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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/4184?offset=10</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41362/genemates-an-r-package-for-detecting-horizontal-gene-co-transfer-between-bacteria-using-gene-gene-associations-controlled-for-population-structure</guid>
	<pubDate>Sat, 07 Mar 2020 05:52:20 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41362/genemates-an-r-package-for-detecting-horizontal-gene-co-transfer-between-bacteria-using-gene-gene-associations-controlled-for-population-structure</link>
	<title><![CDATA[GeneMates: an R package for Detecting Horizontal Gene Co-transfer between Bacteria Using Gene-gene Associations Controlled for Population Structure]]></title>
	<description><![CDATA[<p><span>GeneMates is an R package implementing a network approach to identify horizontal gene co-transfer (HGcoT) between bacteria using whole-genome sequencing (WGS) data. It is particularly useful for investigating intra-species HGcoT, where presence-absence status of acquired genes is usually confounded by bacterial population structure due to clonal reproduction.</span></p>
<p><a href="https://www.biorxiv.org/content/10.1101/2020.02.29.970970v1">https://www.biorxiv.org/content/10.1101/2020.02.29.970970v1</a></p><p>Address of the bookmark: <a href="https://github.com/wanyuac/GeneMates" rel="nofollow">https://github.com/wanyuac/GeneMates</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44791/hibc-human-intestinal-bacteria-collection</guid>
	<pubDate>Wed, 07 May 2025 05:49:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44791/hibc-human-intestinal-bacteria-collection</link>
	<title><![CDATA[HiBC: Human Intestinal Bacteria Collection]]></title>
	<description><![CDATA[<p>The human gut is home to trillions of microorganisms, forming one of the most complex and dynamic microbial ecosystems known to science. The <strong style="font-size: 12.8px;">Human Intestinal Bacteria Collection (HiBC)</strong><span style="font-size: 12.8px; font-weight: normal;"> is a pioneering initiative aimed at cataloging, preserving, and studying the diverse bacterial species that inhabit the human gastrointestinal tract. This curated collection serves as a critical resource for researchers working on microbiome-related health, disease, and therapeutics.</span></p><h2>What is HiBC?</h2><p>The Human Intestinal Bacteria Collection (HiBC) is a comprehensive, high-quality reference repository of bacterial isolates derived from human fecal samples. It focuses on anaerobic and facultative anaerobic bacteria that play pivotal roles in digestion, immune modulation, vitamin synthesis, and pathogen resistance. The collection includes both culturable strains and genomic data from unculturable taxa, bridging the gap between culture-dependent and -independent microbiome studies.</p><h2>Why is HiBC Important?</h2><ol>
<li>
<p><strong>Understanding Microbiome-Host Interactions</strong><br /> HiBC enables deeper insight into the functions of specific bacterial taxa in the gut. With well-characterized isolates, researchers can conduct mechanistic studies to explore how certain bacteria influence metabolism, inflammation, or mental health.</p>
</li>
<li>
<p><strong>Precision Probiotics and Therapeutics</strong><br /> By providing access to native human gut microbes, HiBC supports the development of next-generation probiotics, live biotherapeutic products (LBPs), and fecal microbiota transplantation (FMT) alternatives.</p>
</li>
<li>
<p><strong>Standardization and Reproducibility</strong><br /> With standardized cultivation and genomic protocols, HiBC ensures consistency across microbiome research studies, improving reproducibility and comparability of findings.</p>
</li>
<li>
<p><strong>Antimicrobial Resistance (AMR) Surveillance</strong><br /> HiBC includes metadata on antibiotic resistance genes (ARGs), helping track the spread of AMR in commensal gut bacteria and understanding its implications for human health.</p>
</li>
</ol><h2>Key Features of HiBC</h2><ul>
<li>
<p><strong>Culturable Bacteria Repository:</strong> A living collection of anaerobic and facultative strains isolated from healthy and diseased individuals worldwide.</p>
</li>
<li>
<p><strong>Metadata-rich Entries:</strong> Each isolate is annotated with host details (age, health status, diet), geographical origin, phenotypic traits, and antibiotic susceptibility profiles.</p>
</li>
<li>
<p><strong>Whole Genome Sequencing (WGS):</strong> High-quality genome assemblies for most strains to support functional and comparative genomics.</p>
</li>
<li>
<p><strong>Interactive Database Access:</strong> User-friendly search and filtering options for strain selection based on taxonomy, function, or clinical relevance.</p>
</li>
<li>
<p><strong>Cross-linking with Other Databases:</strong> Integration with NCBI, GOLD, and Human Microbiome Project (HMP) data for broader context and validation.</p>
</li>
</ul><h2>Applications of HiBC</h2><ul>
<li>
<p>Microbiome-based diagnostics and biomarker discovery</p>
</li>
<li>
<p>Host-microbe interaction studies in gnotobiotic mouse models</p>
</li>
<li>
<p>Gut microbiome modulation through diet, drugs, or engineered bacteria</p>
</li>
<li>
<p>Longitudinal studies of gut flora across age, geography, and lifestyle</p>
</li>
<li>
<p>Environmental and evolutionary microbiology of human-associated bacteria</p>
</li>
</ul><h2>Accessing HiBC</h2><p>Researchers and interested parties can explore the HiBC database through its official website: <a href="https://www.hibc.rwth-aachen.de/" target="_new">https://www.hibc.rwth-aachen.de/</a>. The platform offers comprehensive information on bacterial isolates, including taxonomy, cultivation conditions, and genomic data, facilitating advanced research in human gut microbiome studies.</p><h2>Final Thoughts</h2><p>The <strong>HiBC</strong> is a cornerstone resource in the rapidly evolving field of microbiome research. As science moves toward personalized medicine and microbial therapeutics, having a reliable and diverse collection of human gut bacteria is not just useful &mdash; it's essential. Whether you're a microbiologist, clinician, computational biologist, or biotechnologist, HiBC offers tools to accelerate discovery and innovation in gut microbiome science.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41033/clark-fast-accurate-and-versatile-sequence-classification-system</guid>
	<pubDate>Sat, 15 Feb 2020 01:49:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41033/clark-fast-accurate-and-versatile-sequence-classification-system</link>
	<title><![CDATA[CLARK: Fast, accurate and versatile sequence classification system]]></title>
	<description><![CDATA[<p><span></span><a href="http://dx.doi.org/10.1186/s12864-015-1419-2"><strong>CLARK</strong></a><span>, a method based on a supervised sequence classification using discriminative&nbsp;</span><em>k</em><span>-mers. Considering two distinct specific classification problems (see the article for details), namely (1) the taxonomic classification of metagenomic reads to known bacterial genomes, and (2) the assignment of BAC clones and transcript to chromosome arms/centromeres (in the absence of a finished assembly for the reference genome), CLARK outperforms in classification speed and precision the best state-of-the-art methods.</span></p>
<p><span><a href="http://clark.cs.ucr.edu/Spaced/">http://clark.cs.ucr.edu/Spaced/</a></span></p><p>Address of the bookmark: <a href="http://clark.cs.ucr.edu/Spaced/" rel="nofollow">http://clark.cs.ucr.edu/Spaced/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/22761/pit-bioinformatics-group</guid>
  <pubDate>Tue, 16 Jun 2015 14:34:26 -0500</pubDate>
  <link></link>
  <title><![CDATA[PIT Bioinformatics Group]]></title>
  <description><![CDATA[
<p>PIT Bioinformatics Group solves problems in bioinformatics and  computational biology. Recent developed online tools:</p>

