<?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/37233?offset=360</link>
	<atom:link href="https://bioinformaticsonline.com/related/37233?offset=360" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33014/synteny-portal-a-web-based-application-portal-for-synteny-block-analysis</guid>
	<pubDate>Wed, 24 May 2017 10:39:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33014/synteny-portal-a-web-based-application-portal-for-synteny-block-analysis</link>
	<title><![CDATA[Synteny Portal: a web-based application portal for synteny block analysis]]></title>
	<description><![CDATA[<p><span>Synteny Portal, a versatile web-based application portal for constructing, visualizing and browsing synteny blocks. With Synteny Portal, users can easily (i) construct synteny blocks among multiple species by using prebuilt alignments in the UCSC genome browser database, (ii) visualize and download syntenic relationships as high-quality images, (iii) browse synteny blocks with genetic information and (iv) download the details of synteny blocks to be used as input for downstream synteny-based analyses, all in an intuitive and easy-to-use web-based interface. We believe that Synteny Portal will serve as a highly valuable tool that will enable biologists to easily perform comparative genomics studies by compensating limitations of existing tools. Synteny Portal is freely available at&nbsp;</span><a href="http://bioinfo.konkuk.ac.kr/synteny_portal" target="pmc_ext">http://bioinfo.konkuk.ac.kr/synteny_portal</a><span>.</span></p>
<p>http://bioinfo.konkuk.ac.kr/synteny_portal/</p><p>Address of the bookmark: <a href="http://bioinfo.konkuk.ac.kr/synteny_portal/" rel="nofollow">http://bioinfo.konkuk.ac.kr/synteny_portal/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36746/soap2-short-oligonucleotide-analysis-package-2</guid>
	<pubDate>Wed, 23 May 2018 10:09:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36746/soap2-short-oligonucleotide-analysis-package-2</link>
	<title><![CDATA[SOAP2 : Short Oligonucleotide Analysis Package 2]]></title>
	<description><![CDATA[SOAPaligner/soap2 is a member of the SOAP (Short Oligonucleotide Analysis Package). It is an updated version of SOAP software for short oligonucleotide alignment. The new program features in super fast and accurate alignment for huge amounts of short reads generated by Illumina/Solexa Genome Analyzer. Compared to soap v1, it is one order of magnitude faster. It require only 2 minutes aligning one million single-end reads onto the human reference genome. Another remarkable improvement of SOAPaligner is that it now supports a wide range of the read length.

SOAPaligner benefitted in time and space efficiency by a revolution in the basic data structures and algorithms used.The core algorithms and the indexing data structures (2way-BWT) are developed by the algorithms research group of the Department of Computer Science, the University of Hong Kong (T.W. Lam, Alan Tam, Simon Wong, Edward Wu and S.M. Yiu).<p>Address of the bookmark: <a href="http://soap.genomics.org.cn/soapaligner.html" rel="nofollow">http://soap.genomics.org.cn/soapaligner.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38378/gwaspro-a-high-performance-genome-wide-association-analysis-server</guid>
	<pubDate>Fri, 07 Dec 2018 08:04:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38378/gwaspro-a-high-performance-genome-wide-association-analysis-server</link>
	<title><![CDATA[GWASpro: A High-Performance Genome-Wide Association Analysis Server]]></title>
	<description><![CDATA[<p>GWASpro supports building complex design matrices, by which complex experimental designs that may include replications, treatments, locations and times, can be accounted for in the linear mixed model (LMM). GWASpro is optimized to handle GWAS data that may consist of up to 10 million markers and 10,000 samples from replicable lines or hybrids. GWASpro provides an interface that significantly reduces the learning curve for new GWAS investigators.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://bioinfo.noble.org/GWASPRO/" rel="nofollow">https://bioinfo.noble.org/GWASPRO/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41991/sequence-ontology-bioinformatics-analysis-soba-tool-to-provide-a-simple-statistical-and-graphical-summary-of-an-annotated-genome</guid>
