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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/2882?offset=80</link>
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	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17966/internship-program-for-bioinformatics-biotechnology-professionals-no-of-vacancy-2</guid>
  <pubDate>Wed, 08 Oct 2014 01:10:08 -0500</pubDate>
  <link></link>
  <title><![CDATA[Internship Program for Bioinformatics / Biotechnology Professionals (No. Of Vacancy: 2)]]></title>
  <description><![CDATA[
<p>ArrayGen is offering an Internship Program for Post graduate Bioinformatics / Biotechnology students and professionals. ArrayGen Technologies provide an excellent opportunity to gain research experience and explore if a scientific career is right for you. 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>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34485/phyloxml-xml-for-evolutionary-biology-and-comparative-genomics</guid>
	<pubDate>Wed, 29 Nov 2017 10:04:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34485/phyloxml-xml-for-evolutionary-biology-and-comparative-genomics</link>
	<title><![CDATA[phyloXML:  XML for evolutionary biology and comparative genomics]]></title>
	<description><![CDATA[<p><a href="http://www.biomedcentral.com/1471-2105/10/356/">phyloXML</a><span>&nbsp;(</span><a href="http://www.phyloxml.org/examples_syntax/phyloxml_syntax_example_1.html">example</a><span>) is an&nbsp;</span><a href="http://en.wikipedia.org/wiki/XML">XML</a><span>&nbsp;language designed to describe phylogenetic trees (or networks) and associated data. PhyloXML provides elements for commonly used features, such as taxonomic information, gene names and identifiers, branch lengths, support values, and gene duplication and speciation events. Using these standardized elements allows interoperability between various applications and databases. Furthermore, both due to extensible nature of XML itself and the provision of &lt;property&gt; elements by phyloXML, extensibility as well as domain specific applications are ensured. The structure of phyloXML is described by&nbsp;</span><a href="http://en.wikipedia.org/wiki/XML_Schema_%28W3C%29">XML Schema Definition (XSD)</a><span>&nbsp;language.</span></p><p>Address of the bookmark: <a href="http://www.phyloxml.org/" rel="nofollow">http://www.phyloxml.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36267/pspairwise-sequentially-markovian-coalescent-psmc-model</guid>
	<pubDate>Thu, 19 Apr 2018 05:29:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36267/pspairwise-sequentially-markovian-coalescent-psmc-model</link>
	<title><![CDATA[PSPairwise Sequentially Markovian Coalescent (PSMC) model]]></title>
	<description><![CDATA[<p><span>Implementation of the Pairwise Sequentially Markovian Coalescent (PSMC) model</span></p><p>Address of the bookmark: <a href="https://github.com/lh3/psmc" rel="nofollow">https://github.com/lh3/psmc</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/38649/ngs-platforms-launched-by-bgi%E2%80%99s-mgi-tech</guid>
	<pubDate>Thu, 10 Jan 2019 04:42:06 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/38649/ngs-platforms-launched-by-bgi%E2%80%99s-mgi-tech</link>
	<title><![CDATA[NGS Platforms launched by BGI’s MGI Tech]]></title>
	<description><![CDATA[<p>MGI Tech Co., Ltd. (MGI), a subsidiary of BGI Group, is committed to enabling effective and affordable healthcare solutions for all. Based on its proprietary technology, MGI produces sequencing devices, equipment, consumables and reagents to support life science research, medicine and healthcare. MGI's multi-omics platforms include genetic sequencing, mass spectrometry and medical imaging. Providing real-time, comprehensive, life-long solutions, its mission&nbsp;is to&nbsp;develop and promote advanced life science tools for future healthcare.</p><p>MGI, a subsidiary of global genomics leader BGI Group, announced pricing and its first early access customer for the new ultra high-throughput sequencer, MGISEQ-T7, saying it has driven down sequencing cost to&nbsp;$5&nbsp;per gigabyte, with exceptionally high accuracy. Such innovations are helping more people to realize the benefits of genomic information.</p><p>In October, MGI launched the MGISEQ-T7, a highly flexible production-scale platform that is the most powerful sequencer to date. It can produce as many as 60 whole human genomes in one day. The instrument sells for&nbsp;$1 million.