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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38692?offset=20</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</guid>
	<pubDate>Thu, 13 Aug 2020 10:06:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</link>
	<title><![CDATA[PyParanoid: a pipeline for rapid identification of homologous gene families in a set of genomes]]></title>
	<description><![CDATA[<p>PyParanoid is a pipeline for rapid identification of homologous gene families in a set of genomes - a central task of any comparative genomics analysis. The "gold standard" for identifying homologs is to use reciprocal best hits (RBHs) which depends on performing a all-vs-all sequence comparison, usually using BLAST, to determine homology. However, these methods are computationally expensive, requiring&nbsp;O(n2)&nbsp;resources to identify RBHs. This is problematic, as the modern deluge of sequencing data means that comparative genomics analyses could be performed on datasets of thousands of strains.</p><p>Address of the bookmark: <a href="https://github.com/ryanmelnyk/PyParanoid" rel="nofollow">https://github.com/ryanmelnyk/PyParanoid</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</guid>
	<pubDate>Sat, 03 Jun 2023 19:19:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</link>
	<title><![CDATA[homologizer: Phylogenetic phasing of gene copies into polyploid subgenomes]]></title>
	<description><![CDATA[<p dir="auto">This tutorial describes the usage of&nbsp;<code>homologizer</code>&nbsp;to phase gene copies into polyploid subgenomes. The tutorial is an abbreviated version of a soon-to-be published paper in Methods in Molecular Biology. Please see that paper for many more details and practical considerations for running&nbsp;<code>homologizer</code>&nbsp;analyses. If you use&nbsp;<code>homologizer</code>, please cite the paper in which we first describe the method:</p>
<ul dir="auto">
<li>Freyman, W.A., Johnson, M.G., and C.J. Rothfels. 2022. Homologizer: phylogenetic phasing of gene copies into polyploid subgenomes.&nbsp;<em>bioRxiv</em>&nbsp;<a href="https://www.biorxiv.org/content/10.1101/2020.10.22.351486v4">2020.10.22.351486v4</a></li>
</ul>
<p dir="auto"><code>homologizer</code>&nbsp;is implemented in&nbsp;<code>RevBayes</code>. Please see&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>&nbsp;to download and install&nbsp;<code>RevBayes</code>. For users without previous&nbsp;<code>RevBayes</code>&nbsp;experience, we recommend the tutorials at&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>.</p><p>Address of the bookmark: <a href="https://github.com/wf8/homologizer" rel="nofollow">https://github.com/wf8/homologizer</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29583/graph-genome-suite</guid>
	<pubDate>Fri, 28 Oct 2016 07:59:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29583/graph-genome-suite</link>
	<title><![CDATA[Graph Genome Suite]]></title>
	<description><![CDATA[<p><span>Seven Bridges is the biomedical data analysis company accelerating breakthroughs in genomics research for cancer, drug development and precision medicine. We build self-improving systems to analyze millions of genomes, including the&nbsp;</span><strong>Graph Genome Suite</strong><span>&nbsp;&mdash; the most advanced population genomics tools in the world.</span></p><p>Address of the bookmark: <a href="https://www.sbgenomics.com/graph/" rel="nofollow">https://www.sbgenomics.com/graph/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38745/osprey-network-visualization-system</guid>
	<pubDate>Sun, 20 Jan 2019 05:34:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38745/osprey-network-visualization-system</link>
	<title><![CDATA[Osprey: Network Visualization System]]></title>
	<description><![CDATA[<p>Osprey is a software platform for the visualization of complex biological interaction networks. Osprey builds data-rich graphical representations from&nbsp;<a href="http://geneontology.org/" title="GENE ONTOLOGY CONSORTIUM">Gene Ontology (GO)</a>&nbsp;annotated interaction data maintained by the&nbsp;<a href="https://thebiogrid.org/" title="The BioGRID">BioGRID</a>.</p>
