<?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/27696?offset=190</link>
	<atom:link href="https://bioinformaticsonline.com/related/27696?offset=190" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35131/giggle-a-search-engine-for-large-scale-integrated-genome-analysis</guid>
	<pubDate>Wed, 10 Jan 2018 03:10:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35131/giggle-a-search-engine-for-large-scale-integrated-genome-analysis</link>
	<title><![CDATA[GIGGLE: a search engine for large-scale integrated genome analysis]]></title>
	<description><![CDATA[<p><span>GIGGLE is a genomics search engine that identifies and ranks the significance of genomic loci shared between query features and thousands of genome interval files. GIGGLE (</span><a href="https://github.com/ryanlayer/giggle">https://github.com/ryanlayer/giggle</a><span>) scales to billions of intervals and is over three orders of magnitude faster than existing methods. Its speed extends the accessibility and utility of resources such as ENCODE, Roadmap Epigenomics, and GTEx by facilitating data integration and hypothesis generation.</span></p>
<p>https://www.nature.com/articles/nmeth.4556</p><p>Address of the bookmark: <a href="https://github.com/ryanlayer/giggle" rel="nofollow">https://github.com/ryanlayer/giggle</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39441/snakepipes-a-toolkit-based-on-snakemake-and-python-for-analysis-of-ngs-data</guid>
	<pubDate>Thu, 30 May 2019 04:06:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39441/snakepipes-a-toolkit-based-on-snakemake-and-python-for-analysis-of-ngs-data</link>
	<title><![CDATA[snakepipes: A toolkit based on snakemake and python for analysis of NGS data]]></title>
	<description><![CDATA[<p><span><span>snakePipes are flexible and powerful workflows built using&nbsp;</span><a href="https://github.com/maxplanck-ie/snakepipes/blob/master/snakemake.readthedocs.io">snakemake</a><span>&nbsp;that simplify the analysis of NGS data.</span></span></p>
<ul>
<li>DNA-mapping*</li>
<li>ChIP-seq*</li>
<li>RNA-seq*</li>
<li>ATAC-seq*</li>
<li>scRNA-seq</li>
<li>Hi-C</li>
<li>Whole Genome Bisulfite Seq/WGBS</li>
</ul>
<p><span>(*Also available in "allele-specific" mode)</span></p>
<p><span>snakePipes can be installed via conda : </span></p>
<p><span>'conda install -c mpi-ie -c bioconda -c conda-forge snakePipes'. </span></p>
<p><span>Source code (</span><a href="https://github.com/maxplanck-ie/snakepipes" target="">https://github.com/maxplanck-ie/snakepipes</a><span>) and documentation (</span><a href="https://snakepipes.readthedocs.io/en/latest/" target="">https://snakepipes.readthedocs.io/en/latest/</a><span>) are available online.</span></p><p>Address of the bookmark: <a href="https://github.com/maxplanck-ie/snakepipes" rel="nofollow">https://github.com/maxplanck-ie/snakepipes</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/42206/pollard-lab</guid>
  <pubDate>Fri, 25 Sep 2020 20:20:50 -0500</pubDate>
  <link></link>
  <title><![CDATA[Pollard Lab]]></title>
  <description><![CDATA[
<p>We are a bioinformatics research lab focused on developing novel methods and using them to study genome evolution, organization, and regulation. Our mission is to decode biomedical knowledge that is missed without rigorous statistical approaches.</p>

<p>http://docpollard.org/</p>

<p>Tools</p>

<p>http://docpollard.org/resources/software/</p>
]]></description>
</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/bookmarks/view/43766/genometools-the-versatile-open-source-genome-analysis-software</guid>
	<pubDate>Wed, 02 Feb 2022 04:00:21 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43766/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><img src="http://genometools.org/images/annotation.png" alt="image" style="border: 0px;"></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>http://genometools.org/pub/</p><p>Address of the bookmark: <a href="http://genometools.org/" rel="nofollow">http://genometools.org/</a></p>]]></description>
	<dc:creator>Neel</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/researchlabs/view/43817/bioinfo-lab</guid>
  <pubDate>Fri, 04 Mar 2022 00:17:00 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinfo Lab]]></title>
  <description><![CDATA[
<p>The Institute of Bioinformatics conducts internationally renowned research and provides profound education in bioinformatics. Its research focuses on development and application of machine learning and statistical methods in biology and medicine.</p>

<p>Contact:<br />Computer Science Building (Science Park 3)<br />Altenberger Str. 69, A-4040 Linz, Austria<br />Tel. +43 732 2468 4520 / Fax +43 732 2468 4539<br />E-mail secretary@bioinf.jku.at</p>

<p>http://www.bioinf.jku.at/</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/915/researcher-in-computer-sciencebiology</guid>
  <pubDate>Mon, 15 Jul 2013 18:38:40 -0500</pubDate>
  <link></link>
  <title><![CDATA[Researcher in computer science/biology]]></title>
  <description><![CDATA[
<p>Researcher in Computer Science at the Computational Biology Unit - temporary employment</p>

