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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31568?offset=130</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28891/lumpy</guid>
	<pubDate>Thu, 25 Aug 2016 08:05:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28891/lumpy</link>
	<title><![CDATA[LUMPY]]></title>
	<description><![CDATA[<p>A probabilistic framework for structural variant discovery.</p>
<p>Ryan M Layer, Colby Chiang, Aaron R Quinlan, and Ira M Hall. 2014. "LUMPY: a Probabilistic Framework for Structural Variant Discovery." Genome Biology 15 (6): R84.&nbsp;<a href="http://dx.doi.org/10.1186/gb-2014-15-6-r84">doi:10.1186/gb-2014-15-6-r84</a>.</p>
<p>More at&nbsp;https://github.com/arq5x/lumpy-sv</p><p>Address of the bookmark: <a href="https://github.com/arq5x/lumpy-sv" rel="nofollow">https://github.com/arq5x/lumpy-sv</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28922/ka-ks-and-kaks-calculations</guid>
	<pubDate>Mon, 29 Aug 2016 11:44:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28922/ka-ks-and-kaks-calculations</link>
	<title><![CDATA[Ka, Ks and Ka/Ks calculations]]></title>
	<description><![CDATA[<p>gKaKs is a codon-based genome-level Ka/Ks computation pipeline developed and based on programs from four widely used packages: BLAT, BLASTALL (including bl2seq, formatdb and fastacmd), PAML (including codeml and yn00) and KaKs_Calculator (including 10 substitution rate estimation methods). gKaKs can automatically detect and eliminate frameshift mutations and premature stop codons to compute the substitution rates (Ka, Ks and Ka/Ks) between a well-annotated genome and a non-annotated genome or even a poorly assembled scaffold dataset. It is especially useful for newly sequenced genomes that have not been well annotated.&nbsp;</p>
<p>Look for KaKs calculation:</p>
<p>https://github.com/fumba/kaks-calculator</p>
<p>http://longlab.uchicago.edu/?q=gKaKs</p>
<p>http://www.ncbi.nlm.nih.gov/pubmed/23314322</p><p>Address of the bookmark: <a href="http://longlab.uchicago.edu/?q=gKaKs" rel="nofollow">http://longlab.uchicago.edu/?q=gKaKs</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28997/braker-pipeline-for-fully-automated-prediction-of-protein-coding-genes-with-genemark-eset-and-augustus-in-novel-eukaryotic-genomes</guid>
	<pubDate>Thu, 01 Sep 2016 08:02:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28997/braker-pipeline-for-fully-automated-prediction-of-protein-coding-genes-with-genemark-eset-and-augustus-in-novel-eukaryotic-genomes</link>
	<title><![CDATA[BRAKER: pipeline for fully automated prediction of protein coding genes with GeneMark-ES/ET and AUGUSTUS in novel eukaryotic genomes]]></title>
	<description><![CDATA[<p><span>Gene finding in eukaryotic genomes is notoriously difficult to automate. The task is to design a work flow with a minimal set of tools that would reach state-of-the-art performance across a wide range of species. GeneMark-ET is a gene prediction tool that incorporates RNA-Seq data into unsupervised training and subsequently generates ab initio gene predictions. AUGUSTUS is a gene finder that usually requires supervised training and uses information from RNA-Seq reads in the prediction step. Complementary strengths of GeneMark-ET and AUGUSTUS provided motivation for designing a new combined tool for automatic gene prediction.</span></p>
<p>http://www.ncbi.nlm.nih.gov/pubmed/26559507</p><p>Address of the bookmark: <a href="http://bioinf.uni-greifswald.de/bioinf/braker/" rel="nofollow">http://bioinf.uni-greifswald.de/bioinf/braker/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29112/sybil</guid>
	<pubDate>Wed, 07 Sep 2016 03:20:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29112/sybil</link>
	<title><![CDATA[Sybil]]></title>
	<description><![CDATA[<p><span>The Sybil software package provides a primarily web-based front-end to comparative genome datasets warehoused in a chado relational database. It was developed by the bioinformatics department at The Institute for Genomic Research (</span><a href="http://www.tigr.org/">TIGR</a><span>) and development continues at the J. Craig Venter Institute (</span><a href="http://jcvi.org/">JCVI</a><span>) and the Institute for Genome Sciences (</span><a href="http://igs.umaryland.edu/">IGS</a><span>) at the University of Maryland: Baltimore. Sybil has been used at TIGR/JCVI, IGS, NYU, New York Medical College, Novartis Vaccines and University of Maryland: College Park to support a number of research projects that involve comparative genome analysis. The following sections provide some high-level technical details about the overall architecture and external dependencies of the Sybil package.</span></p><p>Address of the bookmark: <a href="http://sybil.sourceforge.net/" rel="nofollow">http://sybil.sourceforge.net/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29635/r-graphs</guid>
	<pubDate>Fri, 04 Nov 2016 10:48:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29635/r-graphs</link>