<p>Osprey is developed by the&nbsp;<a href="http://www.tyerslab.com/">TyersLab</a>&nbsp;and is a part of the&nbsp;<a href="https://thebiogrid.org/" title="The BioGRID">BioGRID</a>&nbsp;family of software. It utilizes both&nbsp;<a href="https://www.mysql.com/" title="MySQL Database">MySQL</a>&nbsp;and&nbsp;<a href="http://openjdk.java.net/" title="OpenJDK">Java</a>&nbsp;to operate and is compatible with&nbsp;<a href="https://www.microsoft.com/en-us/windows/" title="Microsoft Windows">Windows</a>,&nbsp;<a href="http://www.ubuntu.com/">Linux</a>, and&nbsp;<a href="http://www.apple.com/" title="Apple">Apple</a>&nbsp;operating systems.</p>
<p>These works were published in&nbsp;<strong>Breitkreutz, BJ., Stark, C., Tyers M. "Osprey: A Network Visualization System." Genome Biology 2003 4(3):R22</strong>&nbsp;<a href="http://genomebiology.com/2003/4/3/R22" title="Genome Biology">[Genome Biology]</a>&nbsp;<a href="http://genomebiology.com/content/pdf/gb-2003-4-3-r22.pdf" title="Osprey PDF">[PDF]</a>&nbsp;<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;list_uids=12620107&amp;dopt=Abstract" title="Pubmed">[PubMed]</a>&nbsp;and supported by the&nbsp;<a href="http://www.nih.gov/" title="NIH">National Institutes of Health</a>,&nbsp;<a href="http://www.cihr-irsc.gc.ca/" title="CIHR">Canadian Institutes of Health Research</a>, and&nbsp;<a href="http://www.genomecanada.ca/en/" title="Genome Canada">Genome Canada</a>.</p><p>Address of the bookmark: <a href="https://osprey.thebiogrid.org/" rel="nofollow">https://osprey.thebiogrid.org/</a></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/35386/list-of-visualization-tools-for-network-biology</guid>
	<pubDate>Mon, 29 Jan 2018 05:12:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/35386/list-of-visualization-tools-for-network-biology</link>
	<title><![CDATA[List of visualization tools for network biology]]></title>
	<description><![CDATA[<p>Network analysis&nbsp;is any structured technique used to mathematically analyze a circuit (a &ldquo;network&rdquo; of interconnected components). The&nbsp;<span>Network analysis provides the ability to quantify associations between individuals, which makes it possible to infer details about the network as a whole at the species and/or population level.&nbsp;</span>Few tools published in BMC are listed here https://bmcbioinformatics.biomedcentral.com/articles/sections/networks-analysis.</p><p><img src="https://www.dropbox.com/pri/get/Public/Link%20to%20network.gif?_subject_uid=85115969&amp;raw=1&amp;revision_id=BBqs9eYx7G_faj5J33ExdjmtF8nXK2xrN5dUBsKyTLZQ9RB_hGM-YFmWZMBzbQZfRvjYzfs65HbQYrHRyoikxsQscSFTn1Nud2QeJ8KGfVI5wv4Kzp6froKOmPZu8ZygfKo&amp;size=1280x960&amp;size_mode=3&amp;w=AABQaErsFIz5ZjVZSxXvKaSVUkY5ob1Yjk0x7dghy0X7zw" alt="image" style="border: 0px; border: 0px;"></p><p>Following are the list of standalone applications for network analysis:</p><p>Arena 3D</p><p>3D visualization of multi-layer networks</p><p>http://www.arena3d.org</p><p>Biana</p><p>Data integration and network management</p><p>http://sbi.imim.es/web/BIANA.php</p><p>BioLayout Express 3D&nbsp;</p><p>2D/3D network visualization</p><p>http://www.biolayout.org/</p><p>BiologicalNetworks&nbsp;</p><p>Efficient integrated multi-level analysis of microarray, sequence, regulatory and other data</p><p>http://www.biologicalnetworks.org</p><p>BioMiner</p><p>Modeling, analyzing and visualizing biochemical pathways and networks</p><p>http://www.zbi.uni-saarland.de/chair/projects/BioMiner</p><p>Cell Illustrator&nbsp;</p><p>Petri nets for modeling and simulating biological networks</p><p>http://www.cellillustrator.com</p><p>COPASI</p><p>Analysis of biochemical networks and their dynamics</p><p>http://www.copasi.org/</p><p>Cytoscape&nbsp;</p><p>Network visualization and analysis. Over 200 plugins [60]</p><p>http://www.cytoscape.org/</p><p>Dizzy</p><p>Chemical kinetics stochastic simulation software</p><p>http://magnet.systemsbiology.net/software/Dizzy/</p><p>DyCoNet</p><p>Gephi plugin that can be used to identify dynamic communities in networks</p><p>https://github.com/juliemkauffman/DyCoNet</p><p>GENeVis&nbsp;</p><p>Network and pathway visualization</p><p>http://tinyurl.com/genevis/</p><p>GEPHI&nbsp;</p><p>Interactive visualization and exploration for any network and complex system, dynamic and hierarchical graph.