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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/43804?offset=60</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35106/alien-hunter-prediction-of-putative-horizontal-gene-transfer-hgt-events</guid>
	<pubDate>Sun, 07 Jan 2018 19:11:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35106/alien-hunter-prediction-of-putative-horizontal-gene-transfer-hgt-events</link>
	<title><![CDATA[Alien_Hunter : prediction of putative Horizontal Gene Transfer (HGT) events]]></title>
	<description><![CDATA[<p>Alien_hunter is an application for the prediction of putative Horizontal Gene Transfer (HGT) events with the implementation of Interpolated Variable Order Motifs (IVOMs).</p>
<p>An IVOM approach exploits compositional biases using variable order motif distributions and captures more reliably the local composition of a sequence compared to fixed-order methods. Optionally the predictions can be parsed into a 2-state 2nd order Hidden Markov Model (HMM), in a change-point detection framework, to optimize the localization of the boundaries of the predicted regions. The predictions (embl format) can be automatically loaded into the freely available Artemis genome viewer.</p><p>Address of the bookmark: <a href="http://www.sanger.ac.uk/science/tools/alien-hunter" rel="nofollow">http://www.sanger.ac.uk/science/tools/alien-hunter</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37827/genomethreader-gene-prediction-software</guid>
	<pubDate>Wed, 03 Oct 2018 15:34:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37827/genomethreader-gene-prediction-software</link>
	<title><![CDATA[GenomeThreader: Gene Prediction Software]]></title>
	<description><![CDATA[<p><em>GenomeThreader</em><span>&nbsp;is a software tool to compute gene structure predictions. The gene structure predictions are calculated using a similarity-based approach where additional cDNA/EST and/or protein sequences are used to predict gene structures via spliced alignments.&nbsp;</span><em>GenomeThreader</em><span>&nbsp;was motivated by disabling limitations in&nbsp;</span><a href="http://bioinformatics.iastate.edu/cgi-bin/gs.cgi"><em>GeneSeqer</em></a><span>, a popular gene prediction program which is widely used for plant genome annotation.</span></p><p>Address of the bookmark: <a href="http://genomethreader.org/" rel="nofollow">http://genomethreader.org/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45306/the-genes-that-travel-together-a-genomic-detective-story</guid>
	<pubDate>Fri, 11 Sep 2026 13:00:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45306/the-genes-that-travel-together-a-genomic-detective-story</link>
	<title><![CDATA[The Genes That Travel Together: A Genomic Detective Story]]></title>
	<description><![CDATA[<p>Imagine looking through thousands of microbial genomes and discovering two genes that repeatedly appear together. The obvious conclusion is that they must somehow be connected&mdash;that perhaps they work together, participate in the same pathway, or depend on each other. But evolution has a way of leaving misleading clues. What if these two genes are found together simply because they were inherited from the same ancient ancestor? In that case, their apparent association may have little to do with their biological function; it may simply be a reflection of shared evolutionary history. This is the intriguing problem addressed by CORGIAS (https://github.com/ynishimuraLv/corgias), a computational framework developed to distinguish genuine gene associations from correlations created by common ancestry.</p><p>Instead of asking only whether two genes occur together across genomes, CORGIAS asks a deeper question: did these genes actually evolve together, repeatedly gaining or losing their presence in concert, or are they merely travelling together because of their inherited history? The framework introduces two complementary approaches, Ancestral State Adjustment (ASA) and the Simultaneous EVolution test (SEV), which incorporate evolutionary information into the search for gene associations. This distinction becomes increasingly important as genome sequencing continues to uncover enormous numbers of microbial genomes, many from organisms that have never been cultured and whose genes remain functionally mysterious. In this growing genomic landscape, simply finding a gene is no longer enough&mdash;we need clues about what that gene might be doing. CORGIAS approaches this problem almost like a genomic detective: rather than treating every association as evidence, it reconstructs the evolutionary story behind the association and asks whether the evidence survives that history. By doing so, it offers a way to separate coincidence from biological connection and potentially uncover functional relationships hidden within the vast microbial genomic landscape. The broader message is beautifully simple: genes do not evolve in isolation, and understanding what they do may require us to look beyond where they are today and reconstruct how they arrived there. Sometimes, the most important clue in a genome is not the gene itself, but the evolutionary journey it has taken.</p><p>More at&nbsp;https://academic.oup.com/nargab/article/7/4/lqaf182/8377910?</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/38443/genoplotr-plot-gene-and-genome-maps-project</guid>
	<pubDate>Wed, 12 Dec 2018 08:33:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38443/genoplotr-plot-gene-and-genome-maps-project</link>
	<title><![CDATA[genoPlotR - plot gene and genome maps project!]]></title>
	<description><![CDATA[<p>genoPlotR is a R package to produce reproducible, publication-grade graphics of gene and genome maps. It allows the user to read from usual format such as protein table files and blast results, as well as home-made tabular files.</p>
<h3>Features</h3>
<ul>
<li>Linear representation of several segments of DNA</li>
<li>Comparisons represented by areas between the segments (like Artemis, for example)</li>
