structure</a></div><p>Visualize protein sequence motifs on the 3D protein structures.</p></div><div><div><a href="http://myhits.isb-sib.ch/cgi-bin/motif_scan">MotifScan</a></div><p>Find presence of any known protein motif (Prosite and Pfam) in a protein sequence.</p></div><div><div><a href="http://bioinfo3d.cs.tau.ac.il/MultiBind">MultiBind -- Multiple Alignment of Protein Binding Sites</a></div><p>Recognize spatial chemical binding patterns common to a set of protein structures.</p></div><div><div><a href="http://mendel.imp.univie.ac.at/myristate/SUPLpredictor.htm">NMT -- The MYR Predictor</a></div><p>Analyze proteins for the presence of N-terminal N-myristoylation site.</p></div><div><div><a href="http://www.cbs.dtu.dk/services/NetNGlyc/">NetNGlyc -- N-Glycosylation sites prediction tool</a></div><p>Find the presence of N-Glycosylation sites in human proteins.</p></div><div><div><a href="http://www.cbs.dtu.dk/services/NetOGlyc/">NetOGly 3.1 -- O-glycosylation sites prediction tool</a></div><p>Find the presence of O-GalNAc (mucin type) glycosylation sites in mammalian proteins.</p></div><div><div><a href="http://www.cbs.dtu.dk/services/NetPhos/">NetPhos 2.0 -- Phosphorylation sites predictions</a></div><p>Analyze eukaryotic proteins for the presence of serine, threonine and tyrosine phosphorylation sites.</p></div><div><div><a href="http://www.cbs.dtu.dk/services/NetPhosK/">NetPhosK 1.0 Server -- kinase specific eukaryotic protein phosphorylation sites prediction tool</a></div><p>Find possible kinase specific phosphorylation sites in eukaryotic proteins.</p></div><div><div><a href="http://networkin.info/search.php">NetworKIN -- a resource for exploring cellular phosphorylation networks</a></div><div>&nbsp;</div></div><div><div><a href="http://neuroproteomics.scs.uiuc.edu/neuropred.html">NeuroPred -- a tool to predict cleavage sites in neuropeptide precursors and provide the masses of the resulting peptides</a></div><p>Predict cleavage sites at basic amino acid locations in neuropeptide precursor sequences.</p></div><div><div><a href="http://www.ebi.ac.uk/patentdata/nr/">Non-Redundant Patent Sequences - Patented Sequence Database</a></div><p>Find information about patented nucleotide and protein sequences.</p></div><div><div><a href="http://www.cbs.dtu.dk/databases/OGLYCBASE/">O-GLYCBASE</a></div><p>Search for information about glycoproteins with O-linked and C-linked glycosylation sites.</p></div><div><div><a href="http://www.pandora.cs.huji.ac.il/">PANDORA -- Protein ANnotation Diagram ORiented Analysis</a></div><p>Find information about protein sequence annotations.</p></div><div><div><a href="http://sunserver.cdfd.org.in:8080/protease/PAR_3D/index.html">PAR-3D -- Protein Active site Residue - 3D structural motif</a></div><p>A server to predict protein active site residues.</p></div><div><div><a href="http://wwwmgs.bionet.nsc.ru/mgs/gnw/pdbsite/">PDBSite -- a database of the 3D structure of protein functional sites</a></div><p>Search for structural and functional information on the protein functional sites.</p></div><div><div><a href="http://wwwmgs.bionet.nsc.ru/mgs/systems/fastprot/pdbsitescan.html">PDBSiteScan -- A program for searching for active, binding and posttranslational modification sites in the 3D structures of proteins</a></div><p>Search 3D protein fragments similar in structure to known active, binding and posttranslational modification sites.</p></div><div><div><a href="http://pedant.gsf.de/">PEDANT -- Protein Extraction, Description and ANalysis Tool</a></div><p>Conduct genome wide functional and structural analysis.</p></div><div><div><a href="http://phosida.org/">PHOSIDA -- Phosphorylation site database</a></div><p>Search for phosphorylation data of any protein of interest.</p></div><div><div><a href="http://www.phosphorylation.biochem.vt.edu/">PHOSPHORYLATION SITE DATABASE</a></div><p>Search for information on prokaryotic proteins that undergo serine, threonine, or tyrosine phosphorylation.</p></div><div><div><a href="http://www.jcvi.org/pn-utility/web/smarty_wrapper/about.php">PNU -- Protein Naming Utility</a></div><p>Determine correct names for proteins.