</p><p>The T7 enables simultaneous but independent operation of up to four flow cells, which means different applications such as single-cell RNA sequencing, whole exome sequencing and whole genome sequencing can be run in different flow cells at the same time. This helps to reduce costs, allowing MGI to offer the most competitive sequencing price in the market.</p><p><span>Powered by DNBseq&trade;, MGISEQ delivers quality data with accuracy for SNP and Indel calling rate of 99.9% and 99%, respectively, along with decreased duplication rate down to less than 2 percent, and almost zero Index mis-assignment rate.</span></p><p><span><span>SOURCE MGI</span></span></p><p>https://www.bgi.com/global/company/news/bgis-mgi-tech-launches-two-new-ngs-platforms/</p><p>http://en.mgitech.cn/</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40834/nucleus-python-and-c-code-for-reading-and-writing-genomics-data</guid>
	<pubDate>Sun, 02 Feb 2020 08:14:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40834/nucleus-python-and-c-code-for-reading-and-writing-genomics-data</link>
	<title><![CDATA[Nucleus: Python and C++ code for reading and writing genomics data.]]></title>
	<description><![CDATA[<p>Nucleus is a library of Python and C++ code designed to make it easy to read, write and analyze data in common genomics file formats like SAM and VCF. In addition, Nucleus enables painless integration with the TensorFlow machine learning framework, as anywhere a genomics file is consumed or produced, a TensorFlow tfrecords file may be used instead.</p><p>Address of the bookmark: <a href="https://github.com/google/nucleus" rel="nofollow">https://github.com/google/nucleus</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42143/sibelia-a-comparative-genomics-tool</guid>
	<pubDate>Sat, 22 Aug 2020 02:49:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42143/sibelia-a-comparative-genomics-tool</link>
	<title><![CDATA[Sibelia: A comparative genomics tool]]></title>
	<description><![CDATA[<p><strong>Sibelia</strong>: A comparative genomics tool: It assists biologists in analysing the genomic variations that correlate with pathogens, or the genomic changes that help microorganisms adapt in different environments. Sibelia will also be helpful for the evolutionary and genome rearrangement studies for multiple strains of microorganisms.&nbsp;</p>
<p><strong>Sibelia</strong>&nbsp;is useful in finding: (1) shared regions, (2) regions that present in one group of genomes but not in others, (3) rearrangements that transform one genome to other genomes.</p>
<p>More at&nbsp;<a href="http://bioinf.spbau.ru/sibelia">http://bioinf.spbau.ru/sibelia</a></p>
<p>Sibelia docs&nbsp;<a href="http://gensoft.pasteur.fr/docs/Sibelia/3.0.7/SIBELIA.md">http://gensoft.pasteur.fr/docs/Sibelia/3.0.7/SIBELIA.md</a></p><p>Address of the bookmark: <a href="https://github.com/bioinf/Sibelia" rel="nofollow">https://github.com/bioinf/Sibelia</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43046/postdoctoral-fellow-for-a-large-scale-microbial-comparative-genomics</guid>
  <pubDate>Thu, 29 Apr 2021 08:44:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[postdoctoral fellow for a large-scale microbial comparative genomics !]]></title>
  <description><![CDATA[
<p>Asaf Levy hiring a postdoctoral fellow for a large-scale microbial comparative genomics project at the Hebrew University of Jerusalem (Israel). <br />The project is a continuation of Levy Asaf et al. Nature Genetics 2018 paper.<br />Requirements: <br />1.Experience with programming in at least one programming language, preferably Python.<br />2.A PhD in bioinformatics/computational biology<br />3.At least one first authorship publication in a good journal, preferably more.<br />4.Good communication skills in English <br />5.Ability to enter and study in Israel (not applicable for Pakistani people, for example). <br />6.Ability to work in a team.<br />Please send CV to alevy@mail.huji.ac.il</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</guid>
	<pubDate>Thu, 17 Feb 2022 05:37:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</link>
	<title><![CDATA[Comparative genomics visualisation tools !]]></title>
	<description><![CDATA[<p>Comparative genomics visualisation tools !</p><p>Address of the bookmark: <a href="https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative" rel="nofollow">https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/33965/a-national-workshop-on-dna-barcoding-and-phylogenetics-09-th-%E2%80%93-12-th-august-2017-andhra-university-visakhapatnam-ap-india</guid>