	<title><![CDATA[R Graphs !!]]></title>
	<description><![CDATA[<p><span>The blog is a collection of script examples with example data and output plots. R produce excellent quality graphs for data analysis, science and business presentation, publications and other purposes. Self-help codes and examples are provided. Enjoy nice graphs !!</span></p><p>Address of the bookmark: <a href="http://rgraphgallery.blogspot.be/" rel="nofollow">http://rgraphgallery.blogspot.be/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29679/comparative-genomics-educational-material-and-papers-bookmarks</guid>
	<pubDate>Wed, 09 Nov 2016 16:23:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29679/comparative-genomics-educational-material-and-papers-bookmarks</link>
	<title><![CDATA[Comparative genomics educational material and papers bookmarks]]></title>
	<description><![CDATA[<p><span>Alignment of the porcine genome against seven other mammalian genomes (</span><a href="http://www.nature.com/nature/journal/v491/n7424/full/nature11622.html#supplementary-information">Supplementary Information</a><span>) identified homologous synteny blocks (HSBs). Using porcine HSBs and stringent filtering criteria, 192 pig-specific evolutionary breakpoint regions (EBRs) were located. The number of porcine EBRs </span><span>is comparable to the number of bovine-lineage-specific EBRs (100) reported earlier using a slightly lower resolution (500</span><span><span>&thinsp;</span></span><span>kilobases (kb)), indicating that both lineages evolved with an average rate of ~2.1 large-scale rearrangements per million years after the divergence from a common cetartiodactyl ancestor ~60</span><span><span>&thinsp;</span></span><span>Myr ago</span><sup><a href="http://www.nature.com/nature/journal/v491/n7424/full/nature11622.html#ref2" title="Meredith, R. W. et al. Impacts of the Cretaceous Terrestrial Revolution and KPg extinction on mammal diversification. Science 334, 521-524 (2011)">2</a></sup><span>. This rate compares to ~1.9 rearrangements per million years within the primate lineage (</span><a href="http://www.nature.com/nature/journal/v491/n7424/full/nature11622.html#supplementary-information">Supplementary Table 11</a><span>). A total of 20 and 18 cetartiodactyl EBRs (shared by pigs and cattle) were detected using the pig and human genomes as a reference, respectively.</span></p><p>Address of the bookmark: <a href="http://www.nature.com/nature/journal/v491/n7424/abs/nature11622.html" rel="nofollow">http://www.nature.com/nature/journal/v491/n7424/abs/nature11622.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/29915/professor-all-levels-in-bioinformatics-and-computational-biology</guid>
  <pubDate>Tue, 22 Nov 2016 05:43:38 -0600</pubDate>
  <link></link>
  <title><![CDATA[Professor (all levels) in Bioinformatics and Computational Biology]]></title>
  <description><![CDATA[
<p>King Abdullah University of Science and Technology (KAUST) (kaust.edu.sa) is seeking a highly motivated and skilled faculty member for the Bioinformatics track whose research focuses on development of methods and tools for Bioinformatics and Computational Biology.<br />KAUST is an international, graduate-level research university dedicated to advancing science and technology through interdisciplinary research, education, and innovation. Located on the shores of the Red Sea in Saudi Arabia, KAUST offers superb research facilities, generous assured research funding, and internationally competitive salaries, attracting top international faculty, scientists, engineers, and students to conduct fundamental and goal-oriented research to address the world’s pressing scientific and technological challenges in the areas of food, water, energy, and the environment.<br />The successful applicant is expected to develop world-leading research in domain of bioinformatics/computational biology with focus on development of novel computational approaches for efficient and accurate methods of analyzing biological phenomena at molecular level. The faculty member will be part of the Computational Bioscience Research Center (CBRC) within the Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division. The position will remain open until filled.<br /> <br />Requirements:<br /> <br />PhD or equivalent in a Computer Science, Mathematics or Engineering discipline. Candidates should be well-established within the research field relevant to the position grade. They should demonstrate original research and experience at the highest international level.<br /> <br />Responsibilities and tasks:<br /> <br />Research competence in the following areas is preferred:<br />Analysis of next generation sequencing (NGS) and other ‘omics’ data (e.g. CAGE, ChIP-Seq, DHS, RNA-Seq, Ribo-Seq, proteomic, metabolic and NMR spectra, etc.).<br />Signaling, regulatory and metabolic pathways analysis.<br />Development of tools (web-based and standalone) suited for efficient computational biology/bioinformatics.<br /> <br /> <br />Visit cemse.kaust.edu.sa to apply.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30090/standardized-velvet-assembly-report</guid>
