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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29992?offset=170</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28164/greengenes-database</guid>
	<pubDate>Wed, 29 Jun 2016 10:03:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28164/greengenes-database</link>
	<title><![CDATA[Greengenes database]]></title>
	<description><![CDATA[<p>The greengenes web application provides access to the 2011 version of the greengenes 16S rRNA gene sequence alignment for browsing, blasting, probing, and downloading. The data and tools presented by greengenes can assist the researcher in choosing phylogenetically specific probes, interpreting microarray results, and aligning/annotating novel sequences. If you are an ARB user, you can use greengenes to keep your own local database current.</p><p>Address of the bookmark: <a href="http://greengenes.lbl.gov/cgi-bin/nph-index.cgi" rel="nofollow">http://greengenes.lbl.gov/cgi-bin/nph-index.cgi</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33006/avid-a-global-alignment-program</guid>
	<pubDate>Wed, 24 May 2017 05:19:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33006/avid-a-global-alignment-program</link>
	<title><![CDATA[AVID: A Global Alignment Program]]></title>
	<description><![CDATA[<p>A new global alignment method called AVID. The method is designed to be fast, memory efficient, and practical for sequence alignments of large genomic regions up to megabases long. We present numerous applications of the method, ranging from the comparison of assemblies to alignment of large syntenic genomic regions and whole genome human/mouse alignments. We have also performed a quantitative comparison of AVID with other popular alignment tools. To this end, we have established a format for the representation of alignments and methods for their comparison. These formats and methods should be useful for future studies. The tools we have developed for the alignment comparisons, as well as the AVID program, are publicly available. See Web Site References section for AVID Web address and Web addresses for other programs discussed in this paper.</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC430967/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC430967/</a></p>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27961/nearhgt</guid>
	<pubDate>Wed, 22 Jun 2016 05:41:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27961/nearhgt</link>
	<title><![CDATA[NearHGT]]></title>
	<description><![CDATA[<p>Horizontal gene transfer (HGT), the transfer of genetic material between organisms, is crucial for genetic innovation and the evolution of genome architecture. Existing HGT detection algorithms rely on a strong phylogenetic signal distinguishing the transferred sequence from ancestral (vertically derived) genes in its recipient genome. Detecting HGT between closely related species or strains is challenging, as the phylogenetic signal is usually weak and the nucleotide composition is normally nearly identical. Nevertheless, there is a great importance in detecting HGT between congeneric species or strains, especially in clinical microbiology, where understanding the emergence of new virulent and drug-resistant strains is crucial, and often time-sensitive.</p>
<p>We developed a novel, self-contained technique named&nbsp;<em>Near HGT</em>, based on the&nbsp;<em>synteny index</em>, to measure the divergence of a gene from its native genomic environment and used it to identify candidate HGT events between closely related strains. The method confirms candidate transferred genes based on the&nbsp;<em>constant relative mutability</em>&nbsp;(CRM). Using CRM, the algorithm assigns a confidence score based on &ldquo;unusual&rdquo; sequence divergence. A gene exhibiting exceptional deviations according to both synteny and mutability criteria, is considered a validated HGT product. We first employed the technique to a set of three&nbsp;<em>E. coli</em>&nbsp;strains and detected several highly probable horizontally acquired genes. We then compared the method to existing HGT detection tools using a larger strain data set.</p>
<p>When combined with additional approaches our new algorithm provides richer picture and brings us closer to the goal of detecting all newly acquired genes in a particular strain.</p>
<p><strong>Availability:</strong><span>&nbsp;The method is publicly available at</span><a href="http://research.haifa.ac.il/~ssagi/software/nearHGT.zip">http://research.haifa.ac.il/~ssagi/software/nearHGT.zip</a></p><p>Address of the bookmark: <a href="http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004408" rel="nofollow">http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004408</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36216/crusview</guid>
	<pubDate>Thu, 12 Apr 2018 09:22:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36216/crusview</link>
	<title><![CDATA[CrusView]]></title>
	<description><![CDATA[<p><span>CrusView&nbsp;is a java based tool for karyotype/genome visualization and comparison of crucifer&nbsp;Species. It also integrates an binary version of KGBassembler and a&nbsp;post-modification step for its assembling result.</span></p><p>Address of the bookmark: <a href="http://www.cmbb.arizona.edu/?page_id=250" rel="nofollow">http://www.cmbb.arizona.edu/?page_id=250</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</guid>
	<pubDate>Thu, 23 Jun 2016 07:26:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</link>
	<title><![CDATA[WgSim]]></title>
	<description><![CDATA[<p>Reads simulator</p>
<p>Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simulate diploid genomes with SNPs and insertion/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution sequencing errors. It does not generate INDEL sequencing errors, but this can be partly compensated by simulating INDEL polymorphisms.<br><br>Wgsim outputs the simulated polymorphisms, and writes the true read coordinates as well as the number of polymorphisms and sequencing errors in read names. One can evaluate the accuracy of a mapper or a SNP caller with wgsim_eval.pl that comes with the package.<br><br></p><p>Address of the bookmark: <a href="https://github.com/lh3/wgsim" rel="nofollow">https://github.com/lh3/wgsim</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39017/macse-multiple-alignment-of-coding-sequences-accounting-for-frameshifts-and-stop-codons</guid>
	<pubDate>Mon, 18 Feb 2019 04:21:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39017/macse-multiple-alignment-of-coding-sequences-accounting-for-frameshifts-and-stop-codons</link>
