<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/40604?offset=410</link>
	<atom:link href="https://bioinformaticsonline.com/related/40604?offset=410" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38762/katuali-is-a-flexible-consensus-pipeline-implemented-in-snakemake-to-basecall-assemble-and-polish-oxford-nanopore-technologies-sequencing-data</guid>
	<pubDate>Tue, 22 Jan 2019 06:26:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38762/katuali-is-a-flexible-consensus-pipeline-implemented-in-snakemake-to-basecall-assemble-and-polish-oxford-nanopore-technologies-sequencing-data</link>
	<title><![CDATA[Katuali is a flexible consensus pipeline implemented in Snakemake to basecall, assemble, and polish Oxford Nanopore Technologies&#039; sequencing data]]></title>
	<description><![CDATA[<ul>
<li>Run a pipeline processing fast5s to a consensus in a single command.</li>
<li>Recommended fixed "standard" and "fast" pipelines.</li>
<li>Interchange basecaller, assembler, and consensus components of the pipelines simply by changing the target filepath.</li>
<li>Seemless distribution of tasks over local or distributed compute.</li>
<li>Highly configurable.</li>
<li>Open source (Mozilla Public License 2.0).</li>
</ul>
<p>Documentation can be found at&nbsp;<a href="https://nanoporetech.github.io/katuali/">https://nanoporetech.github.io/katuali/</a>.</p><p>Address of the bookmark: <a href="https://github.com/nanoporetech/katuali" rel="nofollow">https://github.com/nanoporetech/katuali</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39856/tritex-sequence-assembly-pipeline-for-triticeae-genomes</guid>
	<pubDate>Tue, 20 Aug 2019 09:47:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39856/tritex-sequence-assembly-pipeline-for-triticeae-genomes</link>
	<title><![CDATA[TRITEX sequence assembly pipeline for Triticeae genomes]]></title>
	<description><![CDATA[<div>
<p>The pipeline is open-source and hosted in a public Bitbucket&nbsp;<a href="https://bitbucket.org/tritexassembly/tritexassembly.bitbucket.io/src/master/">repository</a>.</p>
</div>
<div>
<p>TRITEX has been run on highly inbred genotypes of barley (<em>Hordeum vulgare</em>), tetraploid wheat (<em>Triticum turgidum</em>) and hexaploid wheat (<em>T. aestivum</em>) with reasonable results: super-scaffold N50 values in the range of dozens of Mb and pseudomolecules with better gene space representation than a BAC-by-BAC assembly. It has never been tested and is not expected to work on heterozygous or autopolyploid genomes.</p>
</div>
<div>
<p>A protocol for generating chromosome-conformation capture sequencing (Hi-C) data suitable for use with the pipeline is described in&nbsp;<a href="https://bio-protocol.org/e2955">Himmelbach et al. 2018</a>. Refer to the&nbsp;<a href="https://www.10xgenomics.com/resources/technical-notes/">technical notes</a>&nbsp;of 10X Genomics on how to generate Chromium data.</p>
</div><p>Address of the bookmark: <a href="https://tritexassembly.bitbucket.io/" rel="nofollow">https://tritexassembly.bitbucket.io/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41030/slr-superscaffolder-a-scaffold-assemble-pipeline-for-stlfr-reads</guid>
	<pubDate>Fri, 14 Feb 2020 14:23:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41030/slr-superscaffolder-a-scaffold-assemble-pipeline-for-stlfr-reads</link>
	<title><![CDATA[SLR-superscaffolder: A scaffold assemble pipeline for stLFR reads.]]></title>
	<description><![CDATA[<p>This is a scaffold assembler designed for stLFR reads[1]. It uses the link-reads information from stLFR reads to assemble contigs to scaffolds.</p>
<p>Here is an illustration of this pipeline:</p>
<p>&nbsp;<img src="https://github.com/BGI-Qingdao/SLR-superscaffolder/raw/master/image.png" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/BGI-Qingdao/SLR-superscaffolder" rel="nofollow">https://github.com/BGI-Qingdao/SLR-superscaffolder</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</guid>
	<pubDate>Mon, 17 Aug 2020 05:25:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</link>
