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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/32048?offset=30</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31375/cocacola-binning-metagenomic-contigs-using-sequence-composition-read-coverage-co-alignment-and-paired-end-read-linkage</guid>
	<pubDate>Tue, 07 Mar 2017 08:50:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31375/cocacola-binning-metagenomic-contigs-using-sequence-composition-read-coverage-co-alignment-and-paired-end-read-linkage</link>
	<title><![CDATA[COCACOLA (binning metagenomic contigs using sequence COmposition, read CoverAge, CO-alignment, and paired-end read LinkAge)]]></title>
	<description><![CDATA[<p>COCACOLA is a general framework that combines different types of information: sequence COmposition, CoverAge across multiple samples, CO-alignment to reference genomes and paired-end reads LinkAge to automatically bin contigs into OTUs. Furthermore, COCACOLA seamlessly embraces customized prior knowledge to facilitate binning accuracy.</p>
<p>News: Python version of COCACOLA is available now!</p><p>Address of the bookmark: <a href="https://github.com/younglululu/COCACOLA" rel="nofollow">https://github.com/younglululu/COCACOLA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31552/multigenome-assembly</guid>
	<pubDate>Tue, 14 Mar 2017 04:41:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31552/multigenome-assembly</link>
	<title><![CDATA[Multigenome assembly]]></title>
	<description><![CDATA[<p>This project contains scripts and tutorials on how to assemble individual microbial genomes from metagenomes, as described in:</p>
<p>Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes</p>
<p>Mads Albertsen, Philip Hugenholtz, Adam Skarshewski, Gene W. Tyson, K&aring;re L. Nielsen and Per .H. Nielsen</p>
<p>Nature Biotechnology 2013, doi:&nbsp;<a href="http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.2579.html">10.1038/nbt.2579</a></p>
<p>See the associated&nbsp;<a href="http://madsalbertsen.github.io/multi-metagenome/">online guide</a>&nbsp;for detailed information.</p>
<p>https://github.com/MadsAlbertsen/multi-metagenome</p><p>Address of the bookmark: <a href="https://github.com/MadsAlbertsen/multi-metagenome" rel="nofollow">https://github.com/MadsAlbertsen/multi-metagenome</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32465/tetra-nucleotide-analysis</guid>
	<pubDate>Thu, 04 May 2017 05:07:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32465/tetra-nucleotide-analysis</link>
	<title><![CDATA[Tetra-Nucleotide Analysis]]></title>
	<description><![CDATA[<p>A tetra-nucleotide is a fragment of DNA sequence with 4 bases (e.g. AGTC or TTGG). Pride&nbsp;<em>et al.</em>&nbsp;(2003) showed that the frequency of tetra-nucleotides in bacterial genomes contain useful, albeit weak, phylogenetic signals. Even though tetra-nucleotide analysis (TNA) utilizes the information of whole genome, it is evident that it cannot replace other alignment-based phylogenetic methods such as&nbsp;<a href="https://chunlab.wordpress.com/orthoani/">OrthoANI</a>&nbsp;or&nbsp;16S rRNA phylogeny. However, TNA can be useful for&nbsp;phylogenetic characterization when whole genome or 16S rRNA gene information is not available. For example, a partial genomic fragment obtained from a metagenome can be identified by TNA (Teeling&nbsp;<em>et al.</em>, 2004). TNA is also fast enough that it can be&nbsp;used&nbsp;as a search engine against a large genome database.</p><p>Address of the bookmark: <a href="https://chunlab.wordpress.com/tetra-nucleotide-analysis/" rel="nofollow">https://chunlab.wordpress.com/tetra-nucleotide-analysis/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32730/ncbi-prokaryotic-genome-annotation-pipeline</guid>
	<pubDate>Tue, 16 May 2017 08:56:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32730/ncbi-prokaryotic-genome-annotation-pipeline</link>
	<title><![CDATA[NCBI Prokaryotic Genome Annotation Pipeline]]></title>
	<description><![CDATA[<p>NCBI Prokaryotic Genome Annotation Pipeline is designed to annotate bacterial and archaeal genomes (chromosomes and plasmids).</p>