</p></div><div><div><a href="http://mbs.cbrc.jp/poodle/poodle-s.html">POODLE-S -- Predicition Of Order and Disorder by machine LEarning</a></div><p>Web application for predicting protein disorder by using physicochemical features and reduced amino acid set of a position-specific scoring matrix.</p></div><div><div><a href="http://gemdock.life.nctu.edu.tw/ppisearch/">PPISearch -- Protein-Protein Interaction Search</a></div><p>Find homologous protein-protein interactions across multiple species.</p></div><div><div><a href="http://www.ebi.ac.uk/ppsearch/">PPSearch</a></div><p>Search your query sequence against PROSITE pattern database for protein motifs.</p></div><div><div><a href="http://pridb.gdcb.iastate.edu/">PRIDB -- Protein-RNA Interface DataBase</a></div><p>Find information about protein-RNA complexes from the Protein Data Bank (PDB).</p></div><div><div><a href="http://umber.sbs.man.ac.uk/dbbrowser/PRINTS/">PRINTS and its automatic supplement, prePRINTS -- A compendium of protein fingerprints</a></div><p>Search for protein fingerprints.</p></div><div><div><a href="http://www.expasy.org/prosite/">PROSITE</a></div><p>Identify protein families and domains for a given protein sequence.</p></div><div><div><a href="http://www.imtech.res.in/raghava/prrdb/">PRRDB -- Pattern Recognition Receptor Database</a></div><p>A comprehensive database of pattern-recognition receptors and their ligands.</p></div><div><div><a href="http://www.arabidopsis.org/cgi-bin/patmatch/nph-patmatch.pl">PatMatch -- a program for finding patterns in peptide and nucleotide sequences</a></div><p>Search for short nucleotide or peptide sequences such as cis-elements in nucleotide sequences or small domains and motifs in protein sequences.</p></div><div><div><a href="http://pepcyber.umn.edu/PPEP/">PepCyber:P~PEP -- a database of human protein protein interactions mediated by phosphoprotein-binding domains</a></div><p>Database specialized in documenting human PPBD-containing proteins and PPBD-mediated interactions.</p></div><div><div><a href="http://us.expasy.org/tools/peptidecutter/">PeptideCutter -- protein cleavage sites prediction tool</a></div><p>Predicts potential protease cleavage sites and sites cleaved by chemicals in a given protein sequence.</p></div><div><div><a href="http://phobius.binf.ku.dk/">Phobius -- A combined transmembrane topology and signal peptide predictor</a></div><p>Predict combined transmembrane topology and signal peptides.</p></div><div><div><a href="http://phospho.elm.eu.org/">Phospho.ELM -- a database of phosphorylation sites</a></div><p>Search for eukaryotic phosphorylation sites.</p></div><div><div><a href="http://www.phospho3d.org/">Phospho3D -- a database of three-dimensional structures of protein phosphorylation sites</a></div><p>Search for 3D structure and functional annotation of phosphorylation sites in proteins.</p></div><div><div><a href="http://www.phosphosite.org/">PhosphoSite -- A bioinformatics resource dedicated to physiological protein phosphorylation.</a></div><p>Search the database of in vivo phosphorylation sites of human and mouse proteins</p></div><div><div><a href="http://pxgrid.med.monash.edu.au/polyq/">PolyQ -- Polyglutamine Database</a></div><p>Find information about polyglutamine (polyQ) repeats.</p></div><div><div><a href="http://www.ebi.ac.uk/pratt/">Pratt Protein motif and pattern discovery</a></div><p>Find the presence of protein motifs and patterns in an amino acid sequence.</p></div><div><div><a href="http://www.predisi.de/">PrediSi -- Prediction of Signal Peptides and their Cleavage Positions</a></div><p>Predict signal peptide sequences and their cleavage positions in bacterial and eukaryotic amino acid sequences.</p></div><div><div><a href="http://www.ebi.ac.uk/thornton-srv/databases/ProFunc/">ProFunc -- a server for predicting protein function from 3D structure</a></div><p>Predict protein functions based on known structures.