	<title><![CDATA[SqueezeMeta: a fully automated metagenomics pipeline, from reads to bins]]></title>
	<description><![CDATA[<p>SqueezeMeta is a full automatic pipeline for metagenomics/metatranscriptomics, covering all steps of the analysis. SqueezeMeta includes multi-metagenome support allowing the co-assembly of related metagenomes and the retrieval of individual genomes via binning procedures. Thus, SqueezeMeta features several unique characteristics:</p>
<ol>
<li>Co-assembly procedure with read mapping for estimation of the abundances of genes in each metagenome</li>
<li>Co-assembly of a large number of metagenomes via merging of individual metagenomes</li>
<li>Includes binning and bin checking, for retrieving individual genomes</li>
<li>The results are stored in a database, where they can be easily exported and shared, and can be inspected anywhere using a web interface.</li>
<li>Internal checks for the assembly and binning steps inform about the consistency of contigs and bins, allowing to spot potential chimeras.</li>
<li>Metatranscriptomic support via mapping of cDNA reads against reference metagenomes</li>
</ol><p>Address of the bookmark: <a href="https://github.com/jtamames/SqueezeMeta" rel="nofollow">https://github.com/jtamames/SqueezeMeta</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43062/jcvi-utility-libraries</guid>
	<pubDate>Sat, 08 May 2021 22:04:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43062/jcvi-utility-libraries</link>
	<title><![CDATA[JCVI utility libraries]]></title>
	<description><![CDATA[<p><span>Collection of Python libraries to parse bioinformatics files, or perform computation related to assembly, annotation, and comparative genomics.</span></p><p>Address of the bookmark: <a href="https://github.com/tanghaibao/jcvi" rel="nofollow">https://github.com/tanghaibao/jcvi</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44373/mitohifi-a-python-pipeline-for-mitochondrial-genome-assembly-from-pacbio-high-fidelity-reads</guid>
	<pubDate>Tue, 05 Sep 2023 07:31:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44373/mitohifi-a-python-pipeline-for-mitochondrial-genome-assembly-from-pacbio-high-fidelity-reads</link>
	<title><![CDATA[MitoHiFi: a python pipeline for mitochondrial genome assembly from PacBio high fidelity reads]]></title>
	<description><![CDATA[<p dir="auto">MitoHiFi v3.2 is a python pipeline distributed under&nbsp;<a href="https://github.com/marcelauliano/MitoHiFi/blob/master/LICENSE">MIT License</a>&nbsp;!</p>
<p dir="auto">MitoHiFi was first developed to assemble the mitogenomes for a wide range of species in the Darwin Tree of Life Project (DToL)</p>
<p dir="auto">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-023-05385-y&nbsp;</p>
<p dir="auto"><a href="https://github.com/marcelauliano/MitoHiFi/blob/master/docs/dtol-logo-round-300x132.png" target="_blank"><img src="https://github.com/marcelauliano/MitoHiFi/raw/master/docs/dtol-logo-round-300x132.png" alt="" style="border: 0px; border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/marcelauliano/MitoHiFi" rel="nofollow">https://github.com/marcelauliano/MitoHiFi</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44595/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</guid>
	<pubDate>Sat, 06 Jul 2024 04:29:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44595/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</link>
	<title><![CDATA[SqueezeMeta: a fully automated metagenomics pipeline, from reads to bins]]></title>
	<description><![CDATA[<p dir="auto">SqueezeMeta is a full automatic pipeline for metagenomics/metatranscriptomics, covering all steps of the analysis. SqueezeMeta includes multi-metagenome support allowing the co-assembly of related metagenomes and the retrieval of individual genomes via binning procedures. Thus, SqueezeMeta features several unique characteristics:</p>
<ol dir="auto">
<li>Co-assembly procedure with read mapping for estimation of the abundances of genes in each metagenome</li>