<p>- Budapest Reference Connectome: View a parametrizable connectome (brain graph).<br />- AmphoraNet: The webserver implementation of the AMPHORA2 workflow for phylogenetic analysis of metagenomic shotgun sequencing data.<br />- AmphoraVizu: Chart visualization for metagenomics analysis tools AMPHORA2 and AmphoraNet.<br />- SCARF: Free online association rule mining tool.</p>

<p>More at: http://pitgroup.org</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</guid>
	<pubDate>Thu, 18 Jun 2020 06:58:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</link>
	<title><![CDATA[sunbeam: A robust, extensible metagenomics pipeline]]></title>
	<description><![CDATA[<p><span>Sunbeam is a pipeline written in&nbsp;</span><a href="http://snakemake.readthedocs.io/">snakemake</a><span>&nbsp;that simplifies and automates many of the steps in metagenomic sequencing analysis. It uses&nbsp;</span><a href="http://conda.io/">conda</a><span>&nbsp;to manage dependencies, so it doesn't have pre-existing dependencies or admin privileges, and can be deployed on most Linux workstations and clusters. To read more, check out&nbsp;</span><a href="https://microbiomejournal.biomedcentral.com/articles/10.1186/s40168-019-0658-x">our paper in Microbiome</a><span>.</span></p>
<p><span><a href="https://sunbeam.readthedocs.io/en/latest/">https://sunbeam.readthedocs.io/en/latest/</a></span></p><p>Address of the bookmark: <a href="https://github.com/sunbeam-labs/sunbeam" rel="nofollow">https://github.com/sunbeam-labs/sunbeam</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44529/contigextender-a-new-approach-to-improving-de-novo-sequence-assembly-for-viral-metagenomics-data</guid>
	<pubDate>Wed, 08 May 2024 07:32:45 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44529/contigextender-a-new-approach-to-improving-de-novo-sequence-assembly-for-viral-metagenomics-data</link>
	<title><![CDATA[ContigExtender: a new approach to improving de novo sequence assembly for viral metagenomics data]]></title>
	<description><![CDATA[<p dir="auto">ContigExtender, was developed to extend contigs, complementing de novo assembly. ContigExtender employs a novel recursive Overlap Layout Candidates (r-OLC) strategy that explores multiple extending paths to achieve longer and highly accurate contigs. ContigExtender is effective for extending contigs significantly in in silico synthesized and real metagenomics datasets.</p>
<p dir="auto">More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953547/</p>
<p dir="auto"><a href="https://camo.githubusercontent.com/72dc78177cd84dd0c667a2922a9fd984fb548b5ec94b11f9a547211a4adba3b1/68747470733a2f2f692e696d6775722e636f6d2f7734516944496a2e706e67" target="_blank"><img src="https://camo.githubusercontent.com/72dc78177cd84dd0c667a2922a9fd984fb548b5ec94b11f9a547211a4adba3b1/68747470733a2f2f692e696d6775722e636f6d2f7734516944496a2e706e67" alt="extension process" title="extension process" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/dengzac/contig-extender" rel="nofollow">https://github.com/dengzac/contig-extender</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6954/workshop-on-population-and-metagenomics-analysis-nerc</guid>
  <pubDate>Sun, 01 Dec 2013 14:25:45 -0600</pubDate>
  <link></link>
  <title><![CDATA[Workshop on population and metagenomics analysis @ NERC]]></title>
  <description><![CDATA[
<p>Workshop Overview</p>

