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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31714?</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36880/jvarkit-java-utilities-for-bioinformatics</guid>
	<pubDate>Fri, 08 Jun 2018 09:31:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36880/jvarkit-java-utilities-for-bioinformatics</link>
	<title><![CDATA[Jvarkit : Java utilities for Bioinformatics]]></title>
	<description><![CDATA[Collection of Java tool kits for bioinformatics works:

Jvarkit : Java utilities for Bioinformatics<p>Address of the bookmark: <a href="http://lindenb.github.io/jvarkit/" rel="nofollow">http://lindenb.github.io/jvarkit/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</guid>
	<pubDate>Fri, 20 May 2016 11:01:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</link>
	<title><![CDATA[RCircos: an R package for Circos 2D track plots]]></title>
	<description><![CDATA[<p>RCircos package provides a simple and flexible way to make Circos 2D track plots with R and could be easily integrated into other R data processing and graphic manipulation pipelines for presenting large-scale multi-sample genomic research data. It can also serve as a base tool to generate complex Circos images.</p>
<p>More at https://bitbucket.org/henryhzhang/rcircos/src</p><p>Address of the bookmark: <a href="https://bitbucket.org/henryhzhang/rcircos/src" rel="nofollow">https://bitbucket.org/henryhzhang/rcircos/src</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29635/r-graphs</guid>
	<pubDate>Fri, 04 Nov 2016 10:48:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29635/r-graphs</link>
	<title><![CDATA[R Graphs !!]]></title>
	<description><![CDATA[<p><span>The blog is a collection of script examples with example data and output plots. R produce excellent quality graphs for data analysis, science and business presentation, publications and other purposes. Self-help codes and examples are provided. Enjoy nice graphs !!</span></p><p>Address of the bookmark: <a href="http://rgraphgallery.blogspot.be/" rel="nofollow">http://rgraphgallery.blogspot.be/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/12787/integrative-genomics-viewer-igv-tutorial</guid>
	<pubDate>Sat, 12 Jul 2014 15:16:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/12787/integrative-genomics-viewer-igv-tutorial</link>
	<title><![CDATA[Integrative Genomics Viewer (IGV) tutorial]]></title>
	<description><![CDATA[<p>The <a href="http://www.broadinstitute.org/igv/">Integrative Genomics Viewer (IGV)</a> from the Broad Center allows you to view several types of data files involved in any NGS analysis that employs a reference genome, including how reads from a dataset are mapped, gene annotations, and predicted genetic variants.</p>
<p>http://www.broadinstitute.org/igv/</p><p>Address of the bookmark: <a href="https://wikis.utexas.edu/display/bioiteam/Integrative+Genomics+Viewer+%28IGV%29+tutorial" rel="nofollow">https://wikis.utexas.edu/display/bioiteam/Integrative+Genomics+Viewer+%28IGV%29+tutorial</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/44284/tools-for-geospatial-data-analysis</guid>
	<pubDate>Wed, 22 Mar 2023 02:10:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/44284/tools-for-geospatial-data-analysis</link>
	<title><![CDATA[Tools for Geospatial data analysis !]]></title>
	<description><![CDATA[<div><div><div><div><div><div><div><div><div><div><p>Geospatial data is becoming increasingly important in many fields, including urban planning, environmental science, public health, and more. These tools can help you work with data from a variety of sources, including satellite imagery, GPS data, and other forms of spatial data. They can help you visualize data, perform complex analysis, and even create maps and other visualizations.</p><p>The list includes some of the most popular and widely used geospatial tools available in Python. These tools can help you work with data from a variety of sources and in a variety of formats. Some of the tools are focused on visualization, such as Cartopy, Folium, and Contextily, which allow you to create interactive maps and other visualizations. Other tools are more focused on data manipulation and analysis, such as Fiona, GeoPandas, and Rasterio, which allow you to manipulate and analyze spatial data in a variety of ways.