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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/34569?offset=490</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40505/decostar-reconstructing-the-ancestral-organization-of-genes-or-genomes-using-reconciled-phylogenies</guid>
	<pubDate>Fri, 03 Jan 2020 13:28:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40505/decostar-reconstructing-the-ancestral-organization-of-genes-or-genomes-using-reconciled-phylogenies</link>
	<title><![CDATA[DeCoSTAR: Reconstructing the Ancestral Organization of Genes or Genomes Using Reconciled Phylogenies]]></title>
	<description><![CDATA[<p>DeCoSTAR computes adjacency evolutionary scenarios using a scoring scheme based on a weighted sum of adjacency gains and breakages. Solutions, both optimal and near-optimal, are sampled according to the Boltzmann&ndash;Gibbs distribution centered around parsimonious solutions, and statistical supports on ancestral and extant adjacencies are provided. DeCoSTAR supports the features of previously contributed tools that reconstruct ancestral adjacencies, namely DeCo, DeCoLT, ART-DeCo, and DeClone. In a few minutes, DeCoSTAR can reconstruct the evolutionary history of domains inside genes, of gene fusion and fission events, or of gene order along chromosomes, for large data sets including dozens of whole genomes from all kingdoms of life.</p><p>Address of the bookmark: <a href="https://github.com/YoannAnselmetti/DeCoSTAR_pipeline" rel="nofollow">https://github.com/YoannAnselmetti/DeCoSTAR_pipeline</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35418/karyoploter-plot-whole-genomes-with-arbitrary-data</guid>
	<pubDate>Fri, 02 Feb 2018 03:24:28 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35418/karyoploter-plot-whole-genomes-with-arbitrary-data</link>
	<title><![CDATA[karyoploteR: plot whole genomes with arbitrary data]]></title>
	<description><![CDATA[<p><span><a href="http://bioconductor.org/packages/karyoploteR">karyoploteR</a></span><span>&nbsp;is an R package to create karyoplots, that is, representations of whole genomes with arbitrary data plotted on them. It is inspired by the R base graphics system and does not depend on other graphics packages. The aim of karyoploteR is to offer the user an easy way to plot data along the genome to get broad genome-wide view to facilitate the identification of genome wide relations and distributions.</span></p><p>Address of the bookmark: <a href="https://bernatgel.github.io/karyoploter_tutorial/" rel="nofollow">https://bernatgel.github.io/karyoploter_tutorial/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</guid>
	<pubDate>Wed, 27 Dec 2017 00:04:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</link>
	<title><![CDATA[Recovery of complete genomes from metagenomes]]></title>
	<description><![CDATA[<p>This project contains scripts and tutorials on how to assemble individual microbial genomes from metagenomes, as described in:</p>
<p><strong>Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes</strong></p>
<p><a href="http://personprofil.aau.dk/120257">Mads Albertsen</a>,&nbsp;<a href="http://ecogenomic.org/users/phil-hugenholtz">Philip Hugenholtz</a>,&nbsp;<a href="http://ecogenomic.org/users/adam-skarshewski">Adam Skarshewski</a>,&nbsp;<a href="http://www.ecogenomic.org/users/gene-tyson">Gene W. Tyson</a>,&nbsp;<a href="http://personprofil.aau.dk/103057">K&aring;re L. Nielsen</a>&nbsp;and&nbsp;<a href="http://personprofil.aau.dk/105842">Per .H. Nielsen</a></p>
<p>Nature Biotechnology 2013, doi:&nbsp;<a href="http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.2579.html">10.1038/nbt.2579</a></p><p>Address of the bookmark: <a href="http://madsalbertsen.github.io/multi-metagenome/" rel="nofollow">http://madsalbertsen.github.io/multi-metagenome/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</guid>
	<pubDate>Mon, 14 May 2018 04:02:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</link>
	<title><![CDATA[Digest: In silico restriction digest of complete genomes]]></title>