</p><p>https://gephi.org</p><p>Igraph</p><p>Collection of network analysis tools with the emphasis on efficiency, portability and ease of use</p><p>http://igraph.sourceforge.net</p><p>Medusa</p><p>Semantic and multi-edged simple networks</p><p>https://sites.google.com/site/medusa3visualization/</p><p>NAViGaTOR</p><p>Visualizing and analyzing protein-protein interaction networks</p><p>http://tinyurl.com/navigator1/</p><p>N-Browse</p><p>Interactive graphical browser for biological networks</p><p>http://www.gnetbrowse.org/</p><p>NeAT</p><p>Topological and clustering analysis of networks</p><p>http://rsat.ulb.ac.be/neat/</p><p>Ondex&nbsp;</p><p>Data integration and visualization of large networks</p><p>http://www.ondex.org/</p><p>Osprey</p><p>Visualization and annotation of biological networks</p><p>http://biodata.mshri.on.ca/osprey/servlet/Index</p><p>Pajek&nbsp;</p><p>Analysis and visualization of large networks and social network analysis</p><p>http://vlado.fmf.uni-lj.si/pub/networks/pajek/</p><p>PathwayAssist&nbsp;</p><p>Navigation and analysis of biological pathways, gene regulation networks and protein interaction maps.</p><p>http://www.ariadnegenomics.com/downloads/</p><p>PIVOT&nbsp;</p><p>Layout algorithms for visualizing protein interactions and families</p><p>http://acgt.cs.tau.ac.il/pivot/</p><p>ProCope&nbsp;</p><p>Prediction and evaluation of protein complexes from purification data experiments</p><p>http://www.bio.ifi.lmu.de/Complexes/ProCope/</p><p>ProViz&nbsp;</p><p>Visualization and exploration of interaction networks. Gene Ontology and PSI-MI formats supported</p><p>http://cbi.labri.fr/eng/proviz.htm</p><p>SpectralNET&nbsp;</p><p>Network analysis and visualizations. Scatter plots and dimensionality reduction algorithms</p><p>https://www.broadinstitute.org/software/spectralnet</p><p>Tulip&nbsp;</p><p>Enables the development of algorithms, visual encodings, interaction techniques, data models and domain-specific visualizations</p><p>http://tulip.labri.fr/TulipDrupal/</p><p>VANESA&nbsp;</p><p>Automatic reconstruction and analysis of biological networks and Petri nets based on life-science database information</p><p>http://agbi.techfak.uni-bielefeld.de/vanesa/</p><p>VANTED&nbsp;</p><p>Network reconstruction, data visualization, integration of various data types, network simulation</p><p>http://tinyurl.com/vanted/</p><p>yEd</p><p>Creation of diagrams manually and import external data</p><p>http://tinyurl.com/yEdGraph/</p><p>Web tools for network analysis</p><p>APID&nbsp;</p><p>Unified protein-protein interactions from BIND, BioGRID, DIP, HPRD, IntAct and MINT</p><p>http://bioinfow.dep.usal.es/apid/</p><p>Arcadia&nbsp;</p><p>Translates text-based descriptions of biological networks (SBML files) into standardized diagrams (Systems Biology Graphical Notation Process Description maps)</p><p>http://arcadiapathways.sourceforge.net/</p><p>AVIS&nbsp;</p><p>Viewer for signaling networks</p><p>http://actin.pharm.mssm.edu/AVIS2</p><p>bioPIXIE&nbsp;</p><p>Discovery of biological networks from diverse functional genomic data</p><p>http://pixie.princeton.edu/pixie</p><p>CellPublisher</p><p>Interactive representations of biochemical processes</p><p>http://cellpublisher.gobics.de/</p><p>Graphle</p><p>Distributed network exploration and visualization of interactive large, dense graphs</p><p>http://tinyurl.com/graphle/</p><p>GraphWeb&nbsp;</p><p>Web server for graph-based analysis of biological networks</p><p>http://biit.cs.ut.ee/graphweb/</p><p>Hubba</p><p>Web-based