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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36837?offset=340</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32868/pollux-platform-independent-error-correction-of-single-and-mixed-genomes</guid>
	<pubDate>Fri, 19 May 2017 09:41:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32868/pollux-platform-independent-error-correction-of-single-and-mixed-genomes</link>
	<title><![CDATA[Pollux: platform independent error correction of single and mixed genomes]]></title>
	<description><![CDATA[<p><span>Pollux: General-purpose error corrector that corrects errors introduced by Illumina, Ion Torrent, and Roche 454 sequencing technologies and can be applied to single- or mixed-genome data. In addition to correcting substitution errors, we locate and correct insertion, deletion, and homopolymer errors while remaining sensitive to low coverage areas of sequencing projects. Using published data sets, we correct 94% of Illumina MiSeq errors, 88% of Ion Torrent PGM errors, 85% of Roche 454 GS Junior errors. Introduced errors are 20 to 70 times more rare than successfully corrected errors. Furthermore, we show that the quality of assemblies improves when reads are corrected by our software.</span></p>
<p><span>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-014-0435-6</span></p><p>Address of the bookmark: <a href="https://github.com/emarinier/pollux" rel="nofollow">https://github.com/emarinier/pollux</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44599/p10k-the-protist-10000-genomes</guid>
	<pubDate>Sat, 06 Jul 2024 08:29:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44599/p10k-the-protist-10000-genomes</link>
	<title><![CDATA[P10K: The Protist 10,000 Genomes]]></title>
	<description><![CDATA[<p><span>The Protist 10,000 Genomes (P10K) Project aims to decipher the genome sequences and construct a comprehensive database resource containing over 10,000 species of protists, encompassing representatives from every major clade. Samples were collected from diverse habitats, and the genome information was acquired through de novo sequencing, genome re-annotation, and integration of publicly available data. Serving as a centralized data portal for the project, the P10K database primarily focuses on delivering high-quality curation and facilitating efficient retrieval of protist genome data.</span></p><p>Address of the bookmark: <a href="https://ngdc.cncb.ac.cn/p10k/" rel="nofollow">https://ngdc.cncb.ac.cn/p10k/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33887/gview-a-java-application-for-viewing-and-examining-prokaryotic-genomes-in-a-circular-or-linear-context</guid>
	<pubDate>Fri, 14 Jul 2017 07:47:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33887/gview-a-java-application-for-viewing-and-examining-prokaryotic-genomes-in-a-circular-or-linear-context</link>
	<title><![CDATA[GView: A Java application for viewing and examining prokaryotic genomes in a circular or linear context]]></title>
	<description><![CDATA[<p>GView is a Java application for viewing and examining prokaryotic genomes in a circular or linear context. It accepts standard sequence file formats and an optional style specification file to generate customizable, publication quality genome maps in bitmap and scalable vector graphics formats. GView features an interactive pan-and-zoom interface, a command-line interface for incorporation in genome analysis pipelines, and a public Application Programming Interface for incorporation in other Java applications.</p>
<p><strong>Availability:</strong>&nbsp;GView is a freely available application licensed under the GNU Public License. The application, source code, documentation, file specifications, tutorials and image galleries are available at&nbsp;<a href="http://gview.ca/" target="pmc_ext">http://gview.ca</a></p>
<p><strong>Contact:</strong>&nbsp;<a href="mailto:dev@null">ac.cg.cpsa-cahp@raalesmod.nav.yrag</a></p>
<p>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995121/</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995121/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995121/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</guid>
	<pubDate>Wed, 27 Dec 2017 00:04:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</link>
	<title><![CDATA[Recovery of complete genomes from metagenomes]]></title>
	<description><![CDATA[<p>This project contains scripts and tutorials on how to assemble individual microbial genomes from metagenomes, as described in:</p>
<p><strong>Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes</strong></p>
<p><a href="http://personprofil.aau.dk/120257">Mads Albertsen</a>,&nbsp;<a href="http://ecogenomic.org/users/phil-hugenholtz">Philip Hugenholtz</a>,&nbsp;<a href="http://ecogenomic.org/users/adam-skarshewski">Adam Skarshewski</a>,&nbsp;<a href="http://www.ecogenomic.org/users/gene-tyson">Gene W. Tyson</a>,&nbsp;<a href="http://personprofil.aau.dk/103057">K&aring;re L. Nielsen</a>&nbsp;and&nbsp;<a href="http://personprofil.aau.dk/105842">Per .H. Nielsen</a></p>
<p>Nature Biotechnology 2013, doi:&nbsp;<a href="http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.2579.html">10.1038/nbt.2579</a></p><p>Address of the bookmark: <a href="http://madsalbertsen.github.io/multi-metagenome/" rel="nofollow">http://madsalbertsen.github.io/multi-metagenome/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</guid>
	<pubDate>Mon, 14 May 2018 04:02:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</link>
	<title><![CDATA[Digest: In silico restriction digest of complete genomes]]></title>
	<description><![CDATA[<p><span>This tool allows to retrieve number of cleavages yielded by commercially available endonucleases in up-to-date sequenced prokaryotic genomes. When the number of fragments is bellow 50, Pulse Field gel Electrophoresis (PFGE) is simulated.</span></p>
