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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38646?offset=50</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37259/epiviz-an-interactive-visualization-tool-for-functional-genomics-data</guid>
	<pubDate>Mon, 09 Jul 2018 05:27:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37259/epiviz-an-interactive-visualization-tool-for-functional-genomics-data</link>
	<title><![CDATA[Epiviz: an interactive visualization tool for functional genomics data.]]></title>
	<description><![CDATA[<p><span>Epiviz is an interactive visualization tool for functional genomics data. It supports genome navigation like other genome browsers, but allows multiple visualizations of data within genomic regions using scatterplots, heatmaps and other user-supplied visualizations. It also includes data from the&nbsp;</span><a href="http://barcode.luhs.org/" target="_blank">Gene Expression Barcode project</a><span>&nbsp;for transcriptome visualization. It has a flexible plugin framework so users can add</span><a href="http://d3js.org/" target="_blank">d3</a><span>&nbsp;visualizations. You can see a video tour&nbsp;</span><a href="http://youtu.be/099c4wUxozA" target="_blank">here</a><span>.</span></p>
<p><span>https://bioconductor.org/packages/release/bioc/html/epivizr.html</span></p>
<p><span>https://github.com/epiviz</span></p>
<p><span>https://github.com/epiviz/epiviz</span></p><p>Address of the bookmark: <a href="https://epiviz.github.io/" rel="nofollow">https://epiviz.github.io/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38561/hawkeye-an-interactive-visual-analytics-tool-for-genome-assemblies</guid>
	<pubDate>Tue, 01 Jan 2019 11:56:17 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38561/hawkeye-an-interactive-visual-analytics-tool-for-genome-assemblies</link>
	<title><![CDATA[Hawkeye: an interactive visual analytics tool for genome assemblies]]></title>
	<description><![CDATA[<p><span>Genome sequencing remains an inexact science, and genome sequences can contain significant errors if they are not carefully examined. Hawkeye is our new visual analytics tool for genome assemblies, designed to aid in identifying and correcting assembly errors. Users can analyze all levels of an assembly along with summary statistics and assembly metrics, and are guided by a ranking component towards likely mis-assemblies. Hawkeye is freely available and released as part of the open source AMOS project&nbsp;</span><span><a href="http://amos.sourceforge.net/hawkeye"><span>http://amos.sourceforge.net/hawkeye</span></a></span><span>.</span></p>
<p>https://genomebiology.biomedcentral.com/articles/10.1186/gb-2007-8-3-r34</p><p>Address of the bookmark: <a href="http://amos.sourceforge.net/wiki/index.php?title=Hawkeye" rel="nofollow">http://amos.sourceforge.net/wiki/index.php?title=Hawkeye</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40598/mitoz-a-toolkit-for-animal-mitochondrial-genome-assembly-annotation-and-visualization</guid>
	<pubDate>Fri, 24 Jan 2020 04:09:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40598/mitoz-a-toolkit-for-animal-mitochondrial-genome-assembly-annotation-and-visualization</link>
	<title><![CDATA[MitoZ: a toolkit for animal mitochondrial genome assembly, annotation and visualization]]></title>
	<description><![CDATA[<p><span>MitoZ is a Python3-based toolkit which aims to automatically filter pair-end raw data (fastq files), assemble genome, search for mitogenome sequences from the genome assembly result, annotate mitogenome (genbank file as result), and mitogenome visualization. MitoZ is available from&nbsp;</span><code>https://github.com/linzhi2013/MitoZ</code><span>.</span></p>
<p><span><a href="https://academic.oup.com/nar/article/47/11/e63/5377471">https://academic.oup.com/nar/article/47/11/e63/5377471</a></span></p><p>Address of the bookmark: <a href="https://github.com/linzhi2013/MitoZ" rel="nofollow">https://github.com/linzhi2013/MitoZ</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44318/proksee-in-depth-characterization-and-visualization-of-bacterial-genomes</guid>
	<pubDate>Tue, 09 May 2023 19:38:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44318/proksee-in-depth-characterization-and-visualization-of-bacterial-genomes</link>
	<title><![CDATA[Proksee: in-depth characterization and visualization of bacterial genomes]]></title>
	<description><![CDATA[<p><span>Proksee is an expert system for genome assembly, annotation and visualization. To begin using Proksee, provide a complete genome sequence, sequencing reads or a CGView/Proksee map JSON file.</span></p><p>Address of the bookmark: <a href="https://proksee.ca/" rel="nofollow">https://proksee.ca/</a></p>]]></description>
	<dc:creator>LEGE</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/40221/dash-a-web-application-framework-that-provides-pure-python-abstraction-around-html-css-and-javascript</guid>