service to explore the essential nodes in a network</p><p>http://hub.iis.sinica.edu.tw/Hubba</p><p>NetworkBLAST&nbsp;</p><p>Analysis of protein interaction networks across species to infer protein complexes that are conserved in evolution</p><p>http://www.cs.tau.ac.il/~bnet/networkblast.htm</p><p>Pathview&nbsp;</p><p>Tool set for pathway-based data integration and visualization</p><p>http://Pathview.r-forge.r-project.org/</p><p>PINA&nbsp;</p><p>Integrated platform for protein interaction network construction, filtering, analysis, visualization and management</p><p>http://cbg.garvan.unsw.edu.au/pina/home.do</p><p>ReMatch&nbsp;</p><p>Web-based tool for integration of user-given stoichiometric metabolic models into a database collected from public data sources</p><p>http://www.cs.helsinki.fi/group/sysfys/software/rematch/</p><p>SNOW&nbsp;</p><p>Gene mapping on a reference or human protein-protein interaction network that SNOW hosts</p><p>http://snow.bioinfo.cipf.es</p><p>STITCH&nbsp;</p><p>Resource to explore known and predicted interactions of chemicals and proteins</p><p>http://stitch.embl.de/</p><p>STRING</p><p>Protein interaction networks and integration of data such as genomic context, high-throughput experiments, conserved coexpression and previous knowledge derived from the literature</p><p>http://string-db.org</p><p>TVNViewer&nbsp;</p><p>An interactive visualization tool for exploring networks that change over time or space</p><p>http://www.sailing.cs.cmu.edu/main/?page_id=545</p><p>tYNA&nbsp;</p><p>System for managing, comparing and mining multiple networks</p><p>http://tyna.gersteinlab.org/tyna/</p><p>VisANT&nbsp;</p><p>Visualization, mining, analysis and modeling of biological networks, metabolic networks and ecosystems</p><p>http://visant.bu.edu/</p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40611/deepvariant-an-analysis-pipeline-that-uses-a-deep-neural-network-to-call-genetic-variants-from-next-generation-dna-sequencing-data</guid>
	<pubDate>Sat, 25 Jan 2020 13:28:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40611/deepvariant-an-analysis-pipeline-that-uses-a-deep-neural-network-to-call-genetic-variants-from-next-generation-dna-sequencing-data</link>
	<title><![CDATA[DeepVariant : an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.]]></title>
	<description><![CDATA[<p><span>DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.</span></p>
<p><span><span>DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data. DeepVariant relies on&nbsp;</span><a href="https://github.com/google/nucleus">Nucleus</a><span>, a library of Python and C++ code for reading and writing data in common genomics file formats (like SAM and VCF) designed for painless integration with the&nbsp;</span><a href="https://www.tensorflow.org/">TensorFlow</a><span>&nbsp;machine learning framework.</span></span></p>
<p><span><a href="https://ai.googleblog.com/2017/12/deepvariant-highly-accurate-genomes.html">https://ai.googleblog.com/2017/12/deepvariant-highly-accurate-genomes.html</a></span></p>
<p><span><a href="https://www.biorxiv.org/content/10.1101/092890v6">https://www.biorxiv.org/content/10.1101/092890v6</a></span></p>
<p><span><img src="https://4.bp.blogspot.com/-2KlXZO60sWE/WiGc8qlZfxI/AAAAAAAACOs/s1pNiKI8jsAvJLr1E_po5udDO8eObm_awCLcBGAs/s640/image3.png" width="640" height="427" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/google/deepvariant" rel="nofollow">https://github.com/google/deepvariant</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44497/graphpath-a-graph-attention-model-for-molecular-stratification-with-interpretability-based-on-the-pathway-pathway-interaction-network</guid>
	<pubDate>Wed, 27 Mar 2024 20:51:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44497/graphpath-a-graph-attention-model-for-molecular-stratification-with-interpretability-based-on-the-pathway-pathway-interaction-network</link>
