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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28164?</link>
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	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31300/clgenomics</guid>
	<pubDate>Fri, 03 Mar 2017 09:57:28 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31300/clgenomics</link>
	<title><![CDATA[CLgenomics]]></title>
	<description><![CDATA[<p>CLgenomics is a standalone desktop software specifically designed for bacterial genome analysis. This program has a powerful multi-genome browser, which enables rapid and responsive exploration of bacterial genomes.</p>
<p>To use CLgenomics, individual genome data (genome sequences + annotation details) are compiled and saved in a specially formatted file called CLG (ChunLab Genomics).&nbsp;Each CLG file corresponds with one bacterial genome. If multiple genomes are being considered and compared, multiple CLG files are needed. ChunLab offers &gt;40,000 CLG files of publicly available Bacterial and Archaeal genomes.</p><p>Address of the bookmark: <a href="https://chunlab.wordpress.com/clgenomics-software/" rel="nofollow">https://chunlab.wordpress.com/clgenomics-software/</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43292/bioinformatics-scientist-production-bioinformatics-south-san-francisco-ca</guid>
  <pubDate>Thu, 19 Aug 2021 08:45:24 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics Scientist, Production Bioinformatics @ South San Francisco, CA]]></title>
  <description><![CDATA[
<p>wist is looking for a Bioinformatics Scientist to join our Production Bioinformatics Team. You will work alongside research scientists, software engineers and data scientists to further deliver on our mission to expand access to best-in-class synthetic biology and next-generation sequencing applications. You will be developing and engineering tools to better evaluate and build hardened, production quality pipelines, optimize data quality, and automate lab and bioinformatics processes. Our ideal candidate is an organized problem solver with a background in developing and building novel production-quality bioinformatics tools and packages. Equally excellent communication skills and a proven ability to work independently are required.</p>

