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	<title><![CDATA[BOL: Related items]]></title>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44527/alvis-a-tool-for-contig-and-read-alignment-visualisation-and-chimera-detection</guid>
	<pubDate>Wed, 08 May 2024 07:02:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44527/alvis-a-tool-for-contig-and-read-alignment-visualisation-and-chimera-detection</link>
	<title><![CDATA[Alvis: a tool for contig and read ALignment VISualisation and chimera detection]]></title>
	<description><![CDATA[<p><span>Alvis, a simple command line tool that can generate visualisations for a number of common alignment analysis tasks. Alvis is a fast and portable tool that accepts input in a variety of alignment formats and will output production ready vector images. Additionally, Alvis will highlight potentially chimeric reads or contigs, a common source of misassemblies.</span></p>
<p>More at&nbsp;https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-021-04056-0</p><p>Address of the bookmark: <a href="https://github.com/SR-Martin/alvis" rel="nofollow">https://github.com/SR-Martin/alvis</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<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>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/29110/structural-variants-ppt</guid>
	<pubDate>Wed, 07 Sep 2016 03:16:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/29110/structural-variants-ppt</link>
	<title><![CDATA[Structural variants PPT]]></title>
	<description><![CDATA[<p>1000 Genomes data tutorial at ASHG</p><p>Structural variants presentation by</p><p>Jan Korbel</p><p>European Molecular Biology Laboratory (EMBL) Heidelberg Genome Biology Research Unit</p><p>Reference:&nbsp;</p><p>https://www.genome.gov/pages/research/der/1000genomesprojecttutorials/structuralvariants-jankorbel.pdf</p>]]></description>
	<dc:creator>Jit</dc:creator>
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