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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/989?offset=100</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36846/gblocks-eliminates-poorly-aligned-positions-and-divergent-regions-of-a-dna-or-protein-alignment</guid>
	<pubDate>Sat, 02 Jun 2018 07:36:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36846/gblocks-eliminates-poorly-aligned-positions-and-divergent-regions-of-a-dna-or-protein-alignment</link>
	<title><![CDATA[Gblocks: eliminates poorly aligned positions and divergent regions of a DNA or protein alignment]]></title>
	<description><![CDATA[<p><a href="http://molevol.cmima.csic.es/castresana/Gblocks.html">Gblocks</a><span>&nbsp;eliminates poorly aligned positions and divergent regions of a DNA or protein alignment so that it becomes more suitable for phylogenetic analysis. This server implements the most important features of the Gblocks program to make its use as simple as possible without loosing the functionality that it is necessary in most of the cases. Other options can be changed in the stand-alone program. You can see here an&nbsp;</span><a href="http://molevol.cmima.csic.es/castresana/Gblocks_server/nad3.pir-gb.htm">example output file</a><span>&nbsp;showing the blocks selected from a protein alignment. Further information can be found in the&nbsp;</span><a href="http://molevol.cmima.csic.es/castresana/Gblocks/Gblocks_documentation.html">online documentation</a><span>.&nbsp;</span></p><p>Address of the bookmark: <a href="http://molevol.cmima.csic.es/castresana/Gblocks_server.html" rel="nofollow">http://molevol.cmima.csic.es/castresana/Gblocks_server.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38501/fgenesh-program-for-predicting-multiple-genes-in-genomic-dna-sequences</guid>
	<pubDate>Thu, 20 Dec 2018 11:55:08 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38501/fgenesh-program-for-predicting-multiple-genes-in-genomic-dna-sequences</link>
	<title><![CDATA[FGENESH - Program for predicting multiple genes in genomic DNA sequences]]></title>
	<description><![CDATA[<p>FGENESH is the fastest (50-100 times faster than GenScan) and most accurate gene finder available - see the figure and the table below. In recent rice genome sequencing projects, it was cited "the most successful (gene finding) program (Yu&nbsp;<em>et al</em>. (2002) Science 296:79) and was used to produce 87% of all high-evidence predicted genes (Goff&nbsp;<em>et al</em>. (2002) Science 296:79).</p><p>Address of the bookmark: <a href="http://www.softberry.com/berry.phtml?topic=fgenesh&amp;group=help&amp;subgroup=gfind" rel="nofollow">http://www.softberry.com/berry.phtml?topic=fgenesh&amp;group=help&amp;subgroup=gfind</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40856/3d-de-novo-assembly-3d-dna-pipeline</guid>
	<pubDate>Sun, 02 Feb 2020 13:41:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40856/3d-de-novo-assembly-3d-dna-pipeline</link>
	<title><![CDATA[3D de novo assembly (3D DNA) pipeline]]></title>
	<description><![CDATA[<p>For a detailed description of the pipeline and how it integrates with other tools designed by the Aiden Lab see&nbsp;<a href="http://aidenlab.org/assembly/manual_180322.pdf">Genome Assembly Cookbook</a>&nbsp;on&nbsp;<a href="http://aidenlab.org/assembly">http://aidenlab.org/assembly</a>.</p>
<p>For the original version of the pipeline and to reproduce the Hs2-HiC and the AaegL4 genomes reported in&nbsp;<a href="http://science.sciencemag.org/content/356/6333/92">(Dudchenko et al.,&nbsp;<em>Science</em>, 2017)</a>&nbsp;see the&nbsp;<a href="https://github.com/theaidenlab/3d-dna/tree/745779bdf64db6e55bddb70c24e9b58825938c33">original commit</a>.</p>
<p>For the detailed description of the merge section see&nbsp;<a href="https://github.com/theaidenlab/AGWG-merge">https://github.com/theaidenlab/AGWG-merge</a>.</p><p>Address of the bookmark: <a href="https://github.com/theaidenlab/3d-dna" rel="nofollow">https://github.com/theaidenlab/3d-dna</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42023/encode3-a-collection-of-research-articles-and-related-content-describing-the-encyclopedia-of-dna-elements-its-datasets-and-tools</guid>
	<pubDate>Sat, 08 Aug 2020 08:25:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42023/encode3-a-collection-of-research-articles-and-related-content-describing-the-encyclopedia-of-dna-elements-its-datasets-and-tools</link>
