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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38172?</link>
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	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</guid>
	<pubDate>Fri, 19 Jan 2018 15:03:51 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</link>
	<title><![CDATA[BioCircos.js is an open source interactive Javascript library to interactive display biological data on the web]]></title>
	<description><![CDATA[<p><a href="http://bioinfo.ibp.ac.cn/biocircos/index.php">BioCircos.js</a>&nbsp;is an open source interactive&nbsp;<code>Javascript</code>&nbsp;library which provides an easy way to interactive display biological data on the web. It implements a raster-based&nbsp;<code>SVG</code>&nbsp;visualization using the open source Javascript framework jquery.js. BioCircos.js is multiplatform and works in all major internet browsers (<strong>Internet Explorer</strong>,&nbsp;<strong>Mozilla Firefox</strong>,&nbsp;<strong>Google Chrome</strong>,&nbsp;<strong>Safari</strong>,&nbsp;<strong>Opera</strong>). Its speed is determined by the client&rsquo;s hardware and internet browser. For smoothest user experience, we recommend&nbsp;<strong>Google Chrome</strong>.</p>
<p>BioCircos.js provides&nbsp;<strong>SNP</strong>,&nbsp;<strong>CNV</strong>,&nbsp;<strong>HEATMAP</strong>,&nbsp;<strong>LINK</strong>,&nbsp;<strong>LINE</strong>,&nbsp;<strong>SCATTER</strong>,&nbsp;<strong>ARC</strong>,&nbsp;<strong>TEXT</strong>, and&nbsp;<strong>HISTGRAM</strong>modules to display genome-wide genetic variations (SNPs, CNVs and chromosome rearrangement), gene expression and biomolecule interactions. BioCircos.js also provides&nbsp;<strong>BACKGROUND</strong>&nbsp;module to display background and axis circles. Tooltips showing detailed information of SVG elements are also provided.</p>
<p><a href="http://bioinfo.ibp.ac.cn/biocircos/document/demo/pages/paper01.html">Demo</a></p><p>Address of the bookmark: <a href="http://bioinfo.ibp.ac.cn/biocircos/document/index.html" rel="nofollow">http://bioinfo.ibp.ac.cn/biocircos/document/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44904/termal-a-fast-and-interactive-terminal-based-viewer-for-multiple-sequence-alignments</guid>
	<pubDate>Mon, 22 Sep 2025 23:51:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44904/termal-a-fast-and-interactive-terminal-based-viewer-for-multiple-sequence-alignments</link>
	<title><![CDATA[Termal: a fast and interactive terminal-based viewer for multiple sequence alignments]]></title>
	<description><![CDATA[<p>termal, a fast, interactive, terminal-based viewer for multiple sequence alignments (MSAs), designed for use on remote systems such as high-performance computing (HPC) clusters.</p>
<p>https://academic.oup.com/bioinformaticsadvances/advance-article/doi/10.1093/bioadv/vbaf208/8257678?login=true</p><p>Address of the bookmark: <a href="https://github.com/sib-swiss/termal" rel="nofollow">https://github.com/sib-swiss/termal</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
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	<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/38598/zenbu-a-collaborative-omics-data-integration-and-interactive-visualization-system</guid>
	<pubDate>Fri, 04 Jan 2019 13:35:26 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38598/zenbu-a-collaborative-omics-data-integration-and-interactive-visualization-system</link>
	<title><![CDATA[ZENBU: a collaborative, omics data integration and interactive visualization system]]></title>
	<description><![CDATA[<p><span>ZENBU</span><span>&nbsp;</span><span>is a data integration, data analysis, and visualization system enhanced for RNAseq, ChipSeq, CAGE and other types of next-generation-sequence-tag (NGS) based data. ZENBU allows for novel data exploration through "on-demand" data processing and interactive linked-visualizations and is able to make many-views from the same primary sequence alignment data which users can uploaded from BAM, BED, GFF and tab-text files.&nbsp;<br>Please check our&nbsp;<a href="http://fantom.gsc.riken.jp/zenbu/wiki">documentation wiki</a>&nbsp;for details on how to use the system, or check out some of the views above.</span></p><p>Address of the bookmark: <a href="http://fantom.gsc.riken.jp/zenbu/" rel="nofollow">http://fantom.gsc.riken.jp/zenbu/</a></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36758/pbalign-maps-pacbio-reads-to-reference-sequences-and-saves-alignments-to-a-bam-file</guid>
	<pubDate>Thu, 24 May 2018 10:06:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36758/pbalign-maps-pacbio-reads-to-reference-sequences-and-saves-alignments-to-a-bam-file</link>
	<title><![CDATA[pbalign: maps PacBio reads to reference sequences and saves alignments to a BAM file]]></title>