<p>Genome annotation is a multi-level process that includes prediction of protein-coding genes, as well as other functional genome units such as structural RNAs, tRNAs, small RNAs, pseudogenes, control regions, direct and inverted repeats, insertion sequences, transposons and other mobile elements.</p>
<p>NCBI has developed an automatic prokaryotic genome annotation pipeline that combines&nbsp;<em>ab initio</em>&nbsp;gene prediction algorithms with homology based methods. The first version of NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP;&nbsp;<a href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=pubmed&amp;dopt=Abstract&amp;list_uids=18416670">see Pubmed Article</a>) developed in 2005 has been replaced with an upgraded version that is capable of processing a larger data volume. You can find a more detailed description of the new version of&nbsp;the pipeline in&nbsp;<a href="https://www.ncbi.nlm.nih.gov/books/NBK174280/">NCBI Handbook chapter</a>. NCBI's annotation pipeline depends on several internal databases and is not currently available for download or use outside of the NCBI environment.</p>
<p>https://www.ncbi.nlm.nih.gov/genome/annotation_prok/</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/genome/annotation_prok/" rel="nofollow">https://www.ncbi.nlm.nih.gov/genome/annotation_prok/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40948/bio7-an-integrated-development-environment-for-ecological-modeling-scientific-image-analysis-and-statistical-analysis</guid>
	<pubDate>Fri, 07 Feb 2020 23:32:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40948/bio7-an-integrated-development-environment-for-ecological-modeling-scientific-image-analysis-and-statistical-analysis</link>
	<title><![CDATA[Bio7: an integrated development environment for ecological modeling, scientific image analysis and statistical analysis]]></title>
	<description><![CDATA[<p><span>The application Bio7 is an integrated development environment for ecological modeling, scientific image analysis and statistical analysis. The application itself is based on an RCP-Eclipse-Environment (Rich-Client-Platform) which offers a huge flexibility in configuration and extensibility because of its plug-in structure and the possibility of customization.</span></p>
<p><a href="https://bio7.org/about/">https://bio7.org/about/</a></p><p>Address of the bookmark: <a href="https://bio7.org/home-2/" rel="nofollow">https://bio7.org/home-2/</a></p>]]></description>
	<dc:creator>Nidhi Rajput</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44734/data-visualization-in-bioinformatics-useful-and-eye-catching-plots-for-data-analysis</guid>
	<pubDate>Sat, 14 Dec 2024 12:41:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44734/data-visualization-in-bioinformatics-useful-and-eye-catching-plots-for-data-analysis</link>
	<title><![CDATA[Data Visualization in Bioinformatics: Useful and Eye-Catching Plots for Data Analysis]]></title>
	<description><![CDATA[<p>Data visualization is a cornerstone of bioinformatics, enabling researchers to interpret complex datasets effectively. With a plethora of data types&mdash;genomic sequences, expression profiles, protein interactions, and more&mdash;the right visualizations can make or break an analysis. This blog highlights some of the most useful and visually compelling plots for bioinformatics data analysis, along with tools to create them.</p><h4><strong>1. Heatmaps: Exploring Patterns in High-Dimensional Data</strong></h4><p>Heatmaps are a go-to visualization for representing high-dimensional datasets, such as gene expression or metabolomics data. They use color gradients to display data intensity, making patterns and clusters easily detectable.</p><ul>
<li>
<p><strong>Applications</strong>: Gene expression analysis, pathway enrichment, methylation studies.</p>
</li>
<li>
<p><strong>Tools</strong>: Seaborn (Python), ComplexHeatmap (R), Morpheus (web-based).</p>
</li>
</ul><p><strong>Tip</strong>: Add dendrograms to visualize clustering of rows and columns for hierarchical relationships.</p><h4><strong>2. Volcano Plots: Highlighting Differential Features</strong></h4><p>Volcano plots are indispensable for identifying significantly differentially expressed genes or proteins. They plot the log2 fold change against &ndash;log10(p-value), making it easy to spot statistically significant changes.</p><ul>
