<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/989?offset=80</link>
	<atom:link href="https://bioinformaticsonline.com/related/989?offset=80" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<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>
<item>
	<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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</guid>
	<pubDate>Tue, 26 Nov 2013 17:34:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</link>
	<title><![CDATA[DNA tale of 3 to 4 years old Serbia boy]]></title>
	<description><![CDATA[<p><span>The genome of a young boy found underground at Mal&rsquo;ta near Lake Baikal of eastern Siberia around 24,000 years ago came out as close relative of Europeans and Native Indians.</span></p><p><span>Link:</span></p><p><span><a href="http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0">http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0</a></span></p><p>&nbsp;</p><p><a href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html">http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10237/genome-of-rainbow-trout-sequenced</guid>
	<pubDate>Fri, 25 Apr 2014 10:36:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10237/genome-of-rainbow-trout-sequenced</link>
	<title><![CDATA[Genome of Rainbow Trout Sequenced]]></title>
	<description><![CDATA[<p>Major finding:</p><p><span>&ldquo;In humans and most vertebrates the duplication events were older so there are fewer duplicated genes still present. Most of the duplicated genes get lost or modified so much that they are no longer recognizable as duplicates over time. In the trout and salmon we can see an earlier stage in the process and many duplicated genes are still present,&rdquo; said Dr Gary Thorgaard of Washington State University, a co-author of the paper published in the journal Nature Communications.</span></p><p><span>Source:</span></p><p><span>http://www.sci-news.com/genetics/science-genome-rainbow-trout-01877.html</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10378/real-time-sequencing</guid>
	<pubDate>Sun, 04 May 2014 18:16:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10378/real-time-sequencing</link>
	<title><![CDATA[Real time Sequencing]]></title>
	<description><![CDATA[<p><span>&ldquo;... we now know we can do high-throughput sequencing at any location on Earth,&rdquo; Moroz said.</span></p><p><span>Source:</span></p><p><span>http://news.ufl.edu/2014/04/28/real-time-genome-sequencing-at-sea/</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/11365/drawback-of-exome-sequencing</guid>
	<pubDate>Mon, 02 Jun 2014 05:46:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/11365/drawback-of-exome-sequencing</link>
	<title><![CDATA[Drawback of Exome Sequencing]]></title>
	<description><![CDATA[<p><span><span>Dr Eric Londin, Assistant Professor, Thomas Jefferson University, USA, stated that analysis of 44 exome datasets from four different testing kits showed that they missed a high proportion of clinically relevant regions in the 56 ACMG genes. "At least one gene in each exome method was missing more than 40 percent of disease-causing genetic variants, and we found that the worst-performing method missed more than 90 percent of such variants in four of the 56 genes," he says.</span><br /></span></p><p><span><strong>Source</strong>:&nbsp;http://www.eurekalert.org/pub_releases/2014-05/esoh-pco052914.php</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

</channel>
</rss>