	<pubDate>Tue, 05 Nov 2019 06:39:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40221/dash-a-web-application-framework-that-provides-pure-python-abstraction-around-html-css-and-javascript</link>
	<title><![CDATA[Dash: a web application framework that provides pure Python abstraction around HTML, CSS, and JavaScript.]]></title>
	<description><![CDATA[<p style="margin-top: 0px; margin-bottom: 0.75rem;">Dash is a web application framework that provides pure Python abstraction around HTML, CSS, and JavaScript.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">Dash Bio is a suite of bioinformatics components that make it simpler to analyze and visualize bioinformatics data and interact with them in a Dash application.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">The source can be found on GitHub at<span>&nbsp;</span><a href="https://github.com/plotly/dash-bio">plotly/dash-bio</a>.</p>
<p style="margin-top: 0px; margin-bottom: 0.75rem;">These docs are using Dash Bio version 0.1.4.</p><p>Address of the bookmark: <a href="https://dash.plot.ly/dash-bio" rel="nofollow">https://dash.plot.ly/dash-bio</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35565/circosjs-d3-library-to-build-circular-graphs</guid>
	<pubDate>Tue, 13 Feb 2018 06:57:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35565/circosjs-d3-library-to-build-circular-graphs</link>
	<title><![CDATA[circosJS: d3 library to build circular graphs]]></title>
	<description><![CDATA[<p>Circos is a javascript library to easily build interactive graphs in a circular layout. It's based on&nbsp;<a href="https://d3js.org/">d3.js</a>. It aims to be a javascript version of the&nbsp;<a href="http://circos.ca/">Circos</a>&nbsp;software.</p>
<p>You should consider using Circos to show:</p>
<ul>
<li>relationships between entities</li>
<li>periodical data</li>
</ul><p>Address of the bookmark: <a href="https://github.com/nicgirault/circosJS" rel="nofollow">https://github.com/nicgirault/circosJS</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38166/pygenometracks-standalone-program-and-library-to-plot-beautiful-genome-browser-tracks</guid>
	<pubDate>Fri, 09 Nov 2018 12:34:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38166/pygenometracks-standalone-program-and-library-to-plot-beautiful-genome-browser-tracks</link>
	<title><![CDATA[pyGenomeTracks: Standalone program and library to plot beautiful genome browser tracks]]></title>
	<description><![CDATA[<p>pyGenomeTracks aims to produce high-quality genome browser tracks that are highly customizable. Currently, it is possible to plot:</p>
<ul>
<li>bigwig</li>
<li>bed (many options)</li>
<li>bedgraph</li>
<li>links (represented as arcs)</li>
<li>Hi-C matrices (if&nbsp;<a href="http://hicexplorer.readthedocs.io/">HiCExplorer</a>&nbsp;is installed)</li>
</ul><p>Address of the bookmark: <a href="https://github.com/deeptools/pyGenomeTracks" rel="nofollow">https://github.com/deeptools/pyGenomeTracks</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29343/accnet</guid>
	<pubDate>Fri, 07 Oct 2016 05:22:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29343/accnet</link>
	<title><![CDATA[AccNET]]></title>
	<description><![CDATA[<p><span>AccNET is a Perl application that presents a new way to study the accessory genome of a given set of organisms. Using the proteomes of these organisms, AccNET create a bipartite network compatible with common network analysis platforms. AccNET collects phylogenetic and functional information in a network improving the analysis capability. Networks offer a new perspective of organism organization through elements acquired by horizontal gene transfers and not constricted by hierarchical structures.</span></p>
<p><span>More at&nbsp;https://www.youtube.com/watch?v=vdGuy1GAJrQ</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/accnet/" rel="nofollow">https://sourceforge.net/projects/accnet/</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges</guid>
	<pubDate>Sat, 02 Jul 2022 11:41:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges</link>
	<title><![CDATA[JASMINE: Jointly Accurate Sv Merging with Intersample Network Edges]]></title>
	<description><![CDATA[<p><span>This tool is used to merge structural variants (SVs) across samples. Each sample has a number of SV calls, consisting of position information (chromosome, start, end, length), type and strand information, and a number of other values. Jasmine represents the set of all SVs across samples as a network, and uses a modified minimum spanning forest algorithm to determine the best way of merging the variants such that each merged variants represents a set of analogous variants occurring in different samples.</span></p><p>Address of the bookmark: <a href="https://github.com/mkirsche/Jasmine" rel="nofollow">https://github.com/mkirsche/Jasmine</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

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