	<pubDate>Fri, 09 Dec 2016 03:59:59 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30090/standardized-velvet-assembly-report</link>
	<title><![CDATA[Standardized velvet assembly report]]></title>
	<description><![CDATA[<p>Requirements:</p>
<ul>
<li>velvet (velveth velvetg should be in your PATH)</li>
<li>R (with Sweave)</li>
<li>pdflatex (usually part of TeTeX)</li>
<li>ggplot2 (from R prompt type install.packages("ggplot2","proto","xtable"))</li>
<li>Perl</li>
</ul>
<p>Optional:</p>
<ul>
<li>BLAT or BLAST (to generate alignments against a reference genome). If using BLAT, add faToTwoBit,gfClient,gfServer to your PATH. If using BLAST, add blastall and formatdb.</li>
</ul>
<p>Edit permute.sh to your liking, paying particular attention to the kmer, cvCut, expCov, and other flags</p>
<p>To Run:</p>
<ol>
<li><code>perl fastaAllSize mysequences.fa &gt; mysequences.stat or gunzip -c mysequences.fa.gz | fastaAllSize &gt; mysequences.stat</code>&nbsp;Substitute fastqAllSize for fastq files.</li>
<li><code>./permute.sh mysequences</code>&nbsp;(leave out the .fa)</li>
</ol>
<p>https://github.com/leipzig/standardized-velvet-assembly-report</p><p>Address of the bookmark: <a href="https://github.com/leipzig/standardized-velvet-assembly-report" rel="nofollow">https://github.com/leipzig/standardized-velvet-assembly-report</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30897/finestructure-v2-globetrotter</guid>
	<pubDate>Mon, 13 Feb 2017 08:40:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30897/finestructure-v2-globetrotter</link>
	<title><![CDATA[fineSTRUCTURE v2 &amp; GLOBETROTTER]]></title>
	<description><![CDATA[<p>Software available at this site</p>
<div>
<ul>
<li><a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/finestructure_info.html">FineSTRUCTURE version 2</a>, a pipeline for running ChromoPainter and FineSTRUCTURE for population inference. A GUI is available for interpretation. Download from the <a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/finestructure.html">Downloads</a> page.</li>
<li><a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/finestructureR.html">FineSTRUCTURE R scripts</a>, a facility for exploring the results when the GUI is unavailable.</li>
<li><a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/globetrotter.html">GLOBETROTTER</a>, the admixture dating method based on ChromoPainter. Download from the <a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/finestructure.html">Downloads</a> page.</li>
<li><a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/admixture.html">AdmixturePainting</a>, A set of R tools to inmterpret the results of ADMIXTURE and STRUCTURE-like mixture models.</li>
<li><a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/radpainter.html">RADpainter</a>, finestructure and ChromoPainter for RAD tag data used for non-model organisms.</li>
<li>Scripts to perform many types of conversion. Included in the main software download from the <a href="https://people.maths.bris.ac.uk/%7Emadjl/finestructure/finestructure.html">Downloads</a> page.</li>
</ul>
What this page is This page provides information about and downloads for <strong>methodology for Chromosome Painting</strong>. It is not a facility to analyse your genome. Sorry if you were misled by the punchy name!<br> About Chromosome Painting Painting is an efficient way of identifying important haplotype information from dense genotype data. It describes ancestry in an efficient way suitable for a range of further analyses, including population identification and admixture dating.</div><p>Address of the bookmark: <a href="http://paintmychromosomes.com/" rel="nofollow">http://paintmychromosomes.com/</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30971/hiveplot</guid>
	<pubDate>Thu, 16 Feb 2017 11:39:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30971/hiveplot</link>
	<title><![CDATA[HivePlot]]></title>
	<description><![CDATA[<p>The&nbsp;<em>hive plot</em>&nbsp;is a rational visualization method for drawing networks. Nodes are mapped to and positioned on radially distributed linear axes &mdash; this mapping is based on network structural properties. Edges are drawn as curved links. Simple and interpretable.</p>
<p>The purpose of the hive plot is to establish a new baseline for visualization of large networks &mdash; a method that is both general and tunable and useful as a starting point in visually exploring network structure.</p>
<p>More at&nbsp;http://www.hiveplot.com/</p><p>Address of the bookmark: <a href="http://www.hiveplot.com/" rel="nofollow">http://www.hiveplot.com/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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