<li>Co-assembly of a large number of metagenomes via merging of individual metagenomes</li>
<li>Includes binning and bin checking, for retrieving individual genomes</li>
<li>The results are stored in a database, where they can be easily exported and shared, and can be inspected anywhere using a web interface.</li>
<li>Internal checks for the assembly and binning steps inform about the consistency of contigs and bins, allowing to spot potential chimeras.</li>
<li>Metatranscriptomic support via mapping of cDNA reads against reference metagenomes</li>
</ol><p>Address of the bookmark: <a href="https://github.com/jtamames/SqueezeMeta" rel="nofollow">https://github.com/jtamames/SqueezeMeta</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36918/p-rna-scaffolder-a-fast-and-accurate-genome-scaffolder-using-paired-end-rna-sequencing-reads</guid>
	<pubDate>Tue, 12 Jun 2018 08:14:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36918/p-rna-scaffolder-a-fast-and-accurate-genome-scaffolder-using-paired-end-rna-sequencing-reads</link>
	<title><![CDATA[P_RNA_scaffolder: a fast and accurate genome scaffolder using paired-end RNA-sequencing reads]]></title>
	<description><![CDATA[P_RNA_scaffolder, a fast and accurate tool using paired-end RNA-sequencing reads to scaffold genomes. This tool aims to improve the completeness of both protein-coding and non-coding genes. After this tool was applied to scaffolding human contigs, the structures of both protein-coding genes and circular RNAs were almost completely recovered and equivalent to those in a complete genome, especially for long proteins and long circular RNAs.<p>Address of the bookmark: <a href="http://www.fishbrowser.org/software/P_RNA_scaffolder/" rel="nofollow">http://www.fishbrowser.org/software/P_RNA_scaffolder/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37650/p-rna-scaffolder-a-fast-and-accurate-genome-scaffolder-using-paired-end-rna-sequencing-reads</guid>
	<pubDate>Fri, 07 Sep 2018 05:19:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37650/p-rna-scaffolder-a-fast-and-accurate-genome-scaffolder-using-paired-end-rna-sequencing-reads</link>
	<title><![CDATA[P_RNA_scaffolder: a fast and accurate genome scaffolder using paired-end RNA-sequencing reads]]></title>
	<description><![CDATA[<p><span>P_RNA_scaffolder is a novel scaffolding tool using Pair-end RNA-seq to scaffold genome fragments. The method is suitable for most genomes. The program could utilize Illumina Paired-end RNA-sequencing reads from target speciesies. Our method provides another practical alternative to existing mate-pair_based approaches or other Protein-based approaches (for instance,&nbsp;</span><a href="http://www.fishbrowser.org/software/PEP_scaffolder/">PEP_scaffolder&nbsp;</a><span>) for scaffolding genome sequences. The most important feature of this method is to improve the completeness of gene regions and long-coding gene regions (for instance,&nbsp;</span><a href="http://circrna.org/">circRNA</a><span>).</span></p><p>Address of the bookmark: <a href="http://www.fishbrowser.org/software/P_RNA_scaffolder/#" rel="nofollow">http://www.fishbrowser.org/software/P_RNA_scaffolder/#</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/7986/list-of-bioinformatics-open-source-projectssoftware</guid>
	<pubDate>Tue, 21 Jan 2014 14:28:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/7986/list-of-bioinformatics-open-source-projectssoftware</link>
	<title><![CDATA[List of bioinformatics open source projects/software.]]></title>
