<?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/43364?offset=540</link>
	<atom:link href="https://bioinformaticsonline.com/related/43364?offset=540" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43997/tools-for-rna-classification</guid>
	<pubDate>Tue, 08 Nov 2022 03:39:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43997/tools-for-rna-classification</link>
	<title><![CDATA[Tools for RNA classification]]></title>
	<description><![CDATA[<p><span>barrnap</span>&nbsp;-&nbsp;<a href="https://github.com/tseemann/barrnap" target="_blank">https://github.com/tseemann/barrnap</a></p><p><span>CPAT</span>&nbsp;-&nbsp;<a href="https://github.com/liguowang/cpat" target="_blank">https://github.com/liguowang/cpat</a>,&nbsp;<a href="http://lilab.research.bcm.edu/" target="_blank">http://lilab.research.bcm.edu/</a>&nbsp;(web server)</p><p><span>CPC2</span>&nbsp;-&nbsp;<a href="https://github.com/gao-lab/CPC2_standalone" target="_blank">https://github.com/gao-lab/CPC2_standalone</a>,&nbsp;<a href="http://cpc2.gao-lab.org/" target="_blank">http://cpc2.gao-lab.org/</a>&nbsp;(web server)</p><p><span>Infernal</span>&nbsp;-&nbsp;<a href="http://eddylab.org/infernal/" target="_blank">http://eddylab.org/infernal/</a>,&nbsp;<a href="https://github.com/EddyRivasLab/infernal" target="_blank">https://github.com/EddyRivasLab/infernal</a></p><p><span>NCBI RefSeq</span>&nbsp;-&nbsp;<a href="https://www.ncbi.nlm.nih.gov/refseq/" target="_blank">https://www.ncbi.nlm.nih.gov/refseq/</a></p><p><span>Rfam</span>&nbsp;-&nbsp;<a href="http://rfam.xfam.org/" target="_blank">http://rfam.xfam.org/</a>,&nbsp;<a href="https://docs.rfam.org/en/latest/index.html" target="_blank">https://docs.rfam.org/en/latest/index.html</a></p><p><span>SILVA</span>&nbsp;-&nbsp;<a href="https://www.arb-silva.de/" target="_blank">https://www.arb-silva.de/</a></p><p><span>RNAmmer</span>&nbsp;-&nbsp;<a href="http://www.cbs.dtu.dk/services/RNAmmer/" target="_blank">http://www.cbs.dtu.dk/services/RNAmmer/</a>&nbsp;(web server, standalone download link)</p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44401/bioinformatics-tools-for-phylogeny</guid>
	<pubDate>Mon, 06 Nov 2023 03:09:59 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44401/bioinformatics-tools-for-phylogeny</link>
	<title><![CDATA[Bioinformatics Tools for Phylogeny !]]></title>
	<description><![CDATA[<p><span>Direct access to the individual tools available on this server.</span></p><table summary="list of individual tools">
<thead>
<tr><th>Multiple Alignment:</th><th>Phylogeny:</th><th>Tree viewers:</th><th>Utilities:</th></tr>
</thead>
<tbody>
<tr>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=muscle">MUSCLE</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=phyml">PhyML</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=treedyn">TreeDyn</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=gblocks">Gblocks</a></td>
</tr>
<tr>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=tcoffee">T-Coffee</a>&nbsp;/&nbsp;<a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=expresso">3DCoffee</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=tnt">TNT</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=drawgram">Drawgram</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=jalview">Jalview</a></td>
</tr>
<tr>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=clustalw">ClustalW</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=bionj">BioNJ</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=drawtree">Drawtree</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=readseq">Readseq</a></td>
</tr>
<tr>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=probcons">ProbCons</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=mrbayes">MrBayes</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/one_task.cgi?task_type=atv">ATV (A Tree Viewer)</a></td>
<td><a href="http://phylogeny.lirmm.fr/phylo_cgi/data_converter.cgi">Built-in converter</a></td>
</tr>
</tbody>
</table>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44718/mycology-research-resources-for-bioinformaticians-unlocking-the-fungal-kingdom</guid>
	<pubDate>Fri, 13 Dec 2024 11:21:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44718/mycology-research-resources-for-bioinformaticians-unlocking-the-fungal-kingdom</link>
	<title><![CDATA[Mycology Research Resources for Bioinformaticians: Unlocking the Fungal Kingdom]]></title>
