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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44252?offset=70</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44557/fundamentals-of-data-visualization-by-claus-o-wilke</guid>
	<pubDate>Sat, 08 Jun 2024 16:07:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44557/fundamentals-of-data-visualization-by-claus-o-wilke</link>
	<title><![CDATA[Fundamentals of Data Visualization by Claus O. Wilke]]></title>
	<description><![CDATA[<p><span><span>The book is meant as a guide to making visualizations that accurately reflect the data, tell a story, and look professional. It has grown out of my experience of working with students and postdocs in my laboratory on thousands of data visualizations. Over the years, I have noticed that the same issues arise over and over. I have attempted to collect my accumulated knowledge from these interactions in the form of this book.</span></span></p>
<p><span>The entire book is written in R Markdown, using RStudio as my text editor and the&nbsp;</span><span>bookdown</span><span>&nbsp;package to turn a collection of markdown documents into a coherent whole. The book&rsquo;s source code is hosted on GitHub, at&nbsp;</span><a href="https://github.com/clauswilke/dataviz">https://github.com/clauswilke/dataviz</a><span>.&nbsp;</span></p><p>Address of the bookmark: <a href="https://clauswilke.com/dataviz/" rel="nofollow">https://clauswilke.com/dataviz/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4552/imtech-lab</guid>
  <pubDate>Sun, 15 Sep 2013 09:41:04 -0500</pubDate>
  <link></link>
  <title><![CDATA[IMTECH Lab]]></title>
  <description><![CDATA[
<p>Computer Aided Protein Structure Prediction; Identification of Vaccine<br />Candidates (T-Epitope prediction); Analysis of Nucleotide/Protein Sequences; Development of Web Server/</p>

<p>Software; Creation of Public Domain Resources in Biology<br />Present Status::</p>

<p>Developing prediction methods for gene, beta-turn, secondary structure and MHC-binding sites.<br />Area of Interest ::</p>

<p>Comparison of force field simulations. Analysis of DNA-protein interactions using molecular mechanics methods.Drug Target Identification using in silico biology.</p>

<p>More @ http://www.imtech.res.in/bic/index.php?option=com_content&amp;view=article&amp;id=65</p>

<p>PIs: http://www.imtech.res.in/bic/index.php?option=com_content&amp;view=article&amp;id=69</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28200/machine-learning</guid>
	<pubDate>Fri, 01 Jul 2016 12:57:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28200/machine-learning</link>
	<title><![CDATA[Machine Learning !!!]]></title>
	<description><![CDATA[<p>In machine learning, computers apply&nbsp;<strong>statistical learning</strong>&nbsp;techniques to automatically identify patterns in data. These techniques can be used to make highly accurate predictions.</p>
<p><em>Keep scrolling.</em>&nbsp;Using a data set about homes, we will create a machine learning model to distinguish homes in New York from homes in San Francisco.</p><p>Address of the bookmark: <a href="http://www.r2d3.us/visual-intro-to-machine-learning-part-1/" rel="nofollow">http://www.r2d3.us/visual-intro-to-machine-learning-part-1/</a></p>]]></description>
	<dc:creator>Gudiya Pal</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/39826/data-scientist-mwd</guid>
  <pubDate>Wed, 07 Aug 2019 03:19:46 -0500</pubDate>
  <link></link>
  <title><![CDATA[Data Scientist (m/w/d)]]></title>
  <description><![CDATA[
<p>https://uk-erlangen.concludis.de/prj/shw/b8b26f24186191c7af8a25e2cc6115ca_0/27008/Data_Scientist_m_w_d.htm?b=0</p>