	<description><![CDATA[<p>Open source software is software that can be freely used, changed, and shared (in modified or unmodified form) by anyone. Open source software is made by many people, and distributed under licenses that comply with the Open Source Definition.The Open Source Initiative (OSI) is a global non-profit that supports and promotes the open source movement. Followings are the OS bioinformatics projects/software :</p><p><strong>.NET Bio</strong></p><p>http://blogs.msdn.com/b/msr_er/archive/2011/10/18/microsoft-biology-foundation-evolves-into-new-toolkit-net-bio.aspx</p><p>A language-neutral bioinformatics toolkit built using the Microsoft 4.0 .NET Framework to help developers, researchers, and scientists.</p><p><strong>AMPHORA</strong> ("AutoMated Phylogenomic infeRence Application")</p><p>http://wolbachia.biology.virginia.edu/WuLab/Software.html</p><p><a href="http://en.wikipedia.org/wiki/Metagenomics" title="Metagenomics">Metagenomics</a> analysis software</p><p><strong>Anduril</strong></p><p>http://www.anduril.org/anduril/site/</p><p>Component-based <a href="http://en.wikipedia.org/wiki/Workflow" title="Workflow">workflow</a> framework for data analysis</p><p>Armadillo workflow platform</p><p>Tool for designing and executing phylogenetic workflows</p><p><strong>AutoDock</strong></p><p>http://autodock.scripps.edu/</p><p>suite of automated docking tools</p><p><strong>Biochemical Algorithms Library (BALL)</strong></p><p>http://www.ball-project.org/</p><p>C++ library and framework for molecular modeling and visualization designed for rapid prototyping</p><p><strong>Bio4j</strong></p><p>http://bio4j.com/</p><p>Bio4j is a <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">bioinformatics</a> platform and <a href="http://en.wikipedia.org/wiki/Chart" title="Chart">graph</a> based <a href="http://en.wikipedia.org/wiki/Database" title="Database">database</a> built around most data available in <a href="http://en.wikipedia.org/wiki/UniProt" title="UniProt">UniProt</a> KB(<a href="http://en.wikipedia.org/wiki/Swiss-Prot" title="Swiss-Prot">Swiss-Prot</a> + <a href="http://en.wikipedia.org/wiki/TrEMBL" title="TrEMBL">TrEMBL</a>), <a href="http://en.wikipedia.org/wiki/Gene_Ontology" title="Gene Ontology">Gene Ontology</a> (GO), <a href="http://en.wikipedia.org/w/index.php?title=UniRef&amp;action=edit&amp;redlink=1" title="UniRef (page does not exist)">UniRef</a> (50,90,100), <a href="http://en.wikipedia.org/wiki/RefSeq" title="RefSeq">RefSeq</a>, <a href="http://en.wikipedia.org/wiki/National_Center_for_Biotechnology_Information" title="National Center for Biotechnology Information">NCBI</a> taxonomy, and Expasy Enzyme DB</p><p><strong>Bioclipse</strong></p><p>www.bioclipse.net</p><p>Visual platform for <a href="http://en.wikipedia.org/wiki/Cheminformatics" title="Cheminformatics">chemo</a>- and <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">bioinformatics</a> based on the <a href="http://en.wikipedia.org/wiki/Eclipse_%28software%29" title="Eclipse (software)">Eclipse</a> Rich Client Platform (RCP).</p><p><strong>Bioconductor</strong></p><p>http://www.bioconductor.org/</p><p><a href="http://en.wikipedia.org/wiki/R_%28programming_language%29" title="R (programming language)">R (programming language)</a> language toolkit</p><p><strong>Bioinformatics Learning Tutorial (BLT)</strong></p><p>http://sourceforge.net/projects/biotutorial/</p><p>Educational <a href="http://en.wikipedia.org/wiki/Interactive_tutorials" title="Interactive tutorials">interactive tutorials</a> and 3D animations for Replication, Transcription, and Translation</p><p><strong>BioHaskell</strong></p><p>http://biohaskell.org/</p><p><a href="http://en.wikipedia.org/wiki/Haskell_%28programming_language%29" title="Haskell (programming language)">Haskell (programming language)</a></p><p><strong>BioJava</strong></p><p>http://biojava.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Java_%28programming_language%29" title="Java (programming language)">Java (programming language)</a></p><p><strong>BioMOBY</strong></p><p>http://biomoby.org/</p><p>registry of <a href="http://en.wikipedia.org/wiki/Web_services" title="Web services">web services</a></p><p><strong>BioPerl</strong></p><p>http://www.bioperl.