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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36398?offset=90</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33789/i-pv-interactive-protein-sequence-visualization</guid>
	<pubDate>Mon, 03 Jul 2017 07:52:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33789/i-pv-interactive-protein-sequence-visualization</link>
	<title><![CDATA[I-PV: Interactive Protein Sequence Visualization]]></title>
	<description><![CDATA[<p><span>I-PV is a interactive data visualization software designed for inspection of protein sequences and mutation information. It is mainly used for Genetics and Bioinformatics. So what exactly makes it standout?</span></p>
<p><span>http://i-pv.org/ipv_rec</span></p><p>Address of the bookmark: <a href="http://i-pv.org/" rel="nofollow">http://i-pv.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44882/fantasia</guid>
	<pubDate>Wed, 20 Aug 2025 02:48:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44882/fantasia</link>
	<title><![CDATA[FANTASIA]]></title>
	<description><![CDATA[<p dir="auto">FANTASIA is an advanced pipeline for the automatic functional annotation of protein sequences using state-of-the-art protein language models. It integrates deep learning embeddings and in-memory similarity searches, retrieving reference vectors from a PostgreSQL database with pgvector, to associate Gene Ontology (GO) terms with proteins.</p>
<p>https://www.nature.com/articles/s42003-025-08651-2</p><p>Address of the bookmark: <a href="https://github.com/CBBIO/FANTASIA" rel="nofollow">https://github.com/CBBIO/FANTASIA</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/5254/mike-ritchie-lab</guid>
  <pubDate>Wed, 02 Oct 2013 15:25:45 -0500</pubDate>
  <link></link>
  <title><![CDATA[Mike Ritchie Lab]]></title>
  <description><![CDATA[
<p>Mike Ritchie Lab primary research focus is the detection of susceptibility genes for common diseases such as cancer, diabetes, hypertension, and cardiovascular disease, among others. The approaches will involve the development and application of new statistical methods with a focus on the detection of gene-gene interactions associated with human disease.</p>

<p>Gene expression and protein expression patterns between normal and non-normal tissues is a growing area of research that may lead to the identification of candidate genes for understanding the etiology of common, complex diseases. </p>

<p>Lab homepage @ http://ritchielab.psu.edu/ritchielab/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26409/ucsc-genome-browser-and-blat-software</guid>
	<pubDate>Thu, 18 Feb 2016 03:18:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26409/ucsc-genome-browser-and-blat-software</link>
	<title><![CDATA[UCSC Genome Browser and Blat software !]]></title>
	<description><![CDATA[<p>This directory contains Genome Browser and Blat application binaries built for standalone <br>command-line use on various supported Linux and UNIX platforms. To determine which set of binaries <br>to download, type "uname -a" on the command line to display your machine type. In most cases the <br>usage statement for the application can be viewed by running the binary with no arguments. <br><br>The UCSC Genome Browser and Blat software are free for academic, nonprofit, and personal use. A <br>license is required for commercial download and installation of these binaries, with the exception <br>of items built from the following source code directories, which are freely available for all uses:<br><br>&nbsp;- kent/src/utils (includes big* tools)<br>&nbsp;- kent/src/lib<br>&nbsp;- kent/src/hg/autoSql<br>&nbsp;- kent/src/hg/autoXml<br><br>For information about commercial licensing of the Genome Browser software, see <br>http://genome.ucsc.edu/license/. The Blat and In-Silico PCR software may be commercially<br>licensed through Kent Informatics (http://www.kentinformatics.com).</p>
<p>More at http://hgdownload.cse.ucsc.edu/admin/exe/</p><p>Address of the bookmark: <a href="http://hgdownload.cse.ucsc.edu/admin/exe/" rel="nofollow">http://hgdownload.cse.ucsc.edu/admin/exe/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27432/gkno</guid>