<p>More at https://boards.greenhouse.io/twistbioscience/jobs/3135495?gh_src=9ecc0b941us</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/39606/amity-university-bioinformatics-summer-program-kolkata</guid>
	<pubDate>Tue, 11 Jun 2019 21:27:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/39606/amity-university-bioinformatics-summer-program-kolkata</link>
	<title><![CDATA[Amity University Bioinformatics Summer Program - Kolkata]]></title>
	<description><![CDATA[<p>Registrations are now open for the 2019 Summer Bioinformatics Training program at Amity University, Kolkata. The program will focus on introductory topics for life science students. We will review important history, topics and challenges bioinformatics can help address in the context of basic research, discovery and industry.</p><p>Read more: https://edu.t-bio.info/amity-university-summer-bioinformatics-program-registrations-are-open/</p>]]></description>
	<dc:creator>eliabrodsky</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32485/bacterial-genome-assembly</guid>
	<pubDate>Fri, 05 May 2017 06:11:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32485/bacterial-genome-assembly</link>
	<title><![CDATA[Bacterial genome assembly !!]]></title>
	<description><![CDATA[<p>This tutorial will serve as an example of how to use free and open-source genome assembly and secondary scaffolding tools to generate high quality assemblies of&nbsp;bacterial sequence data. The bacterial sample used in this tutorial will be referred&nbsp;to simply&nbsp;as &ldquo;Species&rdquo; since it is&nbsp;live data. This data is paired-end data, meaning that there are forward and reverse reads, which we will designate as Sample_R1.fastq and Sample_R2.fastq, respectively.</p>
<p>https://github.com/jennomics/WorkflowPaper/blob/master/Genome%20Assembly%20and%20Annotation.md</p><p>Address of the bookmark: <a href="http://bioinformatics.uconn.edu/bacterial-genome-assembly-tutorial/" rel="nofollow">http://bioinformatics.uconn.edu/bacterial-genome-assembly-tutorial/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44731/exploring-bacterial-comparative-genomics-a-bioinformatics-approach</guid>
	<pubDate>Sat, 14 Dec 2024 12:31:14 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44731/exploring-bacterial-comparative-genomics-a-bioinformatics-approach</link>
	<title><![CDATA[Exploring Bacterial Comparative Genomics: A Bioinformatics Approach]]></title>
	<description><![CDATA[<p>In the world of microbiology, bacteria have long fascinated scientists for their diversity, adaptability, and crucial roles in ecosystems and human health. Comparative genomics&mdash;a field that involves analyzing and comparing the genomes of different organisms&mdash;has revolutionized our understanding of bacterial evolution, adaptation, and pathogenicity. By leveraging bioinformatics tools and techniques, researchers can uncover genomic insights that were once hidden. This blog delves into the principles, methodologies, and applications of bacterial comparative genomics from a bioinformatics perspective.</p><h4><strong>What is Bacterial Comparative Genomics?</strong></h4><p>Comparative genomics involves the systematic comparison of genomes across different bacterial species or strains. This approach allows scientists to:</p><ul>
<li>
<p>Identify conserved and unique genes.</p>
</li>
<li>
<p>Explore genetic determinants of pathogenicity.</p>
</li>
<li>
<p>Understand bacterial evolution and phylogenetics.</p>
</li>
<li>
<p>Investigate horizontal gene transfer and its role in antibiotic resistance.</p>
</li>
</ul><p>Bioinformatics is central to these analyses, enabling the processing and interpretation of large-scale genomic data.</p><h4><strong>Key Steps in Bacterial Comparative Genomics</strong></h4><ol>
<li>
<p><strong>Genome Sequencing and Assembly</strong>: The process begins with obtaining high-quality bacterial genome sequences. Advances in next-generation sequencing (NGS) technologies have made it faster and more affordable to sequence bacterial genomes. Tools such as SPAdes and Velvet are commonly used for genome assembly.</p>
</li>
<li>
<p><strong>Genome Annotation</strong>: Annotating a genome involves identifying genes, regulatory elements, and other genomic features. Automated tools like Prokka and RAST provide functional annotations, allowing researchers to predict the roles of genes and proteins.</p>
</li>
<li>
<p><strong>Genome Alignment</strong>: Aligning genomes is crucial for identifying conserved regions, single-nucleotide polymorphisms (SNPs), and structural variations. Tools like Mauve and progressiveMauve are commonly employed for whole-genome alignments.</p>
</li>
<li>
<p><strong>Comparative Analyses</strong>:</p>
<ul>
<li>
<p><strong>Core and Pan-genome Analysis</strong>: The core genome consists of genes shared across all strains of a species, while the pan-genome includes all genes found in any strain. Software like Roary and BPGA can perform core and pan-genome analyses.</p>
</li>
<li>
<p><strong>Phylogenetic Analysis</strong>: Comparative genomics often involves reconstructing evolutionary relationships. Tools such as MEGA and IQ-TREE facilitate phylogenetic tree construction based on genomic data.</p>
