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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/43319?offset=120</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41571/wego-simple-but-useful-tool-for-visualizing-comparing-and-plotting-go-gene-ontology-annotation-results</guid>
	<pubDate>Sun, 12 Apr 2020 10:02:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41571/wego-simple-but-useful-tool-for-visualizing-comparing-and-plotting-go-gene-ontology-annotation-results</link>
	<title><![CDATA[WEGO : simple but useful tool for visualizing, comparing and plotting GO (Gene Ontology) annotation results]]></title>
	<description><![CDATA[<p><span>WEGO (Web Gene Ontology Annotation Plot) is a simple but useful tool for visualizing, comparing and plotting GO (Gene Ontology) annotation results. As the GO vocabulary became more and more popular, WEGO was widely adopted and used in many researches. Therefore we have updated WEGO 2.0 in 2018. Here are some changes we&rsquo;ve made:</span><br><span>1. The limit of input file numbers was cancelled. Now the users could upload as many files as they want with one operation.</span><br><span>2. We have added the reference data of 9 species for users selection.</span><br><span>3. Besides the traditional WEGO histogram, WEGO 2.0 outputs an additional type of bar graph showing GO terms with significant gene number differences.</span></p><p>Address of the bookmark: <a href="http://wego.genomics.org.cn/" rel="nofollow">http://wego.genomics.org.cn/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38166/pygenometracks-standalone-program-and-library-to-plot-beautiful-genome-browser-tracks</guid>
	<pubDate>Fri, 09 Nov 2018 12:34:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38166/pygenometracks-standalone-program-and-library-to-plot-beautiful-genome-browser-tracks</link>
	<title><![CDATA[pyGenomeTracks: Standalone program and library to plot beautiful genome browser tracks]]></title>
	<description><![CDATA[<p>pyGenomeTracks aims to produce high-quality genome browser tracks that are highly customizable. Currently, it is possible to plot:</p>
<ul>
<li>bigwig</li>
<li>bed (many options)</li>
<li>bedgraph</li>
<li>links (represented as arcs)</li>
<li>Hi-C matrices (if&nbsp;<a href="http://hicexplorer.readthedocs.io/">HiCExplorer</a>&nbsp;is installed)</li>
</ul><p>Address of the bookmark: <a href="https://github.com/deeptools/pyGenomeTracks" rel="nofollow">https://github.com/deeptools/pyGenomeTracks</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40991/jtools-more-efficient-presentation-of-regression-analyses</guid>
	<pubDate>Tue, 11 Feb 2020 23:10:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40991/jtools-more-efficient-presentation-of-regression-analyses</link>
	<title><![CDATA[jtools : more efficient presentation of regression analyses]]></title>
	<description><![CDATA[<p>This package consists of a series of functions created by the author (Jacob) to automate otherwise tedious research tasks. At this juncture, the unifying theme is the more efficient presentation of regression analyses. There are a number of functions for other programming and statistical purposes as well. Support for the&nbsp;<code>survey</code>&nbsp;package&rsquo;s&nbsp;<code>svyglm</code>&nbsp;objects as well as weighted regressions is a common theme throughout.</p>
<p><strong>Notice:</strong>&nbsp;As of&nbsp;<code>jtools</code>&nbsp;version 2.0.0, all functions dealing with interactions (e.g.,&nbsp;<code>interact_plot()</code>,&nbsp;<code>sim_slopes()</code>,&nbsp;<code>johnson_neyman()</code>) have been moved to a new package, aptly named&nbsp;<a href="https://interactions.jacob-long.com/"><code>interactions</code></a>.</p><p>Address of the bookmark: <a href="https://cran.r-project.org/web/packages/jtools/readme/README.html" rel="nofollow">https://cran.r-project.org/web/packages/jtools/readme/README.html</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44208/circos-visualization</guid>
	<pubDate>Mon, 06 Mar 2023 06:01:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44208/circos-visualization</link>
	<title><![CDATA[Circos visualization !]]></title>
	<description><![CDATA[<p>Circos visualization</p>
<p>https://wlcb.oit.uci.edu/modules/index.html</p><p>Address of the bookmark: <a href="https://wlcb.oit.uci.edu/NG-Circos" rel="nofollow">https://wlcb.oit.uci.edu/NG-Circos</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30236/pyscaf</guid>