	<pubDate>Fri, 20 May 2016 18:56:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27432/gkno</link>
	<title><![CDATA[GKNO]]></title>
	<description><![CDATA[<p><span>gkno opens the world of complex bioinformatic analysis to people of all level of computational expertise. This site contains documentation, tutorials and information on all the tools that comprise gkno.</span></p>
<p><span>http://gkno.me/how-to/install.html</span></p>
<p><span>http://gkno.me/software.html</span></p><p>Address of the bookmark: <a href="http://gkno.me/" rel="nofollow">http://gkno.me/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/32713/salzberg-lab</guid>
  <pubDate>Mon, 15 May 2017 05:14:01 -0500</pubDate>
  <link></link>
  <title><![CDATA[Salzberg lab]]></title>
  <description><![CDATA[
<p>We are a computational biology lab that develops novel methods for analysis of DNA and RNA sequences. Our research includes software for aligning and assembling RNA-seq data, whole-genome assembly, and microbiome analysis. We work closely with biomedical scientists to apply these methods to current problems arising in a broad spectrum of biological and medical research areas. We’re also part of the Center for Computational Biology, a group of 20+ faculty members and their labs at Johns Hopkins working on computational, statistical, and mathematical methods that can turn massive genomic data sets into biologically and clinically useful information.</p>

<p>https://salzberg-lab.org/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34470/simngs-and-simlibrary-%E2%80%93-software-for-simulating-next-gen-sequencing-data</guid>
	<pubDate>Tue, 28 Nov 2017 06:49:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34470/simngs-and-simlibrary-%E2%80%93-software-for-simulating-next-gen-sequencing-data</link>
	<title><![CDATA[simNGS and simLibrary – Software for Simulating Next-Gen Sequencing Data]]></title>
	<description><![CDATA[<p>simNGS is software for simulating observations from Illumina sequencing machines using the statistical models behind the AYB base-calling software. By default, observations only incorporate noise due to sequencing and do not incorporate effects from more esoteric sources of noise that may be present in real data ("dust", bubbles, merged clusters, sequence-heterogeneous clusters, etc). Many of these additional sources may optionally applied.</p>
<p>simNGS takes fasta format sequences and a file describing the covariance of noise between bases and cycles observed in an actual run of the machine, randomly generates noisy intensities representing the signals for the sequence at each cycle and calculates likelihoods for all possible base calls.</p><p>Address of the bookmark: <a href="https://www.ebi.ac.uk/goldman-srv/simNGS/" rel="nofollow">https://www.ebi.ac.uk/goldman-srv/simNGS/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41678/gridss-the-genomic-rearrangement-identification-software-suite</guid>
	<pubDate>Sun, 17 May 2020 10:27:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41678/gridss-the-genomic-rearrangement-identification-software-suite</link>
	<title><![CDATA[GRIDSS: the Genomic Rearrangement IDentification Software Suite]]></title>
	<description><![CDATA[<p>GRIDSS is a module software suite containing tools useful for the detection of genomic rearrangements. GRIDSS includes a genome-wide break-end assembler, as well as a structural variation caller for Illumina sequencing data. GRIDSS calls variants based on alignment-guided positional de Bruijn graph genome-wide break-end assembly, split read, and read pair evidence.</p><p>Address of the bookmark: <a href="https://github.com/PapenfussLab/gridss" rel="nofollow">https://github.com/PapenfussLab/gridss</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/33842/awesome-perl-frameworks-libraries-and-software-part-5</guid>
	<pubDate>Fri, 07 Jul 2017 04:12:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/33842/awesome-perl-frameworks-libraries-and-software-part-5</link>
	<title><![CDATA[Awesome perl frameworks, libraries and software - PART 5]]></title>