<li>
<p><strong>Applications</strong>: RNA-seq, proteomics, and metabolomics.</p>
</li>
<li>
<p><strong>Tools</strong>: ggplot2 (R), EnhancedVolcano (R), Plotly (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use color to highlight significant features and label key genes or proteins.</p><h4><strong>3. PCA Plots: Reducing Complexity with Principal Component Analysis</strong></h4><p>Principal Component Analysis (PCA) plots are used to reduce dimensionality and uncover trends or clusters in data. They provide insights into sample variability and grouping.</p><ul>
<li>
<p><strong>Applications</strong>: Transcriptomics, metabolomics, microbiome studies.</p>
</li>
<li>
<p><strong>Tools</strong>: scikit-learn + Matplotlib (Python), prcomp (R), ClustVis (web-based).</p>
</li>
</ul><p><strong>Tip</strong>: Annotate clusters with metadata to enhance interpretability.</p><h4><strong>4. Manhattan Plots: Genome-Wide Association Studies</strong></h4><p>Manhattan plots visualize p-values across the genome, making it easy to identify significant associations in genome-wide studies. They resemble city skylines, with the highest peaks indicating loci of interest.</p><ul>
<li>
<p><strong>Applications</strong>: GWAS, QTL mapping.</p>
</li>
<li>
<p><strong>Tools</strong>: qqman (R), Matplotlib (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use alternating colors for chromosomes and highlight significant SNPs for clarity.</p><h4><strong>5. Circular Plots (Circos): Visualizing Genomic Relationships</strong></h4><p>Circular plots are ideal for visualizing relationships across the genome, such as structural variations, gene duplications, or synteny.</p><ul>
<li>
<p><strong>Applications</strong>: Comparative genomics, structural variation studies.</p>
</li>
<li>
<p><strong>Tools</strong>: Circos (standalone), Rcircos (R), pyCircos (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Keep the plot clean and avoid overcrowding to maintain readability.</p><h4><strong>6. Sankey Diagrams: Tracking Data Flows</strong></h4><p>Sankey diagrams visualize flows or relationships between categories, often used to track changes in gene expression or pathway enrichment across conditions.</p><ul>
<li>
<p><strong>Applications</strong>: Pathway analysis, gene set enrichment analysis.</p>
</li>
<li>
<p><strong>Tools</strong>: Plotly (Python), networkD3 (R).</p>
</li>
</ul><p><strong>Tip</strong>: Use gradients or distinct colors to highlight key transitions.</p><h4><strong>7. Network Graphs: Mapping Interactions</strong></h4><p>Network graphs represent relationships between entities, such as protein-protein interactions or gene regulatory networks. Nodes represent entities, and edges represent relationships.</p><ul>
<li>
<p><strong>Applications</strong>: Systems biology, interactomics.</p>
</li>
<li>
<p><strong>Tools</strong>: Cytoscape (standalone), igraph (R), NetworkX (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use edge thickness or node size to represent interaction strength or centrality.</p><h4><strong>8. Violin Plots: Visualizing Data Distribution</strong></h4><p>Violin plots combine a boxplot with a density plot, showing the distribution and variability of data.</p><ul>
<li>
<p><strong>Applications</strong>: Single-cell RNA-seq, quantitative trait analysis.</p>
</li>
<li>
<p><strong>Tools</strong>: Seaborn (Python), ggplot2 (R).</p>
</li>
</ul><p><strong>Tip</strong>: Split violins by groups for side-by-side comparisons.</p><h4><strong>9. Time-Series Plots: Monitoring Changes Over Time</strong></h4><p>Time-series plots display changes in variables across time points, useful for tracking gene expression dynamics or metabolic fluxes.</p><ul>
<li>
<p><strong>Applications</strong>: Time-course experiments, cell cycle studies.</p>
</li>
<li>
<p><strong>Tools</strong>: Matplotlib (Python), ggplot2 (R).</p>
</li>
</ul><p><strong>Tip</strong>: Smooth the data to highlight trends while avoiding overfitting.</p><h4><strong>10. Genome Tracks: Visualizing Genomic Features</strong></h4><p>Genome tracks display multiple layers of genomic data, such as gene annotations, sequencing coverage, and epigenetic marks.</p><ul>