<p>The Department of Informatics is a vacant position as a researcher in computer science, related to Computational Biology Unit (CBU), for 3 years.<br /> <br />The position is part of CBU Service Group and will focus on bioinformatic analysis project and especially the analysis of high-throughput data, including NGS (sequencing), and proteomics data.<br /> <br />The successful candidate will be part of the Norwegian bioinformatics platform's national helpdesk within the project ELIXIR.NO<br /> <br />Applicants must hold a PhD in a relevant subject such as computer science, mathematics, molecular biology and also possess expertise and experience in bioinformatics statistics and analysis of data from high-throughput molecular experiment.<br /> <br />Basic programming or scripting skills are required. Experience in Python, R, Perl, Linux-based operating systems and moreover knowledge of databases and web programming will be a strength for applicants.<br /> <br />We expect enthusiasm and independence and moreover the ability to work in an interdisciplinary team environment.<br /> <br />Good knowledge of English is required.<br /> <br />Salaries start at level 57 (code 1109/LR 24.1) by appointment. Further promotion occurs after<br />service seniority in the position (at grade 57-65). Of particularly highly qualified applicants may be considered a higher salary.<br /> <br />Further information about the position is available from the chair of the CBU, <br />Professor Inge Jonassen, e-mail: Inge.Jonassen @ ii.uib.no<br /> <br />The successful applicant must comply with the guidelines that apply at any given time the position.<br /> <br />State employment shall as far as possible reflect the diversity of the population. It is therefore an objective to achieve a balanced age and sex composition and the recruitment of persons with immigrant backgrounds. Persons with immigrant background are requested to apply for the position.<br /> <br />Women are particularly encouraged to apply. If the experts find that several applicants have approximately equivalent qualifications, the rules on equal in the Personnel Regulations for Academic Positions will be applied.<br /> <br />University of Bergen applies the principles of public openness when recruiting staff to scientific positions.<br /> <br />Information about the applicant may be made public even though the applicant has requested not to be named in the list of applicants. If the request does not host admitted to the result, the applicant shall be notified of this.<br /> <br />Send application, CV, certificates, diplomas, undergraduate work and a list of publications (list of publications) online by clicking on https://www.jobbnorge.no/jobbsoknet/login.aspx?returnurl=/jobbsoknet/jobapplication.aspx?jobid=95196<br /> <br />You need to upload certified translations into English or a Scandinavian language of appendices, such as diplomas and transcripts.<br /> <br />Applications sent by email to individuals at the institute will not be considered.<br /> <br />Deadline: 9 August 2013</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/2054/postdoc-positions-mammalian-transcriptome-evolution-at-sib</guid>
  <pubDate>Mon, 12 Aug 2013 19:58:33 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoc Positions - Mammalian Transcriptome Evolution at SIB]]></title>
  <description><![CDATA[
<p>BIOINFORMATICS POSTDOC IN FUNCTIONAL EVOLUTIONARY GENOMICS</p>

<p>Center for Integrative Genomics, University of Lausanne, Switzerland</p>

<p>Two postdoctoral positions (2 years with possible extensions up to 5 years) are available immediately in the evolutionary genomics group of Henrik Kaessmann.</p>

<p>We are seeking highly qualified and enthusiastic applicants with strong skills in computational biology/bioinformatics, preferably also with experience in data mining and comparative or evolutionary genome analysis.</p>

<p>We have been interested in a range of topics related to the functional evolution of genomes from primates (e.g., the emergence of new genes and their functions) and other mammals (e.g., the origin and evolution of mammalian sex chromosomes). In the framework of a recently launched series of projects, a large amount of transcriptome and genome (e.g., epigenome) data are being produced by the wet lab unit of the group using next generation sequencing technologies for a unique collection of tissues from representative mammals and outgroup species (e.g., birds). Topics of current projects based on these data include the origins and/or evolution of protein-coding genes, alternative splicing, microRNAs, long noncoding RNAs, and dosage compensation.</p>

<p>The postdoctoral fellow will perform integrated evolutionary/bioinformatics analyses based on data produced in the lab and available genomic data. The specific project will be developed together with the candidate.</p>

<p>The language of the institute is English, and its members form an international group that is rapidly expanding. The institute is located in Lausanne, a beautiful city at Lake Geneva.</p>

<p>For more information on the group and our institute more generally, please refer to our website: http://www.unil.ch/cig/page7858_en.html</p>

<p>Please submit a CV, statement of research interest, and names of three references to: Henrik Kaessmann (Henrik.Kaessmann@unil.ch).</p>

<p>Webpage : http://www.unil.ch/cig/page7858.html</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/2423/cancers-origins-revealed</guid>
	<pubDate>Thu, 15 Aug 2013 13:06:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/2423/cancers-origins-revealed</link>
	<title><![CDATA[Cancer's origins revealed]]></title>
	<description><![CDATA[<p>Researchers have provided the first comprehensive compendium of mutational processes that drive tumour development. Together, these mutational processes explain most mutations found in 30 of the most common cancer types. This new understanding of cancer development could help to treat and prevent a wide-range of cancers.<br /><br />More at &gt;&gt; http://www.sanger.ac.uk/about/press/2013/130814.html</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>

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