	<description><![CDATA[<p>Mycology, the study of fungi, is a field that bridges ecology, medicine, and biotechnology. With advancements in bioinformatics, researchers now have unprecedented opportunities to explore the fungal kingdom at molecular, genetic, and ecological levels. From understanding pathogenic fungi to harnessing fungal enzymes for industrial applications, the potential is vast.</p><p>To fully leverage these opportunities, bioinformaticians require specialized tools and databases. This blog highlights essential resources for mycology research, focusing on databases, tools, and platforms tailored for fungal biology.</p><h4><strong>1. Fungal Databases</strong></h4><h5><strong>1.1. MycoCosm</strong></h5><p><strong>Website</strong>: <a target="_new">MycoCosm</a><br />Developed by the DOE Joint Genome Institute, MycoCosm is a comprehensive portal for fungal genomics. It offers genomic and transcriptomic data for a wide range of fungi, including saprobes, pathogens, and symbionts.</p><ul>
<li><strong>Key Features</strong>: Genome browsers, comparative genomics tools, and functional annotations.</li>
<li><strong>Best For</strong>: Large-scale studies on fungal evolution and ecology.</li>
</ul><h5><strong>1.2. FungiDB</strong></h5><p><strong>Website</strong>: <a href="https://fungidb.org/" target="_new">FungiDB</a><br />FungiDB is an integrated genomic resource for fungal pathogens and non-pathogens. It provides access to genome sequences, transcriptomic data, and functional annotations.</p><ul>
<li><strong>Key Features</strong>: Advanced search options, BLAST, and pathway analysis tools.</li>
<li><strong>Best For</strong>: Studying fungal pathogenesis and host-pathogen interactions.</li>
</ul><h5><strong>1.3. Index Fungorum</strong></h5><p><strong>Website</strong>: <a href="http://www.indexfungorum.org/" target="_new">Index Fungorum</a><br />This nomenclatural database provides information on the scientific names of fungi. It&rsquo;s an essential resource for taxonomists and researchers focused on fungal biodiversity.</p><ul>
<li><strong>Key Features</strong>: Taxonomic hierarchy and synonymy tracking.</li>
<li><strong>Best For</strong>: Identifying and classifying fungal species.</li>
</ul><h5><strong>1.4. UNITE</strong></h5><p><strong>Website</strong>: <a target="_new">UNITE</a><br />UNITE is a specialized database for fungal ITS (Internal Transcribed Spacer) sequences, often used in fungal identification and phylogenetics.</p><ul>
<li><strong>Key Features</strong>: Curated reference datasets and community annotations.</li>
<li><strong>Best For</strong>: Environmental mycology and microbial ecology studies.</li>
</ul><h4><strong>2. Analytical Tools</strong></h4><h5><strong>2.1. Funannotate</strong></h5><p><strong>Repository</strong>: <a href="https://github.com/nextgenusfs/funannotate" target="_new">GitHub - Funannotate</a><br />Funannotate is a genome annotation tool designed for fungi. It supports tasks like gene prediction, functional annotation, and orthology analysis.</p><ul>
<li><strong>Best For</strong>: Annotating newly sequenced fungal genomes.</li>
</ul><h5><strong>2.2. BUSCO (Benchmarking Universal Single-Copy Orthologs)</strong></h5><p><strong>Website</strong>: <a target="_new">BUSCO</a><br />BUSCO evaluates genome assembly and annotation completeness using orthologs. It includes a fungal-specific dataset.</p><ul>
<li><strong>Best For</strong>: Assessing the quality of fungal genome assemblies.</li>
</ul><h5><strong>2.3. Pathogen-Host Interactions Database (PHI-base)</strong></h5><p><strong>Website</strong>: <a href="http://www.phi-base.org/" target="_new">PHI-base</a><br />PHI-base is a manually curated resource containing information on pathogen-host interactions, including fungal pathogens.</p><ul>
<li><strong>Best For</strong>: Exploring virulence factors and host-pathogen relationships.</li>
</ul><h4><strong>3. Visualization Platforms</strong></h4><h5><strong>3.1. Cytoscape</strong></h5><p><strong>Website</strong>: <a href="https://cytoscape.org/" target="_new">Cytoscape</a><br />A powerful tool for visualizing molecular interaction networks, Cytoscape can be used to study protein-protein interactions, gene networks, and metabolic pathways in fungi.</p><ul>
<li><strong>Best For</strong>: Network biology and functional genomics.</li>
</ul><h5><strong>3.2. iTOL (Interactive Tree of Life)</strong></h5><p><strong>Website</strong>: <a target="_new">iTOL</a><br />iTOL is an interactive tool for visualizing phylogenetic trees.</p><ul>
<li><strong>Best For</strong>: Displaying fungal phylogenies and comparing evolutionary relationships.</li>