	<title><![CDATA[MACSE: Multiple Alignment of Coding SEquences Accounting for Frameshifts and Stop Codons]]></title>
	<description><![CDATA[<p>MACSE aligns coding NT sequences with respect to their AA translation while allowing NT sequences to contain multiple frameshifts and/or stop codons. MACSE is hence the first automatic solution to align protein-coding gene datasets containing non-functional sequences (pseudogenes) without disrupting the underlying codon structure. It has also proved useful in detecting undocumented frameshifts in public database sequences and in aligning next-generation sequencing reads/contigs against a reference coding sequence.</p>
<p>For further details about the underlying algorithm see the original publication:<br><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0022594" target="_new">MACSE: Multiple Alignment of Coding SEquences accounting for frameshifts and stop codons.<br>Vincent Ranwez, S&eacute;bastien Harispe, Fr&eacute;d&eacute;ric Delsuc, Emmanuel JP Douzery<br>PLoS One 2011, 6(9): e22594</a>.</p><p>Address of the bookmark: <a href="https://bioweb.supagro.inra.fr/macse/index.php?menu=releases" rel="nofollow">https://bioweb.supagro.inra.fr/macse/index.php?menu=releases</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28121/kaiju</guid>
	<pubDate>Mon, 27 Jun 2016 11:23:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28121/kaiju</link>
	<title><![CDATA[Kaiju]]></title>
	<description><![CDATA[<p>Kaiju is a program for the taxonomic classification of metagenomic high-throughput sequencing reads. Each read is directly assigned to a taxon within the NCBI taxonomy by comparing it to a reference database containing microbial and viral protein sequences.</p>
<p>By default, Kaiju uses either the available complete genomes from NCBI RefSeq or the microbial subset of the non-redundant protein database <em>nr</em> used by NCBI BLAST, optionally also including fungi and microbial eukaryotes.</p>
<p>Kaiju translates reads into amino acid sequences, which are then searched in the database using a modified backward search on a memory-efficient implementation of the Burrows-Wheeler transform, which finds maximum exact matches (MEMs), optionally allowing mismatches in the protein alignment. The search can process up to millions of reads per minute using, for example, only 10 GB RAM with a protein database comprising 4821 microbial genomes. Kaiju can also be used for querying any other protein database without taxonomic classification, using either protein or nucleotide queries.</p>
<p>Kaiju is described in <a href="http://www.nature.com/ncomms/2016/160413/ncomms11257/full/ncomms11257.html">Menzel, P. et al. (2016) Fast and sensitive taxonomic classification for metagenomics with Kaiju. <em>Nat. Commun.</em> 7:11257</a> (open access).</p><p>Address of the bookmark: <a href="http://kaiju.binf.ku.dk/" rel="nofollow">http://kaiju.binf.ku.dk/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43952/elastic-blast</guid>
	<pubDate>Tue, 06 Sep 2022 18:14:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43952/elastic-blast</link>
	<title><![CDATA[Elastic BLAST !]]></title>
	<description><![CDATA[<p><a href="https://blast.ncbi.nlm.nih.gov/doc/elastic-blast/elasticblast.html?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=elasticblast-top3-20220823">ElasticBLAST</a>&nbsp;is a new way to&nbsp;<a href="https://blast.ncbi.nlm.nih.gov/?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=elasticblast-top3-20220823">BLAST</a>&nbsp;large numbers of queries, faster and on the cloud. Here are the top three reasons you should use ElasticBLAST:</p>
<h6><strong><img src="https://i0.wp.com/ncbiinsights.ncbi.nlm.nih.gov/wp-content/uploads/2022/08/ElasticBLAST_Larger-e1659978198941.png?resize=150%2C120&amp;ssl=1" alt="" width="150" height="120" style="border: 0px;">1. ElasticBLAST can handle much LARGER queries!&nbsp;</strong></h6>
<p>ElasticBLAST can search query sets that have&nbsp;<em>hundreds to millions of sequences</em>&nbsp;and against BLAST databases of all sizes.</p>
<h6><span><img src="https://i0.wp.com/ncbiinsights.ncbi.nlm.nih.gov/wp-content/uploads/2022/08/ElasticBLAST_Faster.png?resize=150%2C120&amp;ssl=1" alt="" width="150" height="120" style="border: 0px;">2. ElasticBLAST is FASTER</span></h6>
<p>ElasticBLAST distributes your searches across multiple cloud instances to process them simultaneously. The ability to scale resources in this way allows you to process large numbers of queries in a shorter time than you could with BLAST+.</p>
<h6><img src="https://i0.wp.com/ncbiinsights.ncbi.nlm.nih.gov/wp-content/uploads/2022/08/ElasticBLAST_Easy.png?resize=150%2C120&amp;ssl=1" alt="" width="150" height="120" style="border: 0px;">3. ElasticBLAST is EASY to run on the cloud<strong><br></strong></h6>
<p>ElasticBLAST is easy to set up using our step-by-step instructions&nbsp;<span>(</span><a href="https://blast.ncbi.nlm.nih.gov/doc/elastic-blast/quickstart-aws.html?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=elasticblast-top3-20220823" target="_blank"><span><span>Amazon Web&nbsp;</span><span>Services (AWS)</span></span></a><span>,&nbsp;</span><a href="https://blast.ncbi.nlm.nih.gov/doc/elastic-blast/quickstart-gcp.html?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=elasticblast-top3-20220823" target="_blank"><span>Google Cloud Platform (GCP)</span></a><span><span>)</span>&nbsp;<span>and</span>&nbsp;<span>allows&nbsp;</span><span>you&nbsp;</span><span>to leverage the power of</span><span>&nbsp;the&nbsp;</span><span>cloud. Once configured, i</span><span>t</span>&nbsp;<span>manages the software and database installation, handles partitioning of the BLAST workload among the various instances, and deallocates cloud resources when the searches are done.</span></span></p>
<p><span><span>ElasticBLAST</span>&nbsp;<span>also&nbsp;</span><span>selects the instance (</span><span>i.e.,</span><span>&nbsp;machine) type for you based on database size. Of course, you can also choose the instance type manually if you prefer</span><span>.&nbsp;</span></span></p><p>Address of the bookmark: <a href="https://blast.ncbi.nlm.nih.gov/doc/elastic-blast/" rel="nofollow">https://blast.ncbi.nlm.nih.gov/doc/elastic-blast/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/28425/advertisement-for-junior-research-fellowjrf-at-school-of-computational-and-integrative-sciences-jawaharlal-nehru-university</guid>
  <pubDate>Thu, 14 Jul 2016 07:24:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[Advertisement for Junior Research Fellow(JRF)  at School of Computational and Integrative Sciences  Jawaharlal Nehru University]]></title>
  <description><![CDATA[
<p>Advertisement for Junior Research Fellow(JRF) - (1)</p>