</p></div><div><div><a href="http://bioinfo41.weizmann.ac.il/promate/promateus.html">ProMateus--an open research approach to protein-binding sites analysis</a></div><p>Predict the location of potential protein-protein binding sites for unbound proteins.</p></div><div><div><a href="http://www.proteus.cs.huji.ac.il/">ProTeus -- identifying signatures in protein termini</a></div><p>Identify short linear signatures in protein termini.</p></div><div><div><a href="http://genius.embnet.dkfz-heidelberg.de/menu/cgi-bin/w2h-open/w2h.open/w2h.startthis?SIMGO=w2h%2ewelcome">ProtSweep -- protein annotation by homology</a></div><p>Analyze and identify newly obtained protein sequences.</p></div><div><div><a href="http://protemot.csbb.ntu.edu.tw/">Protemot -- prediction of protein binding sites with automatically extracted geometrical templates</a></div><p>Predict protein binding sites in a protein sequence based on geometrical analysis of protein tertiary substructures.</p></div><div><div><a href="http://quasimotifinder.tau.ac.il/">QuasiMotiFinder -- protein annotation by searching for evolutionarily conserved motif-like patterns</a></div><p>Search for evolutionarily conserved motif-like patterns in protein sequences.</p></div><div><div><a href="http://bindr.gdcb.iastate.edu/RNABindR">RNABindR -- software for prediction of RNA binding residues in proteins</a></div><p>Web-based server for analyzing and predicting RNA binding sites in proteins.</p></div><div><div><a href="http://caps.ncbs.res.in/scanmot/scanmot.html">SCANMOT -- searching for similar sequences using a simultaneous scan of multiple sequence motifs</a></div><p>Search for similarities between proteins by simultaneous matching of multiple motifs.</p></div><div><div><a href="http://bioinf.fbb.msu.ru/SDPpred/">SDPpred -- A Tool for Prediction of Amino Acid Residues that Determine Differences in Functional Specificity of Homologous Proteins</a></div><p>Predict residues in protein sequences that determine the proteins' functional specificity.</p></div><div><div><a href="http://tamm.mit.edu/SDR/">SDR -- Specificity Determining Residues Database</a></div><p>Predict specificity-determining residues in protein families.</p></div><div><div><a href="http://bioware.ucd.ie/~slimdisc/">SLiMDisc -- Short, Linear Motif Discovery</a></div><p>Find shared motifs in proteins with a common attribute.</p></div><div><div><a href="http://sumosp.biocuckoo.org/">SUMOsp -- a web server for sumoylation site prediction</a></div><p>Conduct in silico sumoylation sites prediction.</p></div><div><div><a href="http://oxytricha.princeton.edu/SWAKK/">SWAKK -- a web server for detecting positive selection in proteins using a sliding window substitution rate analysis</a></div><p>Detect protein sequence section under positive evolution selection.</p></div><div><div><a href="http://www.expasy.org/tools/scanprosite/">ScanProsite</a></div><p>Search for motifs and patterns within protein sequences.</p></div><div><div><a href="http://www.expasy.org/tools/scanprosite/">ScanProsite -- detection of PROSITE signature matches and ProRule-associated functional and structural residues in proteins</a></div><p>Detect patterns, profiles and motifs in a protein sequence.</p></div><div><div><a href="http://scansite.mit.edu/">ScanSite 2.0 -- Proteome-wide prediction of cell signaling interactions using short sequence motifs</a></div><p>Search for motifs within proteins that are likely to be phosphorylated by specific protein kinases or bind to domains such as SH2 domains, 14-3-3 domains or PDZ domains.</p></div><div><div><a href="http://sepresa.bio-x.cn/">SePreSA -- SErver for the PREdiction of populations susceptible to Serious Adverse drug reaction</a></div><p>Find information about populations carrying polymorphisms within protein binding pockets that make them susceptible to serious adverse drug reaction (SADR).</p></div><div><div><a href="http://motif.genome.jp/">Sequence Motif Search</a></div><p>Search the presence of a motif in either amino acid sequence or nucleotide sequence.</p></div><div><div><a href="http://www.csbio.sjtu.edu.cn/bioinf/Signal-3L/">Signal-3L -- A 3-layer approach for predicting signal peptides</a></div><p>Predict signal peptides.