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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44889?offset=30</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44311/jbrowse-2-a-modular-genome-browser-with-views-of-synteny-and-structural-variation</guid>
	<pubDate>Tue, 25 Apr 2023 20:58:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44311/jbrowse-2-a-modular-genome-browser-with-views-of-synteny-and-structural-variation</link>
	<title><![CDATA[JBrowse 2: a modular genome browser with views of synteny and structural variation]]></title>
	<description><![CDATA[<ul dir="auto">
<li>igvjs - a create-react-app with igv package from npm installed. the igv.js is instrumented to output "DONE" to the console when finished, and to have an increased fetchSizeLimit (which is otherwise git in CRAM longread tests)</li>
<li>jb2-web - stock instance of jbrowse-web v1.7.5</li>
<li>jb1 - stock instance of jbrowse 1 v1.16.11</li>
<li>jb2 embedded - a create-react-app with @jbrowse/react-linear-genome-view</li>
</ul><p>Address of the bookmark: <a href="https://github.com/GMOD/jb2profile" rel="nofollow">https://github.com/GMOD/jb2profile</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37666/ensembl-variation-calculated-variant-consequences</guid>
	<pubDate>Sun, 09 Sep 2018 19:17:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37666/ensembl-variation-calculated-variant-consequences</link>
	<title><![CDATA[Ensembl Variation - Calculated variant consequences]]></title>
	<description><![CDATA[<p><span>For each variant that is mapped to the reference genome, we identify all overlapping Ensembl transcripts. We then use a rule-based approach to predict the effects that each allele of the variant may have on each transcript. The set of consequence terms, defined by the&nbsp;</span><a href="http://www.sequenceontology.org/">Sequence Ontology</a><span>&nbsp;(SO), that can be currently assigned to each combination of an allele and a transcript is shown in the table below. Note that each allele of each variant may have a different effect in different transcripts.</span></p>
<p><span><img src="https://www.ensembl.org/info/genome/variation/prediction/consequences.jpg" width="1280" height="570" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://www.ensembl.org/info/genome/variation/prediction/predicted_data.html" rel="nofollow">https://www.ensembl.org/info/genome/variation/prediction/predicted_data.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29917/gojs</guid>
	<pubDate>Tue, 22 Nov 2016 08:25:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29917/gojs</link>
	<title><![CDATA[GoJS]]></title>
	<description><![CDATA[<p><strong>GoJS</strong> is a feature-rich JavaScript library for implementing custom interactive diagrams and complex visualizations across modern web browsers and platforms. <strong>GoJS</strong> makes constructing JavaScript diagrams of complex nodes, links, and groups easy with customizable templates and layouts.</p>
<p><strong>GoJS</strong> offers many advanced features for user interactivity such as drag-and-drop, copy-and-paste, in-place text editing, tooltips, context menus, automatic layouts, templates, data binding and models, transactional state and undo management, palettes, overviews, event handlers, commands, and an extensible tool system for custom operations.</p>
<p><strong>GoJS</strong> is pure JavaScript, so users get interactivity without requiring round-trips to servers and without plugins. <strong>GoJS</strong> normally runs completely in the browser, rendering to an HTML5 Canvas element or SVG without any server-side requirements. <strong>GoJS</strong> does not depend on any JavaScript libraries or frameworks, so it should work with any HTML or JavaScript framework or with no framework at all. &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</p>
<p>More at&nbsp;http://gojs.net/latest/index.html</p><p>Address of the bookmark: <a href="http://gojs.net/latest/index.html" rel="nofollow">http://gojs.net/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38039/vgsc-a-web-based-vector-graph-toolkit-of-genome-synteny-and-collinearity</guid>
	<pubDate>Tue, 30 Oct 2018 10:46:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38039/vgsc-a-web-based-vector-graph-toolkit-of-genome-synteny-and-collinearity</link>
	<title><![CDATA[VGSC: A Web-Based Vector Graph Toolkit of Genome Synteny and Collinearity]]></title>