	<pubDate>Wed, 26 Jul 2017 00:37:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/33965/a-national-workshop-on-dna-barcoding-and-phylogenetics-09-th-%E2%80%93-12-th-august-2017-andhra-university-visakhapatnam-ap-india</link>
	<title><![CDATA[A National Workshop on "DNA Barcoding and Phylogenetics" 09 th – 12 th August, 2017 @ Andhra University, Visakhapatnam, A.P., India]]></title>
	<description><![CDATA[<p>DNA Barcoding is an emerging global standard for&nbsp;identifying species using gene sequences, and it has far reaching&nbsp;applications for society and the study of&nbsp;biodiversity on Earth. DNA Barcoding began during<br />recent decades with the proposal that organisms could be&nbsp;assigned to their correct species using a short gene&nbsp;sequence from a standardized position in the genome. By&nbsp;using genetic data rather than morphological features,&nbsp;barcoding can identify specimens that challenge the most&nbsp;expert taxonomist: larval forms, eggs, damaged or&nbsp;partial specimens (including gut contents and fecal&nbsp;matter), and derivative forms (e.g., fish filets). Since&nbsp;its introduction, barcoding has proven effective as an&nbsp;identification system for a wide range of taxonomic&nbsp;groups and for varied applications of importance to&nbsp;science and society.<br />The current Workshop aims to introduce about the&nbsp;current emerging trends and applications of Molecular<br />Phylogenetics and Evolution studies and to provide&nbsp;hands on training on molecular biology and&nbsp;bioinformatics tools in Molecular Phylogenetics&nbsp;research.</p><p>For registration Kindly follow the Link</p><p>http://andhrauniversity.edu.in/webnew/admin/docs/Broucher-for-National-workshop-Aug-2017-18072017.pdf</p><p>&nbsp;</p><p>&nbsp;</p>]]></description>
	<dc:creator>M JAGANNATH</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44720/a-beginners-guide-to-using-kraken-for-taxonomic-classification</guid>
	<pubDate>Fri, 13 Dec 2024 11:29:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44720/a-beginners-guide-to-using-kraken-for-taxonomic-classification</link>
	<title><![CDATA[A Beginner&#039;s Guide to Using Kraken for Taxonomic Classification]]></title>
	<description><![CDATA[<div>Kraken is a popular bioinformatics tool designed for fast and accurate taxonomic classification of metagenomic sequences. Its efficiency and precision make it a go-to resource for analyzing microbial communities, including bacteria, viruses, archaea, and fungi. Whether you're new to bioinformatics or experienced in the field, Kraken is an indispensable tool for taxonomic analysis.</div><div><div><div><div dir="auto"><div><div><p>In this blog, we&rsquo;ll walk through the basics of Kraken, from installation to running an analysis, and highlight its key features and applications.</p><h4><strong>What is Kraken?</strong></h4><p>Kraken is a sequence classification tool that assigns taxonomic labels to DNA sequences using exact k-mer matching. It uses a reference database of genomes, dividing sequences into k-mers and identifying matches in a computationally efficient way.</p><h4><strong>Key Features of Kraken</strong></h4><ul>
<li><strong>Speed</strong>: Kraken processes data much faster than alignment-based methods.</li>
<li><strong>Accuracy</strong>: It uses a precise k-mer matching algorithm for high-resolution taxonomic assignments.</li>
<li><strong>Scalability</strong>: It can handle large metagenomic datasets.</li>
<li><strong>Custom Databases</strong>: You can build and use custom databases tailored to your research needs.</li>
</ul><h4><strong>Installing Kraken</strong></h4><ol>
<li>
<p><strong>System Requirements</strong></p>
<ul>
<li>A Unix-based operating system (Linux/macOS).</li>
<li>Sufficient computational resources for database building (RAM and disk space).</li>
</ul>
</li>
<li>
<p><strong>Installation Steps</strong></p>
<ul>
<li>Clone the Kraken repository from GitHub:
<div>
<div>&nbsp;</div>
<div dir="ltr"><code>git <span style="font-size: 12.8px; font-weight: normal;">clone</span> https://github.com/DerrickWood/kraken.git <span style="font-size: 12.8px; font-weight: normal;">cd</span> kraken </code></div>
</div>
</li>
<li>Compile the Kraken binaries:
<div>
<div>&nbsp;</div>
<div dir="ltr"><code>make </code></div>
