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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/8798?offset=30</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32154/decostar-detection-of-co-evolution</guid>
	<pubDate>Fri, 14 Apr 2017 06:27:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32154/decostar-detection-of-co-evolution</link>
	<title><![CDATA[DeCoSTAR - Detection of Co-evolution]]></title>
	<description><![CDATA[<p><span>DeCoSTAR is a software which aims at reconstructing ancestral gene or genome organizations, in the form of sets of neighborhood relations -adjacencies- between pairs of ancestral genes or gene domains.</span><br><span>Ancestral genes or domains are deduced from reconciled gene trees in a context of birth, speciation, duplication, loss, transfer, which are either given as input or computed with the&nbsp;</span><a href="http://mbb.univ-montp2.fr/MBB/download_sources/16__TERA">ecceTERA package</a><span>, to which DeCoSTAR is integrated. DeCoSTAR constructs parsimonious scenarios of gains and breakages of adjacencies, and contains in particular all the features of previous software DeCo, DeCoLT, ArtDeCo and DeClone. It provides statistical supports on ancestral adjacencies, or the possibility to handle badly assembled genomes.&nbsp;</span><br><span>DeCoSTAR is able to reconstruct the histories of domains inside genes, including gene fusion and fission events, as well as ancestral genome structures for dozens of whole genomes from all kingdoms of life in a few minutes.</span></p><p>Address of the bookmark: <a href="http://pbil.univ-lyon1.fr/software/DeCoSTAR/" rel="nofollow">http://pbil.univ-lyon1.fr/software/DeCoSTAR/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35252/hgt-finder-a-new-tool-for-horizontal-gene-transfer-finding-and-application-to-aspergillus-genomes</guid>
	<pubDate>Wed, 17 Jan 2018 05:03:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35252/hgt-finder-a-new-tool-for-horizontal-gene-transfer-finding-and-application-to-aspergillus-genomes</link>
	<title><![CDATA[HGT-Finder: A New Tool for Horizontal Gene Transfer Finding and Application to Aspergillus genomes]]></title>
	<description><![CDATA[<p><span>HGT-Finder: </span></p>
<p><span>(i) can be used for HGT detection in both prokaryotes and eukaryotes, </span></p>
<p><span>(ii) can report a statistical&nbsp;</span><em>P</em><span>&nbsp;value for each gene to indicate how likely it is to be horizontally transferred, and </span></p>
<p><span>(iii) is fully automated (requires minimal human intervention), as well as very easy to install and run.&nbsp;</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626719/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626719/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37954/biogps-spotlight-on-the-gene-expression-atlas</guid>
	<pubDate>Thu, 18 Oct 2018 12:15:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37954/biogps-spotlight-on-the-gene-expression-atlas</link>
	<title><![CDATA[BioGPS: Spotlight on the Gene Expression Atlas]]></title>
	<description><![CDATA[<p>BioGPS opened 2016 with a publication in Nucleic Acids Research, right after the New Year holiday. Throughout the year, new designs for the site were being created, reviewed, adjusted, reviewed, adjusted, and more review/adjustments in anticipation of a site redesign for 2017. A Plugin registration Blitz was held in March and April; followed by a Plugin Review Blitz in May. The BioGPS spotlight series was also restarted, with spotlights on BGEE, Intermine, and other Intermine-related plugins.</p>
<p>There were ~910,000 requests made to BioGPS in 2016. Requests to BioGPS peaked in March and at the lowest in December.</p><p>Address of the bookmark: <a href="http://biogps.org/" rel="nofollow">http://biogps.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44770/nvidia-and-arc-institute-unveil-evo-2-a-breakthrough-ai-for-dna-design</guid>
	<pubDate>Fri, 21 Feb 2025 10:39:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44770/nvidia-and-arc-institute-unveil-evo-2-a-breakthrough-ai-for-dna-design</link>
	<title><![CDATA[NVIDIA and Arc Institute Unveil Evo 2: A Breakthrough AI for DNA Design]]></title>