	<title><![CDATA[ENCODE3: A collection of research articles and related content describing the Encyclopedia of DNA Elements, its datasets and tools.]]></title>
	<description><![CDATA[<p>How cells, tissues and organisms interpret the information encoded in the genome has vital implications for our understanding of development, health and disease. Launched in 2003, the ENCyclopedia Of DNA Elements (ENCODE) project has the aim of mapping the functional elements in the human genome (later expanded to include model organisms).</p><p>During the first phase of ENCODE, published in 2007, microarray-based technologies were used to detect regions associated with transcription factors, certain histone modifications and open chromatin within a pre-specified 1% of the human genome.</p><p>ENCODE&rsquo;s second phase saw a switch to sequencing-based technologies, the addition of new assay types and the analysis of functional elements genome-wide, described in a collection of research articles in 2012.</p><p><span>The&nbsp;</span><a href="https://www.nature.com/articles/s41586-020-2493-4">Encyclopedia paper of ENCODE 3</a><span>, published in&nbsp;</span><em>Nature</em><span>, gives an overview of the various assays that were performed in human and mouse cell lines and tissues and describes a Registry of human and mouse candidate&nbsp;</span><em>cis</em><span>-regulatory elements (cCREs).</span></p><p>More at&nbsp;<a href="https://www.nature.com/immersive/d42859-020-00027-2/index.html">https://www.nature.com/immersive/d42859-020-00027-2/index.html</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44329/metabuli-%EB%B6%84%EB%A6%AC-improves-metagenomic-read-classification</guid>
	<pubDate>Sat, 03 Jun 2023 20:15:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44329/metabuli-%EB%B6%84%EB%A6%AC-improves-metagenomic-read-classification</link>
	<title><![CDATA[Metabuli 분리 improves metagenomic read classification]]></title>
	<description><![CDATA[<p><span>Metabuli 분리 improves metagenomic read classification through metamers, DNA-AA k-mers, to be sensitive and specific, recovering 99% and 98% of DNA or AA classifiers.</span></p>
<p>&nbsp;</p>
<p><span><span>Metabuli is metagenomic classifier that jointly analyze both DNA and amino acid (AA) sequences. DNA-based classifiers can make specific classifications, exploiting point mutations to distinguish close taxa. AA-based classifiers have higher sensitivity in detecting homology between query and reference sequences, leverageing higher conservation of AA sequences. Metabuli combines the information of both sequence types using a novel k-mer structure,&nbsp;</span><em>metamer</em><span>, to enable both specific and sensitive characterization of metagenomic samples. In addition, it can classify reads against a database of any size as long as it fits in the hard disk.</span> </span></p><p>Address of the bookmark: <a href="https://github.com/steineggerlab/Metabuli" rel="nofollow">https://github.com/steineggerlab/Metabuli</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44663/svbyeye-r-package-to-visualize-alignments-between-two-or-multiple-dna-sequences</guid>
	<pubDate>Tue, 17 Sep 2024 02:34:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44663/svbyeye-r-package-to-visualize-alignments-between-two-or-multiple-dna-sequences</link>
	<title><![CDATA[SVbyEye: R Package to visualize alignments between two or multiple DNA sequences]]></title>
	<description><![CDATA[<p dir="auto">R Package to visualize alignments between two or multiple DNA sequences including<br>a number of functionalities to facilitate processing of alignments in PAF format.</p>
<p dir="auto"><span>SVbyEye, an open-source R package to visualize and annotate sequence-to-sequence alignments along with various functionalities to process alignments in PAF format. The tool facilitates the characterization of complex SVs in the context of sequence homology helping resolve the mechanisms underlying their formation. Availability and implementation SVbyEye is available at https://github.com/daewoooo/SVbyEye.</span></p>
<p dir="auto">Author: David Porubsky</p><p>Address of the bookmark: <a href="https://github.com/daewoooo/SVbyEye" rel="nofollow">https://github.com/daewoooo/SVbyEye</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/42693/dna-rna-meme</guid>
	<pubDate>Thu, 28 Jan 2021 11:23:14 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/42693/dna-rna-meme</link>
	<title><![CDATA[DNA RNA MEME]]></title>
