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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/42619?offset=40</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36849/glean-an-unsupervised-learning-system-to-integrate-disparate-sources-of-gene-structure-evidence</guid>
	<pubDate>Sat, 02 Jun 2018 07:38:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36849/glean-an-unsupervised-learning-system-to-integrate-disparate-sources-of-gene-structure-evidence</link>
	<title><![CDATA[GLEAN: an unsupervised learning system to integrate disparate sources of gene structure evidence]]></title>
	<description><![CDATA[<p><span>GLEAN is an unsupervised learning system to integrate disparate sources of gene structure evidence (gene model predictions, EST/protein genomic sequence alignments, SAGE/peptide tags, etc) to produce a consensus gene prediction, without prior training.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/glean-gene/" rel="nofollow">https://sourceforge.net/projects/glean-gene/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</guid>
	<pubDate>Tue, 15 Jan 2019 09:39:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</link>
	<title><![CDATA[GeNeCK (Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks]]></title>
	<description><![CDATA[<p><strong>GeNeCK</strong><span>&nbsp;(Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks based on gene expression data and optional hub gene information.</span></p>
<p><span><span>It efficiently constructs gene networks from expression data. It allows the user to use ten different network construction methods (such as partial correlation-, likelihood-, Bayesian- and mutual information-based methods) and integrates the resulting networks from multiple methods. Hub gene information, if available, can be incorporated to enhance performance.</span></span></p>
<p><span><span><span>GeNeCK is an efficient and easy-to-use web application for gene regulatory network construction. It can be accessed at&nbsp;</span><span><a href="http://lce.biohpc.swmed.edu/geneck" target="_blank"><span>http://lce.biohpc.swmed.edu/geneck</span></a></span></span></span></p><p>Address of the bookmark: <a href="http://lce.biohpc.swmed.edu/geneck/" rel="nofollow">http://lce.biohpc.swmed.edu/geneck/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42362/magic-a-tool-for-predicting-transcription-factors-and-cofactors-driving-gene-sets-using-encode-data</guid>
	<pubDate>Thu, 26 Nov 2020 11:05:04 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42362/magic-a-tool-for-predicting-transcription-factors-and-cofactors-driving-gene-sets-using-encode-data</link>
	<title><![CDATA[MAGIC: A tool for predicting transcription factors and cofactors driving gene sets using ENCODE data]]></title>
	<description><![CDATA[<p><span>The algorithm presented herein,&nbsp;</span><strong>M</strong><span>ining&nbsp;</span><strong>A</strong><span>lgorithm for&nbsp;</span><strong>G</strong><span>enet</span><strong>I</strong><span>c&nbsp;</span><strong>C</strong><span>ontrollers (MAGIC), uses ENCODE ChIP-seq data to look for statistical enrichment of TFs and cofactors in gene bodies and flanking regions in gene lists without an&nbsp;</span><em>a priori</em><span>&nbsp;binary classification of genes as targets or non-targets. When compared to other TF mining resources, MAGIC displayed favourable performance in predicting TFs and cofactors that drive gene changes in 4 settings: </span></p>
<p><span>1) A cell line expressing or lacking single TF, </span></p>
<p><span>2) Breast tumors divided along PAM50 designations </span></p>
<p><span>3) Whole brain samples from WT mice or mice lacking a single TF in a particular neuronal subtype </span></p>
<p><span>4) Single cell RNAseq analysis of neurons divided by Immediate Early Gene expression levels. </span></p>
<p><span>In summary, MAGIC is a standalone application that produces meaningful predictions of TFs and cofactors in transcriptomic experiments.</span></p>
<p><span>More at&nbsp;https://uwmadison.app.box.com/s/8j90e5h2rjrsz3bacaxnq8kor2o64vyg</span></p><p>Address of the bookmark: <a href="https://github.com/asroopra/MAGIC" rel="nofollow">https://github.com/asroopra/MAGIC</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33826/geneprof-analysis-of-high-throughput-sequencing-experiment</guid>
	<pubDate>Wed, 05 Jul 2017 16:47:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33826/geneprof-analysis-of-high-throughput-sequencing-experiment</link>
	<title><![CDATA[GeneProf: analysis of high-throughput sequencing experiment]]></title>
	<description><![CDATA[<div>GeneProf is a web-based, graphical software suite that allows users to analyse data produced using high-throughput sequencing platforms (RNA-seq and ChIP-seq; "Next-Generation Sequencing" or NGS): Next-gen analysis for next-gen data!</div>
<p>Some of GeneProf's highlights include:</p>
<ul>
<li><strong>Easy-to-use web-based interface:</strong>Access your data at any time from any computer with a working internet connection -- no need to install software! (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_introduction.jsp#section:SystemRequirements">Section 'System Requirements'</a>).</li>