<li>
<p><strong>Applications</strong>: ChIP-seq, ATAC-seq, whole-genome sequencing.</p>
</li>
<li>
<p><strong>Tools</strong>: IGV (standalone), pyGenomeTracks (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Stack related tracks for direct comparisons.</p><h4><strong>11. UpSet Plots: Visualizing Set Intersections</strong></h4><p>UpSet plots are a powerful alternative to Venn diagrams for visualizing intersections between multiple datasets.</p><ul>
<li>
<p><strong>Applications</strong>: Overlap analysis for gene sets, pathways, or variants.</p>
</li>
<li>
<p><strong>Tools</strong>: UpSetR (R), ComplexUpset (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use bar plots to represent the size of each intersection for added clarity.</p><h4><strong>12. Ridge Plots: Comparing Distributions</strong></h4><p>Ridge plots visualize the distributions of multiple datasets, stacked for easy comparison.</p><ul>
<li>
<p><strong>Applications</strong>: Transcriptomics, single-cell RNA-seq.</p>
</li>
<li>
<p><strong>Tools</strong>: ggridges (R), Matplotlib (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use transparency and consistent scaling for better readability.</p><h4><strong>13. Chord Diagrams: Visualizing Connections Between Groups</strong></h4><p>Chord diagrams illustrate relationships between categories, such as shared genes between pathways or overlaps in regulatory elements.</p><ul>
<li>
<p><strong>Applications</strong>: Pathway overlap, synteny, co-expression networks.</p>
</li>
<li>
<p><strong>Tools</strong>: Circlize (R), Holoviews (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use distinct colors for each group to emphasize relationships.</p><h4><strong>14. Treemaps: Hierarchical Data Representation</strong></h4><p>Treemaps visualize hierarchical data as nested rectangles, with area proportional to data size.</p><ul>
<li>
<p><strong>Applications</strong>: Ontology enrichment, pathway analysis.</p>
</li>
<li>
<p><strong>Tools</strong>: Treemapify (R), Plotly (Python).</p>
</li>
</ul><p><strong>Tip</strong>: Use colors to represent additional variables, like significance or enrichment scores.</p><h4><strong>15. T-SNE/UMAP Plots: Dimensionality Reduction for Clustering</strong></h4><p>T-SNE and UMAP plots are great for visualizing high-dimensional data in two dimensions while preserving local or global structure.</p><ul>
<li>
<p><strong>Applications</strong>: Single-cell transcriptomics, clustering analyses.</p>
</li>
<li>
<p><strong>Tools</strong>: scikit-learn (Python), Seurat (R).</p>
</li>
</ul><p><strong>Tip</strong>: Combine with metadata annotations for better cluster interpretation.</p><h4><strong>Bringing It All Together</strong></h4><p>The choice of visualization can significantly impact the insights gained from bioinformatics data. By selecting plots tailored to your data type and analysis goals, you can effectively communicate your findings and make your research more impactful. Whether you&rsquo;re a seasoned bioinformatician or a beginner, mastering these visualizations will elevate your analyses and presentations.</p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/17176/arvados</guid>
	<pubDate>Sat, 20 Sep 2014 16:54:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/17176/arvados</link>
	<title><![CDATA[Arvados]]></title>
	<description><![CDATA[<p>Arvados is a free and open&nbsp;source bioinformatics&nbsp;platform for genomic and&nbsp;biomedical data. User can&nbsp;Store | Organize | Compute | Share the data for free.&nbsp;</p>
<p><img src="https://arvados.org/images/dax.png" width="400" height="535" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://arvados.org/" rel="nofollow">https://arvados.org/</a></p>]]></description>
	<dc:creator>Martin Jones</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27696/methylkit</guid>
	<pubDate>Fri, 03 Jun 2016 10:09:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27696/methylkit</link>
	<title><![CDATA[methylKit]]></title>
