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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27961?</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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36583/eugi-a-novel-resource-for-studying-genomic-islands-to-facilitate-horizontal-gene-transfer-detection-in-eukaryotes</guid>
	<pubDate>Sat, 12 May 2018 07:26:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36583/eugi-a-novel-resource-for-studying-genomic-islands-to-facilitate-horizontal-gene-transfer-detection-in-eukaryotes</link>
	<title><![CDATA[EuGI: a novel resource for studying genomic islands to facilitate horizontal gene transfer detection in eukaryotes]]></title>
	<description><![CDATA[<p><span>SWGIS v2.0 along with the EuGI database, which houses GIs identified in 66 different eukaryotic species, and the EuGI web-resource, provide the first comprehensive resource for studying HGT in eukaryotes.</span></p>
<p>https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-018-4724-8</p><p>Address of the bookmark: <a href="https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-018-4724-8" rel="nofollow">https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-018-4724-8</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</guid>
	<pubDate>Wed, 22 Jun 2016 05:37:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</link>
	<title><![CDATA[DarkHorse]]></title>
	<description><![CDATA[<p><em>DarkHorse</em>&nbsp;is a bioinformatic method for rapid, automated identification and ranking of phylogenetically atypical proteins on a genome-wide basis. It works by selecting potential ortholog matches from a reference database of amino acid sequences, then using these matches to calculate a lineage probability index (LPI) score for each genome protein.</p>
<p>LPI scores are inversely proportional to the phylogenetic distance between database match sequences and the query genome. These scores are useful not only for large-scale<em>de novo</em>&nbsp;predictions of horizontally transferred proteins, but can also serve as an independent quality control test for potential horizontal transfer candidates identified by alternative methods, especially those based on nucleic acid signatures. Candidates having high LPI scores are unlikely to have been horizontally transferred, since they are highly conserved among closely related organisms.</p>
<p>One unique and powerful feature of the DarkHorse HGT Candidate database is the opportunity to explore the phylogenetic background of potential HGT donors as well as recipients. The breadth of the database allows not only query sequences, but also their database match partners to be evaluated for sequence similarity or novelty compared to taxonomically related organisms.</p>
<p><em>DarkHorse</em>&nbsp;is configurable for varying degrees of phylogenetic granularity and protein sequence conservation. Users should consult the&nbsp;<a href="http://darkhorse.ucsd.edu/#references">references</a>&nbsp;cited below for a complete explanation of parameter selection and result interpretation. A brief&nbsp;<a href="http://darkhorse.ucsd.edu/tutorial.html">tutorial</a>&nbsp;page is also available on-line.</p><p>Address of the bookmark: <a href="http://darkhorse.ucsd.edu/download.html" rel="nofollow">http://darkhorse.ucsd.edu/download.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41969/shadowcaster-a-hybrid-approach-for-the-detection-of-horizontal-gene-transfer-events-in-prokaryotes</guid>
	<pubDate>Tue, 14 Jul 2020 06:42:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41969/shadowcaster-a-hybrid-approach-for-the-detection-of-horizontal-gene-transfer-events-in-prokaryotes</link>
	<title><![CDATA[ShadowCaster: a hybrid approach for the detection of horizontal gene transfer events in prokaryotes]]></title>
	<description><![CDATA[<p><span>ShadowCaster implements an evolutionary model to calculate Bayesian likelihoods for each &lsquo;alien genes&rsquo; with an unusual sequence composition according to the host genome background to detect HGT events in prokaryotes.</span></p>
<p><a href="https://www.mdpi.com/2073-4425/11/7/756/htm">https://www.mdpi.com/2073-4425/11/7/756/htm</a></p>
<p><a href="https://shadowcaster.readthedocs.io/en/latest/">https://shadowcaster.readthedocs.io/en/latest/</a></p>
<p><a href="https://github.com/dani2s/ShadowCaster_testData">https://github.com/dani2s/ShadowCaster_testData</a></p><p>Address of the bookmark: <a href="https://github.com/dani2s/ShadowCaster" rel="nofollow">https://github.com/dani2s/ShadowCaster</a></p>]]></description>
	<dc:creator>Jit</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/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/opportunity/view/10262/research-fellow-phd-candidate-in-computational-biology-%E2%80%93-2-positions</guid>
  <pubDate>Fri, 25 Apr 2014 20:19:58 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research fellow (PhD candidate) in computational biology – 2 positions]]></title>
  <description><![CDATA[
<p>At the Department of Informatics two 4-year positions as research fellow are available in the field of computational biology connected to the Computational Biology Unit. The positions are linked to the project “Integrated genomics - linking transcriptional and translational regulation over developmental time” supported by the Bergen Research Foundation</p>