	<description><![CDATA[<p>Explain the DNA and RNA with picture ...</p>]]></description>
	<dc:creator>Neel</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/42693" length="41627" type="image/jpeg" />
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38215/pwhatshap-a-parallel-high-performance-version-of-whatshap</guid>
	<pubDate>Wed, 14 Nov 2018 08:20:27 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38215/pwhatshap-a-parallel-high-performance-version-of-whatshap</link>
	<title><![CDATA[pWhatsHap: a parallel, high-performance version of WhatsHap]]></title>
	<description><![CDATA[<div id="ASec4">
<p>Given the potential relevance of efficient haplotyping in several analysis pipelines, we have designed and engineered&nbsp;pWhatsHap, a parallel, high-performance version of&nbsp;WhatsHap.&nbsp;pWhatsHap&nbsp;is embedded in a toolkit developed in Python and supports genomics datasets in standard file formats. Building on&nbsp;WhatsHap,&nbsp;pWhatsHap&nbsp;exhibits the same complexity exploring a number of possible solutions which is exponential in the coverage of the dataset. The parallel implementation on multi-core architectures allows for a relevant reduction of the execution time for haplotyping, while the provided results enjoy the same high accuracy as that provided by&nbsp;WhatsHap, which increases with coverage.</p>
</div>
<p>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-016-1170-y</p><p>Address of the bookmark: <a href="https://bitbucket.org/whatshap/whatshap" rel="nofollow">https://bitbucket.org/whatshap/whatshap</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4195/barber-pole-worm-sheep-pathogen-sequenced</guid>
	<pubDate>Tue, 03 Sep 2013 16:32:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4195/barber-pole-worm-sheep-pathogen-sequenced</link>
	<title><![CDATA[Barber pole worm , sheep pathogen sequenced !!!]]></title>
	<description><![CDATA[<p>Haemonchus contortus is a highly pathogenic parasitic nematode of that can infect a large number of wild and domesticated ruminant species and is the most economically important parasite of sheep and goats worldwide. Scientists at the Wellcome Trust Sanger Institute have sequenced the genome of the barber's pole worm (Haemonchus contortus), which will help to explore the this tropical parasite which&nbsp;been disseminated around the world by livestock movement.&nbsp;</p><p>H. contortus is a member of the superfamily trichostrongyloidea (Strongylida) which contains most of the economically important parasitic nematodes of grazing livestock. These parasites cost the global livestock industry billions of dollars per annum in lost production and drug costs.&nbsp;A common type of clover may be a preventative or palliative for the disease. However, some particular breeds of sheep, such as the Gulf Coast Native from the Southern United States, have been shown to have developed special resistance to H. contortus.</p><p>Getting the full genome can help to tackle the problem and understand the resistance mechanism with an ease. Moreover, the genome could now provide a comprehensive understanding of how treatments against parasitic worms work and point to further new treatments and vaccines.&nbsp;By comparing the genome of the barber's pole worm with those of worms that have acquired drug resistance, researchers expect to reveal information about how and why resistance has occurred. Till now, researchers have uncovered essential information in the fight against drug resistance in worms.</p><p>Reference:</p><p><a href="http://www.fwi.co.uk/articles/28/08/2013/140758/researchers-close-in-on-worm-resistance-in-sheep.htm">http://www.fwi.co.uk/articles/28/08/2013/140758/researchers-close-in-on-worm-resistance-in-sheep.htm</a></p><p><a href="http://www.sciencedaily.com/releases/2013/08/130828103351.htm?utm_source=feedburner&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+sciencedaily%2Fplants_animals+(ScienceDaily%3A+Plants+%26+Animals+News)">http://www.sciencedaily.com/releases/2013/08/130828103351.htm?utm_source=feedburner&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+sciencedaily%2Fplants_animals+(ScienceDaily%3A+Plants+%26+Animals+News)</a></p><p>Image source: Wikipedia</p><p><img src="http://upload.wikimedia.org/wikipedia/commons/8/8e/Haemonchus_contortus.jpg" alt="image" width="800" height="533" style="border: 0px; border: 0px;"></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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