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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36723?offset=460</link>
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	<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/35619/tallymer-method-to-compute-k-mer-frequencies-and-its-application-to-annotate-large-repetitive-plant-genomes</guid>
	<pubDate>Thu, 15 Feb 2018 10:21:02 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35619/tallymer-method-to-compute-k-mer-frequencies-and-its-application-to-annotate-large-repetitive-plant-genomes</link>
	<title><![CDATA[Tallymer: method to compute K-mer frequencies and its application to annotate large repetitive plant genomes]]></title>
	<description><![CDATA[<p>Tallymer is based on enhanced suffix arrays. This gives a much larger flexibility concerning the choice of the&nbsp;<span>k</span>-mer size. Tallymer can process large data sizes of several billion bases. We used it in a variety of applications to study the genomes of maize and other plant species. In particular, Tallymer was used to index a set whole genome shotgun sequences from maize (B73) (total size 10<sup>9</sup>&nbsp;bp).&nbsp;<br>Tallymer was effective in a variety of applications to aid genome annotation in maize, despite limitations imposed by the relatively low coverage of sequence available.</p>
<p>A manual can be found&nbsp;<a href="https://www.zbh.uni-hamburg.de/fileadmin/gi/tallymer/tallymer.pdf" target="_blank" title="tallymer.pdf (111 KB)">here</a>.</p><p>Address of the bookmark: <a href="https://www.zbh.uni-hamburg.de/forschung/arbeitsgruppe-genominformatik/software/tallymer.html" rel="nofollow">https://www.zbh.uni-hamburg.de/forschung/arbeitsgruppe-genominformatik/software/tallymer.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36800/genomemapper-simultaneous-alignment-of-short-reads-against-multiple-genomes</guid>
	<pubDate>Fri, 25 May 2018 09:29:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36800/genomemapper-simultaneous-alignment-of-short-reads-against-multiple-genomes</link>
	<title><![CDATA[GenomeMapper: Simultaneous alignment of short reads against multiple genomes]]></title>
	<description><![CDATA[GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference. If you are unsure which one is the appropriate GenomeMapper, you might want to use the latter

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768987/<p>Address of the bookmark: <a href="http://1001genomes.org/software/genomemapper.html" rel="nofollow">http://1001genomes.org/software/genomemapper.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39867/gepard-allows-the-calculation-of-dotplots-even-for-large-sequences-like-chromosomes-or-bacterial-genomes</guid>
	<pubDate>Mon, 26 Aug 2019 11:38:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39867/gepard-allows-the-calculation-of-dotplots-even-for-large-sequences-like-chromosomes-or-bacterial-genomes</link>
	<title><![CDATA[Gepard: allows the calculation of dotplots even for large sequences like chromosomes or bacterial genomes]]></title>
	<description><![CDATA[<p>Gepard (German: "cheetah", Backronym for "GEnome PAir - Rapid Dotter") allows the calculation of dotplots even for large sequences like chromosomes or bacterial genomes. Reference: Krumsiek J, Arnold R, Rattei T. Gepard: A rapid and sensitive tool for creating dotplots on genome scale. Bioinformatics 2007; 23(8): 1026-8. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/17309896" target="_blank">17309896</a></p>
<p><a href="http://cube.univie.ac.at/gepard">http://cube.univie.ac.at/gepard</a></p><p>Address of the bookmark: <a href="https://github.com/univieCUBE/gepard" rel="nofollow">https://github.com/univieCUBE/gepard</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</guid>
	<pubDate>Mon, 17 Feb 2020 05:38:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</link>
	<title><![CDATA[Chromonomer: a tool set for repairing and enhancing assembled genomes through integration of genetic maps and conserved synteny]]></title>
	<description><![CDATA[<p>Chromonomer is a program designed to integrate a genome assembly with a genetic map. Chromonomer tries very hard to identify and remove markers that are out of order in the genetic map, when considered against their local assembly order; and to identify scaffolds that have been incorrectly assembled according to the genetic map, and split those scaffolds.</p><p>Address of the bookmark: <a href="http://catchenlab.life.illinois.edu/chromonomer/" rel="nofollow">http://catchenlab.life.illinois.edu/chromonomer/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42325/published-a-dataset-of-363-genomes-from-approximately-92-percent-of-bird-families</guid>
	<pubDate>Thu, 19 Nov 2020 07:04:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42325/published-a-dataset-of-363-genomes-from-approximately-92-percent-of-bird-families</link>
	<title><![CDATA[Published a dataset of 363 genomes from approximately 92 percent of bird families]]></title>
	<description><![CDATA[<div>A research team published a dataset of 363 genomes from approximately 92 percent of bird families and showed the significance of sampling dense organisms for biodiversity research. The study was jointly conducted by Chinese and international institutions and museums and was led by researchers from the Kunming Institute of Zoology (KIZ) of the Chinese Academy of Sciences (CAS). Total of 267 were newly published among the 363 sequenced genomes.&nbsp;They were mainly taken from samples of avian tissue kept in museums around the world, enabling researchers to sequence rare and endangered birds' genomes.</div><div>&nbsp;</div><div>Its descendants have adapted to a wide variety of ecological niches since the first bird formed more than 150 million years ago, giving rise to small, hovering hummingbirds, plunge-diving pelicans and showy paradise birds. More than 10,000 bird species live on the planet today - and now scientists are well on their way to capturing a full genetic image of that diversity.</div><div>&nbsp;</div><div>B10K is expanding its efforts to encompass the next stage of avian classification with 363 genomes complete. The team will sequence thousands of extra genomes in this process, attempting to represent each of the approximately 2,300 bird genera.</div><div>&nbsp;</div><div><img src="https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41586-020-2873-9/MediaObjects/41586_2020_2873_Fig1_HTML.png?as=webp" alt="image" style="border: 0px;"></div><div>&nbsp;</div><div>The genomic resource is expected to provide new insights on evolutionary processes in cross-species comparative studies and assist in efforts to protect species, according to the research findings reported as a cover story in the journal Nature.</div><div>&nbsp;</div><div>Ref at&nbsp;Dense sampling of bird diversity increases power of comparative genomics&nbsp;https://www.nature.com/articles/s41586-020-2873-9</div>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<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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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39671/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</guid>
	<pubDate>Sat, 06 Jul 2019 03:48:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39671/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</link>
	<title><![CDATA[Flye: Fast and accurate de novo assembler for single molecule sequencing reads]]></title>
	<description><![CDATA[<p><span>Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes raw PB / ONT reads as input and outputs polished contigs. Flye also includes a special mode for metagenome assembly.</span></p><p>Address of the bookmark: <a href="https://github.com/fenderglass/Flye" rel="nofollow">https://github.com/fenderglass/Flye</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42477/hifiasm-a-haplotype-resolved-assembler-for-accurate-hifi-reads</guid>
	<pubDate>Thu, 24 Dec 2020 10:03:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42477/hifiasm-a-haplotype-resolved-assembler-for-accurate-hifi-reads</link>
	<title><![CDATA[Hifiasm: a haplotype-resolved assembler for accurate Hifi reads]]></title>
	<description><![CDATA[<p><span>Hifiasm is a fast haplotype-resolved de novo assembler for PacBio Hifi reads. It can assemble a human genome in several hours and works with the California redwood genome, one of the most complex genomes sequenced so far. Hifiasm can produce primary/alternate assemblies of quality competitive with the best assemblers. It also introduces a new graph binning algorithm and achieves the best haplotype-resolved assembly given trio data.</span></p><p>Address of the bookmark: <a href="https://github.com/chhylp123/hifiasm" rel="nofollow">https://github.com/chhylp123/hifiasm</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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