</li>
<li>
<p><strong>Functional Enrichment Analysis</strong>: To understand the biological significance of unique or shared genes, functional enrichment analysis using databases like GO (Gene Ontology) and KEGG is essential.</p>
</li>
</ul>
</li>
</ol><div>&nbsp;<strong style="font-size: 1em;">Recommended Bioinformatics Tools for Comparative Genomics</strong></div><p>Here are some additional bioinformatics tools that can aid bacterial comparative genomics:</p><ul>
<li>
<p><strong>OrthoFinder</strong>: For accurate ortholog identification across multiple genomes.</p>
</li>
<li>
<p><strong>PanOCT</strong>: Specifically designed for pan-genome clustering and annotation.</p>
</li>
<li>
<p><strong>FASTANI</strong>: A tool for calculating Average Nucleotide Identity (ANI) for microbial genome comparisons.</p>
</li>
<li>
<p><strong>CIRCOS</strong>: For visually comparing genomic data through circular genome plots.</p>
</li>
<li>
<p><strong>Galaxy Platform</strong>: A user-friendly web-based platform offering numerous genomic analysis tools.</p>
</li>
<li>
<p><strong>BLAST</strong>: Essential for sequence alignment and similarity searches.</p>
</li>
<li>
<p><strong>PhyloSift</strong>: Focused on phylogenetic analysis of microbial genomes using marker genes.</p>
</li>
</ul><p>These tools, in combination with the methods discussed, provide a robust framework for conducting comprehensive comparative genomic studies.</p><h4><strong>Applications of Bacterial Comparative Genomics</strong></h4><ol>
<li>
<p><strong>Understanding Pathogenicity</strong>: Comparative genomics helps identify virulence factors that distinguish pathogenic strains from non-pathogenic relatives. For instance, comparing genomes of <em>Escherichia coli</em> strains has revealed key genetic determinants of pathogenicity in enterohemorrhagic strains.</p>
</li>
<li>
<p><strong>Antibiotic Resistance Research</strong>: The spread of antibiotic resistance genes through horizontal gene transfer is a major global concern. Comparative analyses can trace the origins and dissemination of resistance genes, aiding in the development of countermeasures.</p>
</li>
<li>
<p><strong>Microbial Ecology and Evolution</strong>: By studying genomic variations, researchers can understand how bacteria adapt to different environments. This is particularly relevant for extremophiles and symbiotic bacteria.</p>
</li>
<li>
<p><strong>Vaccine Development</strong>: Identifying conserved antigens across pathogenic strains is critical for vaccine design. Comparative genomics has been instrumental in developing vaccines against pathogens like <em>Neisseria meningitidis</em>.</p>
</li>
<li>
<p><strong>Biotechnology Applications</strong>: Comparative studies can uncover unique metabolic pathways in bacteria, paving the way for applications in bioremediation, synthetic biology, and industrial microbiology.</p>
</li>
</ol><h4><strong>Challenges in Bacterial Comparative Genomics</strong></h4><p>While the field has made significant strides, several challenges remain:</p><ul>
<li>
<p><strong>Data Overload</strong>: The rapid growth of sequencing data requires robust computational infrastructure and efficient algorithms.</p>
</li>
<li>
<p><strong>Genome Plasticity</strong>: High rates of horizontal gene transfer and genome rearrangements in bacteria complicate comparative analyses.</p>
</li>
<li>
<p><strong>Annotation Accuracy</strong>: Automated annotation tools are not infallible, and manual curation is often needed for high-confidence results.</p>
</li>
<li>
<p><strong>Interpreting Non-Coding Regions</strong>: Understanding the functional significance of non-coding genomic regions remains a challenge.</p>
</li>
</ul><h4><strong>Future Directions</strong></h4><p>The integration of bacterial comparative genomics with other &lsquo;omics&rsquo; approaches&mdash;such as transcriptomics, proteomics, and metabolomics&mdash;promises a more comprehensive understanding of bacterial biology. Additionally, advancements in machine learning and artificial intelligence are likely to further enhance bioinformatics analyses, enabling the prediction of complex phenotypes from genomic data.</p><h4><strong>Conclusion</strong></h4><p>Bacterial comparative genomics, driven by bioinformatics, continues to unravel the complexities of bacterial life. From combating antibiotic resistance to uncovering the secrets of microbial evolution, this interdisciplinary field holds immense potential for addressing pressing challenges in microbiology and beyond. As technology advances, so too will our ability to harness the power of comparative genomics for scientific and societal benefit.</p>]]></description>
	<dc:creator>LEGE</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/41905/research-associate-bioinformatics-in-iisc-recruitment-2020</guid>
  <pubDate>Tue, 23 Jun 2020 21:53:34 -0500</pubDate>
  <link></link>
  <title><![CDATA[Research Associate Bioinformatics in IISc Recruitment 2020]]></title>
  <description><![CDATA[
<p>Research Associate Bioinformatics in IISc Recruitment 2020</p>