</p><p>The list also includes some tools for working with specific types of geospatial data. For example, the H3 library is designed specifically for working with hexagonal grids, while PySAL is focused on spatial econometrics and spatial analysis. Whether you are a data scientist, GIS specialist, or geospatial enthusiast, these tools are sure to enhance your work and help you achieve your goals.</p><p>In summary, this list is an excellent resource for anyone working with geospatial data in Python. It contains a wide range of tools for working with different types of data, and can help you visualize data, perform complex analysis, and create maps and other visualizations. If you're looking to enhance your skills in geospatial analysis, this list is definitely worth checking out.</p></div></div></div><div><p>These tools are:</p><ul>
<li>ArcGIS - <a href="https://lnkd.in/dgC6sKJH" target="_new">https://lnkd.in/dgC6sKJH</a></li>
<li>Cartopy - <a href="https://lnkd.in/dc8ijXRg" target="_new">https://lnkd.in/dc8ijXRg</a></li>
<li>Contextily - <a href="https://lnkd.in/dTdQsmKX" target="_new">https://lnkd.in/dTdQsmKX</a></li>
<li>Descartes - <a href="https://lnkd.in/dCJykxwW" target="_new">https://lnkd.in/dCJykxwW</a></li>
<li>Fiona - <a href="https://lnkd.in/d8sJ3Q5a" target="_new">https://lnkd.in/d8sJ3Q5a</a></li>
<li>Folium - <a href="https://lnkd.in/dfSsE-MB" target="_new">https://lnkd.in/dfSsE-MB</a></li>
<li>GDAL - <a href="https://lnkd.in/dYBJBaAY" target="_new">https://lnkd.in/dYBJBaAY</a></li>
<li>Geohash - <a href="https://lnkd.in/d_NxJ4_M" target="_new">https://lnkd.in/d_NxJ4_M</a></li>
<li>GeoJSON - <a href="https://lnkd.in/daGs2WYq" target="_new">https://lnkd.in/daGs2WYq</a></li>
<li>GeoPandas - <a href="https://lnkd.in/dBTFKKV3" target="_new">https://lnkd.in/dBTFKKV3</a></li>
<li>Geopy - <a href="https://lnkd.in/dfAzR8Xa" target="_new">https://lnkd.in/dfAzR8Xa</a></li>
<li>Gevent - <a href="http://www.gevent.org/" target="_new">http://www.gevent.org</a></li>
<li>H3 - <a href="https://h3geo.org/docs/" target="_new">https://h3geo.org/docs/</a></li>
<li>OSMnx - <a href="https://lnkd.in/dm3pHgUS" target="_new">https://lnkd.in/dm3pHgUS</a></li>
<li>PyQGIS - <a href="https://lnkd.in/dShWyWVr" target="_new">https://lnkd.in/dShWyWVr</a></li>
<li>PySAL - <a href="https://pysal.org/" target="_new">https://pysal.org</a></li>
<li>Pydeck - <a href="https://lnkd.in/dGBFu-iw" target="_new">https://lnkd.in/dGBFu-iw</a></li>
<li>Pyproj - <a href="https://lnkd.in/dNG9fdkm" target="_new">https://lnkd.in/dNG9fdkm</a></li>
<li>RTree - <a href="https://lnkd.in/dURMiYpU" target="_new">https://lnkd.in/dURMiYpU</a></li>
<li>Rasterio - <a href="https://lnkd.in/dEMC6ve6" target="_new">https://lnkd.in/dEMC6ve6</a></li>
<li>Scikit-mobility - <a href="https://lnkd.in/dpHhaX2J" target="_new">https://lnkd.in/dpHhaX2J</a></li>
<li>Shapely - <a href="https://lnkd.in/d568datK" target="_new">https://lnkd.in/d568datK</a></li>
</ul><p>These tools offer a wide range of capabilities for working with geospatial data, from visualizing and manipulating data to performing complex analysis and modeling. Whether you are a data scientist, GIS specialist, or geospatial enthusiast, these tools are sure to enhance your work and help you achieve your goals.</p></div></div></div></div></div></div></div></div>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27323/cutadapt</guid>
	<pubDate>Fri, 13 May 2016 04:54:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27323/cutadapt</link>
	<title><![CDATA[cutadapt]]></title>
	<description><![CDATA[<p>Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.</p>
<p>Cleaning your data in this way is often required: Reads from small-RNA sequencing contain the 3&rsquo; sequencing adapter because the read is longer than the molecule that is sequenced. Amplicon reads start with a primer sequence. Poly-A tails are useful for pulling out RNA from your sample, but often you don&rsquo;t want them to be in your reads.</p>
<p>Cutadapt helps with these trimming tasks by finding the adapter or primer sequences in an error-tolerant way. It can also modify and filter reads in various ways. Adapter sequences can contain IUPAC wildcard characters. Also, paired-end reads and even colorspace data is supported. If you want, you can also just demultiplex your input data, without removing adapter sequences at all.</p>