	<description><![CDATA[<p>NVIDIA and the Arc Institute have introduced <strong style="font-size: 12.8px;">Evo 2</strong>, a groundbreaking AI model designed to <strong style="font-size: 12.8px;">understand, predict, and generate DNA sequences</strong>. This marks a major advancement in computational biology, offering scientists an unprecedented tool to decode the genetic blueprint of life and even design entirely new biological systems.</p><h3><strong>The Power of Evo 2: AI Meets DNA</strong></h3><p>Evo 2 is <strong>the largest AI model for biology ever created</strong>, trained on an astonishing <strong>9.3 trillion DNA "letters"</strong> (nucleotides) carefully selected from genomes spanning the entire tree of life. This massive dataset ensures that Evo 2 can recognize patterns and relationships in genetic sequences at an unparalleled scale.</p><p>For the first time, scientists can <strong>design DNA with AI</strong>, moving beyond simple sequence analysis to active DNA generation. Evo 2 enables researchers to <strong>predict, modify, and even create entire genetic sequences</strong>, opening new possibilities in medicine, agriculture, and synthetic biology.</p><h3><strong>Decoding the Dark Genome</strong></h3><p>One of the biggest challenges in genetics is understanding the <strong>non-coding regions</strong> of DNA&mdash;vast stretches of the genome that do not code for proteins but play crucial roles in regulating gene expression. These regions control when and how genes are activated, influencing everything from development to disease.</p><p>Evo 2 is designed to <strong>decode these non-coding elements</strong>, helping researchers uncover their functions and use this knowledge to develop gene-based therapies, synthetic life forms, and precision agriculture solutions.</p><h3><strong>From Reading DNA to Writing It</strong></h3><p>To put Evo 2&rsquo;s impact into perspective:</p><ul>
<li><strong>Previous AI models could "read" DNA</strong> like a book, analyzing genetic sequences and identifying patterns.</li>
<li><strong>Evo 2 can "write" entirely new DNA</strong>, designing functional genes, chromosomes, and even full genomes from scratch.</li>
</ul><p>This means scientists can now <strong>engineer biological systems with AI</strong>, designing new proteins, metabolic pathways, and genetic circuits to address real-world challenges.</p><h3><strong>A Step Toward Generative Biology</strong></h3><p>The Arc Institute describes Evo 2 as a major step toward <strong>"generative biology"</strong>&mdash;a revolutionary approach where AI is used to create <strong>novel biological structures</strong> rather than just analyzing existing ones. This could lead to breakthroughs such as:</p><ul>
<li><strong>New medicines</strong>: AI-generated enzymes and proteins tailored for targeted therapies.</li>
<li><strong>Disease-resistant crops</strong>: Genetically optimized plants for higher yield and climate resilience.</li>
<li><strong>Synthetic organisms</strong>: Custom-designed microbes for bioremediation, biofuel production, and industrial applications.</li>
</ul><h3><strong>An Open-Source Revolution</strong></h3><p>Unlike many proprietary AI models, <strong>Evo 2 is open source</strong>, making its capabilities accessible to researchers worldwide. This democratization of AI-driven biology means that scientists from different disciplines can <strong>collaborate, experiment, and innovate</strong>, accelerating discoveries in genetic engineering and synthetic biology.</p><p>With Evo 2, the boundaries of what&rsquo;s possible in <strong>DNA design, genetic engineering, and biological innovation</strong> are being redrawn. The future of life sciences is no longer just about understanding life&rsquo;s code&mdash;it&rsquo;s about writing it.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/35802/bioinformatics-tools-to-detect-horizontal-gene-transfer-hgt-in-genomes</guid>
	<pubDate>Fri, 02 Mar 2018 04:56:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/35802/bioinformatics-tools-to-detect-horizontal-gene-transfer-hgt-in-genomes</link>
	<title><![CDATA[Bioinformatics tools to detect horizontal gene transfer (HGT) in genomes]]></title>