</ul><h4><strong>4. Community Resources</strong></h4><h5><strong>4.1. Mycological Society of America (MSA)</strong></h5><p><strong>Website</strong>: <a href="https://msafungi.org/" target="_new">MSA</a><br />The MSA promotes fungal research and provides access to resources, conferences, and publications.</p><ul>
<li><strong>Best For</strong>: Networking with fungal researchers and accessing recent studies.</li>
</ul><h5><strong>4.2. OpenFungi</strong></h5><p><strong>Website</strong>: <a href="https://openfungi.org/" target="_new">OpenFungi</a><br />OpenFungi is an open-source initiative providing fungal genomic and transcriptomic datasets for research and education.</p><ul>
<li><strong>Best For</strong>: Sharing and accessing public fungal datasets.</li>
</ul><h4><strong>5. Genomics Workflows</strong></h4><h5><strong>5.1. Galaxy</strong></h5><p><strong>Website</strong>: <a href="https://usegalaxy.org/" target="_new">Galaxy Project</a><br />Galaxy offers a web-based platform for reproducible bioinformatics workflows, including tools for fungal genome and transcriptome analysis.</p><ul>
<li><strong>Best For</strong>: User-friendly analysis pipelines without requiring coding skills.</li>
</ul><h5><strong>5.2. Snakemake</strong></h5><p><strong>Repository</strong>: <a target="_new">Snakemake</a><br />A flexible pipeline management tool that supports fungal data processing and analysis.</p><ul>
<li><strong>Best For</strong>: Custom workflows for large-scale fungal datasets.</li>
</ul><h4><strong>Conclusion</strong></h4><p>Fungal research is a rapidly growing field with vast implications for medicine, agriculture, and industry. For bioinformaticians, the availability of specialized resources&mdash;databases, tools, and community platforms&mdash;opens doors to innovative discoveries. Whether you are investigating fungal genomics, studying host-pathogen interactions, or exploring fungal biodiversity, the resources outlined above will empower your research journey.</p><p>Dive into these resources and help unravel the mysteries of the fungal kingdom!</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/35395/comprehensive-list-of-visualization-tools-for-biological-pathways</guid>
	<pubDate>Tue, 30 Jan 2018 06:01:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/35395/comprehensive-list-of-visualization-tools-for-biological-pathways</link>
	<title><![CDATA[Comprehensive list of visualization tools for biological pathways]]></title>
	<description><![CDATA[<p>The study of biological pathways is a key to understand the different processes inside a cell: proteins exert their function not in isolation but in a tightly controlled network of interactions and reactions. Activation of a pathway typically leads to a change of state in the cell. Pathways come in different flavors, depending on their functions in the cell &ndash; the three main types are metabolic pathways, gene regulatory pathways, and signaling pathways. These biological pathways and networks are not only an appropriate approach to visualize molecular reactions. They have also become one leading method in -omics data analysis and visualization.</p><p><img src="https://photos-1.dropbox.com/t/2/AABemz29qAuSTqSzr5mEsQE7JIMxZlU1CBy0E5n0yUVYbA/12/85115969/png/32x32/1/_/1/2/pathway.png/EOfXoUIYrJ8CIAcoBw/01qsT2eykyPvSH-rNpy3cqioDzZPc4i-xULG3BEZvCk?preserve_transparency=1&amp;size=1280x960&amp;size_mode=3" width="800" height="533" alt="image" style="border: 0px;"></p><p>Following are the comprehensive list of visualization tools for biological pathways:</p><p>BiNA</p><p>Drawings of metabolic networks supporting hiding of cofactors and drawing of chemical structures</p><p>http://bina.unipax.info/</p><p>BioTapestry</p><p>Interactive tool for building, visualizing and sharing gene regulatory network models over the web</p><p>http://www.biotapestry.org/</p><p>Caleydo</p><p>Visual analysis framework targeted at biomolecular data. Visualization of interdependencies between multiple datasets</p><p>http://www.caleydo.org/</p><p>CellDesigner</p><p>A modeling tool for biochemical networks</p><p>http://www.celldesigner.org/</p><p>Edinburgh Pathway Editor</p><p>Edit and draw pathway diagrams</p><p>http://epe.sourceforge.net/SourceForge/EPE.html</p><p>GenMAPP</p><p>Visualization of gene expression and other genomic data on maps representing biological pathways and groupings of genes</p><p>http://www.genmapp.org/</p><p>Ingenuity IPA</p><p>Data integration platform and manually annotated pathways</p><p>http://tinyurl.com/IngenuityPath</p><p>JDesigner</p><p>Graphical modeling environment for biochemical reaction