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Perl" title="Perl">Perl</a> language toolkit</p><p><strong>BioPHP</strong></p><p>http://www.biophp.org/</p><p><a href="http://en.wikipedia.org/wiki/PHP" title="PHP">PHP</a> language toolkit</p><p><strong>Biopython</strong></p><p>http://biopython.org/wiki/Main_Page</p><p><a href="http://en.wikipedia.org/wiki/Python_%28programming_language%29" title="Python (programming language)">Python</a> language toolkit</p><p><strong>BioRails</strong></p><p>https://github.com/biorails</p><p>a <a href="http://en.wikipedia.org/wiki/Data_management_system" title="Data management system">data management system</a> designed to support researchers in <a href="http://en.wikipedia.org/wiki/Drug_discovery" title="Drug discovery">drug discovery</a></p><p><strong>BioRuby</strong></p><p>http://bioruby.org/</p><p><a href="http://en.wikipedia.org/wiki/Ruby_%28programming_language%29" title="Ruby (programming language)">Ruby</a> language toolkit</p><p><strong>BioSmalltalk</strong></p><p>https://code.google.com/p/biosmalltalk/</p><p><a href="http://en.wikipedia.org/wiki/Smalltalk_%28programming_language%29" title="Smalltalk (programming language)">Smalltalk</a> language toolkit</p><p><strong>BioUno</strong></p><p>http://www.biouno.org/</p><p><a href="http://en.wikipedia.org/w/index.php?title=BioUno&amp;action=edit&amp;redlink=1" title="BioUno (page does not exist)">BioUno</a> is a project that applies <a href="http://en.wikipedia.org/wiki/Continuous_Integration" title="Continuous Integration">Continuous Integration</a> tools and techniques in <a href="http://en.wikipedia.org/wiki/Bioinformatics" title="Bioinformatics">Bioinformatics</a>. It uses <a href="http://en.wikipedia.org/wiki/Jenkins_%28software%29" title="Jenkins (software)">Jenkins</a> and its plug-in API to create <a href="http://en.wikipedia.org/wiki/Bioinformatics_workflow_management_system" title="Bioinformatics workflow management system">biology workflows</a> and manage <a href="http://en.wikipedia.org/wiki/Computer_clusters" title="Computer clusters">computer clusters</a>.</p><p><strong>caCORE</strong></p><p>&nbsp;</p><p>ontologic representation environment</p><p><strong>caArray</strong></p><p>https://cabig-stage.nci.nih.gov/community/tools/caArray</p><p>ontologic representation environment</p><p><strong>EMBOSS</strong></p><p>http://emboss.sourceforge.net/</p><p>Suite of packages for sequencing, searching, etc.</p><p><strong>Gaggle</strong></p><p>https://www.gaggle.net/</p><p>A framework for interoperability between systems biology software</p><p><strong>Galaxy</strong></p><p>http://galaxyproject.org/</p><p><a href="http://en.wikipedia.org/wiki/Scientific_workflow_system" title="Scientific workflow system">Scientific workflow</a> and <a href="http://en.wikipedia.org/wiki/Data_integration" title="Data integration">data integration</a> system</p><p><strong>GenePattern</strong></p><p>http://www.broadinstitute.org/cancer/software/genepattern/</p><p><a href="http://en.wikipedia.org/wiki/Scientific_workflow_system" title="Scientific workflow system">Scientific workflow system</a> that provides access to more than 150 genomic analysis tools</p><p><strong>GeWorkbench</strong></p><p>http://wiki.c2b2.columbia.edu/workbench/index.php/Home</p><p>Genomic <a href="http://en.wikipedia.org/wiki/Data_integration" title="Data integration">data integration</a> platform</p><p><strong>GMOD</strong></p><p>http://www.gmod.org/wiki/Main_Page</p><p>Toolkit for addressing many common challenges at biological databases.</p><p><strong>GeneProf</strong></p><p>http://www.geneprof.org/GeneProf/</p><p>A web-based, bioinformatics software suite for the analysis of functional genomics experiments, e.g. RNA-seq or ChIP-seq.</p><p><strong>GeneTalk</strong></p><p>http://www.gene-talk.de/</p><p>Tool for filtering sequence variants in <a href="http://en.wikipedia.org/wiki/Variant_Call_Format" title="Variant Call Format">VCF</a> files. Network for scientists and clinicians for expertise and knowledge exchange. Database of annotations aboute sequence variants with clinically relevant information.</p><p><strong>GenGIS</strong></p><p>http://kiwi.cs.dal.ca/GenGIS/Main_Page</p><p>Application that allows users to combine digital map data with information about biological sequences collected from the environment.