<p>Deadline: 30.09.2019</p>

<p>Requirement:<br />Microsoft SQL Server: Administration, Transact-SQL<br />Machine Learning<br />Know Deutsch und Englisch langauge</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44301/carrot2-clustering-engine</guid>
	<pubDate>Fri, 07 Apr 2023 13:11:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44301/carrot2-clustering-engine</link>
	<title><![CDATA[Carrot2 clustering engine]]></title>
	<description><![CDATA[<h2>&nbsp;</h2>
<p>This is the demo application of the&nbsp;<a href="http://project.carrot2.org/" target="_blank">Carrot<sup>2</sup>&nbsp;clustering engine</a>. It uses Carrot<sup>2</sup>'s algorithms to organize search results into thematic folders.</p>
<h3>User interfaces</h3>
<ul>
<li><span><a href="https://search.carrot2.org/#/search/:source">Web Search Clustering</a></span>&nbsp;organizes search results from public search engines into clusters; offers treemap- and pie-chart visualizations of the clusters.</li>
<li><span><a href="https://search.carrot2.org/#/workbench">Clustering Workbench</a></span>&nbsp;clusters content from local files in JSON or Excel format, Solr or Elasticsearch; allows tuning of clustering parameters and exporting results as Excel or JSON.</li>
</ul>
<h3>Search engines</h3>
<ul>
<li><span>Web</span>:&nbsp;<span>web search results provided by&nbsp;<a href="https://etools.ch/" target="_blank">etools.ch</a>. Extensive use may require special arrangements with the&nbsp;<a href="mailto:sschmid@comcepta.com" target="_blank">owner</a>&nbsp;of the etools.ch service.</span></li>
<li><span>PubMed</span>:&nbsp;<span>abstracts of medical papers from the PubMed database provided by NCBI.</span></li>
<li><span>Local file</span>:&nbsp;<span>content read from a local file in Carrot2 XML, JSON, CSV or Excel format.</span></li>
<li><span>Solr</span>:&nbsp;<span>queries an Apache Solr instance.</span></li>
<li><span>Elasticsearch</span>:&nbsp;<span>queries an Elasticsearch instance.</span></li>
</ul>
<h3>Clustering algorithms</h3>
<ul>
<li><span>Lingo</span>:&nbsp;<span>creates well-described flat clusters. Does not scale beyond a few thousand search results. Available as part of the open source&nbsp;<a href="http://project.carrot2.org/" target="_blank">Carrot<sup>2</sup>&nbsp;framework</a>.</span></li>
<li><span>STC</span>:&nbsp;<span>the classic search results clustering algorithm. Produces flat cluster with adequate description, very fast. Available as part of the open source&nbsp;<a href="http://project.carrot2.org/" target="_blank">Carrot<sup>2</sup>&nbsp;framework</a></span></li>
<li><span>k-means</span>:&nbsp;<span>base line clustering algorithm, produces bag-of-words style cluster descriptions. Available as part of the open source&nbsp;<a href="http://project.carrot2.org/" target="_blank">Carrot<sup>2</sup>&nbsp;framework</a></span></li>
</ul><p>Address of the bookmark: <a href="https://search.carrot2.org/#/search/web" rel="nofollow">https://search.carrot2.org/#/search/web</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34420/rita-rapid-identification-of-high-confidence-taxonomic-assignments-for-metagenomic-data</guid>
	<pubDate>Mon, 27 Nov 2017 08:25:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34420/rita-rapid-identification-of-high-confidence-taxonomic-assignments-for-metagenomic-data</link>
	<title><![CDATA[RITA: Rapid identification of high-confidence taxonomic assignments for metagenomic data]]></title>
	<description><![CDATA[<p>RITA is a standalone software package and Web server for taxonomic assignment of metagenomic sequence reads. By combining homology predictions from BLAST or UBLAST with compositional classifications from a Naive Bayes classifier, RITA is able to achieve very high accuracy on short reads. Unlike other hybrid approaches which combine these predictions for all sequences to be classified, RITA uses a pipeline to first identify cases where both types of classifier are in agreement, which constitute the highest-confidence set. Sequences not classified in this manner are subjected to a series of downstream classification steps.</p>
<p>This work has been accepted for publication:</p>
<p>MacDonald NJ, Parks DH, and Beiko RG. Rapid identification of taxonomic assignments. Accepted to&nbsp;<em>Nucleic Acids Research</em>&nbsp;April 4, 2012.</p>
<p>If you have any questions or bug reports, please let us know at &lt;beiko@cs.dal.ca&gt;.</p><p>Address of the bookmark: <a href="http://kiwi.cs.dal.ca/Software/RITA" rel="nofollow">http://kiwi.cs.dal.ca/Software/RITA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</guid>
	<pubDate>Fri, 19 Jan 2018 15:03:51 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</link>
	<title><![CDATA[BioCircos.js is an open source interactive Javascript library to interactive display biological data on the web]]></title>
	<description><![CDATA[<p><a href="http://bioinfo.ibp.ac.cn/biocircos/index.php">BioCircos.js</a>&nbsp;is an open source interactive&nbsp;<code>Javascript</code>&nbsp;library which provides an easy way to interactive display biological data on the web. It implements a raster-based&nbsp;<code>SVG</code>&nbsp;visualization using the open source Javascript framework jquery.js. BioCircos.js is multiplatform and works in all major internet browsers (<strong>Internet Explorer</strong>,&nbsp;<strong>Mozilla Firefox</strong>,&nbsp;<strong>Google Chrome</strong>,&nbsp;<strong>Safari</strong>,&nbsp;<strong>Opera</strong>). Its speed is determined by the client&rsquo;s hardware and internet browser. For smoothest user experience, we recommend&nbsp;<strong>Google Chrome</strong>.</p>
<p>BioCircos.js provides&nbsp;<strong>SNP</strong>,&nbsp;<strong>CNV</strong>,&nbsp;<strong>HEATMAP</strong>,&nbsp;<strong>LINK</strong>,&nbsp;<strong>LINE</strong>,&nbsp;<strong>SCATTER</strong>,&nbsp;<strong>ARC</strong>,&nbsp;<strong>TEXT</strong>, and&nbsp;<strong>HISTGRAM</strong>modules to display genome-wide genetic variations (SNPs, CNVs and chromosome rearrangement), gene expression and biomolecule interactions. BioCircos.js also provides&nbsp;<strong>BACKGROUND</strong>&nbsp;module to display background and axis circles. Tooltips showing detailed information of SVG elements are also provided.</p>
<p><a href="http://bioinfo.ibp.ac.cn/biocircos/document/demo/pages/paper01.html">Demo</a></p><p>Address of the bookmark: <a href="http://bioinfo.ibp.ac.cn/biocircos/document/index.html" rel="nofollow">http://bioinfo.ibp.ac.cn/biocircos/document/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37205/afterqc-automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</guid>
	<pubDate>Fri, 29 Jun 2018 03:26:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37205/afterqc-automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</link>
	<title><![CDATA[AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data]]></title>
	<description><![CDATA[Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
AfterQC can simply go through all fastq files in a folder and then output three folders: good, bad and QC folders, which contains good reads, bad reads and the QC results of each fastq file/pair.
Currently it supports processing data from HiSeq 2000/2500/3000/4000, Nextseq 500/550, MiniSeq...and other Illumina 1.8 or newer formats

