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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/33887?offset=100</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44313/orthovenn3-an-integrated-platform-for-exploring-and-visualizing-orthologous-data-across-genomes</guid>
	<pubDate>Tue, 02 May 2023 00:48:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44313/orthovenn3-an-integrated-platform-for-exploring-and-visualizing-orthologous-data-across-genomes</link>
	<title><![CDATA[OrthoVenn3: an integrated platform for exploring and visualizing orthologous data across genomes]]></title>
	<description><![CDATA[<p><span>OrthoVenn3 is a powerful tool for comparative genomics analysis, used as a web server for full genome comparisons, annotation, and evolutionary analysis of orthologous clusters across multiple species. It has already been used by thousands of users from over 60 countries.</span></p><p>Address of the bookmark: <a href="https://orthovenn3.bioinfotoolkits.net/" rel="nofollow">https://orthovenn3.bioinfotoolkits.net/</a></p>]]></description>
	<dc:creator>Abhi</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>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34461/drawid-user-friendly-java-software-for-chromosome-measurements-and-idiogram-drawing</guid>
	<pubDate>Mon, 27 Nov 2017 16:03:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34461/drawid-user-friendly-java-software-for-chromosome-measurements-and-idiogram-drawing</link>
	<title><![CDATA[DRAWID: user-friendly Java software for chromosome measurements and idiogram drawing]]></title>
	<description><![CDATA[<p>"DRAWID has number of advantages including a user-friendly interactive interface, possibility for simultaneous chromosome and FISH/GISH/banding signal measurement and idiogram drawing as well as number of useful functions facilitating the procedure of chromosome analysis," explain the scientists.</p>
<p>"The output of the program is Microsoft XL table and publish-ready idiogram picture."</p>
<div>
<p>Find their paper openly published with us at:&nbsp;<a href="https://doi.org/10.3897/compcytogen.v11i4.20830" target="_blank">https://doi.org/10.3897/compcytogen.v11i4.20830</a></p>
</div><p>Address of the bookmark: <a href="https://compcytogen.pensoft.net/articles.php?id=20830" rel="nofollow">https://compcytogen.pensoft.net/articles.php?id=20830</a></p>]]></description>
	<dc:creator>Robert M Willioms</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/39302/understanding-reads-mapping-and-flags</guid>
	<pubDate>Thu, 25 Apr 2019 09:06:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/39302/understanding-reads-mapping-and-flags</link>
	<title><![CDATA[Understanding reads mapping and flags !]]></title>
	<description><![CDATA[<p><strong>Linear Alignment:</strong>&nbsp;An alignment of a read to a single reference sequence that may&nbsp;<q>include insertions, deletions, skips and clipping</q>,&nbsp;<span style="text-decoration: underline;">but may not include direction changes</span>&nbsp;(i.e. one portion of the alignment on forward strand and another portion of alignment on reverse strand).<sup id="fnref:1"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:1"><br /></a></sup></p><p><strong>Chimeric Alignment:</strong>&nbsp;An alignment of a read that cannot be represented as a linear alignment. Typically, one of the linear alignments in a chimeric alignment is considered the &ldquo;representative&rdquo; alignment, and the others are called &ldquo;supplementary&rdquo; and are distinguished by the supplementary alignment flag.<sup id="fnref:1:1"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:1"><br /></a></sup></p><p>Chimeric reads are indicative of structural variation in DNA-seq and it may indicate the presence of&nbsp;<a href="https://en.wikipedia.org/wiki/Chimeric_gene">chimeric genes</a>&nbsp;in RNA-seq.<sup id="fnref:2"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:2"><br /></a></sup></p><p>In short, chimeric reads can be split in to two or more parts, each part would be mapped to reference(it&rsquo;s not&nbsp;<a href="https://www.biostars.org/p/119537/">hard-clipped</a>), the total length of the mapped part is longger than read length.<sup id="fnref:3"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:3"><br /></a></sup></p><p><strong>Representative alignment:</strong>&nbsp;A chimeric alignment that is represented as a set of linear alignments that do not have large overlaps typically has one linear alignment that is considered the representative alignment.<sup id="fnref:4"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:4"><br /></a></sup></p><p>One read can align to multiple positions, we can find one alignmnet position which sequence do not have large overlaps, it called representative alighment, for other alignment positions, we called them supplementary alignment.</p><p>It seems that GATK can realignment those representative reads to the correctly position via&nbsp;<q>RealignerTargetCreator and IndelRealigner</q>. (WARNING: I am not quite sure if I understand this correctly. If someone could help me, please leave me a message below, thanks, thanks.)</p><p><strong>Supplementary Alignment:</strong>&nbsp;A chimeric reads but not a representative reads.</p><p><strong>Primary Alignment and Secondary Alignment:</strong>&nbsp;A read may map ambiguously to multiple locations, e.g. due to repeats.&nbsp;<strong>Only one of the multiple read alignments is considered primary</strong>,<span style="text-decoration: underline;">&nbsp;and this decision may be arbitrary</span>. All other alignments have the secondary alignment flag.<sup id="fnref:5"><a href="https://yulijia.net/en/bioinformatics/2015/12/21/Linear-Chimeric-Supplementary-Primary-and-Secondary-Alignments.html#fn:5"><br /></a></sup></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</guid>