networks</p><p>http://jdesigner.sourceforge.net/Site/JDesigner.html</p><p>KaPPA View</p><p>Plant pathways</p><p>http://kpv.kazusa.or.jp/</p><p>KEGG Atlas</p><p>Interactive Kyoto Encyclopedia of Genes and Genomes pathways</p><p>http://www.genome.jp/kegg/</p><p>Omix&nbsp;</p><p>Visualizing multi-omics data in metabolic networks</p><p>https://www.omix-visualization.com</p><p>PathVisio&nbsp;</p><p>Biological pathway analysis software that allows drawing, editing and analysis of biological pathways</p><p>http://www.pathvisio.org/</p><p>VitaPad&nbsp;</p><p>Application to visualize biological pathways and map experimental data to them</p><p>http://tinyurl.com/vitapad/</p><p>Web tools for pathways</p><p>ArrayXPath&nbsp;</p><p>Mapping and visualizing microarray gene-expression data and integrated biological pathway resources using SVG</p><p>http://tinyurl.com/ArrayXPath/</p><p>GEPAT&nbsp;</p><p>Integrated analysis of transcriptome data in genomic, proteomic and metabolic contexts</p><p>http://gepat.sourceforge.net/</p><p>iPath&nbsp;</p><p>Web-based tool for the visualization, analysis and customization of pathway maps</p><p>http://pathways.embl.de/</p><p>Kegg-Based Viewer&nbsp;</p><p>KEGG-based pathway visualization tool for complex high-throughput data</p><p>http://www.g-language.org/data/marray/</p><p>MapMan&nbsp;</p><p>User-driven tool that displays large datasets onto diagrams of metabolic pathways or other processes</p><p>http://mapman.gabipd.org/web/guest/mapman</p><p>MetPA&nbsp;</p><p>Analysis and visualization of metabolomic data within the biological context of metabolic pathways</p><p>http://metpa.metabolomics.ca</p><p>Omics Viewer&nbsp;</p><p>Data mapping on BioCyc pathways (collection of 5500 pathway/genome databases)</p><p>http://www.biocyc.org/</p><p>Pathway Explorer</p><p>Interactive Java drawing tool for the construction of biological pathway diagrams in a visual way and the annotation of the components and interactions between them</p><p>http://genome.tugraz.at/pathwayexplorer/pathwayexplorer_description.shtml</p><p>Pathway projector&nbsp;</p><p>Zoomable pathway browser using KEGG atlas and Google Maps API</p><p>http://www.g-language.org/PathwayProjector/</p><p>PATIKA&nbsp;</p><p>Integrated environment composed of a central database and a visual editor, built around an extensive ontology and an integration framework</p><p>http://www.cs.bilkent.edu.tr/~patikaweb/</p><p>Reactome SkyPainter&nbsp;</p><p>Visualization of over-represented pathways and reactions from gene lists</p><p>http://www.reactome.org/skypainter-2</p><p>WikiPathways</p><p>Wiki-based, open, public platform dedicated to the curation of biological pathways by and for the scientific community</p><p>http://www.wikipathways.org/</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35057/ectools-long-read-correction-and-other-correction-tools</guid>
	<pubDate>Fri, 05 Jan 2018 04:02:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35057/ectools-long-read-correction-and-other-correction-tools</link>
	<title><![CDATA[ECTOOLS: Long Read Correction and other Correction tools]]></title>
	<description><![CDATA[<p>Long Read Correction and other Correction tools</p>
<p>This package is a loose collection of scripts. To run the correction<br>routine see the section below. Descriptions of the other scripts<br>are at the bottom of this file.</p>
<p>Contact: gurtowsk@cshl.edu</p>
<p>In short, the correction algorithm takes as input the unitigs from a short read assembly and uses them to correct long read data. More background information for the algorithm can be found:<br>http://schatzlab.cshl.edu/presentations/2013-06-18.PBUserMeeting.pdf</p><p>Address of the bookmark: <a href="https://github.com/jgurtowski/ectools" rel="nofollow">https://github.com/jgurtowski/ectools</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36842/gap-filling-or-contigs-extensions-tools</guid>
	<pubDate>Fri, 01 Jun 2018 08:07:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36842/gap-filling-or-contigs-extensions-tools</link>
	<title><![CDATA[Gap filling or Contigs extensions tools !]]></title>
	<description><![CDATA[
<p>There are many tools to perform gap filling using Illumina short reads, for example "GapFiller: a de novo assembly approach to fill the gap within paired reads" or "Toward almost closed genomes with GapFiller". There are also some tools like GAPresolution that can help to perform local re-assemblies using 454 reads. We used GAPresolution but it is not a very good software, it is useful only in some specific situations.</p>