	<pubDate>Mon, 19 Dec 2016 14:20:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30236/pyscaf</link>
	<title><![CDATA[pyScaf]]></title>
	<description><![CDATA[<p>pyScaf orders contigs from genome assemblies utilising several types of information:</p>
<ul>
<li>paired-end (PE) and/or mate-pair libraries (<a href="https://github.com/lpryszcz/pyScaf#ngs-based-scaffolding">NGS-based mode</a>)</li>
<li>long reads (<a href="https://github.com/lpryszcz/pyScaf#scaffolding-based-on-long-reads">NGS-based mode</a>)</li>
<li>synteny to the genome of some related species (<a href="https://github.com/lpryszcz/pyScaf#reference-based-scaffolding">reference-based mode</a>)</li>
</ul>
<p>Scaffolding&nbsp;</p>
<p>In reference-based mode, pyScaf uses synteny to the genome of closely related species in order to order contigs and estimate distances between adjacent contigs.</p>
<p>Contigs are aligned globally (end-to-end) onto reference chromosomes, ignoring:</p>
<ul>
<li>matches not satisfying cut-offs (<code>--identity</code>&nbsp;and&nbsp;<code>--overlap</code>)</li>
<li>suboptimal matches (only best match of each query to reference is kept)</li>
<li>and removing overlapping matches on reference.</li>
</ul>
<p>In preliminary tests, pyScaf performed superbly on simulated heterozygous genomes based on&nbsp;<em>C. parapsilosis</em>&nbsp;(13 Mb; CANPA) and&nbsp;<em>A. thaliana</em>&nbsp;(119 Mb; ARATH) chromosomes, reconstructing correctly all chromosomes always for CANPA and nearly always for ARATH (<a href="https://www.dropbox.com/sh/bb7lwggo40xrwtc/AAAZ7pByVQQQ-WhUXZVeJaZVa/pyScaf?dl=0">Figures in dropbox</a>,&nbsp;<a href="https://docs.google.com/spreadsheets/d/1InBExy-qKDLj-upd8tlPItVSKc4mLepZjZxB31ii9OY/edit#gid=2036953672">CANPA table</a>,&nbsp;<a href="https://docs.google.com/spreadsheets/d/1InBExy-qKDLj-upd8tlPItVSKc4mLepZjZxB31ii9OY/edit#gid=1920757821">ARATH table</a>).<br>Runs took ~0.5 min for CANPA on&nbsp;<code>4 CPUs</code>&nbsp;and ~2 min for ARATH on&nbsp;<code>16 CPUs</code>.</p>
<p><span>Important remarks:</span></p>
<ul>
<li>Reduce your assembly before (fasta2homozygous.py) as any redundancy will likely break the synteny.</li>
<li>pyScaf works better with contigs than scaffolds, as scaffolds are often affected by mis-assemblies (no&nbsp;<em>de novo assembler</em>&nbsp;/ scaffolder is perfect...), which breaks synteny.</li>
<li>pyScaf works very well if divergence between reference genome and assembled contigs is below 20% at nucleotide level.</li>
<li>pyScaf deals with large rearrangements ie. deletions, insertion, inversions, translocations.&nbsp;<span>Note however, this is experimental implementation!</span></li>
<li>Consider closing gaps after scaffolding.</li>
</ul><p>Address of the bookmark: <a href="https://github.com/lpryszcz/pyScaf" rel="nofollow">https://github.com/lpryszcz/pyScaf</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35550/circoletto-visualizing-sequence-similarity-with-circos</guid>
	<pubDate>Fri, 09 Feb 2018 10:23:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35550/circoletto-visualizing-sequence-similarity-with-circos</link>
	<title><![CDATA[Circoletto: visualizing sequence similarity with Circos]]></title>
	<description><![CDATA[<p><span>Circoletto, an online visualization tool based on Circos, which provides a fast, aesthetically pleasing and informative overview of sequence similarity search results.</span></p>
<p>Online version and downloadable software package for offline use (source code in PERL) freely available at&nbsp;<a href="http://bat.ina.certh.gr/tools/circoletto/" target="">http://bat.ina.certh.gr/tools/circoletto/</a></p>
<p><strong>Contact:</strong><a href="mailto:ndarz@certh.gr" target="">ndarz@certh.gr</a></p><p>Address of the bookmark: <a href="http://tools.bat.infspire.org/circoletto/" rel="nofollow">http://tools.bat.infspire.org/circoletto/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/2882/phylogenetics</guid>
	<pubDate>Fri, 23 Aug 2013 03:53:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/2882/phylogenetics</link>
	<title><![CDATA[Phylogenetics]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/fQwI90bkJl4" frameborder="0" allowfullscreen></iframe>006 - Phylogenetics

Paul Andersen discusses the specifics of phylogenetics.  The evolutionary relationships of organisms are discovered through both morphological and molecular data.  A specific type of phylogenetic tree, the cladogram, is also covered.