	<description><![CDATA[<p>Horizontal gene transfer (HGT), the &ldquo;non-sexual movement of genetic material between two organisms&rdquo; , is relatively common in prokaryotes&nbsp;and single-celled eukaryotes, but a number of factors combine to make it far rarer in multicellular eukaryotes. In order for a eukaryotic species to gain a gene by HGT, foreign DNA must enter the host nucleus, integrate into the genome, and in more complex organisms it must enter the sequestered germline in order to be transmitted to offspring. Once there, it must not experience strong negative selection, despite potential for genetic incompatibility with the host genome and mismatch between the niche of the donor and the host. Over the longer term, foreign DNA may become &ldquo;domesticated&rdquo; in the recipient genome and provide novel function.</p><p>Following are the popular tool to detect HGT in genomes:</p><p><a href="http://www.trex.uqam.ca/index.php?action=hgt&amp;project=trex">T-REX</a>&nbsp;/&nbsp;<a href="http://www.trex.uqam.ca/download/hgt-detection_3.22.zip">3.22</a></p><p>HGT detection /&nbsp;download &amp; compile</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/20525630">20525630</a></p><p>&nbsp;</p><p><a href="http://compbio.engr.uconn.edu/software/RANGER-DTL/">RANGER-DTL</a>&nbsp;/&nbsp;<a href="http://compbio.engr.uconn.edu/software/RANGER-DTL/Linux.zip">2.0</a></p><p>HGT detection /&nbsp;download binary</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/22689773">22689773</a></p><p>&nbsp;</p><p><a href="https://bioinfocs.rice.edu/phylonet">PhyloNet</a>&nbsp;/&nbsp;<a href="https://bioinfocs.rice.edu/sites/g/files/bxs266/f/kcfinder/files/PhyloNet_3.6.1.jar">3.6.1</a></p><p>HGT detection /&nbsp;download binary</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/18662388">18662388</a></p><p>&nbsp;</p><p><a href="https://www.cs.hmc.edu/~hadas/jane/index.html">Jane</a>&nbsp;/&nbsp;<a href="https://www.cs.hmc.edu/~hadas/jane/form.html">4.01</a></p><p>HGT detection /&nbsp;download binary (!license!)</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/20181081">20181081</a></p><p>&nbsp;</p><p><a href="http://www.tree-puzzle.de/">TREE-PUZZLE</a>&nbsp;/&nbsp;<a href="http://www.tree-puzzle.de/tree-puzzle-5.3.rc16-linux.tar.gz">5.3.rc16</a></p><p>HGT detection /&nbsp;download &amp; compile</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/11934758">11934758</a></p><p>&nbsp;</p><p><a href="http://www.sigmath.es.osaka-u.ac.jp/shimo-lab/prog/consel/">CONSEL</a>&nbsp;/&nbsp;<a href="http://www.sigmath.es.osaka-u.ac.jp/shimo-lab/prog/consel/pub/cnsls020.tgz">0.20</a></p><p>HGT detection /&nbsp;download</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/11751242">11751242</a></p><p>&nbsp;</p><p><a href="http://darkhorse.ucsd.edu/">DarkHorse</a>&nbsp;/&nbsp;<a href="http://darkhorse.ucsd.edu/DarkHorse-1.5_rev170.tar.gz">1.5 rev170</a></p><p>HGT detection /&nbsp;download &amp; install</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/17274820">17274820</a></p><p>&nbsp;</p><p><a href="https://github.com/DittmarLab/HGTector">HGTector</a>&nbsp;/&nbsp;<a href="https://github.com/DittmarLab/HGTector/archive/wgshgt.zip">0.2.1</a></p><p>HGT detection /&nbsp;git clone</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/25159222">25159222</a></p><p>&nbsp;</p><p><a href="http://www5.esu.edu/cpsc/bioinfo/software/EGID/">EGID</a>&nbsp;/&nbsp;<a href="http://www5.esu.edu/cpsc/bioinfo/software/EGID/EGID_1.0.tar.gz">1.0</a></p><p>HGT detection /&nbsp;download</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/22355228">22355228</a></p><p>&nbsp;</p><p><a href="http://exon.gatech.edu/GeneMark/">GeneMarkS</a>&nbsp;/&nbsp;<a href="http://exon.gatech.edu/GeneMark/license_download.cgi">4.30</a></p><p>HGT detection / download binary (!license!)</p><p><a href="https://www.ncbi.nlm.nih.gov/pubmed/9461475">9461475</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</guid>
	<pubDate>Fri, 14 Dec 2018 04:10:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</link>
	<title><![CDATA[EGAD: Ultra-fast functional analysis of gene networks]]></title>
	<description><![CDATA[<p><span>With the EGAD (Extending &lsquo;Guilt-by-Association&rsquo; by Degree) package, we present a series of highly efficient tools to calculate functional properties in networks based on the guilt-by-association principle. These allow rapid controlled comparisons and analyses. Two of the core features are: a function prediction algorithm which is fully vectorized (neighbor_voting), allowing network characterization across even thousands of functional groups to be accomplished in minutes in cross-validation and an analytic determination of the optimal prior to guess candidates genes across multiple functional sets (calculate_multifunc, auc_multifunc).</span></p><p>Address of the bookmark: <a href="https://github.com/sarbal/EGAD" rel="nofollow">https://github.com/sarbal/EGAD</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41814/gggenes-a-ggplot2-extension-for-drawing-gene-arrow-maps</guid>