<p>Essential Qualifications: Ph.D. (Bioinformatics/ Biophysics/ Biotechnology or any other stream of biological/ physical sciences) with a minimum of two publications in reputed peer reviewed journals in the area of structural bioinformatics or biophysics or biomolecular modeling/ simulation.</p>

<p>Job description: Development of bioinformatics tools and algorithms/software for structure based analysis of biomolecular systems. Programmatic access to major biomolecular databases using APIs Knowledge based prediction and analysis of biomolecular structure, function and interactions. Docking/simulations for inhibitor design.</p>

<p>Desirable Qualifications (Research Associate/s): i)  Strong computer programming skills (in Python/PERL/PHP or C++ or object oriented database management systems like MySQL etc or scripting languages under LINUX/UNIX environment). </p>

<p>ii) Extensive experience in computational analysis of biomolecular structure/interactions and usage of advanced biomolecular simulation softwares. iii) Adequate knowledge of major databases, webservers and softwares in the area of biomolecular structure/function and drug design. iv)  Familiarity with Parallel Programming environments and experience in usage of high-end HPC clusters.</p>

<p>The candidates must highlight their experience in above mentioned fields/topics in their CV. Initial appointment will be for a period of 1 year, subject to extension after review of performance.</p>

<p>Emoluments: As per DST, GOI norms and commensurate with experience.</p>

<p>More at https://www.iisc.ac.in/positions-open/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27463/bpipe-a-tool-for-running-and-managing-bioinformatics-pipelines</guid>
	<pubDate>Sat, 21 May 2016 22:42:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27463/bpipe-a-tool-for-running-and-managing-bioinformatics-pipelines</link>
	<title><![CDATA[Bpipe - a tool for running and managing bioinformatics pipelines]]></title>
	<description><![CDATA[<p>Bpipe provides a platform for running big bioinformatics jobs that consist of a series of processing stages - known as 'pipelines'.</p>
<ul>
<li>January 20th, 2016 - New! Bpipe 0.9.9 released!</li>
<li>Download <a href="http://download.bpipe.org/versions/bpipe-0.9.9.tar.gz">latest</a>, <a href="http://download.bpipe.org">all</a></li>
<li><a href="http://docs.bpipe.org">Documentation</a></li>
<li><a href="https://groups.google.com/forum/#%21forum/bpipe-discuss">Mailing List</a> (Google Group)</li>
</ul>
<p>Bpipe has been published in <a href="http://bioinformatics.oxfordjournals.org/content/early/2012/04/11/bioinformatics.bts167.abstract">Bioinformatics</a>! If you use Bpipe, please cite:</p>
<p><em>Sadedin S, Pope B &amp; Oshlack A, Bpipe: A Tool for Running and Managing Bioinformatics Pipelines, Bioinformatics</em></p><p>Address of the bookmark: <a href="http://docs.bpipe.org/" rel="nofollow">http://docs.bpipe.org/</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43272/bioinformatics-head-bioinformatics-manager-iii-cancer-genomics-research-laboratory-at-frederick-national-laboratory</guid>
  <pubDate>Wed, 18 Aug 2021 00:19:48 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics Head (Bioinformatics Manager III), Cancer Genomics Research Laboratory at  Frederick National Laboratory]]></title>
  <description><![CDATA[
<p>Frederick National Laboratory seeking an enthusiastic, creative, and seasoned bioinformatics professional to join our leadership team and direct the exceptional Bioinformatics Group at the Cancer Genomics Research Laboratory (CGR).  CGR has a diverse team of bioinformatics and computational scientists that support all areas of bioinformatics and data analysis (infrastructure, data QC, pipeline development and maintenance, data curation and sharing, methodology development, statistical analyses, machine learning approaches, and scientific interpretation).</p>

<p>More at https://leidosbiomed.csod.com/ats/careersite/jobdetails.aspx?site=4&amp;c=leidosbiomed&amp;id=2040</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/2778/mom-knows-best</guid>
	<pubDate>Thu, 22 Aug 2013 13:30:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/2778/mom-knows-best</link>
	<title><![CDATA[Mom Knows Best]]></title>
	<description><![CDATA[<p>We always get instructions to wash our hands, sterilize kitchen stuff and bla bla. However, recent findings suggest something else. Perhaps we can't survive, or will face lots of problems if bacteria&rsquo;s colonies are absent in mother womb. Please find the detail sources of microbial transmission in humans from mother to child in recently published PLOS paper.</p><p><a href="http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001631">http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001631</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31024/dagchainer-computing-chains-of-syntenic-genes-in-complete-genomes</guid>
	<pubDate>Fri, 17 Feb 2017 16:13:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31024/dagchainer-computing-chains-of-syntenic-genes-in-complete-genomes</link>
	<title><![CDATA[DAGchainer: Computing Chains of Syntenic Genes in Complete Genomes]]></title>
	<description><![CDATA[<p>The DAGchainer software computes chains of syntenic genes found within complete genome sequences. As input, DAGchainer accepts a list of gene pairs with sequence homology along with their genome coordinates. Using a scoring function which accounts for the distance between neighboring genes on each DNA molecule and the BLAST E-value score between homologs, maximally scoring chains of ordered gene pairs are computed and reported. This algorithm can be used to mine large evolutionary conserved regions of genomes between two organisms. Alternatively, by examining colinear sets of homologous genes found within a single genome, segmental genome duplications can be revealed.</p>
<p>This software distribution includes both the DAGchainer utility and a Java-based graphical interface that allows the inputs and outputs to be navigated and interrogated dynamically.</p><p>Address of the bookmark: <a href="http://dagchainer.sourceforge.net/" rel="nofollow">http://dagchainer.sourceforge.net/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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