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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/4090?offset=1180</link>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/44400/pevzner-lab</guid>
  <pubDate>Thu, 02 Nov 2023 05:39:26 -0500</pubDate>
  <link></link>
  <title><![CDATA[Pevzner Lab !]]></title>
  <description><![CDATA[
<p>The laboratory works on genome sequencing, immunoproteogenomics, antibiotics sequencing, and comparative genomics - computational technologies that enabled new applications and allowed scientists to attack biological problems that remained beyond the reach of previous techniques.</p>

<p>https://bioalgorithms.ucsd.edu/research4.html</p>
]]></description>
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<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>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/4094/manufacturing-life-with-j-craig-venter</guid>
	<pubDate>Thu, 29 Aug 2013 08:52:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/4094/manufacturing-life-with-j-craig-venter</link>
	<title><![CDATA[Manufacturing Life with J. Craig Venter]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/PKtozMvSsBk" frameborder="0" allowfullscreen></iframe>J. Craig Venter, CEO of Synthetic Genomics, talks about finding genomic-driven solutions to address global needs such as new sources of energy, food and vaccines in an interview with James Bennet, Editor-in-Chief of The Atlantic. This program is introduced by Pradeep Khosla, the new chancellor of the University of California, San Diego.  Series: "The Atlantic Meets The Pacific" [11/2012] [Public Affairs] [Show ID: 24359]
The Atlantic Meets the Pacific playlist: http://goo.gl/5V8Yb
The Atlantic Meets the Pacific on UCTV: http://www.uctv.tv/atlanticpacific
UCTV: http://www.uctv.tv]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/19272/translate2r</guid>
	<pubDate>Fri, 21 Nov 2014 01:16:06 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/19272/translate2r</link>
	<title><![CDATA[translate2R]]></title>
	<description><![CDATA[<p>After their presentation at the international &ldquo;user!&rdquo; conference, data analysis specialist <a href="http://www.eoda.de/en/" target="_blank">eoda</a> starts the public alpha testing of <a href="http://www.eoda.de/en/translate2R.html" target="_blank">translate2R</a>. With the start of alpha testing the innovative migration solution by the company hailing from Kassel discards the working title &ldquo;translateR&rdquo; and takes on the final product brand name &ldquo;translate2R&rdquo;. translate2R is a service for the automated translation of SPSS&reg; syntax to R code, therefore supporting data analysts with a quick and low-risk migration to R.</p><p>The manual translation of many, frequently rather complex SPSS scripts often presents itself as a tedious and error-prone task, and represents a rather large obstacle for many analysts and companies to migrate to a modern, open source data management and analysis tool like R. With translate2R this hurdle will be diminished substantially.</p><p>Find at https://service.eoda.de/translater/?lang=en</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/36191/bioinformatics-workshops-no-coding-required</guid>
	<pubDate>Mon, 09 Apr 2018 13:06:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/36191/bioinformatics-workshops-no-coding-required</link>
	<title><![CDATA[Bioinformatics Workshops - NO CODING REQUIRED]]></title>
	<description><![CDATA[<p><img src="https://edu.t-bio.info/wp-content/uploads/2018/03/t-bioinfo-bioinformatics-workshops.jpg" alt="Bioinformatics Workshops T-BioInfo" width="568" height="319" style="vertical-align: middle; border: 0px;"></p><p>Pine Biotech, Inc., a US-based startup working with the Tauber Bioinformatics Research Center is offering a full curriculum online preparing students without any technical background for real-life challenges with large scale biomedical data. Workshops on processing, analysis and biomedical interpretation of Next Generation Sequencing data cover important up-to-date algorithms and machine learning approaches. The most important thing is that there are virtually no pre-requisites such as coding, biostatistics or advanced medical skills. If you know what gene is and how the genes are expressed, you are ready to take the courses or join our workshops. Learn more:&nbsp;https://edu.t-bio.info/workshops/</p>]]></description>
	<dc:creator>eliabrodsky</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/12111/internship-program-with-arraygen-technolgies</guid>
  <pubDate>Sun, 22 Jun 2014 23:18:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Internship program with ArrayGen Technolgies]]></title>
  <description><![CDATA[
<p>Internship Program for Bioinformatics / Biotechnology Professionals Currently we offer positions to outstanding students interested in Next Generation Sequencing (NGS) data analysis. Applications are accepted throughout the year. Accepted students will be listed on web with their schedules. Accepted students can attend our future workshops and trainings freely at the specified venue.</p>

<p>Interested candidates may email their resume along with a cover letter to careers@arraygen.com</p>