	<pubDate>Tue, 02 Jun 2020 11:43:34 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41814/gggenes-a-ggplot2-extension-for-drawing-gene-arrow-maps</link>
	<title><![CDATA[gggenes: a ggplot2 extension for drawing gene arrow maps.]]></title>
	<description><![CDATA[<p>Install the stable version of gggenes from CRAN:</p>
<p><code><a href="https://www.rdocumentation.org/packages/utils/topics/install.packages">install.packages("gggenes")</a></code></p>
<p>If you want the development version, install it from GitHub:</p>
<p><code><a href="https://www.rdocumentation.org/packages/devtools/topics/reexports">devtools::install_github("wilkox/gggenes")</a></code></p>
<p>More at&nbsp;<a href="https://github.com/wilkox/gggenes">https://github.com/wilkox/gggenes</a></p><p>Address of the bookmark: <a href="http://wilkox.org/gggenes" rel="nofollow">http://wilkox.org/gggenes</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43867/genomeqc-a-quality-assessment-tool-for-genome-assemblies-and-gene-structure-annotations</guid>
	<pubDate>Thu, 19 May 2022 04:29:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43867/genomeqc-a-quality-assessment-tool-for-genome-assemblies-and-gene-structure-annotations</link>
	<title><![CDATA[GenomeQC: a quality assessment tool for genome assemblies and gene structure annotations]]></title>
	<description><![CDATA[<p><span>The GenomeQC web application is implemented in R/Shiny version 1.5.9 and Python 3.6 and is freely available at&nbsp;</span><a href="https://genomeqc.maizegdb.org/">https://genomeqc.maizegdb.org/</a><span>&nbsp;under the GPL license. All source code and a containerized version of the GenomeQC pipeline is available in the GitHub repository&nbsp;</span><a href="https://github.com/HuffordLab/GenomeQC">https://github.com/HuffordLab/GenomeQC</a><span>.</span></p>
<p>https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-6568-2</p><p>Address of the bookmark: <a href="https://github.com/HuffordLab/GenomeQC" rel="nofollow">https://github.com/HuffordLab/GenomeQC</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/1178/r-package-for-visualising-go-enrichment</guid>
	<pubDate>Mon, 22 Jul 2013 12:25:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/1178/r-package-for-visualising-go-enrichment</link>
	<title><![CDATA[R package for visualising GO enrichment]]></title>
	<description><![CDATA[<p>An R package that visualizes the GO enrichment results as word clouds and arranges them together with figures of experimental data. This allows us to draw informative summary plots for analyses such as differential expression or clustering, where for each gene list we display its behaviour in the experiment alongside with its GO annotations.</p><p>Links @ http://raivokolde.github.io/GOsummaries/</p><p>Lab @ http://biit.cs.ut.ee/about/main</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27850/clusterprofiler</guid>
	<pubDate>Thu, 16 Jun 2016 18:57:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27850/clusterprofiler</link>
	<title><![CDATA[clusterProfiler]]></title>
	<description><![CDATA[<p>statistical analysis and visulization of functional profiles for genes and gene clusters<br><br>Bioconductor version: Release (3.3)<br><br>This package implements methods to analyze and visualize functional profiles (GO and KEGG) of gene and gene clusters.<br><br>Author: Guangchuang Yu &lt;guangchuangyu at gmail.com&gt; with contributions from Li-Gen Wang and Giovanni Dall'Olio.<br><br>Maintainer: Guangchuang Yu &lt;guangchuangyu at gmail.com&gt;<br><br>Citation (from within R, enter citation("clusterProfiler")):<br><br>Yu G, Wang L, Han Y and He Q (2012). &ldquo;clusterProfiler: an R package for comparing biological themes among gene clusters.&rdquo; OMICS: A Journal of Integrative Biology, 16(5), pp. 284-287.<br>Installation<br><br>To install this package, start R and enter:<br><br>## try http:// if https:// URLs are not supported<br>source("https://bioconductor.org/biocLite.R")<br>biocLite("clusterProfiler")</p>
<p>https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html</p><p>Address of the bookmark: <a href="https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html" rel="nofollow">https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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