	<pubDate>Fri, 24 Feb 2017 08:56:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</link>
	<title><![CDATA[VAGUE:Velvet Assembler Graphical Front End]]></title>
	<description><![CDATA[<p>VAGUE is a vague acronym for "Velvet Assembler Graphical Front End", which means it is a GUI for the Velvet <em>de novo</em> assembler. The command line version of Velvet can be complicated for beginners to use, but VAGUE makes it clear and simple</p>
<p>More at&nbsp;http://www.vicbioinformatics.com/software.vague.shtml</p><p>Address of the bookmark: <a href="http://www.vicbioinformatics.com/software.vague.shtml" rel="nofollow">http://www.vicbioinformatics.com/software.vague.shtml</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30976/brig</guid>
	<pubDate>Thu, 16 Feb 2017 13:14:25 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30976/brig</link>
	<title><![CDATA[BRIG]]></title>
	<description><![CDATA[<p>BRIG is a free cross-platform (Windows/Mac/Unix) application that can display circular comparisons between a large number of genomes, with a focus on handling genome assembly data. The application is available at:<a href="http://sourceforge.net/projects/brig">http://sourceforge.net/projects/brig</a></p>
<p>If you have any questions or comments, post them on&nbsp;<a href="http://sourceforge.net/tracker/?group_id=328245">one of the trackers</a>&nbsp;on BRIG&rsquo;s SourceForge page:<a href="http://sourceforge.net/tracker/?group_id=328245">http://sourceforge.net/tracker/?group_id=328245</a>.</p>
<p>Features:</p>
<ul>
<li>Images show similarity between a central reference sequence and other sequences as concentric rings.</li>
<li>BRIG will perform all BLAST comparisons and file parsing automatically via a simple GUI.</li>
<li>Contig boundaries and read coverage can be displayed for draft genomes; customized graphs and annotations can be displayed.</li>
<li>Using a user-defined set of genes as input, BRIG can display gene presence, absence, truncation or sequence variation in a set of complete genomes, draft genomes or even raw, unassembled sequence data.</li>
<li>BRIG also accepts SAM-formatted read-mapping files enabling genomic regions present in unassembled sequence data from multiple samples to be compared simultaneously</li>
</ul>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://brig.sourceforge.net/" rel="nofollow">http://brig.sourceforge.net/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31207/laj-viewing-and-manipulating-the-output-from-pairwise-alignment-programs</guid>
	<pubDate>Wed, 01 Mar 2017 08:35:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31207/laj-viewing-and-manipulating-the-output-from-pairwise-alignment-programs</link>
	<title><![CDATA[Laj: viewing and manipulating the output from pairwise alignment programs]]></title>
	<description><![CDATA[<p>Laj is a tool for viewing and manipulating the output from pairwise alignment programs such as <a href="http://bio.cse.psu.edu/">blastz</a>. It can display interactive dotplot, pip, and text representations of the alignments, a diagram showing the locations of exons and repeats, and annotation links to other web sites containing additional information about particular regions.</p>
<p>The program is written in Java in order to provide a graphical user interface that is portable across a variety of computer platforms; indeed its name stands for "Local Alignments with Java". Currently it exists in two forms, a stand-alone application and a web-based applet, with slightly different capabilities.</p><p>Address of the bookmark: <a href="http://www.bx.psu.edu/~ratan/" rel="nofollow">http://www.bx.psu.edu/~ratan/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36216/crusview</guid>
	<pubDate>Thu, 12 Apr 2018 09:22:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36216/crusview</link>
	<title><![CDATA[CrusView]]></title>
	<description><![CDATA[<p><span>CrusView&nbsp;is a java based tool for karyotype/genome visualization and comparison of crucifer&nbsp;Species. It also integrates an binary version of KGBassembler and a&nbsp;post-modification step for its assembling result.</span></p><p>Address of the bookmark: <a href="http://www.cmbb.arizona.edu/?page_id=250" rel="nofollow">http://www.cmbb.arizona.edu/?page_id=250</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</guid>
	<pubDate>Thu, 17 Feb 2022 05:37:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</link>
	<title><![CDATA[Comparative genomics visualisation tools !]]></title>
	<description><![CDATA[<p>Comparative genomics visualisation tools !</p><p>Address of the bookmark: <a href="https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative" rel="nofollow">https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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