<p>Cutadapt comes with an extensive suite of automated tests and is available under the terms of the MIT license.</p>
<p>If you use cutadapt, please cite <a href="http://dx.doi.org/10.14806/ej.17.1.200">DOI:10.14806/ej.17.1.200</a> .</p><p>Address of the bookmark: <a href="https://cutadapt.readthedocs.io/en/stable/installation.html#quickstart" rel="nofollow">https://cutadapt.readthedocs.io/en/stable/installation.html#quickstart</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27847/anvio</guid>
	<pubDate>Thu, 16 Jun 2016 18:15:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27847/anvio</link>
	<title><![CDATA[Anvio]]></title>
	<description><![CDATA[<p>In a nutshell</p>
<p>Anvi&rsquo;o is an analysis and visualization platform for &lsquo;omics data.</p>
<p>Please find the methods paper here: https://peerj.com/articles/1319/</p>
<p>Anvi&rsquo;o would not have been possible without the help of many people who directly or indirectly contributed to its development. Here is the acknowledgements section of our methods paper</p>
<p><span>An analysis and visualization platform for 'omics data</span><span>&nbsp;</span><span><a href="http://merenlab.org/projects/anvio">http://merenlab.org/projects/anvio</a></span></p>
<p><span>Paper&nbsp;https://peerj.com/articles/1839/</span></p><p>Address of the bookmark: <a href="https://github.com/meren/anvio" rel="nofollow">https://github.com/meren/anvio</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</guid>
	<pubDate>Thu, 23 Jun 2016 07:26:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</link>
	<title><![CDATA[WgSim]]></title>
	<description><![CDATA[<p>Reads simulator</p>
<p>Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simulate diploid genomes with SNPs and insertion/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution sequencing errors. It does not generate INDEL sequencing errors, but this can be partly compensated by simulating INDEL polymorphisms.<br><br>Wgsim outputs the simulated polymorphisms, and writes the true read coordinates as well as the number of polymorphisms and sequencing errors in read names. One can evaluate the accuracy of a mapper or a SNP caller with wgsim_eval.pl that comes with the package.<br><br></p><p>Address of the bookmark: <a href="https://github.com/lh3/wgsim" rel="nofollow">https://github.com/lh3/wgsim</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/28290/bioinformatics-tools-and-software</guid>
	<pubDate>Tue, 05 Jul 2016 10:02:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28290/bioinformatics-tools-and-software</link>
	<title><![CDATA[Bioinformatics tools and software]]></title>
	<description><![CDATA[<p><a href="http://drive5.com/usearch">USEARCH &gt;</a><br><span>Extreme high-throughput sequence analysis. Orders of magnitude faster than BLAST.</span>&nbsp;<a href="http://drive5.com/muscle">MUSCLE &gt;</a><br><span>Multiple sequence alignment. Faster and more accurate than CLUSTALW.</span></p>
<p>&nbsp;<a href="http://drive5.com/uparse">UPARSE &gt;</a><br><span>OTU clustering for 16S and other marker genes. Highly accurate OTU sequences and improved diversity measures.</span>&nbsp;<a href="http://drive5.com/uchime">UCHIME &gt;</a><br><span>Chimeric sequence detection.</span>&nbsp;<a href="http://drive5.com/piler">PILER &gt;</a><br><span>De novo genome repeat finder.</span>&nbsp;<a href="http://drive5.com/pilercr">PILER-CR &gt;</a><br><span>Detection of CRISPR repeats in bacterial genomes.</span>&nbsp;<a href="http://drive5.com/qscore">QSCORE &gt;</a><br><span>Compare two multiple alignments for benchmarking.</span>&nbsp;<a href="http://drive5.com/pals">PALS &gt;</a><br><span>Whole-genome alignment.</span>&nbsp;<a href="http://drive5.com/muscle/prefab.htm">PREFAB &gt;</a><br><span>Protein Reference Alignment Database.</span>&nbsp;<a href="http://drive5.com/bench">MSA benchmark collection &gt;</a><br><span>Selected multiple alignment benchmarks in a standardized FASTA format.</span></p><p>Address of the bookmark: <a href="http://drive5.com/software.html" rel="nofollow">http://drive5.com/software.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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