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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36994?offset=90</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/44640/new-blast-core-nucleotide-database-core-nt</guid>
	<pubDate>Tue, 13 Aug 2024 07:12:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/44640/new-blast-core-nucleotide-database-core-nt</link>
	<title><![CDATA[New BLAST Core Nucleotide Database (core_nt)]]></title>
	<description><![CDATA[<p><span>The Core Nucleotide Database (core_nt) is now the default nucleotide BLAST database. Core_nt is also available on the command line. You get faster searches &amp; more focused results.</span></p><p><span><span>Core_nt contains the same eukaryotic transcript and gene-related sequences as nt. The core_nt database is nt without most eukaryotic chromosome sequences. Most nucleotide BLAST searches with core_nt will be similar to the nt database. However, core_nt is better than nt for accomplishing your most common BLAST search goals, such as identifying gene-related sequences like transcript sequences and complete bacterial chromosomes. This is because, in recent years, nt has acquired more low-relevance, non-annotated, and non-gene&nbsp;<span>content.&nbsp;</span></span></span></p><p><span> Learn more:&nbsp;https://ncbiinsights.ncbi.nlm.nih.gov/2024/07/18/new-blast-core-nucleotide-database/</span></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/43656/special-nucleotide-characters-symbols</guid>
	<pubDate>Thu, 16 Dec 2021 23:37:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/43656/special-nucleotide-characters-symbols</link>
	<title><![CDATA[Special Nucleotide Characters / Symbols !]]></title>
	<description><![CDATA[<h2 style="text-align: center;">Nucleotide symbols</h2><table style="margin: auto;" width="95%" border="1" cellpadding="5">
<tbody>
<tr>
<td align="center">Nucleotide symbol</td>
<td align="center">Full Name</td>
</tr>
<tr>
<td align="center">A</td>
<td align="center">Adenine</td>
</tr>
<tr>
<td align="center">C</td>
<td align="center">Cytosine</td>
</tr>
<tr>
<td align="center">G</td>
<td align="center">Guanine</td>
</tr>
<tr>
<td align="center">T</td>
<td align="center">Thymine</td>
</tr>
<tr>
<td align="center">U</td>
<td align="center">Uracil</td>
</tr>
<tr>
<td align="center">R</td>
<td align="center">Guanine / Adenine (purine)</td>
</tr>
<tr>
<td align="center">Y</td>
<td align="center">Cytosine / Thymine (pyrimidine)</td>
</tr>
<tr>
<td align="center">K</td>
<td align="center">Guanine / Thymine</td>
</tr>
<tr>
<td align="center">M</td>
<td align="center">Adenine / Cytosine</td>
</tr>
<tr>
<td align="center">S</td>
<td align="center">Guanine / Cytosine</td>
</tr>
<tr>
<td align="center">W</td>
<td align="center">Adenine / Thymine</td>
</tr>
<tr>
<td align="center">B</td>
<td align="center">Guanine / Thymine / Cytosine</td>
</tr>
<tr>
<td align="center">D</td>
<td align="center">Guanine / Adenine / Thymine</td>
</tr>
<tr>
<td align="center">H</td>
<td align="center">Adenine / Cytosine / Thymine</td>
</tr>
<tr>
<td align="center">V</td>
<td align="center">Guanine / Cytosine / Adenine</td>
</tr>
<tr>
<td align="center">N</td>
<td align="center">Adenine / Guanine / Cytosine / Thymine</td>
</tr>
</tbody>
</table>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43770/chromeister-an-ultra-fast-heuristic-approach-to-detect-conserved-signals-in-extremely-large-pairwise-genome-comparisons</guid>
	<pubDate>Thu, 03 Feb 2022 04:01:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43770/chromeister-an-ultra-fast-heuristic-approach-to-detect-conserved-signals-in-extremely-large-pairwise-genome-comparisons</link>
	<title><![CDATA[chromeister: An ultra fast, heuristic approach to detect conserved signals in extremely large pairwise genome comparisons.]]></title>
	<description><![CDATA[<p>chromeister: An ultra fast, heuristic approach to detect conserved signals in extremely large pairwise genome comparisons.</p>
<p dir="auto">USAGE:</p>
<ul dir="auto">
<li>-query: sequence A in fasta format</li>
<li>-db: sequence B in fasta format</li>
<li>-out: output matrix</li>
<li>-kmer Integer: k&gt;1 (default 32) Use 32 for chromosomes and genomes and 16 for small bacteria</li>
<li>-diffuse Integer: z&gt;0 (default 4) Use 4 for everything - if using large plant genomes you can try using 1</li>
<li>-dimension Size of the output matrix and plot. Integer: d&gt;0 (default 1000) Use 1000 for everything that is not full genome size, where 2000 is recommended</li>