	<description><![CDATA[pbalign aligns PacBio reads to reference sequences, filters aligned reads according to user-specific filtering criteria, and converts the output to either the SAM format or PacBio Compare HDF5 (e.g., .cmp.h5) format. The output Compare HDF5 file will be compatible with Quiver if --forQuiver option is specified.<p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/pbalign" rel="nofollow">https://github.com/PacificBiosciences/pbalign</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39039/dotplotly-generate-an-interactive-dot-plot-from-mummer-or-minimap-alignments</guid>
	<pubDate>Thu, 21 Feb 2019 10:22:17 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39039/dotplotly-generate-an-interactive-dot-plot-from-mummer-or-minimap-alignments</link>
	<title><![CDATA[dotPlotly: Generate an interactive dot plot from mummer or minimap alignments]]></title>
	<description><![CDATA[<p>Create an interactive dot plot from mummer output OR PAF format</p>
<p>R script that makes a plotly interactive and/or static (png/pdf) dot plot.</p>
<p><a href="https://tom-poorten.shinyapps.io/dotplotly_shiny/">Shiny app available for testing</a></p><p>Address of the bookmark: <a href="https://github.com/tpoorten/dotPlotly" rel="nofollow">https://github.com/tpoorten/dotPlotly</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38004/vcfr-a-package-to-manipulate-and-visualize-vcf-data-in-r</guid>
	<pubDate>Thu, 25 Oct 2018 09:05:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38004/vcfr-a-package-to-manipulate-and-visualize-vcf-data-in-r</link>
	<title><![CDATA[vcfR:  a package to manipulate and visualize VCF data in R]]></title>
	<description><![CDATA[<p><span>VcfR is an R package intended to allow easy manipulation and visualization of variant call format (VCF) data. Functions are provided to rapidly read from and write to VCF files. Once VCF data is read into R a parser function extracts matrices from the VCF data for use with typical R functions. This information can then be used for quality control or other purposes. Additional functions provide visualization of genomic data. Once processing is complete data may be written to a VCF file or converted into other popular R objects (e.g., genlight, DNAbin). VcfR provides a link between VCF data and the R environment connecting familiar software with genomic data.</span></p><p>Address of the bookmark: <a href="https://github.com/knausb/vcfR" rel="nofollow">https://github.com/knausb/vcfR</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43870/quip-aggressive-compression-of-fastq-sam-and-bam-files</guid>
	<pubDate>Tue, 24 May 2022 06:31:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43870/quip-aggressive-compression-of-fastq-sam-and-bam-files</link>
	<title><![CDATA[Quip: Aggressive compression of FASTQ, SAM and BAM files.]]></title>
	<description><![CDATA[<p>This will help us to reduce the amount of drive space we take up and decrease data transfer times</p>
<p dir="auto">Quip compresses next-generation sequencing data with extreme prejudice. It supports input and output in the&nbsp;<a href="http://en.wikipedia.org/wiki/Fastq">FASTQ</a>&nbsp;and&nbsp;<a href="http://samtools.sourceforge.net/">SAM/BAM</a>&nbsp;formats, compressing large datasets to as little as 15% of their original size.</p><p>Address of the bookmark: <a href="https://github.com/dcjones/quip" rel="nofollow">https://github.com/dcjones/quip</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40946/free-genomics-data</guid>
	<pubDate>Fri, 07 Feb 2020 14:08:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40946/free-genomics-data</link>
	<title><![CDATA[Free Genomics data !]]></title>
	<description><![CDATA[<p><span>The specimens were collected by the Oxford Wytham Woods and Edinburgh Lohse lab teams. DNA extraction and sequencing was carried out by the Sanger Institute Scientific Operations teams. Assemblies were carried out by the Tree of Life team (Shane McCarthy) and colleagues in Pacific Biosciences (Jonas Korlach).</span></p>
<p><a href="https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/">https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/</a></p><p>Address of the bookmark: <a href="https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/" rel="nofollow">https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37645/lsc-improving-pacbio-long-read-accuracy-by-short-read-alignment</guid>
	<pubDate>Thu, 06 Sep 2018 16:27:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37645/lsc-improving-pacbio-long-read-accuracy-by-short-read-alignment</link>
	<title><![CDATA[LSC: Improving PacBio Long Read Accuracy by Short Read Alignment]]></title>
	<description><![CDATA[<ul>
<li>Added Command line argument support.</li>
<li>Multi-stage execution modes.</li>
<li>Support for parallelization. Now execution proceeds in batches of long reads the size of which can be set by --long_read_batch_size N.</li>
<li>Better compressed intermediate files.</li>
<li>Added utilities folder.</li>
<li>Added support for multiple short read files.</li>
<li>Removed use of configuration file.</li>
</ul><p>Address of the bookmark: <a href="https://www.healthcare.uiowa.edu/labs/au/LSC/" rel="nofollow">https://www.healthcare.uiowa.edu/labs/au/LSC/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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