<p>Take a look at the PRICE software from the DeRisi lab. Its meant to do something very similar. http://derisilab.ucsf.edu/index.php?page=software</p>

<p>You could also look at SSPACE (http://www.baseclear.com/landingpages/basetools-a-wide-range-of-bioinformatics-solutions/sspacev12/), ATLAS tools (http://www.hgsc.bcm.tmc.edu/content/bcm-hgsc-software), and SCARPA (http://compbio.cs.toronto.edu/hapsembler/scarpa.html).</p>

<p>See the PAGIT protocol: http://www.sanger.ac.uk/resources/software/pagit/ </p>

<p>In particular, take a look at the IMAGE tool: http://genomebiology.com/2010/11/4/R41 </p>

<p>Also SOAPdenovo has ha function for scaffolding. Not sure about ABYSS</p>

<p>Here there is a useful explanation of several tools.</p>

<p>https://bioinformaticsonline.com/search?q=scaffolding&amp;entity_type=object&amp;entity_subtype=bookmarks&amp;offset=0&amp;search_type=entities</p>

<p>I could be wrong, but the above answers to your hypothetical scenario appear to miss the point that you aren't interested in assembling the full genome, just the 100 kb part you're interested in. I suggest the following algorithm:</p>

<p>1. Start with the initial assembly C0 of the contigs you have identified as overlapping your region of interest, and the set S of reads those contigs contain. Let C = C0.</p>

<p>2. Repeat:<br />a. Identify paired-end reads (not in C) for which one or both ends align within, or extending, contigs in C.<br />b. Identify unpaired reads that align extending these new paired-end reads.<br />c. Construct a new assembly C' from C and the new reads identified in (a) and (b).<br />d. Trim C' so it does not extend more than 100 kb to either end of C0. Set C = C'.<br />e. Let S' denote the reads that contribute to C'. If S' does not contain any reads not present in S, stop. Otherwise, Set S = S'.</p>

<p>3. If you don't have a complete assembly of the region of interest, generate an STS for each end of each contig, probe a library for clones including these STSes, subclone these clones into a paired-end sequencing vector, and generate paired-end reads for this library; then try steps (1) and (2) again, adding these new sequencing reads to what you had before.</p>