<p>Applications are invited for a post in DST, India funded Project entitled: "Positive and negative impacts of macromolecular crowding agents during target site location by DNA binding proteins – origin of optimal search at physiological ionic concentration (Reference Number: ECR/2016/000188) ''. The selected candidate will be appointed purely on temporary basis, initially for two years as a JRF that may be extended to one year of SRF based on the performance.</p>

<p>Position: Junior Research Fellow (1)</p>

<p>Qualifications &amp; Experience: Candidate must have a consistently good academic record with at least 60% marks in all throughout and must have qualified NET/GATE.</p>

<p>Desirable: Basic knowledge in the field of biophysics, molecular simulations and computational biology are desirable.</p>

<p>Salary: Consolidated Rs. 25,000 per month.</p>

<p>Tenure: The project duration is for three years and the selected candidate would be appointed after an interview. Appointment will be purely on temporary basis as stipulated by the existing rules of the University.</p>

<p>Interested candidates need to send an application to the address mentioned below mentioning the name of the project and post applied for (on the cover of the envelope).</p>

<p>The applications along with CV should be mailed at the address given below. Name, address, contact number and e. mail address of two referees must be enclosed with the application. The last date for the application is July 31st 2016.</p>

<p>Dr. Arnab Bhattacharjee (Principal Investigator) <br />Assistant Professor <br />School of Computational and Integrative Sciences <br />Jawaharlal Nehru University <br />New Delhi-110067 <br />E-mail: arnab@jnu.ac.in</p>

<p>Note: 1. Only shortlisted candidates will be communicated to appear in the interview at SCIS, JNU and no other communications in this regard will be entertained.</p>

<p>2. No TA/DA will be paid for appearing in interview.</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42965/nucl2vec-local-alignment-of-dna-sequences-using-distributed-vector-representation</guid>
	<pubDate>Tue, 16 Mar 2021 05:45:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42965/nucl2vec-local-alignment-of-dna-sequences-using-distributed-vector-representation</link>
	<title><![CDATA[Nucl2Vec: Local alignment of DNA sequences using Distributed Vector Representation]]></title>
	<description><![CDATA[<p><span>We demonstrate a novel approach for</span><span>local alignment of DNA reads with respect to reference genome.</span><span>For this process we have used Skip-gram model for creating</span><span>encoding(Nucl2Vec) and k-nearest neighbor for the alignment.</span><span>With our new approach we have reduced computation cost for</span><span>local alignment , while achieving accuracy comparable to existing</span><span>defacto standard BWA-MEM tool.</span> </p>
<p><em>https://prakharg24.github.io/papers/401851.full.pdf</em></p><p>Address of the bookmark: <a href="https://prakharg24.github.io/papers/401851.full.pdf" rel="nofollow">https://prakharg24.github.io/papers/401851.full.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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