<li><strong>Analysis wizards make your life easy:</strong>Step-by-step workflows make it easy to analyse high-throughput data within a minimum of hands-on time. (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_conceptsexplained.jsp#subconcept:AnalysisWizards">SubConcept 'Analysis Wizards'</a>).</li>
<li><strong>Versatile modules:</strong>Advanced users and data analysis experts benefit from GeneProf's broad range of analysis modules, which can be combined freely into sophisticated workflows (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_conceptsexplained.jsp#concept:Workflows">Concept 'Workflows'</a>).</li>
<li><strong>Integrated Analysis:</strong>Analysis of&nbsp;<em>ChIP-seq</em>&nbsp;and&nbsp;<em>RNA-seq</em>&nbsp;data in one place, plus support for the integration of other external data (e.g. from microarrays).</li>
<li><strong>Comprehensive Resource:</strong>GeneProf provides a comprehensive resource of&nbsp;<em>fully analyzed</em>&nbsp;next-generation sequencing data. Experimental results can be easily accessed and compared and the analysis procedures employed to produce the data are fully transparent (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_tutorials.jsp#tutorial:ExaminingPublicNext-GenDatausingGeneProf">Tutorial 'Examining Public Next-Gen Data..'</a>).</li>
<li><strong>Extensibility:</strong>Algorithm developers and computer programmers can develop their own modules and extend GeneProf. Existing software can be easily wrapped in the workflow framework (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_advancedtopics.jsp#section:ModuleDevelopment:AddingnewFunctionalitytoGeneProf">Section 'Module Development: Adding new..'</a>) and data from GeneProf may be used externally (cp.&nbsp;<a href="https://www.geneprof.org/GeneProf/help_advancedtopics.jsp#section:WebAPI:RetrievingDatafromGeneProf">Section 'Web API: Retrieving Data from ..'</a>).</li>
</ul>
<p>&nbsp;</p>
<p>GeneProf is academic software developed at the&nbsp;<a href="http://www.crm.ed.ac.uk/">Centre for Regenerative Medicine</a>&nbsp;/&nbsp;<a href="http://www.crm.ed.ac.uk/about/institute-stem-cell-research">Institute for Stem Cell Research</a>,&nbsp;<a href="http://www.ed.ac.uk/">University of Edinburgh</a>&nbsp;and has benefited from funding by the&nbsp;<a href="http://www.mrc.ac.uk/">Medical Research Council</a>&nbsp;and the&nbsp;<a href="http://www.eurosystemproject.eu/">EU Framework 7 Project "EuroSyStem"</a>.</p><p>Address of the bookmark: <a href="https://www.geneprof.org/GeneProf/index.jsp" rel="nofollow">https://www.geneprof.org/GeneProf/index.jsp</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42941/csa-a-high-throughput-chromosome-scale-assembly-pipeline-for-vertebrate-genomes</guid>
	<pubDate>Wed, 10 Mar 2021 06:13:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42941/csa-a-high-throughput-chromosome-scale-assembly-pipeline-for-vertebrate-genomes</link>
	<title><![CDATA[CSA: A high-throughput chromosome-scale assembly pipeline for vertebrate genomes]]></title>
	<description><![CDATA[<p>The pipeline can use information from scaffolded assemblies (for example from HiC or 10X Genomics), or even from diverged (~65-100 Mya) reference genomes for ordering the contigs and thus support the assembly process. This typically results in improved contig N50 when compared to current state of the art methods.</p>
<p><img src="https://github.com/HMPNK/CSA2.6/raw/master/Fig1.png" alt="image" style="border: 0px;"></p>
<p>For smaller vertebrate genomes (~1 Gbp) chromosome scale assemblies can be achieved within 12h on high-end Desktop computers (Intel i7, 12 CPU threads, 128 GB RAM). Larger mammalian genomes (~3Gbp) can be processed within 15-18 h on server equipment (Xeon, 96 CPU threads, 1TB RAM).</p><p>Address of the bookmark: <a href="https://github.com/HMPNK/CSA2.6" rel="nofollow">https://github.com/HMPNK/CSA2.6</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39630/vespa-very-large-scale-evolutionary-and-selective-pressure-analyses</guid>
	<pubDate>Sat, 22 Jun 2019 03:07:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39630/vespa-very-large-scale-evolutionary-and-selective-pressure-analyses</link>
	<title><![CDATA[VESPA: Very large-scale Evolutionary and Selective Pressure Analyses]]></title>
	<description><![CDATA[<p>find the resources we provide here useful in getting you set up to analyse and interpret your data.</p>
<p>To reference VESPA:&nbsp;<a href="https://peerj.com/preprints/1895/">https://peerj.com/preprints/1895/</a></p>
<p>Documentation is now hosted on&nbsp;<a href="http://vespa-evol.readthedocs.io/en/latest/">ReadTheDocs</a></p>
<p>&nbsp;</p>
<h2>&nbsp;</h2><p>Address of the bookmark: <a href="https://github.com/aewebb80/VESPA" rel="nofollow">https://github.com/aewebb80/VESPA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/22761/pit-bioinformatics-group</guid>
  <pubDate>Tue, 16 Jun 2015 14:34:26 -0500</pubDate>
  <link></link>
  <title><![CDATA[PIT Bioinformatics Group]]></title>
  <description><![CDATA[
<p>PIT Bioinformatics Group solves problems in bioinformatics and  computational biology. Recent developed online tools:</p>