	<description><![CDATA[<p><span>VGSC, the Vector Graph toolkit of genome Synteny and Collinearity, and its online service, to visualize the synteny and collinearity in the common graphical format, including both raster (JPEG, Bitmap, and PNG) and vector graphic (SVG, EPS, and PDF).</span><em>&nbsp;</em></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783527/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783527/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45267/when-thousands-of-bacterial-genomes-become-one-giant-map</guid>
	<pubDate>Thu, 27 Aug 2026 10:56:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45267/when-thousands-of-bacterial-genomes-become-one-giant-map</link>
	<title><![CDATA[When Thousands of Bacterial Genomes Become One Giant Map]]></title>
	<description><![CDATA[<p>Imagine trying to understand a city by studying just one house.</p><p>You might learn a lot about that house&mdash;the rooms, the doors, the furniture&mdash;but you would miss the bigger story: the streets, the neighborhoods, and all the ways the city changes from one place to another.</p><p>Something similar happens when scientists study bacterial genomes one at a time.</p><p>Over the past decade, researchers have collected thousands of bacterial genomes. These genomes contain an enormous amount of information about how bacteria survive, adapt, and evolve. But comparing thousands of individual genomes can quickly become a computational maze.</p><p>That is where PANORAMA enters the story.</p><p>Developed by J&eacute;r&ocirc;me Arnoux and colleagues, PANORAMA is a computational tool designed to explore bacterial pangenomes&mdash;the complete collection of genetic possibilities found across a species or group of related organisms. Instead of looking at every genome as an isolated object, the approach represents their shared and variable genetic features as a graph.</p><p>Think of this graph as a giant subway map.</p><p>Some stations appear on almost every route. These represent genes that are highly conserved. Other stations appear only on certain routes, representing genes that some bacteria possess while others do not. By looking at the entire network, scientists can begin to see not just *what genes exist*, but how they are organized and how biological systems are distributed across populations.</p><p>The researchers put PANORAMA to the test using 941 genomes of Pseudomonas aeruginosa, a bacterium important in human health. They used the tool to investigate biological systems, including bacterial defense mechanisms against viruses known as bacteriophages. They then expanded the analysis to more than 6,000 genomes from four Enterobacteriaceae species.</p><p>The result is more than a faster way to process data.</p><p>PANORAMA allows researchers to ask a bigger question: What can an entire microbial species do, genetically speaking?</p><p>By comparing pangenomes, the researchers could identify systems shared between species as well as distinctive features. They could also find recurring genomic locations where genetic material is inserted&mdash;clues that may reveal common evolutionary processes.</p><p>And this is perhaps the most exciting part of the story.</p><p>Every bacterial genome is like a page in a huge evolutionary book. Until recently, reading thousands of those pages together was difficult. PANORAMA provides a way to turn those pages into a map, allowing scientists to see patterns that might disappear when each genome is studied separately.</p><p>The study, published in PLOS Computational Biology in July 2026, presents PANORAMA as a foundation for large-scale comparative pangenomics. The software and accompanying analysis resources are openly available, giving other researchers the opportunity to explore microbial diversity themselves.</p><p>So the story is not really about one bacterium or one genome.</p><p>It is about changing the way we look at life.</p><p>Instead of asking, &ldquo;What is inside this genome?&rdquo;, scientists can increasingly ask, &ldquo;What is the full genetic landscape of this species&mdash;and how did it become this way?&rdquo;</p><p>And sometimes, when you stop looking at one house and finally see the whole city, the most interesting discoveries are hiding in the streets between them.</p><p>Read more at&nbsp;https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013856</p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42198/pggb-the-pangenome-graph-builder</guid>
	<pubDate>Sun, 13 Sep 2020 20:54:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42198/pggb-the-pangenome-graph-builder</link>
	<title><![CDATA[pggb: the pangenome graph builder]]></title>