	<description><![CDATA[<p><em>methylKit</em> is an <a href="http://en.wikipedia.org/wiki/R_%28programming_language%29">R</a> package for DNA methylation analysis and annotation from high-throughput bisulfite sequencing. The package is designed to deal with sequencing data from <a href="http://www.nature.com/nprot/journal/v6/n4/abs/nprot.2010.190.html">RRBS</a> and its variants, but also target-capture methods such as <a href="http://www.halogenomics.com/sureselect/methyl-seq">Agilent SureSelect methyl-seq</a>. In addition, methylKit can deal with base-pair resolution data for 5hmC obtained from Tab-seq or oxBS-seq. It can also handle whole-genome bisulfite sequencing data if proper input format is provided.</p><p>Address of the bookmark: <a href="https://github.com/al2na/methylKit" rel="nofollow">https://github.com/al2na/methylKit</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28117/quin%E2%80%99s-web-server</guid>
	<pubDate>Mon, 27 Jun 2016 10:44:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28117/quin%E2%80%99s-web-server</link>
	<title><![CDATA[QuIN’s web server]]></title>
	<description><![CDATA[<p><span>Recent studies of the human genome have indicated that regulatory elements (e.g. promoters and enhancers) at distal genomic locations can interact with each other via chromatin folding and affect gene expression levels. Genomic technologies for mapping interactions between DNA regions, e.g., ChIA-PET and HiC, can generate genome-wide maps of interactions between regulatory elements. These interaction datasets are important resources to infer distal gene targets of non-coding regulatory elements and to facilitate prioritization of critical loci for important cellular functions. With the increasing diversity and complexity of genomic information and public ontologies, making sense of these datasets demands integrative and easy-to-use software tools. Moreover, network representation of chromatin interaction maps enables effective data visualization, integration, and mining. Currently, there is no software that can take full advantage of network theory approaches for the analysis of chromatin interaction datasets. To fill this gap, we developed a web-based application, QuIN, which enables: 1) building and visualizing chromatin interaction networks, 2) annotating networks with user-provided private and publicly available functional genomics and interaction datasets, 3) querying network components based on gene name or chromosome location, and 4) utilizing network based measures to identify and prioritize critical regulatory targets and their direct and indirect interactions.&nbsp;</span></p>
<p><strong>AVAILABILITY:</strong><span>&nbsp;QuIN&rsquo;s web server is available at&nbsp;</span><a href="http://quin.jax.org/">http://quin.jax.org</a><span>&nbsp;QuIN is developed in Java and JavaScript, utilizing an Apache Tomcat web server and MySQL database and the source code is available under the GPLV3 license available on GitHub:</span><a href="https://github.com/UcarLab/QuIN/">https://github.com/UcarLab/QuIN/</a><span>.</span></p><p>Address of the bookmark: <a href="http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004809" rel="nofollow">http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004809</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28303/fancy-oneliner-for-bioinformatics</guid>
	<pubDate>Thu, 07 Jul 2016 12:05:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28303/fancy-oneliner-for-bioinformatics</link>
	<title><![CDATA[Fancy Oneliner for Bioinformatics !!]]></title>
	<description><![CDATA[<p><span>This webpage lists some of the one-liners that we frequently use in metagenomic analyses. You can click on the following links to browse through different topics. You can copy/paste the commands as they are in your terminal screen, provided you follow the same naming conventions and folder structures as we have. We are sharing these codes with the intention that if they are useful and help you in your analyses, then we will be appropriately credited as considerable effort has been put into devising them.</span></p><p>Address of the bookmark: <a href="http://userweb.eng.gla.ac.uk/umer.ijaz/bioinformatics/oneliners.html" rel="nofollow">http://userweb.eng.gla.ac.uk/umer.ijaz/bioinformatics/oneliners.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>

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