</p><p><strong>GenomeSpace</strong></p><p>http://www.genomespace.org/</p><p>Centralized web application that provides data format transformations and facilitates connections with other bioinformatics tools</p><p><strong>GENtle</strong></p><p>http://directory.fsf.org/wiki/GENtle</p><p>An equivalent to the proprietary <a href="http://en.wikipedia.org/wiki/Vector_NTI" title="Vector NTI">Vector NTI</a>, a tool to analyze and edit <a href="http://en.wikipedia.org/wiki/DNA" title="DNA">DNA</a> sequence files</p><p><strong>Integrated Genome Browser</strong></p><p>http://bioviz.org/igb/</p><p><a href="http://en.wikipedia.org/wiki/Java_%28software_platform%29" title="Java (software platform)">Java</a>-based desktop <a href="http://en.wikipedia.org/wiki/Genome_browser" title="Genome browser">genome browser</a></p><p><strong>Integrative Genomics Viewer (IGV)</strong></p><p>http://www.broadinstitute.org/igv/</p><p>High-performance desktop tool for interactive visual exploration of diverse genomic data</p><p><strong>IntAct</strong></p><p>http://www.ebi.ac.uk/intact/</p><p>molecular interaction database</p><p><strong>InterMine</strong></p><p>http://intermine.github.io/intermine.org/</p><p>Extensive data warehouse system for the analysis and integration of biological datasets</p><p><strong>Java Treeview</strong></p><p>http://jtreeview.sourceforge.net/</p><p>microarray data viewer</p><p><strong>LabKey Server</strong></p><p>http://labkey.com/</p><p>platform for integrating, analyzing and sharing data</p><p><strong>OpenClinica</strong></p><p>https://www.openclinica.com/</p><p>software for capturing and managing data in clinical trials</p><p><a href="http://www.biomedcentral.com/1471-2164/13/512">PromKappa</a></p><p>http://xbioinformatics.wordpress.com/tag/promkappa/</p><p>PromKappa (Promoter analysis by Kappa) software program used for promoter pattern generation and promoter analysis.</p><p><strong>MeV: Multi-Experiment Viewer</strong></p><p>http://www.tm4.org/mev.html</p><p>a desktop application for the analysis, visualization and data-mining of large-scale genomic data</p><p><strong>PathVisio</strong></p><p>http://www.pathvisio.org/</p><p>a desktop software for drawing, analysis and visualization of biological pathways</p><p>REDCRAFT</p><p>software for determining tertiary protein structure given assigned Residual Dipolar Coupling data</p><p>SAM Tools</p><p>Data format (SAM) and accompanying tool suite, for storing large nucleotide sequence alignments</p><p><a href="http://en.wikipedia.org/wiki/Staden_Package" title="Staden Package">Staden Package</a></p><p>Sequence assembly, editing and analysis, primarily consisting of gap4, gap5 and spin.</p><p><a href="http://en.wikipedia.org/wiki/STAMP" title="STAMP">STAMP</a></p><p>Software package for analyzing metagenomic profiles that promotes &lsquo;best practices&rsquo; in choosing appropriate statistical techniques and reporting results.</p><p><a href="http://supfam.org/supraHex">supraHex</a></p><p>An open-source R/Bioconductor package for omics data analysis using a supra-hexagonal map</p><p><a href="http://en.wikipedia.org/wiki/Taverna_workbench" title="Taverna workbench">Taverna workbench</a></p><p>Tool for designing and executing workflows</p><p>TGAC Browser</p><p>Genome Browser, visualisation solutions for big data in the genomic era</p><p>T-REX WebServer</p><p>Bioinformatics and phylogenetics webserver (NJ, PhyML, RAxML, MAFFT, MUSCLE, Newick viewer, <a href="http://en.wikipedia.org/wiki/Horizontal_gene_transfer" title="Horizontal gene transfer">Horizontal gene transfer</a> detection, Reticulograms, Substitution models)</p><p><a href="http://en.wikipedia.org/wiki/UGENE" title="UGENE">UGENE</a></p><p>integrated bioinformatics tools</p><p>Visomics</p><p>bioinformatics tools for omics data</p><p>Genome Analysis Toolkit 1.0 (GATK 1.0)</p><p>a software package to analyse next-generation resequencing data</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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