<p>The fate of a cell is ultimately the product of the regulation of its genes. Gene regulation is a coordinated process acting at multiple levels of which transcription and translation are the most prominent. The Valen group is dedicated to the fundamental question of how transcription and translation is integrated to obtain the desired protein abundance. The recent development of high-throughput next generation sequencing techniques to monitor both active translation and transcription has made it possible to study this connection at the genome scale.</p>

<p>This project aims to elucidate the links between regulation of translation and transcription. The applicant will analyze next generation sequencing data and model gene regulation on a genome-wide level to identify the features that affect the translational output of transcripts. The work will be done in close collaboration with experimental scientists who will test the predictions of the computational models.</p>

<p>Additional information on the position can be obtained by contacting Eivind Valen (eivind.valen@ii.uib.no).</p>

<p>The research fellow must take part in the University’s approved PhD program leading to the degree within a time limit of 3 years. Application for admission to the PhD program, including a project plan outline for the training module, will be worked out in collaboration with the research group in question.</p>

<p>In total, the fellowship period is 4 years, 25 % of this will be allocated to teaching and/or administrative duties. The fellowship period may be reduced if the successful applicant has held previous employment as a research fellow or similar.</p>

<p>http://www.jobbnorge.no/en/available-jobs/job/102235/research-fellow-phd-candidate-in-computational-biology-2-positions</p>
]]></description>
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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>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/14899/post-doc-positions-at-the-institute-of-evolution-university-of-haifa-haifa-israel</guid>
  <pubDate>Thu, 04 Sep 2014 03:59:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Post-Doc Positions at the Institute of Evolution, University of Haifa, Haifa, Israel]]></title>
  <description><![CDATA[
<p>We are looking for independent, motivated, diligent, laborious, dedicated Bioinformaticians as post-doctorate fellows for a project aimed at revealing the mechanisms of cancer-resistance and anti-cancer activity of the hypoxia-tolerant subterranean, blind mole-rat, Spalax along its underground evolutionary adaptations. Our project has captured the interest of the scientific community and we have ample financial support for the studies. Generous fellowships ($30K to $40K according to qualifications and performance) are available, immediately, for Post-Docs experts in bioinformatics with a background of good understanding biological questions. That is that can independently handle raw output data of RNA-seq / miR seq/ Genomic, analyze it and can interpret intelligently the relevant biological background. Outstanding candidates for PhD experienced in Bioinformatics will also be considered. Familiarity with cancer research is an advantage. Experience of writing manuscripts for publication and a publication record in relevant journals are expected. English skills both oral and written are required. American, Western-European or Israeli education is a significant benefit. </p>

<p>Our present objectives is to identify and isolate the substances secreted by Spalax cells, resolve with which components they interact that are active only on cancer cells, in order to unravel the biological mechanisms and pathways that evolved in Spalax cell machinery and ultimately lead to the death of cancer-cells. The study could attest to be a breakthrough in cancer research, using the long lived, hypoxia- and cancer-tolerant Spalax as a significant biological resource for biomedical research that hopefully could open new horizons in treatment and prevention of cancer in humans. </p>

<p>Contact: The applications should be submitted, together with extended CV and bibliography, summary of past accomplishments, and contact information of 3 referees, to Prof of Research Aaron Avivi (aaron@research.haifa.ac.il) AND Dr. Imad Shams (imadshams@gmail.com). (http://bit.ly/1lywShk) aaron@research.haifa.ac.il </p>

<p>More at http://evolution.haifa.ac.il/index.php/29-people/personal-websites/77-personal-site-avivi</p>
]]></description>
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