	<description><![CDATA[<p><span>This tool allows to retrieve number of cleavages yielded by commercially available endonucleases in up-to-date sequenced prokaryotic genomes. When the number of fragments is bellow 50, Pulse Field gel Electrophoresis (PFGE) is simulated.</span></p>
<p>A tool for restriction digest of&nbsp;<a href="http://insilico.ehu.eus/restriction/long_seq/">long</a>user's sequences is available.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://insilico.ehu.es/digest/" rel="nofollow">http://insilico.ehu.es/digest/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</guid>
	<pubDate>Wed, 22 Aug 2018 03:21:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</link>
	<title><![CDATA[GTDB-Tk: A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes.]]></title>
	<description><![CDATA[<p>GTDB-Tk is a software toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. It is computationally efficient and designed to work with recent advances that allow hundreds or thousands of metagenome-assembled genomes (MAGs) to be obtained directly from environmental samples. It can also be applied to isolate and single-cell genomes. The GTDB-Tk is open source and released under the GNU General Public License (Version 3).</p>
<p>GTDB-Tk is&nbsp;<span>under active development and validation</span>. Please independently confirm the GTDB-Tk predictions by manually inspecting the tree and bringing any discrepencies to our attention. Notifications about GTDB-Tk releases will be available through the ACE Twitter account (<a href="https://twitter.com/ace_uq">https://twitter.com/ace_uq</a>).</p><p>Address of the bookmark: <a href="https://github.com/Ecogenomics/GTDBTk" rel="nofollow">https://github.com/Ecogenomics/GTDBTk</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39856/tritex-sequence-assembly-pipeline-for-triticeae-genomes</guid>
	<pubDate>Tue, 20 Aug 2019 09:47:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39856/tritex-sequence-assembly-pipeline-for-triticeae-genomes</link>
	<title><![CDATA[TRITEX sequence assembly pipeline for Triticeae genomes]]></title>
	<description><![CDATA[<div>
<p>The pipeline is open-source and hosted in a public Bitbucket&nbsp;<a href="https://bitbucket.org/tritexassembly/tritexassembly.bitbucket.io/src/master/">repository</a>.</p>
</div>
<div>
<p>TRITEX has been run on highly inbred genotypes of barley (<em>Hordeum vulgare</em>), tetraploid wheat (<em>Triticum turgidum</em>) and hexaploid wheat (<em>T. aestivum</em>) with reasonable results: super-scaffold N50 values in the range of dozens of Mb and pseudomolecules with better gene space representation than a BAC-by-BAC assembly. It has never been tested and is not expected to work on heterozygous or autopolyploid genomes.</p>
</div>
<div>
<p>A protocol for generating chromosome-conformation capture sequencing (Hi-C) data suitable for use with the pipeline is described in&nbsp;<a href="https://bio-protocol.org/e2955">Himmelbach et al. 2018</a>. Refer to the&nbsp;<a href="https://www.10xgenomics.com/resources/technical-notes/">technical notes</a>&nbsp;of 10X Genomics on how to generate Chromium data.</p>
</div><p>Address of the bookmark: <a href="https://tritexassembly.bitbucket.io/" rel="nofollow">https://tritexassembly.bitbucket.io/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41918/phispy-phispy-identifies-prophages-in-bacterial-and-probably-archaeal-genomes</guid>
	<pubDate>Tue, 30 Jun 2020 21:36:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41918/phispy-phispy-identifies-prophages-in-bacterial-and-probably-archaeal-genomes</link>
	<title><![CDATA[PhiSpy: PhiSpy identifies prophages in Bacterial (and probably Archaeal) genomes]]></title>
	<description><![CDATA[<p>PhiSpy identifies prophages in Bacterial (and probably Archaeal) genomes. Given an annotated genome it will use several approaches to identify the most likely prophage regions.</p>
<p>Initial versions of PhiSpy were written by</p>
<p>Sajia Akhter (<a href="mailto:sajia@stanford.edu">sajia@stanford.edu</a>)&nbsp;<a href="http://edwards.sdsu.edu/research/">Edwards Bioinformatics Lab</a></p>
<p>Improvements, bug fixes, and other changes were made by</p>