<p>4. If your average sequencing depth for the region of interest exceeds 25 or so without filling all gaps, it is likely that the remaining gaps represent sequences that are not getting cloned in your sequencing vectors. Try different sequencing vectors.</p>
]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41559/dahak-benchmarking-and-containerization-of-tools-for-analysis-of-complex-non-clinical-metagenomes</guid>
	<pubDate>Thu, 09 Apr 2020 04:56:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41559/dahak-benchmarking-and-containerization-of-tools-for-analysis-of-complex-non-clinical-metagenomes</link>
	<title><![CDATA[Dahak: benchmarking and containerization of tools for analysis of complex non-clinical metagenomes.]]></title>
	<description><![CDATA[<p><span>Dahak is a software suite that integrates state-of-the-art open source tools for metagenomic analyses. Tools in the dahak software suite will perform various steps in metagenomic analysis workflows including data pre-processing, metagenome assembly, taxonomic and functional classification, genome binning, and gene assignment. We aim to deliver the analytical framework as a robust and reliable containerized workflow system, which will be free from dependency, installation, and execution problems typically associated with other open-source bioinformatics solutions. This will maximize the transparency, data provenance (i.e., the process of tracing the origins of data and its movement through the workflow), and reproducibility.</span></p>
<p><span>More at&nbsp;<a href="https://dahak-metagenomics.github.io/dahak/">https://dahak-metagenomics.github.io/dahak/</a></span></p><p>Address of the bookmark: <a href="https://github.com/dahak-metagenomics/dahak" rel="nofollow">https://github.com/dahak-metagenomics/dahak</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42570/breeding-insight</guid>
	<pubDate>Wed, 06 Jan 2021 19:49:21 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42570/breeding-insight</link>
	<title><![CDATA[Breeding Insight]]></title>
	<description><![CDATA[<p><span><span>Breeding Insight&nbsp;at Cornell University will leverage recent improvements in genomics and open source informatics components, and in&nbsp;partnership with small breeding programs, will enable these programs to harness&nbsp;&nbsp;powerful digital tools to accelerate their genetic gains</span></span></p>
<p><span>Breeding Insight is funded by&nbsp;the&nbsp;</span><span><a href="https://www.ars.usda.gov/about-ars/" target="_blank">U.S. Department of Agriculture (USDA) Agricultural Research Service (ARS)</a></span><span>&nbsp;through Cornell University. The USDA ARS delivers scientific solutions to national and global agricultural challenges. As a global leader&nbsp;in agricultural discovery through scientific excellence, ARS is committed to delivering cutting-edge, scientific tools and innovative solutions for American farmers, producers, industry, and communities to support the nourishment and well-being of all people; sustaining our nation&rsquo;s agroecosystems and natural resources; and ensuring the economic competitiveness and excellence of our agriculture.</span></p><p>Address of the bookmark: <a href="https://www.breedinginsight.org/" rel="nofollow">https://www.breedinginsight.org/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44288/upset-plots</guid>
	<pubDate>Fri, 24 Mar 2023 22:30:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44288/upset-plots</link>
	<title><![CDATA[Upset plots !]]></title>
	<description><![CDATA[<p>Upset plots are a type of visualization used to analyze the intersection of sets or categories. They are particularly useful for displaying data with multiple categories and analyzing their overlaps.</p>
<p>In an upset plot, each row represents a category or set, and each column represents a data point. The length of the bar for each category indicates the number of data points that belong to that category. The plot also shows the intersections between categories, represented by overlapping bars.</p>
<p>Upset plots are useful for visualizing complex data with multiple categories and intersections, and can help identify patterns and relationships between categories. They are often used in fields such as bioinformatics, where they can be used to analyze gene expression data or to compare the results of different experimental conditions.</p>
<p>https://jokergoo.github.io/ComplexHeatmap-reference/book/upset-plot.html#example-with-the-genomic-regions</p><p>Address of the bookmark: <a href="https://jokergoo.github.io/ComplexHeatmap-reference/book/upset-plot.html#example-with-the-genomic-regions" rel="nofollow">https://jokergoo.github.io/ComplexHeatmap-reference/book/upset-plot.html#example-with-the-genomic-regions</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33003/surankco-supervised-ranking-of-contigs-in-de-novo-assemblies</guid>
	<pubDate>Wed, 24 May 2017 04:46:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33003/surankco-supervised-ranking-of-contigs-in-de-novo-assemblies</link>
	<title><![CDATA[SuRankCo: supervised ranking of contigs in de novo assemblies]]></title>
	<description><![CDATA[<p><span>SuRankCo is a machine learning based software to score and rank contigs from de novo assemblies of next generation sequencing data. It trains with alignments of contigs with known reference genomes and predicts scores and ranking for contigs which have no related reference genome yet.</span></p>
<p>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-015-0644-7</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/surankco/" rel="nofollow">https://sourceforge.net/projects/surankco/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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