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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38661?offset=60</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43698/mimilook-a-phylogenetic-workflow-for-detection-of-gene-acquisition-in-major-orthologous-groups-of-megavirales</guid>
	<pubDate>Mon, 10 Jan 2022 06:32:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43698/mimilook-a-phylogenetic-workflow-for-detection-of-gene-acquisition-in-major-orthologous-groups-of-megavirales</link>
	<title><![CDATA[MimiLook: A Phylogenetic Workflow for Detection of Gene Acquisition in Major Orthologous Groups of Megavirales]]></title>
	<description><![CDATA[<p><span>This tool detects statistically validated events of gene acquisitions with the help of the T-REX algorithm by comparing individual gene tree with NCBI species tree. In between the steps, the workflow decides about handling paralogs, filtering outputs, identifying Megavirale specific OGs, detection of HGTs, along with retrieval of information about those OGs that are monophyletic with organisms from cellular domains of life.&nbsp;</span></p>
<p>https://www.readcube.com/articles/10.3390%2Fv9040072</p><p>Address of the bookmark: <a href="https://pubmed.ncbi.nlm.nih.gov/28387730/" rel="nofollow">https://pubmed.ncbi.nlm.nih.gov/28387730/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45299/the-gene-detectives-how-a-new-computational-tool-is-helping-us-read-the-history-written-in-our-genes</guid>
	<pubDate>Thu, 10 Sep 2026 21:23:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45299/the-gene-detectives-how-a-new-computational-tool-is-helping-us-read-the-history-written-in-our-genes</link>
	<title><![CDATA[The Gene Detectives: How a New Computational Tool Is Helping Us Read the History Written in Our Genes]]></title>
	<description><![CDATA[<p>Imagine opening an ancient family album with no names, dates, or captions. Some photographs are missing, others have been copied, and a few show people who look almost identical. Your challenge is to discover who is related to whom and reconstruct the family story. In evolutionary biology, scientists face a similar mystery when they study genes. Every genome contains clues about its past, but genes can be duplicated, lost, and changed over millions of years, making their history difficult to trace.</p><p>A recent study published in PLOS Computational Biology introduces REvolutionH-tl 2.0 (https://pypi.org/project/revolutionhtl/), a computational tool designed to help solve this mystery. The software analyzes protein sequences and identifies evolutionary relationships between genes. It can help researchers detect important events such as gene duplication, gene loss, and speciation, allowing them to reconstruct how genes evolved across different organisms.</p><p>What makes the tool especially interesting is its focus on both speed and interpretation. The researchers compared REvolutionH-tl 2.0 with several existing computational tools and reported that it achieved competitive accuracy while requiring less computational time in their tests. The tool also includes visualization features, helping researchers turn complicated genetic data into evolutionary stories that are easier to explore.</p><p>Genes are more than simple sequences of DNA; they are records of life&rsquo;s long history. Each surviving gene carries traces of the changes that shaped it. By bringing together computational analysis and visualization, REvolutionH-tl 2.0 acts like a detective, helping scientists uncover these hidden stories. Ultimately, tools like this can improve our understanding of how genomes evolved and how genes acquired the roles they perform today.</p><p>More at&nbsp;https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013017</p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33651/darkhorse-a-method-for-genome-wide-prediction-of-horizontal-gene-transfer</guid>
	<pubDate>Thu, 22 Jun 2017 07:58:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33651/darkhorse-a-method-for-genome-wide-prediction-of-horizontal-gene-transfer</link>
	<title><![CDATA[DarkHorse: a method for genome-wide prediction of horizontal gene transfer]]></title>
	<description><![CDATA[<p><span>A new approach to rapid, genome-wide identification and ranking of horizontal transfer candidate proteins is presented. The method is quantitative, reproducible, and computationally undemanding. It can be combined with genomic signature and/or phylogenetic tree-building procedures to improve accuracy and efficiency. The method is also useful for retrospective assessments of horizontal transfer prediction reliability, recognizing orthologous sequences that may have been previously overlooked or unavailable. These features are demonstrated in bacterial, archaeal, and eukaryotic examples.</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1852411/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1852411/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</guid>
	<pubDate>Tue, 15 Jan 2019 09:39:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</link>
	<title><![CDATA[GeNeCK (Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks]]></title>
	<description><![CDATA[<p><strong>GeNeCK</strong><span>&nbsp;(Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks based on gene expression data and optional hub gene information.</span></p>
<p><span><span>It efficiently constructs gene networks from expression data. It allows the user to use ten different network construction methods (such as partial correlation-, likelihood-, Bayesian- and mutual information-based methods) and integrates the resulting networks from multiple methods. Hub gene information, if available, can be incorporated to enhance performance.</span></span></p>
<p><span><span><span>GeNeCK is an efficient and easy-to-use web application for gene regulatory network construction. It can be accessed at&nbsp;</span><span><a href="http://lce.biohpc.swmed.edu/geneck" target="_blank"><span>http://lce.biohpc.swmed.edu/geneck</span></a></span></span></span></p><p>Address of the bookmark: <a href="http://lce.biohpc.swmed.edu/geneck/" rel="nofollow">http://lce.biohpc.swmed.edu/geneck/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</guid>
	<pubDate>Thu, 13 Aug 2020 10:06:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</link>
	<title><![CDATA[PyParanoid: a pipeline for rapid identification of homologous gene families in a set of genomes]]></title>
	<description><![CDATA[<p>PyParanoid is a pipeline for rapid identification of homologous gene families in a set of genomes - a central task of any comparative genomics analysis. The "gold standard" for identifying homologs is to use reciprocal best hits (RBHs) which depends on performing a all-vs-all sequence comparison, usually using BLAST, to determine homology. However, these methods are computationally expensive, requiring&nbsp;O(n2)&nbsp;resources to identify RBHs. This is problematic, as the modern deluge of sequencing data means that comparative genomics analyses could be performed on datasets of thousands of strains.</p><p>Address of the bookmark: <a href="https://github.com/ryanmelnyk/PyParanoid" rel="nofollow">https://github.com/ryanmelnyk/PyParanoid</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</guid>
	<pubDate>Sat, 03 Jun 2023 19:19:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</link>
	<title><![CDATA[homologizer: Phylogenetic phasing of gene copies into polyploid subgenomes]]></title>
	<description><![CDATA[<p dir="auto">This tutorial describes the usage of&nbsp;<code>homologizer</code>&nbsp;to phase gene copies into polyploid subgenomes. The tutorial is an abbreviated version of a soon-to-be published paper in Methods in Molecular Biology. Please see that paper for many more details and practical considerations for running&nbsp;<code>homologizer</code>&nbsp;analyses. If you use&nbsp;<code>homologizer</code>, please cite the paper in which we first describe the method:</p>
<ul dir="auto">
<li>Freyman, W.A., Johnson, M.G., and C.J. Rothfels. 2022. Homologizer: phylogenetic phasing of gene copies into polyploid subgenomes.&nbsp;<em>bioRxiv</em>&nbsp;<a href="https://www.biorxiv.org/content/10.1101/2020.10.22.351486v4">2020.10.22.351486v4</a></li>
</ul>
<p dir="auto"><code>homologizer</code>&nbsp;is implemented in&nbsp;<code>RevBayes</code>. Please see&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>&nbsp;to download and install&nbsp;<code>RevBayes</code>. For users without previous&nbsp;<code>RevBayes</code>&nbsp;experience, we recommend the tutorials at&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>.</p><p>Address of the bookmark: <a href="https://github.com/wf8/homologizer" rel="nofollow">https://github.com/wf8/homologizer</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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