	<title><![CDATA[GraphPath: A graph attention model for molecular stratification with interpretability based on the pathway-pathway interaction network]]></title>
	<description><![CDATA[<p><span>Achieving accurate and interpretable clinical predictions requires paramount attention to thoroughly characterizing patients at both the molecular and biological pathway levels. In this paper, we present GraphPath, a biological knowledge-driven graph neural network with multi-head self-attention mechanism that implements the pathway-pathway interaction network. We train GraphPath to classify the cancer status of patients with prostate cancer based on their multi-omics profiling.</span></p>
<p><span><img src="https://github.com/amazingma/GraphPath/raw/main/Figures/GraphPath.png" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/amazingma/GraphPath" rel="nofollow">https://github.com/amazingma/GraphPath</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37987/ropebwt2-incremental-construction-of-fm-index-for-dna-sequences</guid>
	<pubDate>Thu, 25 Oct 2018 04:48:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37987/ropebwt2-incremental-construction-of-fm-index-for-dna-sequences</link>
	<title><![CDATA[RopeBWT2: Incremental construction of FM-index for DNA sequences]]></title>
	<description><![CDATA[<p><span>RopeBWT2 is an tool for constructing the FM-index for a collection of DNA sequences. It works by incrementally inserting one or multiple sequences into an existing pseudo-BWT position by position, starting from the end of the sequences. This algorithm can be largely considered a mixture of&nbsp;</span><a href="http://dx.doi.org/10.1007/978-3-642-21458-5_20">BCR</a><span>&nbsp;and&nbsp;</span><a href="http://dfmi.sourceforge.net/">dynamic FM-index</a><span>. Nonetheless, ropeBWT2 is unique in that it may&nbsp;</span><em>implicitly</em><span>sort the input into reverse lexicographical order (RLO) or reverse-complement lexicographical order (RCLO) while building the index.</span></p><p>Address of the bookmark: <a href="https://github.com/lh3/ropebwt2" rel="nofollow">https://github.com/lh3/ropebwt2</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43447/rna-seq-workflow-gene-level-exploratory-analysis-and-differential-expression</guid>
	<pubDate>Sat, 09 Oct 2021 07:59:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43447/rna-seq-workflow-gene-level-exploratory-analysis-and-differential-expression</link>
	<title><![CDATA[RNA-seq workflow: gene-level exploratory analysis and differential expression]]></title>
	<description><![CDATA[<p><span>Here we walk through an end-to-end gene-level RNA-seq differential expression workflow using Bioconductor packages. We will start from the FASTQ files, show how these were quantified to the reference transcripts, and prepare gene-level count datasets for downstream analysis. We will perform exploratory data analysis (EDA) for quality assessment and to explore the relationship between samples, perform differential gene expression analysis, and visually explore the results.</span></p><p>Address of the bookmark: <a href="http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html" rel="nofollow">http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/1973/webinar-wednesday-21-august-2013-at-noon-edt</guid>
	<pubDate>Sun, 11 Aug 2013 19:31:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/1973/webinar-wednesday-21-august-2013-at-noon-edt</link>
	<title><![CDATA[Webinar: Wednesday 21 August 2013 at Noon EDT]]></title>
	<description><![CDATA[<p>This webinar will describe the use of combinatorial pooling to reconstruct gene sequences within BACs. Recent work in barley has shown that this level of sequence knowledge is sufficient to support critical end-point objectives such as map-based cloning and marker-assisted breeding.</p><p>http://www.extension.org/pages/67926/upcoming-webinar:-selective-sequencing-through-combinatorial-pooling#.UggsVuHyPqU</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>

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