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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37674?offset=290</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36109/sankeynetwork-with-networkd3</guid>
	<pubDate>Fri, 06 Apr 2018 12:07:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36109/sankeynetwork-with-networkd3</link>
	<title><![CDATA[sankeyNetwork with networkD3]]></title>
	<description><![CDATA[<p><span>You can also create&nbsp;</span><a href="http://en.wikipedia.org/wiki/Sankey_diagram">Sankey diagrams</a><span>&nbsp;with&nbsp;</span><code>sankeyNetwork</code><span>. Here is an example using downloaded JSON data:</span></p>
<p><span>https://en.wikipedia.org/wiki/Sankey_diagram</span></p><p>Address of the bookmark: <a href="https://christophergandrud.github.io/networkD3/#sankey" rel="nofollow">https://christophergandrud.github.io/networkD3/#sankey</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/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>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44362/biostats-book</guid>
	<pubDate>Mon, 14 Aug 2023 03:11:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44362/biostats-book</link>
	<title><![CDATA[Biostats book !]]></title>
	<description><![CDATA[<p>https://practical-stats-med-r.netlify.app/</p><p>Address of the bookmark: <a href="https://practical-stats-med-r.netlify.app/" rel="nofollow">https://practical-stats-med-r.netlify.app/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</guid>
	<pubDate>Wed, 21 Aug 2013 07:56:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</link>
	<title><![CDATA[Comparison of Short Read De Novo Alignment Algorithms]]></title>
	<description><![CDATA[<p>Excellent article to introduce different sequencing methods along with tools for de novo assembly of sequencing reads and their relevant references.</p>
<p>Title:&nbsp;<strong>Comparison of Short Read De Novo Alignment Algorithms&nbsp;</strong></p>
<p>Author<strong>: Nikhil Gopal</strong></p><p>Address of the bookmark: <a href="http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf" rel="nofollow">http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</guid>
	<pubDate>Tue, 03 Sep 2013 18:00:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</link>
	<title><![CDATA[Latest paper on comparison of mapping tools]]></title>
	<description><![CDATA[<p>A. Hatem, D. Bozdag, A. E. Toland, U. V. Catalyurek "Benchmarking short sequence mapping tools" BMC Bioinformatics, 14(1):184, 2013.</p>
<p>http://bmi.osu.edu/hpc/software/benchmark/</p>
<p><a href="http://bmi.osu.edu/hpc/software/pmap/pmap.html">http://bmi.osu.edu/hpc/software/pmap/pmap.html</a></p>
<p>Other similiar papers:</p>
<p><a href="http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022">http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022</a></p>
<p><a href="http://bioinformatics.oxfordjournals.org/content/28/24/3169">http://bioinformatics.oxfordjournals.org/content/28/24/3169</a></p>
<p>Some new Mapping tool links:<a href="http://bmi.osu.edu/hpc/software/benchmark/"></a></p>
<p><strong>GSNAP</strong></p>
<p><a href="http://research-pub.gene.com/gmap/"></a><a href="http://research-pub.gene.com/gmap/">http://research-pub.gene.com/gmap/</a></p>
<p><strong>RMAP</strong></p>
<p><a href="http://rulai.cshl.edu/rmap/"></a><a href="http://rulai.cshl.edu/rmap/">http://rulai.cshl.edu/rmap/</a></p>
<p><strong>mrsFAST</strong></p>
<p><a href="http://mrsfast.sourceforge.net/Home"></a><a href="http://mrsfast.sourceforge.net/Home">http://mrsfast.sourceforge.net/Home</a></p>
<p><a href="http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/">http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/</a></p>
<p><strong>BFAST</strong></p>
<p><a href="http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page">http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page</a></p>
<p><strong>SHRiMP (for&nbsp;AB SOLiD color-space reads)</strong></p>
<p><a href="http://compbio.cs.toronto.edu/shrimp/">http://compbio.cs.toronto.edu/shrimp/</a></p>
<p><strong>RazerA 3</strong></p>
<p><a href="http://www.seqan.de/projects/razers/">http://www.seqan.de/projects/razers/</a></p><p>Address of the bookmark: <a href="http://www.biomedcentral.com/1471-2105/14/184" rel="nofollow">http://www.biomedcentral.com/1471-2105/14/184</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/9400/largest-genome-sequenced</guid>
	<pubDate>Fri, 21 Mar 2014 13:57:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/9400/largest-genome-sequenced</link>
	<title><![CDATA[Largest Genome Sequenced]]></title>
	<description><![CDATA[<p>The enormous size of the <strong>loblolly pine genome</strong> having <strong>22 billion base pairs</strong> compared to only 3 billion in the human genome. In other words, it is&nbsp;<strong>seven times</strong> larger than a human&rsquo;s and also the largest and the most complete&nbsp;<strong>conifer<a href="http://en.wikipedia.org/wiki/Pinophyta" target="_blank"></a></strong>&nbsp;genome ever sequenced.</p>
<p><strong>Related Paper:</strong></p>
<p>http://genomebiology.com/2014/15/3/R59/abstract</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://www.news.ucdavis.edu/search/news_detail.lasso?id=10859" rel="nofollow">http://www.news.ucdavis.edu/search/news_detail.lasso?id=10859</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/10243/new-rna-seq-tool</guid>
	<pubDate>Fri, 25 Apr 2014 10:59:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/10243/new-rna-seq-tool</link>
	<title><![CDATA[New RNA Seq tool]]></title>
	<description><![CDATA[<p>"<span>By removing the time-consuming step of read mapping, the authors reported, Sailfish able to provide quantification estimates 20&ndash;30 times faster than current methods without loss of accuracy."</span></p>
<p><span>Tool link:</span></p>
<p><span>http://www.cs.cmu.edu/~ckingsf/software/sailfish/</span></p>
<p><span></span></p><p>Address of the bookmark: <a href="http://www.genengnews.com/gen-news-highlights/lightweight-algorithms-sail-through-rna-sequencing-data/81249765/" rel="nofollow">http://www.genengnews.com/gen-news-highlights/lightweight-algorithms-sail-through-rna-sequencing-data/81249765/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10966/genxpro-gmbh</guid>
	<pubDate>Thu, 22 May 2014 07:18:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10966/genxpro-gmbh</link>
	<title><![CDATA[GenXPro GmbH]]></title>
	<description><![CDATA[<p><strong>GenXPro</strong>&nbsp;GMbH is service provider for entire spectrum of nucleotide-based information&nbsp;of any biological sample. By combining intelligent data reduction techniques and&nbsp;latest next generation sequencing technologies, our service portfolio provides most accurate and cost efficient solutions for&nbsp;transcriptomic-, genomic- or epigenomic research.</p><p><span><span><strong><span>GENXPRO GMBH</span>,&nbsp;</strong></span></span><span>ALTENH&Ouml;FERALLEE 3,&nbsp;</span><span>60438 FRANKFURT MAIN,&nbsp;</span><span>GERMANY</span></p><p><span><span><strong>Website</strong></span>:&nbsp;<a href="http://www.genxpro.info/products_and_services/"></a><a href="http://www.genxpro.info/products_and_services/">http://www.genxpro.info/products_and_services/</a></span></p><p><span><strong>PHONE</strong>: +49 (0)69- 95 73 97 10,&nbsp;FAX: +49 (0)69- 95 73 97 06</span></p><p><span>EMAIL: info@genxpro.de</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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