<p>- Budapest Reference Connectome: View a parametrizable connectome (brain graph).<br />- AmphoraNet: The webserver implementation of the AMPHORA2 workflow for phylogenetic analysis of metagenomic shotgun sequencing data.<br />- AmphoraVizu: Chart visualization for metagenomics analysis tools AMPHORA2 and AmphoraNet.<br />- SCARF: Free online association rule mining tool.</p>

<p>More at: http://pitgroup.org</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</guid>
	<pubDate>Thu, 18 Jun 2020 06:58:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</link>
	<title><![CDATA[sunbeam: A robust, extensible metagenomics pipeline]]></title>
	<description><![CDATA[<p><span>Sunbeam is a pipeline written in&nbsp;</span><a href="http://snakemake.readthedocs.io/">snakemake</a><span>&nbsp;that simplifies and automates many of the steps in metagenomic sequencing analysis. It uses&nbsp;</span><a href="http://conda.io/">conda</a><span>&nbsp;to manage dependencies, so it doesn't have pre-existing dependencies or admin privileges, and can be deployed on most Linux workstations and clusters. To read more, check out&nbsp;</span><a href="https://microbiomejournal.biomedcentral.com/articles/10.1186/s40168-019-0658-x">our paper in Microbiome</a><span>.</span></p>
<p><span><a href="https://sunbeam.readthedocs.io/en/latest/">https://sunbeam.readthedocs.io/en/latest/</a></span></p><p>Address of the bookmark: <a href="https://github.com/sunbeam-labs/sunbeam" rel="nofollow">https://github.com/sunbeam-labs/sunbeam</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44587/lorikeet-strain-resolver-for-metagenomics</guid>
	<pubDate>Sat, 06 Jul 2024 04:21:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44587/lorikeet-strain-resolver-for-metagenomics</link>
	<title><![CDATA[Lorikeet: Strain resolver for metagenomics]]></title>
	<description><![CDATA[<p><span>Lorikeet is a within-species variant analysis pipeline for metagenomic communities that utilizes both long and short reads. Lorikeet utilizes a re-implementaion of the GATK HaplotypeCaller algorithm, performing local re-assembly of potentially active regions within candidate genomes. Called variants can be clustered into likely strains using a combination of UMAP and HDBSCAN.</span></p>
<p><span><img src="https://github.com/rhysnewell/Lorikeet/raw/master/docs/_include/images/lorikeet_logo.png" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/rhysnewell/Lorikeet" rel="nofollow">https://github.com/rhysnewell/Lorikeet</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6954/workshop-on-population-and-metagenomics-analysis-nerc</guid>
  <pubDate>Sun, 01 Dec 2013 14:25:45 -0600</pubDate>
  <link></link>
  <title><![CDATA[Workshop on population and metagenomics analysis @ NERC]]></title>
  <description><![CDATA[
<p>Workshop Overview</p>

<p>A ten-day workshop taking place between 25 February - 6 March 2014 providing detailed hands-on training for population and meta-genomics analysis for researchers with little or no background in mathematics or computing.</p>

<p>Venue: Dartington Hall, Totnes, Devon (nearest train station - Totnes)</p>

<p>Times: 25 February - 6th March 2014.</p>

<p>Arrival evening of Tuesday 25 February 2014. Departure morning of 6th March 2014. The course itself will take place 9am-12pm, 2pm-5pm and on some evenings 7pm-10pm everyday 26 February-5th March. Students are expected to attend the entire course.</p>

<p>Contact: research-events@exeter.ac.uk</p>

<p>Registration</p>

<p>The course itself is free of charged and is funded by a Professional Postgraduate Development Award from NERC.</p>

<p>A total of 30 funded places are available which cover the costs of accommodation and food, but not the cost of transportation to/from the venue.</p>

<p>An additional 10 places are available for participants from industry. The cost of accommodation and meals will need to be covered by the participants.</p>

<p>You should register your interest by 31 December 2013. Participants will be informed by 10th January 2014 as to whether they have been selected. Please note that preference will be given to researchers funded by NERC.</p>

<p>More at http://www.eventbrite.co.uk/e/nerc-workshop-on-population-and-metagenomics-analysis-tickets-8628888237</p>
]]></description>
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