<p>A ten-day workshop taking place between 25 February - 6 March 2014 providing detailed hands-on training for population and meta-genomics analysis for researchers with little or no background in mathematics or computing.</p>

<p>Venue: Dartington Hall, Totnes, Devon (nearest train station - Totnes)</p>

<p>Times: 25 February - 6th March 2014.</p>

<p>Arrival evening of Tuesday 25 February 2014. Departure morning of 6th March 2014. The course itself will take place 9am-12pm, 2pm-5pm and on some evenings 7pm-10pm everyday 26 February-5th March. Students are expected to attend the entire course.</p>

<p>Contact: research-events@exeter.ac.uk</p>

<p>Registration</p>

<p>The course itself is free of charged and is funded by a Professional Postgraduate Development Award from NERC.</p>

<p>A total of 30 funded places are available which cover the costs of accommodation and food, but not the cost of transportation to/from the venue.</p>

<p>An additional 10 places are available for participants from industry. The cost of accommodation and meals will need to be covered by the participants.</p>

<p>You should register your interest by 31 December 2013. Participants will be informed by 10th January 2014 as to whether they have been selected. Please note that preference will be given to researchers funded by NERC.</p>

<p>More at http://www.eventbrite.co.uk/e/nerc-workshop-on-population-and-metagenomics-analysis-tickets-8628888237</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44597/imagine-in-silico-metagenomics-pipeline</guid>
	<pubDate>Sat, 06 Jul 2024 04:32:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44597/imagine-in-silico-metagenomics-pipeline</link>
	<title><![CDATA[iMAGine - in silico MetAGenomics pipeline]]></title>
	<description><![CDATA[<p dir="auto"><span>iMAGine</span>&nbsp;is a metagenomic workflow which includes filtering, assembling, and binning.</p>
<p dir="auto">This workflow includes the following tools which are needed to be installed in the system.</p>
<ol dir="auto">
<li><a href="https://github.com/OpenGene/fastp">fastp</a></li>
<li><a href="https://github.com/ablab/spades">spades assembler</a></li>
<li><a href="https://github.com/ablab/quast">QUAST</a></li>
<li><a href="https://github.com/lh3/bwa">bwa</a></li>
<li><a href="https://github.com/samtools/samtools">samtools</a></li>
<li><a href="https://bitbucket.org/berkeleylab/metabat/src/master/">metabat2</a></li>
<li><a href="https://github.com/Ecogenomics/CheckM">CheckM</a></li>
</ol><p>Address of the bookmark: <a href="https://github.com/avishekdutta14/iMAGine" rel="nofollow">https://github.com/avishekdutta14/iMAGine</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/933/world-of-omics</guid>
	<pubDate>Tue, 16 Jul 2013 17:11:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/933/world-of-omics</link>
	<title><![CDATA[World of Omics]]></title>
	<description><![CDATA[<p>How many variants of "omics" techniques presently in use ?</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4100/should-you-get-sequenced-not-all-bad-genes-predict-disease</guid>
	<pubDate>Thu, 29 Aug 2013 15:10:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4100/should-you-get-sequenced-not-all-bad-genes-predict-disease</link>
	<title><![CDATA[Should you get sequenced? Not all bad genes predict disease]]></title>
	<description><![CDATA[<p><span>&ldquo;What we really don&rsquo;t know yet is whether the predictive aspects of the genome are going to turn out to be beneficial or potentially harmful&rdquo;</span></p>
<p><span><span>&ldquo;As we roll out genomic medicine we are fighting against this society-wide misconception that having the bad gene means you&rsquo;re going to get the disease. That&rsquo;s only true in a very few cases.&rdquo;</span></span></p>
<p><span><span><strong>Source</strong>:Today Health</span></span></p><p>Address of the bookmark: <a href="http://www.today.com/health/should-you-get-sequenced-not-all-bad-genes-predict-disease-8C11017154" rel="nofollow">http://www.today.com/health/should-you-get-sequenced-not-all-bad-genes-predict-disease-8C11017154</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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