<p>A tool for restriction digest of&nbsp;<a href="http://insilico.ehu.eus/restriction/long_seq/">long</a>user's sequences is available.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://insilico.ehu.es/digest/" rel="nofollow">http://insilico.ehu.es/digest/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</guid>
	<pubDate>Wed, 22 Aug 2018 03:21:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</link>
	<title><![CDATA[GTDB-Tk: A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes.]]></title>
	<description><![CDATA[<p>GTDB-Tk is a software toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. It is computationally efficient and designed to work with recent advances that allow hundreds or thousands of metagenome-assembled genomes (MAGs) to be obtained directly from environmental samples. It can also be applied to isolate and single-cell genomes. The GTDB-Tk is open source and released under the GNU General Public License (Version 3).</p>
<p>GTDB-Tk is&nbsp;<span>under active development and validation</span>. Please independently confirm the GTDB-Tk predictions by manually inspecting the tree and bringing any discrepencies to our attention. Notifications about GTDB-Tk releases will be available through the ACE Twitter account (<a href="https://twitter.com/ace_uq">https://twitter.com/ace_uq</a>).</p><p>Address of the bookmark: <a href="https://github.com/Ecogenomics/GTDBTk" rel="nofollow">https://github.com/Ecogenomics/GTDBTk</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</guid>
	<pubDate>Thu, 19 Dec 2019 07:33:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</link>
	<title><![CDATA[HaploTypo: a variant-calling pipeline for phased genomes]]></title>
	<description><![CDATA[<p>An increasing number of phased (i.e. with resolved haplotypes) reference genomes are available. However, most genetic variant calling tools do not explicitly account for haplotype structure. Here, we present HaploTypo, a pipeline tailored to resolve haplotypes in genetic variation analyses. HaploTypo infers the haplotype correspondence for each heterozygous variant called on a phased reference genome.</p>
<div>Availability and Implementation</div>
<p>HaploTypo is implemented in Python 2.7 and Python 3.5, and is freely available at&nbsp;<a href="https://github.com/gabaldonlab/haplotypo" target="">https://github.com/gabaldonlab/haplotypo</a>, and as a Docker image.</p><p>Address of the bookmark: <a href="https://github.com/gabaldonlab/haplotypo" rel="nofollow">https://github.com/gabaldonlab/haplotypo</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41686/catbat-tool-for-taxonomic-classification-of-contigs-and-metagenome-assembled-genomes-mags</guid>
	<pubDate>Mon, 18 May 2020 10:53:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41686/catbat-tool-for-taxonomic-classification-of-contigs-and-metagenome-assembled-genomes-mags</link>
	<title><![CDATA[CAT/BAT: tool for taxonomic classification of contigs and metagenome-assembled genomes (MAGs)]]></title>
	<description><![CDATA[<p>Contig Annotation Tool (CAT) and Bin Annotation Tool (BAT) are pipelines for the taxonomic classification of long DNA sequences and metagenome assembled genomes (MAGs/bins) of both known and (highly) unknown microorganisms, as generated by contemporary metagenomics studies. The core algorithm of both programs involves gene calling, mapping of predicted ORFs against the nr protein database, and voting-based classification of the entire contig / MAG based on classification of the individual ORFs. CAT and BAT can be run from intermediate steps if files are formated appropriately (see <a href="https://github.com/dutilh/CAT#usage">Usage</a>).</p><p>Address of the bookmark: <a href="https://github.com/dutilh/CAT" rel="nofollow">https://github.com/dutilh/CAT</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42357/irscope-an-online-program-to-visualize-the-junction-sites-of-chloroplast-genomes</guid>
	<pubDate>Wed, 25 Nov 2020 19:44:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42357/irscope-an-online-program-to-visualize-the-junction-sites-of-chloroplast-genomes</link>
	<title><![CDATA[IRscope: an online program to visualize the junction sites of chloroplast genomes]]></title>
	<description><![CDATA[<p><span>eMPRess, a software program for phylogenetic tree reconciliation under the duplication-transfer-loss model that systematically addresses the problems of choosing event costs and selecting representative solutions, enabling users to make more robust inferences.</span></p><p>Address of the bookmark: <a href="https://sites.google.com/g.hmc.edu/empress/home" rel="nofollow">https://sites.google.com/g.hmc.edu/empress/home</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</guid>
	<pubDate>Mon, 06 May 2024 06:21:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</link>
	<title><![CDATA[Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes]]></title>
	<description><![CDATA[<p><span>Genomic regulatory blocks are chromosomal regions spanned by long clusters of highly conserved noncoding elements devoted to long-range regulation of developmental genes, often immobilizing other, unrelated genes into long-lasting syntenic arrangements. Synorth&nbsp;</span><a href="http://synorth.genereg.net/" target="_blank">http://synorth.genereg.net/</a><span>&nbsp;is a web resource for exploring and categorizing the syntenic relationships in genomic regulatory blocks across multiple genomes, tracing their evolutionary fate after teleost whole genome duplication at the level of genomic regulatory block loci, individual genes, and their phylogenetic context.</span></p>
<p><span>More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745767/</span></p><p>Address of the bookmark: <a href="http://synorth.genereg.net/" rel="nofollow">http://synorth.genereg.net/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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