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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29635?</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28937/sushi-an-rbioconductor-package-for-visualizing-genomic-data</guid>
	<pubDate>Wed, 31 Aug 2016 08:29:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28937/sushi-an-rbioconductor-package-for-visualizing-genomic-data</link>
	<title><![CDATA[Sushi: An R/Bioconductor package for visualizing genomic data]]></title>
	<description><![CDATA[<p>Sushi: An R/Bioconductor package for visualizing genomic data</p><p>Address of the bookmark: <a href="https://www.bioconductor.org/packages/devel/bioc/vignettes/Sushi/inst/doc/Sushi.pdf" rel="nofollow">https://www.bioconductor.org/packages/devel/bioc/vignettes/Sushi/inst/doc/Sushi.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</guid>
	<pubDate>Wed, 24 Aug 2016 05:36:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</link>
	<title><![CDATA[TGNet]]></title>
	<description><![CDATA[<p><span>Recent technological progress has greatly facilitated&nbsp;</span><em>de novo</em><span>&nbsp;genome sequencing. However,&nbsp;</span><em>de novo</em><span>&nbsp;assemblies consist in many pieces of contiguous sequence (contigs) arranged in thousands of scaffolds instead of small numbers of chromosomes. Confirming and improving the quality of such assemblies is critical for subsequent analysis.&nbsp;</span></p>
<p>Visualization and quality assessment of de novo genome assemblies</p>
<p>Citation</p>
<p>This software is fully described in the paper:<br>Riba-Grognuz, Keller, Falquet, Xenarios &amp; Wurm (2011) Visualization and quality assessment of de novo genome assemblies.</p>
<p>In brief, our scripts create Cytoscape files to visualize transcript evidence that suggests adjacency between scaffolds and contigs.</p>
<p>Software requirements</p>
<p>BLAT (tested with Standalone BLAT v. 32&times;1). Source Binaries .<br>Cytoscape (tested with versions 2.7.0, 2.8.2)<br>a UNIX machine (tested on Mac OS X 10.6 and CentOS 4.6)</p><p>Address of the bookmark: <a href="https://github.com/ksanao/TGNet" rel="nofollow">https://github.com/ksanao/TGNet</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</guid>
	<pubDate>Fri, 20 May 2016 11:01:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</link>
	<title><![CDATA[RCircos: an R package for Circos 2D track plots]]></title>
	<description><![CDATA[<p>RCircos package provides a simple and flexible way to make Circos 2D track plots with R and could be easily integrated into other R data processing and graphic manipulation pipelines for presenting large-scale multi-sample genomic research data. It can also serve as a base tool to generate complex Circos images.</p>
<p>More at https://bitbucket.org/henryhzhang/rcircos/src</p><p>Address of the bookmark: <a href="https://bitbucket.org/henryhzhang/rcircos/src" rel="nofollow">https://bitbucket.org/henryhzhang/rcircos/src</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28855/vcfr</guid>
	<pubDate>Fri, 19 Aug 2016 07:38:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28855/vcfr</link>
	<title><![CDATA[vcfR]]></title>
	<description><![CDATA[<p><span>Most variant calling pipelines result in files containing large quantities of variant information. The&nbsp;</span><a href="http://samtools.github.io/hts-specs/" title="VCF format at hts-specs">variant call format (vcf)</a><span>&nbsp;is an increasingly popular format for this data. The format of these files and their content is discussed in the vignette &lsquo;vcf data.&rsquo; These files are typically intended to be post-processed (i.e., filtered) as an attempt to remove false positives or otherwise problematic sites. The R package vcfR provides tools to facilitate this filtering as well as to visualize the effects of choices made during this process.</span></p><p>Address of the bookmark: <a href="https://cran.r-project.org/web/packages/vcfR/vignettes/visualization_1.html" rel="nofollow">https://cran.r-project.org/web/packages/vcfR/vignettes/visualization_1.html</a></p>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29004/r-chie</guid>
	<pubDate>Thu, 01 Sep 2016 11:47:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29004/r-chie</link>
	<title><![CDATA[R-chie]]></title>
	<description><![CDATA[<p><strong>R-chie</strong><span>&nbsp;allows you to make arc diagrams of RNA secondary structures, allowing for easy comparison and overlap of two structures, rank and display basepairs in colour and to also visualize corresponding multiple sequence alignments and co-variation information.</span><br><strong>R4RNA</strong><span>&nbsp;is the R package powering R-chie, available for&nbsp;</span><a href="http://www.e-rna.org/r-chie/download.cgi">download</a><span>&nbsp;and local use for more customized figures and scripting.</span></p>
<p>http://www.e-rna.org/r-chie/plot.cgi?eg=single</p><p>Address of the bookmark: <a href="http://www.e-rna.org/r-chie/plot.cgi?eg=single" rel="nofollow">http://www.e-rna.org/r-chie/plot.cgi?eg=single</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29487/shinyheatmap</guid>
	<pubDate>Fri, 21 Oct 2016 05:12:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29487/shinyheatmap</link>
	<title><![CDATA[Shinyheatmap]]></title>
	<description><![CDATA[<p><span>Background: Transcriptomics, metabolomics, metagenomics, and other various next-generation sequencing (-omics) fields are known for their production of large datasets. Visualizing such big data has posed technical challenges in biology, both in terms of available computational resources as well as programming acumen. Since heatmaps are used to depict high-dimensional numerical data as a colored grid of cells, efficiency and speed have often proven to be critical considerations in the process of successfully converting data into graphics. For example, rendering interactive heatmaps from large input datasets (e.g., 100k+ rows) has been computationally infeasible on both desktop computers and web browsers. In addition to memory requirements, programming skills and knowledge have frequently been barriers-to-entry for creating highly customizable heatmaps. Results: We propose shinyheatmap: an advanced user-friendly heatmap software suite capable of efficiently creating highly customizable static and interactive biological heatmaps in a web browser. shinyheatmap is a low memory footprint program, making it particularly well-suited for the interactive visualization of extremely large datasets that cannot typically be computed in-memory due to size restrictions. Conclusions: shinyheatmap is hosted online as a freely available web server with an intuitive graphical user interface: http://shinyheatmap.com. The methods are implemented in R, and are available as part of the shinyheatmap project at: https://github.com/Bohdan-Khomtchouk/shinyheatmap.</span></p>