</ul><p>Address of the bookmark: <a href="https://github.com/estebanpw/chromeister" rel="nofollow">https://github.com/estebanpw/chromeister</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/27459/tools-for-searching-repeats-and-palindromic-sequences</guid>
	<pubDate>Sat, 21 May 2016 22:32:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/27459/tools-for-searching-repeats-and-palindromic-sequences</link>
	<title><![CDATA[Tools for Searching Repeats And Palindromic Sequences]]></title>
	<description><![CDATA[<p>What are genomic interspersed repeats?</p><p>In the mid 1960's scientists discovered that many genomes contain stretches of highly repetitive DNA sequences ( see Reassociation Kinetics Experiments, and C-Value Paradox ). These sequences were later characterized and placed into five categories:</p><p><strong>Simple Repeats</strong> - Duplications of simple sets of DNA bases (typically 1-5bp) such as A, CA, CGG etc.<br /><strong>Tandem Repeats</strong> - Typically found at the centromeres and telomeres of chromosomes these are duplications of more complex 100-200 base sequences.<br /><strong>Segmental Duplications</strong> - Large blocks of 10-300 kilobases which are that have been copied to another region of the genome.<br /><strong>Interspersed Repeats</strong><br />Processed Pseudogenes, Retrotranscripts, SINES - Non-functional copies of RNA genes which have been reintegrated into the genome with the assitance of a reverse transcriptase.<br />DNA Transposons<br />Retrovirus Retrotransposons<br />Non-Retrovirus Retrotransposons ( LINES )</p><p>Currently up to 50% of the human genome is repetitive in nature and as improvements are made in detection methods this number is expected to increase.</p><p>On the other hand; In genetics, the term palindrome refers to a sequence of nucleotides along a DNA (deoxyribonucleic acid) or RNA (ribonucleic acid) strand that contains the same series of nitrogenous bases regardless from which direction the strand is analyzed. Akin to a language palindrome&mdash;wherein a word or phrase is spelled the same left-to-right as right-to-left (e.g., the word RADAR or the phrase "able was I ere I saw elba")&mdash;with genetic palindromes it does not matter whether the nucleic acid strand is read starting from the 3' (three prime) end or the 5' (five prime) end of the strand.</p><p>Recent research on palindromes centers on understanding palindrome formation during gene amplification. Other studies have attempted to relate palindrome formation to molecular mechanisms involved in double stranded breaks and in the formation of inverted repeats. Assisted by high speed computers, other groups of scientists link palindrome formation to the conservation of genetic information.</p><p>Related to the direction of transcription by RNA polymerase, DNA strands have upstream and downstream terminus defined by differing chemical groups at each end. The ends of each strand of DNA or RNA are termed the 5' (phosphate bound to the 5' position carbon) and 3' (phosphate bound to the 3' carbon) ends to indicate a polarity within the molecule. Using the letters A, T, C, G, to represent the nitrogenous bases adenine, thymine, cytosine, and guanine found in DNA, and the letters A, U, C, G to represent the nitrogenous bases adenine, uracil, cytosine, guanine found in RNA (Note that uracil in RNA replaces the thymine found in DNA), geneticists usually represent DNA by a series of base codes (e.g., 5' AATCGGATTGCA 3'). The base codes are usually arranged from the 5' end to the 3' end.</p><p>Because of specific base pairing in DNA (i.e., adenine (A) always bonds with (thymine (T) and cytosine (C) always bonds with guanine (G)) the complimentary stand to the sequence 5' AATCGGATTGCA 3' would be 3' TTAGCCTAACGT 5'.</p><p>With palindromes the sequences on the complimentary strands read the same in either direction. For example, a sequence of 5' GAATTC3' on one strand would be complimented by a 3' CTTAAG 5' strand. In either case, when either strand is read from the 5' prime end the sequence is GAATTC. Another example of a palindrome would be the sequence 5' CGAAGC 3' that, when reversed, still reads CGAAGC.</p><p>Palindromes are important sequences within nucleic acids. Often they are the site of binding for specific enzymes (e.g., restriction endobucleases) designed to cut the DNA strands at specific locations (i.e., at palindromes).</p><p>Palindromes may arise from brakeage and chromosomal inversions that form inverted repeats that compliment each other. When a palindrome results from an inversion, it is often referred to as an inverted repeat. For example, the sequence 5' CGAAGC 3', if inverted (reversed 180&deg;), still reads CGAAGC.</p><p>The <a href="http://emboss.open-bio.org/">European Molecular Biology Open Software Suite (EMBOSS)</a> includes some basic tools for finding tandem repeats and inverted repeats (see <a href="http://emboss.open-bio.org/html/use/apbs06.html#GroupsAppsTableNucleicrepeatsR6">B.6.22. Applications in group Nucleic:repeats</a>). There are many on-line services providing the EMBOSS tools, for example:</p><ul>