	<description><![CDATA[<ul>
<li><a href="https://github.com/robelix/sub2srt">robelix/sub2srt</a>&nbsp;- subtitle converter</li>
<li><a href="https://github.com/reyjrar/graphite-scripts">reyjrar/graphite-scripts</a>&nbsp;- A Collections of Scripts for Working with Graphite</li>
<li><a href="https://github.com/regilero/check_nginx_status">regilero/check_nginx_status</a>&nbsp;- Nagios check for nginx status report</li>
<li><a href="https://github.com/omniti-labs/resmon">omniti-labs/resmon</a>&nbsp;- resmon</li>
<li><a href="https://github.com/motemen/App-htmlcat">motemen/App-htmlcat</a>&nbsp;- redirect stdin to web browser</li>
<li><a href="https://github.com/moose/Moo">moose/Moo</a>&nbsp;- Minimalist Object Orientation (with Moose compatibility)</li>
<li><a href="https://github.com/miyagawa/fastpass">miyagawa/fastpass</a>&nbsp;- Tiny, XS free, standalone and preforking FastCGI daemon for PSGI</li>
<li><a href="https://github.com/miyagawa/Filesys-Notify-Simple">miyagawa/Filesys-Notify-Simple</a>&nbsp;- Simple and dumb file system watcher</li>
<li><a href="https://github.com/mhop/fhem-mirror">mhop/fhem-mirror</a>&nbsp;- Branch 'master' is a read-only-mirror of svn://svn.code.sf.net/p/fhem/code which is updated once a day. On branch 'enocean' I am going to add some Enocean-Devices</li>
<li><a href="https://github.com/lopnor/Plack-App-DAV">lopnor/Plack-App-DAV</a>&nbsp;- simple DAV server for Plack</li>
<li><a href="https://github.com/kazuho/url_compress">kazuho/url_compress</a>&nbsp;- a static PPM-based URL compressor / decompressor</li>
<li><a href="https://github.com/jnthn/6model">jnthn/6model</a>&nbsp;- Just a place that I'm keeping some meta-model prototyping; anything that matters will make it to another repo (e.g. nqp-rx one or Rakudo one) at some point.</li>
<li><a href="https://github.com/jasonhancock/nagios-puppetdb">jasonhancock/nagios-puppetdb</a>&nbsp;- Nagios plugins and pnp4nagios templates related to Puppetlab's PuppetDB project.</li>
<li><a href="https://github.com/goccy/p5-Compiler-Parser">goccy/p5-Compiler-Parser</a>&nbsp;- Create Abstract Syntax Tree for Perl5</li>
<li><a href="https://github.com/cgutteridge/Grinder">cgutteridge/Grinder</a>&nbsp;- Create RDF data from spreadsheets or CSV</li>
<li><a href="https://github.com/c9s/Plack-Middleware-OAuth">c9s/Plack-Middleware-OAuth</a>&nbsp;- Plack Middleware for OAuth1 and OAuth2</li>
<li><a href="https://github.com/bzip2-cuda/bzip2-cuda">bzip2-cuda/bzip2-cuda</a>&nbsp;- Parallel implementation of bzip2 using cuda</li>
<li><a href="https://github.com/alanstevens/ChocoPackages">alanstevens/ChocoPackages</a>&nbsp;- Chocolatey Nuget Packages</li>
<li><a href="https://github.com/SoylentNews/slashcode">SoylentNews/slashcode</a>&nbsp;- The slashcode repository for SoylentNews. The initial code base was uploaded as it appeared on Sourceforge as of the last commit in September 2009</li>
<li><a href="https://github.com/Miserlou/XSS-Harvest">Miserlou/XSS-Harvest</a>&nbsp;- XSS Weaponization</li>
</ul>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</guid>
	<pubDate>Wed, 07 Feb 2018 10:44:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</link>
	<title><![CDATA[GenomeTools: The versatile open source genome analysis software]]></title>
	<description><![CDATA[<p>The&nbsp;<em>GenomeTools</em>&nbsp;genome analysis system is a&nbsp;<a href="http://genometools.org/license.html">free</a>&nbsp;collection of bioinformatics&nbsp;<a href="http://genometools.org/tools.html">tools</a>&nbsp;(in the realm of genome informatics) combined into a single binary named&nbsp;<em>gt</em>. It is based on a C library named &ldquo;libgenometools&rdquo; which consists of several modules.</p>
<p>If you are interested in gene prediction, have a look at&nbsp;<a href="http://genomethreader.org/" title="GenomeThreader gene prediction        software"><em>GenomeThreader</em></a>.</p><p>Address of the bookmark: <a href="http://genometools.org/" rel="nofollow">http://genometools.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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