	<description><![CDATA[<p><span>This pangenome graph construction pipeline renders a collection of sequences into a pangenome graph (in the variation graph model). Its goal is to build a graph that is locally directed and acyclic while preserving large-scale variation. Maintaining local linearity is important for the interpretation, visualization, and reuse of pangenome variation graphs.</span></p>
<p><img src="https://raw.githubusercontent.com/pangenome/pggb/master/data/images/DRB1-3123.fa.gz.pggb-s3000-p70-n10-a70-K11-k8-w10000-j5000-W0-e100.smooth.og.viz.png" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/pangenome/pggb" rel="nofollow">https://github.com/pangenome/pggb</a></p>]]></description>
	<dc:creator>biogeek</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43263/jumbodb-tool-for-de-bruijn-graph-construction</guid>
	<pubDate>Tue, 17 Aug 2021 13:33:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43263/jumbodb-tool-for-de-bruijn-graph-construction</link>
	<title><![CDATA[JumboDB: tool for de Bruijn graph construction]]></title>
	<description><![CDATA[<p><span>jumboDB tool for fast de Bruijn graph construction from long sequences (reads or genomes) with very low error rate. JumboDB is not a genome assembler by itself but rather a subroutine that translates a set of reads into compressed de Bruijn graph.</span></p>
<p><span>More at&nbsp;https://github.com/AntonBankevich/jumboDB</span></p><p>Address of the bookmark: <a href="https://github.com/AntonBankevich/jumboDB" rel="nofollow">https://github.com/AntonBankevich/jumboDB</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44887/alfapang-alignment-free-algorithm-for-pangenome-graph-construction</guid>
	<pubDate>Thu, 28 Aug 2025 02:56:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44887/alfapang-alignment-free-algorithm-for-pangenome-graph-construction</link>
	<title><![CDATA[AlfaPang: alignment free algorithm for pangenome graph construction]]></title>
	<description><![CDATA[<p><span>AlfaPang constructs variation graphs, leveraging its alignment-free and reference-free approach, based solely on intrinsic sequence properties. This design allows AlfaPang's runtime and memory usage to scale linearly with the size of input sequences, enabling it to handle significantly larger genome sets compared to other methods.</span></p><p>Address of the bookmark: <a href="https://github.com/AdamCicherski/AlfaPang" rel="nofollow">https://github.com/AdamCicherski/AlfaPang</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35345/rgfa-powerful-and-convenient-handling-of-assembly-graphs</guid>
	<pubDate>Thu, 25 Jan 2018 05:47:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35345/rgfa-powerful-and-convenient-handling-of-assembly-graphs</link>
	<title><![CDATA[RGFA: powerful and convenient handling of assembly graphs]]></title>
	<description><![CDATA[<p><span>RGFA, an implementation of the proposed GFA specification in Ruby. It allows the user to conveniently parse, edit and write GFA files. Complex operations such as the separation of the implicit instances of repeats and the merging of linear paths can be performed. A typical application of RGFA is the editing of a graph, to finish the assembly of a sequence, using information not available to the assembler. We illustrate a use case, in which the assembly of a repetitive metagenomic fosmid insert was completed using a script based on RGFA.</span></p>
<p><span>https://github.com/ggonnella/rgfa</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103826/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103826/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40594/gfaviz-flexible-and-interactive-visualization-of-gfa-sequence-graphs</guid>
	<pubDate>Thu, 23 Jan 2020 07:33:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40594/gfaviz-flexible-and-interactive-visualization-of-gfa-sequence-graphs</link>
	<title><![CDATA[GfaViz: flexible and interactive visualization of GFA sequence graphs]]></title>
	<description><![CDATA[<p><span>GFA (Graphical Fragment Assembly) is an emerging standard format for representing sequence graphs. Although it was originally conceived as a format for sequence assembly (hence the name), and this remains its core application, it is more general, and able to represent many different types of sequence graphs, including scaffolding graphs, alignment graphs, variant graphs and splicing graphs.</span></p><p>Address of the bookmark: <a href="https://github.com/ggonnella/gfaviz" rel="nofollow">https://github.com/ggonnella/gfaviz</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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