<li>Reads from common formats: Genbank, EMBL, blast, Mauve, and from user-generated tab files</li>
<li>Plot several subsegments of the same segment on the same line, separated by a //</li>
<li>Automatic or manual placement of the segments on the plot</li>
<li>Add annotations to all the lines</li>
<li>Create smart, automatic annotations for genomes, based on gene names</li>
<li>Add a user-generated tree</li>
<li>Add a global scale or a scale to each line</li>
<li>Use user-defined graphical functions to represent genes</li>
<li></li>
</ul><p>Address of the bookmark: <a href="http://genoplotr.r-forge.r-project.org/" rel="nofollow">http://genoplotr.r-forge.r-project.org/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38752/hgtector-an-automated-method-facilitating-genome-wide-discovery-of-putative-horizontal-gene-transfers</guid>
	<pubDate>Mon, 21 Jan 2019 06:50:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38752/hgtector-an-automated-method-facilitating-genome-wide-discovery-of-putative-horizontal-gene-transfers</link>
	<title><![CDATA[HGTector: an automated method facilitating genome-wide discovery of putative horizontal gene transfers]]></title>
	<description><![CDATA[<p>A computational pipeline for genome-wide detection of putative horizontal gene transfer (HGT) events based on sequence homology search hit distribution statistics</p>
<p>Authors: Qiyun Zhu (<a href="mailto:qiyunzhu@gmail.com">qiyunzhu@gmail.com</a>), Katharina Dittmar (<a href="mailto:katharinad@gmail.com">katharinad@gmail.com</a>)</p>
<p>Affiliation: Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, USA</p>
<p>Zhu Q, Kosoy M, Dittmar K. HGTector: an automated method facilitating genome-wide discovery of putative horizontal gene transfers.&nbsp;<em style="font-size: 12.8px;">BMC Genomics</em>. 2014. 15:717.</p>
<p>Usage: Simply execute&nbsp;<span style="font-size: 12.8px;">perl HGTector.pl</span>, or, open&nbsp;<span style="font-size: 12.8px;">GUI.html</span>&nbsp;in a web browser to see a step-by-step wizard.</p>
<p>Download&nbsp;<a href="https://github.com/DittmarLab/HGTector/archive/0.2.2.zip">HGTector 0.2.2</a>.</p><p>Address of the bookmark: <a href="https://github.com/DittmarLab/HGTector" rel="nofollow">https://github.com/DittmarLab/HGTector</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42362/magic-a-tool-for-predicting-transcription-factors-and-cofactors-driving-gene-sets-using-encode-data</guid>
	<pubDate>Thu, 26 Nov 2020 11:05:04 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42362/magic-a-tool-for-predicting-transcription-factors-and-cofactors-driving-gene-sets-using-encode-data</link>
	<title><![CDATA[MAGIC: A tool for predicting transcription factors and cofactors driving gene sets using ENCODE data]]></title>
	<description><![CDATA[<p><span>The algorithm presented herein,&nbsp;</span><strong>M</strong><span>ining&nbsp;</span><strong>A</strong><span>lgorithm for&nbsp;</span><strong>G</strong><span>enet</span><strong>I</strong><span>c&nbsp;</span><strong>C</strong><span>ontrollers (MAGIC), uses ENCODE ChIP-seq data to look for statistical enrichment of TFs and cofactors in gene bodies and flanking regions in gene lists without an&nbsp;</span><em>a priori</em><span>&nbsp;binary classification of genes as targets or non-targets. When compared to other TF mining resources, MAGIC displayed favourable performance in predicting TFs and cofactors that drive gene changes in 4 settings: </span></p>
<p><span>1) A cell line expressing or lacking single TF, </span></p>
<p><span>2) Breast tumors divided along PAM50 designations </span></p>
<p><span>3) Whole brain samples from WT mice or mice lacking a single TF in a particular neuronal subtype </span></p>
<p><span>4) Single cell RNAseq analysis of neurons divided by Immediate Early Gene expression levels. </span></p>
<p><span>In summary, MAGIC is a standalone application that produces meaningful predictions of TFs and cofactors in transcriptomic experiments.</span></p>
<p><span>More at&nbsp;https://uwmadison.app.box.com/s/8j90e5h2rjrsz3bacaxnq8kor2o64vyg</span></p><p>Address of the bookmark: <a href="https://github.com/asroopra/MAGIC" rel="nofollow">https://github.com/asroopra/MAGIC</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44476/omark-software-for-proteome-protein-coding-gene-repertoire-quality-assessment</guid>
	<pubDate>Wed, 21 Feb 2024 15:01:20 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44476/omark-software-for-proteome-protein-coding-gene-repertoire-quality-assessment</link>
	<title><![CDATA[OMArk: software for proteome (protein-coding gene repertoire) quality assessment]]></title>
	<description><![CDATA[<p><span>OMArk is a software for proteome (protein-coding gene repertoire) quality assessment. It provides measures of proteome completeness, characterizes the consistency of all protein coding genes with regard to their homologs, and identifies the presence of contamination from other species. OMArk relies on the OMA orthology database, from which it exploits orthology relationships, and on the OMAmer software for fast placement of all proteins into gene families.</span></p><p>Address of the bookmark: <a href="https://github.com/DessimozLab/OMArk" rel="nofollow">https://github.com/DessimozLab/OMArk</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33720/deschrambler</guid>
	<pubDate>Thu, 29 Jun 2017 11:54:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33720/deschrambler</link>
	<title><![CDATA[DESCHRAMBLER]]></title>
	<description><![CDATA[<p>DESCHRAMBLER is shown to produce highly accurate reconstructions using data simulation and by benchmarking it against other reconstruction tools</p>
<p>You can find the detail of reconstructed data at http://bioinfo.konkuk.ac.kr/DESCHRAMBLER/</p><p>Address of the bookmark: <a href="https://github.com/jkimlab/DESCHRAMBLER" rel="nofollow">https://github.com/jkimlab/DESCHRAMBLER</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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