</div>
</li>
<li>Add Kraken to your PATH for easy access:
<div>
<div>&nbsp;</div>
<div dir="ltr"><code><span style="font-size: 12.8px; font-weight: normal;">export</span> PATH=<span style="font-size: 12.8px; font-weight: normal;">$PATH</span>:/path/to/kraken </code></div>
</div>
</li>
</ul>
</li>
</ol><h4><strong>Preparing a Database</strong></h4><p>Kraken requires a database of reference genomes. You can use a pre-built database or create a custom one.</p><ol>
<li>
<p><strong>Downloading a Pre-built Database</strong><br />Kraken offers pre-built databases, such as the <em>MiniKraken</em> database, which is lightweight and suitable for smaller datasets. Download it using:</p>
<div>
<div dir="ltr"><code>kraken-build --download-library minikraken </code></div>
</div>
</li>
<li>
<p><strong>Building a Custom Database</strong><br />To include specific genomes, download FASTA files and build the database:</p>
<div>
<div dir="ltr"><code>kraken-build --download-library bacteria --threads 4 --db my_database kraken-build --build --db my_database </code></div>
</div>
<p>This process may take considerable time and resources, depending on the size of the database.</p>
</li>
</ol><h4><strong>Running Kraken</strong></h4><p>Once the database is ready, you can classify sequences.</p><ol>
<li>
<p><strong>Basic Usage</strong><br />Use the following command to classify sequences:</p>
<div>
<div dir="ltr"><code>kraken --db my_database --threads 4 --fastq-input input_sequences.fastq --output kraken_output.txt </code></div>
</div>
<p>Key options:</p>
<ul>
<li><code>--db</code>: Specifies the database.</li>
<li><code>--threads</code>: Number of threads for parallel processing.</li>
<li><code>--fastq-input</code>: Indicates input file format (FASTQ/FASTA).</li>
</ul>
</li>
<li>
<p><strong>Interpreting Results</strong><br />Kraken generates an output file with columns for sequence IDs, taxonomic classifications, and the confidence score.</p>
</li>
</ol><h4><strong>Visualizing Kraken Results</strong></h4><p>Kraken results can be visualized using tools like <strong>Krona</strong> or converted to human-readable reports using <code>kraken-report</code>.</p><ol>
<li>
<p><strong>Generate a Report</strong></p>
<div>
<div dir="ltr"><code>kraken-report --db my_database kraken_output.txt &gt; kraken_report.txt </code></div>
</div>
</li>
<li>
<p><strong>Krona Visualization</strong><br />Install Krona and convert Kraken output for visualization:</p>
<div>
<div dir="ltr"><code>cut -f2,3 kraken_output.txt | ktImportTaxonomy -o krona_output.html </code></div>
</div>
<p>Open the HTML file in your browser to interactively explore the taxonomic classifications.</p>
</li>
</ol><h4><strong>Advanced Usage</strong></h4><ol>
<li>
<p><strong>Confidence Thresholds</strong><br />Adjust the confidence threshold for classification using the <code>--confidence</code> option. Higher values reduce false positives but may miss some true positives:</p>
<div>
<div dir="ltr"><code>kraken --db my_database --confidence 0.1 --fastq-input input.fastq </code></div>
</div>
</li>
<li>
<p><strong>Paired-End Reads</strong><br />For paired-end sequencing data, use:</p>
<div>
<div dir="ltr"><code>kraken --db my_database --paired reads_1.fastq reads_2.fastq </code></div>
</div>
</li>
<li>
<p><strong>Customizing K-mers</strong><br />Kraken allows you to set custom k-mer lengths during database building for specific applications.</p>
</li>
</ol><h4><strong>Applications of Kraken</strong></h4><ul>
<li><strong>Microbial Ecology</strong>: Characterizing microbial communities in soil, water, and the human microbiome.</li>
<li><strong>Pathogen Detection</strong>: Identifying pathogens in clinical samples.</li>
<li><strong>Fungal Research</strong>: Analyzing fungal diversity in metagenomic datasets.</li>
<li><strong>Environmental Monitoring</strong>: Tracking microbial populations in diverse habitats.</li>
</ul><h4><strong>Conclusion</strong></h4><p>Kraken is a versatile and efficient tool for taxonomic classification in metagenomics. Its speed, accuracy, and flexibility make it a favorite among bioinformaticians. By following this guide, you can set up and use Kraken to unlock insights into microbial and fungal communities, paving the way for discoveries in ecology, medicine, and biotechnology.</p></div></div></div></div></div></div>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

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