Intro Music Atribution
Title: I4dsong_loop_main.wav
Artist: CosmicD
Link to sound: http://www.freesound.org/people/CosmicD/sounds/72556/
Creative Commons Atribution License]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30698/itol-interactive-tree-of-life</guid>
	<pubDate>Tue, 31 Jan 2017 05:56:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30698/itol-interactive-tree-of-life</link>
	<title><![CDATA[iTOL: interactive Tree Of Life]]></title>
	<description><![CDATA[<p><strong>Interactive Tree Of Life</strong><span>&nbsp;is an online tool for the display and manipulation of phylogenetic trees. It provides most of the features available in other tree viewers, and offers a novel circular tree layout, which makes it easy to visualize mid-sized tree (up to several thousand leaves). Trees can be exported to several graphical formats, both bitmap and vector based.</span></p>
<p><img src="http://itol.embl.de/img/home/ex3.png" alt="image" style="border: 0px;"><br><span>There are several pre-computed trees available for display, including the main Tree Of Life, described in&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/16513982">Ciccarelli, et al., 2006</a><span>. In addition to the precomputed trees, users can upload and display personal trees and data, using the 'Data upload' page or through a personal user account.</span></p><p>Address of the bookmark: <a href="http://itol.embl.de/" rel="nofollow">http://itol.embl.de/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/38293/tree-illustrating-the-lack-of-interchromosomal-rearrangement-of-the-microchromosomes</guid>
	<pubDate>Mon, 26 Nov 2018 04:20:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/38293/tree-illustrating-the-lack-of-interchromosomal-rearrangement-of-the-microchromosomes</link>
	<title><![CDATA[Tree illustrating the lack of interchromosomal rearrangement of the microchromosomes.]]></title>
	<description><![CDATA[<p><span>Tree illustrating the lack of interchromosomal rearrangement of the microchromosomes. No interchromosomal microchromosome fusions from the avian ancestor unless otherwise stated (macrochromosomal fusions not listed). The overall pattern of microchromosome stability and rearrangement across the species is illustrated</span></p><p><span><span>Jarvis et al. (2014)</span></span></p><p><span><span>Reference&nbsp;https://link.springer.com/article/10.1007/s00412-018-0685-6</span></span></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/38293" length="291560" type="image/png" />
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43419/senior-bioinformatician-assembly-moore-aquatic-symbiosis-project-tree-of-life</guid>
  <pubDate>Sat, 02 Oct 2021 00:28:30 -0500</pubDate>
  <link></link>
  <title><![CDATA[Senior Bioinformatician (Assembly) Moore Aquatic Symbiosis Project Tree of Life]]></title>
  <description><![CDATA[
<p>You will have some previous experience with genome bioinformatics or other large scale scientific data analysis, or a newly qualified graduate student with data science skills interested in DNA sequence data. While desirable, previous experience with DNA sequencing data is not strictly necessary for the position. We have a strong publication record and culture of producing open data resources and open source software development. This role requires an investigative and solution-oriented mindset and excellent communication skills to work effectively within large national and international consortia. </p>

<p>More at https://jobs.sanger.ac.uk/vacancy/senior-bioinformatician-assembly-moore-aquatic-symbiosis-project-tree-of-life-458923.html</p>
]]></description>
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