<p><span>More at&nbsp;http://biorxiv.org/content/early/2016/09/21/076463&nbsp;</span></p><p>Address of the bookmark: <a href="http://shinyheatmap.com/" rel="nofollow">http://shinyheatmap.com/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31714/krona</guid>
	<pubDate>Wed, 22 Mar 2017 04:47:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31714/krona</link>
	<title><![CDATA[Krona]]></title>
	<description><![CDATA[<p>Krona allows hierarchical data to be explored with zooming, multi-layered pie charts. Krona charts can be created using an <a href="https://github.com/marbl/Krona/wiki/ExcelTemplate">Excel template</a> or <a href="https://github.com/marbl/Krona/wiki/KronaTools">KronaTools</a>, which includes support for several bioinformatics tools and raw data formats. The interactive charts are self-contained and can be viewed with any modern web browser (see <a href="https://github.com/marbl/Krona/wiki/Browser%20support">Browser support</a>).</p>
<p><a href="http://marbl.github.io/Krona/img/screen_mgrast.png"><img src="https://camo.githubusercontent.com/27b71b1f1832523723c3d14dec764e7ad098438c/687474703a2f2f6d6172626c2e6769746875622e696f2f4b726f6e612f696d672f7468756d625f6d67726173742e706e67" width="210" height="167" alt="image" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/marbl/Krona/wiki" rel="nofollow">https://github.com/marbl/Krona/wiki</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27070/venn-diagrams-on-r-studio</guid>
	<pubDate>Mon, 25 Apr 2016 16:22:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27070/venn-diagrams-on-r-studio</link>
	<title><![CDATA[Venn Diagrams on R Studio]]></title>
	<description><![CDATA[<h3>First step: Install &amp; load &ldquo;VennDiagram&rdquo; package.</h3>
<pre><code><span># install.packages('VennDiagram')</span>
<span>library</span><span>(</span><span>VennDiagram</span><span>)</span>
</code></pre>
<h3>Second step: Load data</h3>
<p>Add filepath if &ldquo;catdoge.csv&rdquo; is not in working-directory.</p>
<pre><code><span>d</span> <span>&lt;-</span> <span>read.csv</span><span>(</span><span>"catdoge.csv"</span><span>)</span></code><br><br></pre><p>Address of the bookmark: <a href="http://rstudio-pubs-static.s3.amazonaws.com/13301_6641d73cfac741a59c0a851feb99e98b.html" rel="nofollow">http://rstudio-pubs-static.s3.amazonaws.com/13301_6641d73cfac741a59c0a851feb99e98b.html</a></p>]]></description>
	<dc:creator>Jitendra Prajapati</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/29601/statistics-using-r-with-biological-examples</guid>
	<pubDate>Thu, 03 Nov 2016 04:55:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/29601/statistics-using-r-with-biological-examples</link>
	<title><![CDATA[Statistics Using R   with Biological Examples]]></title>
	<description><![CDATA[<p>This book is a manifestation of my desire to teach researchers in biology a bit more about statistics than an ordinary introductory course covers and to introduce the utilization of R as a tool for analyzing their data. My goal is to reach those with little or no training in higher level statistics so that they can do more of their own data analysis, communicate more with statisticians, and appreciate the great potential statistics has to offer as a tool to answer biological questions. </p><p>This is necessary in light of the increasing use of higher level statistics in biomedical research. I hope it accomplishes this mission and encourage its free distribution and use as a course text or supplement.</p><p>K Seefeld, May 2007</p>]]></description>
	<dc:creator>Neel</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/29601" length="4581031" type="application/pdf" />
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29500/genomescope-open-source-web-tool-to-rapidly-estimate-the-overall-characteristics-of-a-genome-including-genome-size-heterozygosity-rate-and-repeat-content-from-unprocessed-short-reads</guid>
	<pubDate>Fri, 21 Oct 2016 05:46:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29500/genomescope-open-source-web-tool-to-rapidly-estimate-the-overall-characteristics-of-a-genome-including-genome-size-heterozygosity-rate-and-repeat-content-from-unprocessed-short-reads</link>
	<title><![CDATA[GenomeScope: open-source web tool to rapidly estimate the overall characteristics of a genome, including genome size, heterozygosity rate, and repeat content from unprocessed short reads]]></title>
	<description><![CDATA[<div>
<div>
<div>
<div id="content-block-markup">
<div>
<div id="abstract-1">
<p id="p-2">Summary: GenomeScope is an open-source web tool to rapidly estimate the overall characteristics of a genome, including genome size, heterozygosity rate, and repeat content from unprocessed short reads. These features are essential for studying genome evolution, and help to choose parameters for downstream analysis. We demonstrate its accuracy on 324 simulated and 16 real datasets with a wide range in genome sizes, heterozygosity levels, and error rates. Availability and Implementation: http://qb.cshl.edu/genomescope/, https://github.com/schatzlab/genomescope.git</p>
</div>
<span></span></div>
<span></span></div>
</div>
</div>
</div><p>Address of the bookmark: <a href="http://qb.cshl.edu/genomescope/" rel="nofollow">http://qb.cshl.edu/genomescope/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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