	<pubDate>Wed, 22 Jul 2020 10:11:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41991/sequence-ontology-bioinformatics-analysis-soba-tool-to-provide-a-simple-statistical-and-graphical-summary-of-an-annotated-genome</link>
	<title><![CDATA[Sequence Ontology Bioinformatics Analysis (SOBA) tool to provide a simple statistical and graphical summary of an annotated genome]]></title>
	<description><![CDATA[<p><span>We have developed the Sequence Ontology Bioinformatics Analysis (SOBA) tool to provide a simple statistical and graphical summary of an annotated genome. We envisage its use during annotation jamborees, genome comparison and for use by developers for rapid feedback during annotation software development and testing. SOBA also provides annotation consistency feedback to ensure correct use of terminology within annotations, and guides users to add new terms to the Sequence Ontology when required. SOBA is available at http://www.sequenceontology.org/cgi-bin/soba.cgi.</span></p>
<p><span>More at <a href="https://pubmed.ncbi.nlm.nih.gov/20494974/">https://pubmed.ncbi.nlm.nih.gov/20494974/</a></span></p><p>Address of the bookmark: <a href="http://www.sequenceontology.org/cgi-bin/soba.cgi" rel="nofollow">http://www.sequenceontology.org/cgi-bin/soba.cgi</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44539/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</guid>
	<pubDate>Wed, 15 May 2024 14:36:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44539/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</link>
	<title><![CDATA[Bactopia: a Flexible Pipeline for Complete Analysis of Bacterial Genomes]]></title>
	<description><![CDATA[<p dir="auto">Bactopia is a flexible pipeline for complete analysis of bacterial genomes. The goal of Bactopia is to process your data with a broad set of tools, so that you can get to the fun part of analyses quicker!</p>
<p dir="auto">Bactopia can be split into two main parts:&nbsp;<a href="https://bactopia.github.io/latest/beginners-guide/">Bactopia Analysis Pipeline</a>, and&nbsp;<a href="https://bactopia.github.io/latest/bactopia-tools/">Bactopia Tools</a>.</p>
<p dir="auto">Bactopia Analysis Pipeline is the main&nbsp;<em>per-isolate</em>&nbsp;workflow in Bactopia. Built with&nbsp;<a href="https://www.nextflow.io/">Nextflow</a>, input FASTQs (local or available from SRA/ENA) are put through numerous analyses including: quality control, assembly, annotation, minmer sketch queries, sequence typing, and more.</p>
<p dir="auto"><a href="https://github.com/bactopia/bactopia/blob/master/data/bactopia-workflow.png" target="_blank"><img src="https://github.com/bactopia/bactopia/raw/master/data/bactopia-workflow.png" alt="Bactopia Overview" style="border: 0px;"></a></p>
<p dir="auto">Bactopia Tools are a set a independent workflows fo</p><p>Address of the bookmark: <a href="https://github.com/bactopia/bactopia" rel="nofollow">https://github.com/bactopia/bactopia</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33912/mesquite-a-modular-system-for-evolutionary-analysis</guid>
	<pubDate>Tue, 18 Jul 2017 07:42:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33912/mesquite-a-modular-system-for-evolutionary-analysis</link>
	<title><![CDATA[Mesquite: A modular system for evolutionary analysis]]></title>
	<description><![CDATA[<p><span>Mesquite is modular, extendible software for evolutionary biology, designed to help biologists organize and analyze comparative data about organisms. Its emphasis is on phylogenetic analysis, but some of its modules concern population genetics, while others do non-phylogenetic multivariate analysis. Because it is modular, the analyses available depend on the modules installed.</span></p>