<p>Official website: http://www.arraygen.com/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14215/the-8000-years-old-tibetian-gene-mutation</guid>
	<pubDate>Wed, 20 Aug 2014 21:57:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14215/the-8000-years-old-tibetian-gene-mutation</link>
	<title><![CDATA[The 8000 years old Tibetian gene mutation !!!]]></title>
	<description><![CDATA[<p>A new study has provided insight into how gene mutation around 8,000 years ago helped Tibetans' to survive in the thin air on the Tibetan Plateau, where an average elevation is of 14,800 feet.<br /><br />A study led by University of Utah scientists is the first to find a genetic cause for the adaptation, a single DNA base pair change that dates back 8,000 years and demonstrate how it contributes to the Tibetans' ability to live in low oxygen conditions.</p><p>About 8,000 years ago, the gene EGLN1 changed by a single DNA base pair. Today, a relatively short time later on the scale of human history, 88 percent of Tibetans have the genetic variation, and it was virtually absent from closely related lowland Asians. The findings indicate the genetic variation endows its carriers with an advantage.<br /><br />In those without the adaptation, low oxygen caused their blood to become thick with oxygen-carrying red blood cells, an attempt to feed starved tissues, which could cause long-term complications such as heart failure. The researchers found that the newly identified genetic variation protected Tibetans by decreasing the over-response to low oxygen.</p><p>Reference: http://www.nature.com/nature/journal/v512/n7513/abs/nature13408.html</p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14024/grapher</guid>
	<pubDate>Thu, 14 Aug 2014 14:02:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14024/grapher</link>
	<title><![CDATA[GrapheR !!!]]></title>
	<description><![CDATA[<p>What a wonderful gem <em>GrapheR</em> is.... Oh yes it is. <em>GrapheR</em> is a GUI for base graphics in R by http://www.maximeherve.com/. The package provides a graphical user interface for creating base charts in R. It is ideal for beginners in R, as the user interface is very clear and the code is written along side into a text file, allowing users to recreate the charts directly in the console. <br /><br />Adding and changing legends? Messing around with the plotting window settings? It is much easier/quicker with this GUI than reading the help file and trying to understand the various parameters.<br />Here is a little example using the iris data set.<br /><br />library(GrapheR)<br />data(iris)<br />run.GrapheR()<br /><br />This will bring up a window that helps me to create the chart and tweak the various parameters.</p><p><img src="http://4.bp.blogspot.com/-NbnCM1dPh3E/U9aW9YxJ9oI/AAAAAAAABgo/gEPzPhOpf2Y/s1600/GrapheR.png" alt="image" width="878" height="868" style="border: 0px; border: 0px;"><br /><br />Finally, I find the underlying R code in a file created by <em>GrapheR</em>. For more details read also the <a href="http://cran.r-project.org/web/packages/GrapheR/index.html" target="_blank">package vignette</a>, which is available in <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_en.pdf" target="_blank">English</a>, <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_fr.pdf" target="_blank">French</a> and <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_de.pdf" target="_blank">German</a>!</p>]]></description>
	<dc:creator>John Parker</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14186/pybedtools</guid>
	<pubDate>Wed, 20 Aug 2014 01:03:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14186/pybedtools</link>
	<title><![CDATA[pybedtools]]></title>
	<description><![CDATA[<p>pybedtools is a Python wrapper for Aaron Quinlan's BEDtools programs (https://github.com/arq5x/bedtools), which are widely used for genomic interval manipulation or "genome algebra". pybedtools extends BEDTools by offering feature-level manipulations from with Python. See full online documentation, including installation instructions, at http://pythonhosted.org/pybedtools/.</p><p>More at http://pythonhosted.org/pybedtools/</p><p>A powerful toolset for genome arithmetic.http://code.google.com/p/bedtools/</p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17504/postdoc-scientist-bioinformatics-at-ccmb</guid>
  <pubDate>Fri, 26 Sep 2014 19:58:41 -0500</pubDate>
  <link></link>
  <title><![CDATA[PostDoc Scientist Bioinformatics at CCMB]]></title>
  <description><![CDATA[
<p>1. Project Assistant/Junior Research Fellow/ Project Fellow [PA_JRF_PF]</p>

<p>a) M.Sc/or equivalent in biological sciences/related areas [Position Code: PA_JRF_PF_a]<br />b) B.E/B.Tech/ M.Sc in biotechnology/bioinformatics/computer science/Chemistry/Physics or MCA [Position Code: PA_JRF_PF_b]<br />c) M.Sc/or equivalent in wildlife sciences/ecology/environmental sciences or MBBS/BVSc/MVSc. [Position Code: PA_JRF_PF_c]</p>

<p>(Candidates with result awaited are NOT eligible to apply)</p>

<p>Upper Age limit 28years</p>

<p>Rs.12000 / Rs.16000 (as sanctioned by the funding agency)</p>

<p>2. Post Doctoral Fellow/Research Associate in multiple research areas [PDF_RA]</p>

<p>Ph.D. (submitted/awarded) in any branch of biological Sciences. Candidates with Ph.D. in other sciences are also encouraged to apply.</p>

<p>Experience in molecular biology, biochemistry, structural biology, cell biology, infectious disease, conservation genetics, veterinary science, reproductive biology, and molecular diagnostics is desired but not mandatory.</p>

<p>[Position Code: PDF_RA]</p>

<p>UpperAge limit 35years</p>

<p>Rs. 22000- 26000 (as sanctioned by the funding agency)</p>

<p>3. Post Doctoral Scientist Fellow [PDSF]</p>

<p>Ph.D in any of the following areas: bioinformatics, next generation sequencing, high throughput data analysis, proteomics, bio-statistics, computer science, information technology, computer hardware and networking/clustering, parallel processing.<br />[Position Code: PDSF]</p>

<p>Upper Age limit 40 years</p>

<p>Rs. 40000 consolidated (as sanctioned by the funding agency)</p>

<p>Download Application: Last date for apply online: 09th Oct 2014</p>

<p>Advertisement: www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>

<p>Apply online http://www.ccmb.res.in/positions/temp_notif/online_form.html</p>

<p>More at http://www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>
]]></description>
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