</p></div><div><div><a href="http://www.cbs.dtu.dk/services/SignalP/">SignalP -- Machine learning approaches to the prediction of signal peptides, their cleavage sites, and other protein sorting signals</a></div><p>Predict signal peptides and their cleavage sites.</p></div><div><div><a href="http://us.expasy.org/tools/sulfinator/">Sulfinator -- tyrosine sulfation sites prediction tool</a></div><p>Predict the presence of tyrosine sulfation sites in protein sequences</p></div><div><div><a href="http://bioinf-services.charite.de/supersite/">SuperSite -- Ligand Binding Site Database</a></div><p>Look at protein structure from a ligand and binding site perspective.</p></div><div><div><a href="http://www.ch.embnet.org/">Swiss EMBnet node web server</a></div><p>Use a collection of bioinformatics tools at this portal site.</p></div><div><div><a href="http://bioinfo.montp.cnrs.fr/?r=t-reks">T-REKS -- identification of Tandem REpeats in sequences with a K-meanS based algorithm</a></div><p>Find information about tandem repeats in proteins that carry fundamental biological functions and are related to a number of human diseases.</p></div><div><div><a href="http://tmbeta-genome.cbrc.jp/TMFunction/">TMFunction -- The Functional Database of Membrane Proteins</a></div><p>Find information about functional residues in alpha-helical and beta-barrel membrane proteins.</p></div><div><div><a href="http://topdom.enzim.hu/">TOPDOM -- Conservatively Located Domains and Motifs in Transmembrane Proteins</a></div><p>Database of domains and motifs with conservative location in transmembrane proteins.</p></div><div><div><a href="http://motif.stanford.edu/distributions/emotif/">The EMOTIF database</a></div><p>Search for highly conserved and specific protein sequence motifs.</p></div><div><div><a href="http://treedetv2.bioinfo.cnio.es/treedet/index.html">TreeDet -- Predicting Functional Residues in Protein Sequence Alignments</a></div><p>Predict functional sites in protein sequence alignments use different methodologies.</p></div><div><div><a href="http://motif.bmi.ohio-state.edu/ChIPMotifs/">W-ChIPMotifs -- ChIP-based protein Motif discovery web server</a></div><p>Find de novo protein motifs from chromatin immunoprecipitation data.</p></div><div><div><a href="http://feature.stanford.edu/webfeature/">WebFEATURE -- an interactive web tool for identifying and visualizing functional sites on macromolecular structures</a></div><p>Scan query structures for functional sites in both proteins and nucleic acids.</p></div><div><div><a href="http://wwwmgs.bionet.nsc.ru/mgs/programs/panalyst/">WebProAnalyst -- an interactive tool for analysis of quantitative structurex96activity relationships in protein families</a></div><p>Analyze quantitative structure-activity relationship of related protein families.</p></div><div><div><a href="http://motif.stanford.edu/distributions/eblocks/">eBLOCKs -- enumerating conserved protein blocks to achieve maximal sensitivity and specificity</a></div><p>Search for ungapped alignments of highly conserved regions among a protein family or superfamily.</p></div><div><div><a href="http://ef-site.hgc.jp/eF-seek/">eF-seek -- prediction of the functional sites of proteins by searching for similar electrostatic potential and molecular surface shape</a></div><p>Predict the functional sites of proteins.</p></div><div><div><a href="http://firedb.bioinfo.cnio.es/Php/FireStar.php">firestar -- prediction of functionally important residues using structural templates and alignment reliability</a></div><p>An expert system for predicting ligand-binding residues in protein structures.</p></div><div><div><a href="http://caps.ncbs.res.in/imotdb/">iMOTdb -- a comprehensive collection of spatially interacting motifs in proteins</a></div><p>Automatically identify spatially interacting motifs among distantly related proteins sharing similar folds and possessing common ancestral lineage.</p></div>]]></description>
	<dc:creator>Neel</dc:creator>
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