<p>Katelyn McNair&nbsp;<a href="http://edwards.sdsu.edu/research/">Edwards Bioinformatics Lab</a>&nbsp;and Przemyslaw Decewicz&nbsp;<a href="http://ddlemb.com/">DEMB at the University of Warsaw</a></p><p>Address of the bookmark: <a href="https://github.com/linsalrob/PhiSpy" rel="nofollow">https://github.com/linsalrob/PhiSpy</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43090/loretta-a-user-friendly-tool-for-assembling-viral-genomes-from-pacbio-sequence-data</guid>
	<pubDate>Wed, 23 Jun 2021 07:54:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43090/loretta-a-user-friendly-tool-for-assembling-viral-genomes-from-pacbio-sequence-data</link>
	<title><![CDATA[LoReTTA, a user-friendly tool for assembling viral genomes from PacBio sequence data]]></title>
	<description><![CDATA[<p>LoReTTA (Long Read Template-Targeted Assembler), a tool designed for performing <em>de novo</em> assembly of long reads generated from viral genomes on the PacBio platform. LoReTTA exploits a reference genome to guide the assembly process, an approach that has been successful with short reads.</p>
<p>https://academic.oup.com/ve/article/7/1/veab042/6248116</p><p>Address of the bookmark: <a href="https://academic.oup.com/ve/article/7/1/veab042/6248116" rel="nofollow">https://academic.oup.com/ve/article/7/1/veab042/6248116</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44655/ngenomesyn-an-easy-to-use-and-flexible-tool-for-publication-ready-visualization-of-syntenic-relationships-across-multiple-genomes</guid>
	<pubDate>Tue, 10 Sep 2024 04:54:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44655/ngenomesyn-an-easy-to-use-and-flexible-tool-for-publication-ready-visualization-of-syntenic-relationships-across-multiple-genomes</link>
	<title><![CDATA[NGenomeSyn: an easy-to-use and flexible tool for publication-ready visualization of syntenic relationships across multiple genomes]]></title>
	<description><![CDATA[<p>NGenomeSyn: an easy-to-use and flexible tool for publication-ready visualization of syntenic relationships across multiple genomes&nbsp;</p>
<p><img src="https://github.com/hewm2008/NGenomeSyn/raw/main/Example/example2/OUT3.png" alt="image" style="border: 0px;"></p>
<p><span>NGenomeSyn [multiple (N) Genome Synteny], for publication-ready visualization of syntenic relationships of the whole genome or local region and genomic features (e.g. repeats, structural variations, genes) across multiple genomes with a high customization. NGenomeSyn provides an easy way for its users to visualize a large amount of data with a rich layout by simply adjusting options for moving, scaling, and rotation of target genomes. Moreover, NGenomeSyn could be applied on the visualization of relationships on non-genomic data with similar input formats.</span></p>
<p>https://academic.oup.com/bioinformatics/article/39/3/btad121/7072460</p><p>Address of the bookmark: <a href="https://github.com/hewm2008/NGenomeSyn" rel="nofollow">https://github.com/hewm2008/NGenomeSyn</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34141/rami-a-tool-for-identification-and-characterization-of-phylogenetic-clusters-in-microbial-communities</guid>
	<pubDate>Mon, 07 Aug 2017 18:49:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34141/rami-a-tool-for-identification-and-characterization-of-phylogenetic-clusters-in-microbial-communities</link>
	<title><![CDATA[RAMI: a tool for identification and characterization of phylogenetic clusters in microbial communities]]></title>
	<description><![CDATA[<p>RAMI, which clusters related nodes in a phylogenetic tree based on the patristic distance. RAMI also produces indices of cluster properties and other indices used in population and community studies on-the-fly.</p>
<p><strong>Availability:</strong>&nbsp;RAMI is licensed under GNU GPL and can be run or downloaded from&nbsp;<a href="http://www.acgt.se/online.html" target="">http://www.acgt.se/online.html</a>.</p><p>Address of the bookmark: <a href="https://academic.oup.com/bioinformatics/article-lookup/doi/10.1093/bioinformatics/btp051" rel="nofollow">https://academic.oup.com/bioinformatics/article-lookup/doi/10.1093/bioinformatics/btp051</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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