The author has reimplemented this tool in C++ with multithreading support to make it much faster. The new tool is called fastp and can be found at: https://github.com/OpenGene/fastp . If you prefer a C++ based tool, please use fastp instead.

https://github.com/OpenGene/AfterQC<p>Address of the bookmark: <a href="https://github.com/OpenGene/AfterQC" rel="nofollow">https://github.com/OpenGene/AfterQC</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37672/seqmonka-tool-to-visualise-and-analyse-high-throughput-mapped-sequence-data</guid>
	<pubDate>Tue, 11 Sep 2018 04:39:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37672/seqmonka-tool-to-visualise-and-analyse-high-throughput-mapped-sequence-data</link>
	<title><![CDATA[SeqMonk:A tool to visualise and analyse high throughput mapped sequence data]]></title>
	<description><![CDATA[<p>SeqMonk is a program to enable the visualisation and analysis of mapped sequence data. It was written for use with mapped next generation sequence data but can in theory be used for any dataset which can be expressed as a series of genomic positions. It's main features are:</p>
<ul>
<li>Import of mapped data from mapped data (BAM/SAM/bowtie etc)</li>
<li>Creation of data groups for visualisation and analysis</li>
<li>Visualisation of mapped regions against an annotated genome.</li>
<li>Flexible quantitation of the mapped data to allow comparisons between data sets</li>
<li>Statistical analysis of data to find regions of interest</li>
<li>Creation of reports containing data and genome annotation</li>
</ul><p>Address of the bookmark: <a href="http://www.bioinformatics.babraham.ac.uk/projects/seqmonk/" rel="nofollow">http://www.bioinformatics.babraham.ac.uk/projects/seqmonk/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38535/nanopack-visualizing-and-processing-long-read-sequencing-data</guid>
	<pubDate>Tue, 25 Dec 2018 21:20:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38535/nanopack-visualizing-and-processing-long-read-sequencing-data</link>
	<title><![CDATA[NanoPack: visualizing and processing long-read sequencing data]]></title>
	<description><![CDATA[The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible with Linux, Mac OS and the MS Windows 10 subsystem for Linux and are available as a graphical user interface, a web service at http://nanoplot.bioinf.be and command line tools.<p>Address of the bookmark: <a href="https://github.com/wdecoster/nanopack" rel="nofollow">https://github.com/wdecoster/nanopack</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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