<p><span>http://mesquiteproject.wikispaces.com/</span></p><p>Address of the bookmark: <a href="https://github.com/MesquiteProject/MesquiteCore/releases" rel="nofollow">https://github.com/MesquiteProject/MesquiteCore/releases</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34465/rnaseq-data-analysis-links</guid>
	<pubDate>Mon, 27 Nov 2017 16:28:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34465/rnaseq-data-analysis-links</link>
	<title><![CDATA[RNAseq data analysis links !]]></title>
	<description><![CDATA[<p>RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data analysis, including experimental design, quality control, read alignment, quantification of gene and transcript levels, visualization, differential gene expression, alternative splicing, functional analysis, gene fusion detection and eQTL mapping.</p><p><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728800/" target="_blank">A survey of best practices for RNA-seq data analysis</a></p><p><a href="http://www.bioconductor.org/help/workflows/rnaseqGene/" target="_blank">RNA-seq workflow: gene-level exploratory analysis and DE</a></p><p><a href="https://github.com/crazyhottommy/RNA-seq-analysis" target="_blank">RNAseq analysis notes from Tommy Tang</a></p><p><a href="http://web.stanford.edu/group/wonglab/doc/RNA-seq-talk-JSM2010.pdf" target="_blank">Analysis of RNA ‐ Seq Data</a></p><p><a href="https://f1000research.com/articles/5-1408/v2" target="_blank">RNA-seq analysis is easy as 1-2-3 with limma, Glimma and edgeR</a></p><p><a href="http://www.nature.com/nprot/journal/v7/n3/full/nprot.2012.016.html" target="_blank">Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks.</a></p><p><a href="https://www.ebi.ac.uk/training/online/course/ebi-next-generation-sequencing-practical-course/rna-sequencing/rna-seq-analysis-transcriptome" target="_blank">EBI RNA-Seq exercise</a></p><p><a href="https://f1000research.com/articles/5-1574/v1" target="_blank">An open RNA-Seq data analysis pipeline tutorial with an example</a></p><p><a href="https://ycl6.gitbooks.io/rna-seq-data-analysis/rna-seq_analysis_workflow.html" target="_blank">RNA-Seq Analysis Workflow</a></p><p><a href="http://www.nature.com/nprot/journal/v11/n9/full/nprot.2016.095.html" target="_blank">Transcript-level expression analysis of RNA-seq experiments</a></p>]]></description>
	<dc:creator>Robert M Willioms</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/34916/bioinformatics-tools-developed-for-oxford-nanopore-data-analysis</guid>
	<pubDate>Wed, 27 Dec 2017 20:47:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/34916/bioinformatics-tools-developed-for-oxford-nanopore-data-analysis</link>
	<title><![CDATA[Bioinformatics tools developed for Oxford Nanopore data analysis !]]></title>
	<description><![CDATA[<p><span>MinION is the only portable real-time device for DNA and RNA&nbsp;</span><span>sequencing</span><span>. Each consumable flow cell can now generate 10&ndash;20 Gb of DNA&nbsp;</span><span>sequence</span><span>&nbsp;data. Ultra-</span><span>long read lengths are possible (hundreds of kb) as you can choose your fragment length.&nbsp;</span>One of the technical advantages of ONT data is the read length, which offers great prospects for genome assembly. Generally, assemblers are based on several different types of algorithms, such as greedy, overlap-layout-consensus (OLC), de Bruijn graph (DBG), and string graph.</p><p><span>List of analysis tools developed for Oxford Nanopore data</span></p><p>BWA <br />Fast nanopore data tuned alignment tool <br />https://github.com/lh3/bwa</p><p>GraphMap<br />Mapper for long and error-prone reads<br />https://github.com/isovic/graphmap</p><p>LAST<br />Nanopore tuned alignment tool<br />http://last.cbrc.jp/</p><p>LINKS<br />Software tool for long read scaffolding <br />https://github.com/warrenlr/LINKS/</p><p>marginAlign<br />Tools to align nanopore reads to a reference<br />https://github.com/benedictpaten/marginAlign</p><p>minoTour<br />Real time analysis tools<br />http://minotour.nottingham.ac.uk/</p><p>nanoCORR<br />Error-correction tool for nanopore sequence data<br />https://github.com/jgurtowski/nanocorr</p><p>NanoOK<br />Software for nanopore data, quality and error profiles<br />https://documentation.tgac.ac.uk/display/NANOOK/NanoOK</p><p>Nanopolish<br />Nanopore analysis and genome assembly software<br />https://github.com/jts/nanopolish</p><p>nanopore<br />Variant-detection tool for nanopore sequence data<br />https://github.com/mitenjain/nanopore</p><p>Nanocorrect<br />Error-correction tool for nanopore sequence data<br />https://github.com/jts/nanocorrect/</p><p>npReader<br />Real-time conversion and analysis of nanopore reads<br />https://github.com/mdcao/npReader</p><p>poRe<br />Tool for analyzing and visualizing nanopore data<br />https://sourceforge.net/p/rpore/wiki/Home/</p><p>PoreSeq<br />Error-correction and variant-calling software<br />https://github.com/tszalay/poreseq</p><p>Poretools<br />Nanopore sequence analysis and visualization software <br />https://github.com/arq5x/poretools</p><p>SSPACE-LongRead<br />Genome scaffolding tool <br />http://www.baseclear.com/genomics/bioinformatics/basetools/SSPACE-longread</p><p>SMIS<br />Genome scaffolding tool <br />https://sourceforge.net/projects/phusion2/files/smis/</p><p>&nbsp;</p><p>List of assemblers for Oxford Nanopore MinION long reads</p><p>LQS<br />DALIGNER, Celera OLC Nanocorrect, <br />Nanopolish corrector<br />https://github.com/jts/nanopolish</p><p>PBcR<br />HGAP or BLASR, Celera OLC <br />PBcR corrector<br />http://wgs-assembler.sourceforge.net/wiki/index.php/PBcR<br /> &ndash;<br />Canu<br />MHAP, Celera OLC <br />Canu corrector<br />https://github.com/marbl/canu</p><p>Falcon<br />String graph, Celera OLC <br />Falcon corrector<br />https://github.com/PacificBiosciences/falcon</p><p>Miniasm <br />OLC<br />https://github.com/lh3/miniasm</p><p>ra-integrate<br />OLC<br />https://github.com/mariokostelac/ra-integrate/</p><p>ALLPATHS-LG<br />de Bruijn graph <br />ALLPATHS-L corrector<br />https://www.broadinstitute.org/software/allpaths-lg/blog/?page_id=12</p><p>SPAdes <br />de Bruijn graph <br />SPAdes corrector<br />http://bioinf.spbau.ru/spades</p>]]></description>
	<dc:creator>biogeek</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</guid>
	<pubDate>Wed, 07 Feb 2018 10:44:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</link>
	<title><![CDATA[GenomeTools: The versatile open source genome analysis software]]></title>
	<description><![CDATA[<p>The&nbsp;<em>GenomeTools</em>&nbsp;genome analysis system is a&nbsp;<a href="http://genometools.org/license.html">free</a>&nbsp;collection of bioinformatics&nbsp;<a href="http://genometools.org/tools.html">tools</a>&nbsp;(in the realm of genome informatics) combined into a single binary named&nbsp;<em>gt</em>. It is based on a C library named &ldquo;libgenometools&rdquo; which consists of several modules.</p>
<p>If you are interested in gene prediction, have a look at&nbsp;<a href="http://genomethreader.org/" title="GenomeThreader gene prediction        software"><em>GenomeThreader</em></a>.</p><p>Address of the bookmark: <a href="http://genometools.org/" rel="nofollow">http://genometools.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</guid>
	<pubDate>Fri, 14 Dec 2018 04:10:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</link>
	<title><![CDATA[EGAD: Ultra-fast functional analysis of gene networks]]></title>
	<description><![CDATA[<p><span>With the EGAD (Extending &lsquo;Guilt-by-Association&rsquo; by Degree) package, we present a series of highly efficient tools to calculate functional properties in networks based on the guilt-by-association principle. These allow rapid controlled comparisons and analyses. Two of the core features are: a function prediction algorithm which is fully vectorized (neighbor_voting), allowing network characterization across even thousands of functional groups to be accomplished in minutes in cross-validation and an analytic determination of the optimal prior to guess candidates genes across multiple functional sets (calculate_multifunc, auc_multifunc).</span></p><p>Address of the bookmark: <a href="https://github.com/sarbal/EGAD" rel="nofollow">https://github.com/sarbal/EGAD</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

</channel>
</rss>