<li>Wageningen Bioinformatics Webportal <a href="http://emboss.bioinformatics.nl/">EMBOSS explorer</a></li>
<li><a href="http://mobyle.pasteur.fr/">Mobyle@Pasteur</a></li>
<li><a href="http://wsembnet.vital-it.ch/">Soaplab2 Web Services at Vital-IT</a></li>
</ul><p>For more sophisticated repeat finding you will want to look at tools using <a href="http://www.girinst.org/repbase/">Repbase</a> for example:</p><ul>
<li>CENSOR
<ul>
<li><a href="http://www.girinst.org/censor/">CENSOR@GIRI</a></li>
<li><a href="http://www.ebi.ac.uk/Tools/so/censor/">CENSOR@EMBL-EBI</a></li>
</ul>
</li>
<li><a href="http://www.repeatmasker.org/">RepeatMasker</a></li>
<li><a href="http://mummer.sourceforge.net/">MUMmer</a>&nbsp;(scan_for_match)</li>
<li><a href="http://emboss.bioinformatics.nl/cgi-bin/emboss/palindrome">Emboss Palindrome</a></li>
</ul><p>Other nucleotide repeat finding methods found by a couple of web searches:</p><ul>
<li><a href="http://tandem.bu.edu/trf/trf.html">Tandem Repeats Finder</a></li>
<li><a href="http://selab.janelia.org/recon.html">RECON</a></li>
<li><a href="http://www.yandell-lab.org/software/repeatrunner.html">RepeatRunner</a></li>
<li><a href="http://bibiserv.techfak.uni-bielefeld.de/reputer/">REPuter</a></li>
<li><a href="http://210.212.215.200/IMEX/index.html">Imperfect Microsatellite Extractor (IMEx)</a></li>
<li><a href="http://www.imtech.res.in/raghava/srf/">Spectral Repeat Finder (SRF)</a></li>
<li><a href="http://zlab.bu.edu/repfind/form.html">REPFIND</a></li>
<li><a href="http://crispr.u-psud.fr/Server/CRISPRfinder.php">CRISPRfinder</a></li>
<li><a href="http://grail.lsd.ornl.gov/grailexp/">GrailEXP</a></li>
<li><a href="http://alggen.lsi.upc.edu/recerca/search/frame-search.html">CONREPP</a></li>
<li><a href="http://www.biophp.org/minitools/find_palindromes/demo.php%20"><span>find_palindromes</span></a></li>
<li><a href="http://insilico.ehu.eus/palindromes/"><span>Palindrome</span></a></li>
<li><a href="http://emboss.bioinformatics.nl/cgi-bin/emboss/palindrome">EMBOSS Palindrome</a></li>
<li><a href="http://bioinfo.cs.technion.ac.il/projects/Engel-Freund/new.html">Palindrome Search</a></li>
</ul>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39821/gvolante-completeness-assessment-of-genometranscriptome-sequences</guid>
	<pubDate>Tue, 06 Aug 2019 21:37:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39821/gvolante-completeness-assessment-of-genometranscriptome-sequences</link>
	<title><![CDATA[gVolante: Completeness Assessment of Genome/Transcriptome Sequences]]></title>
	<description><![CDATA[<p><strong>gVolante</strong><span>&nbsp;provides an online interface for completeness assessment of user&rsquo;s original or publicly available sequence datasets as well as for browsing results of completeness assessment performed on publicly available genome and transcriptome assemblies.</span></p>
<p><img src="https://gvolante.riken.jp/images/assessment.png" width="937" height="545" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://gvolante.riken.jp/" rel="nofollow">https://gvolante.riken.jp/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<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>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37751/kast-perform-alignment-free-k-tuple-frequency-comparisons-from-sequences</guid>
	<pubDate>Thu, 20 Sep 2018 08:56:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37751/kast-perform-alignment-free-k-tuple-frequency-comparisons-from-sequences</link>
	<title><![CDATA[KAST: Perform Alignment-free k-tuple frequency comparisons from sequences]]></title>
	<description><![CDATA[<p><span>Perform Alignment-free k-tuple frequency comparisons from sequences. This can be in the form of two input files (e.g. a reference and a query) or a single file for pairwise comparisons to be made.</span></p><p>Address of the bookmark: <a href="https://github.com/martinjvickers/KAST" rel="nofollow">https://github.com/martinjvickers/KAST</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38385/decipher-a-software-toolset-for-deciphering-and-managing-biological-sequences-efficiently-using-the-r</guid>
	<pubDate>Sun, 09 Dec 2018 19:06:17 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38385/decipher-a-software-toolset-for-deciphering-and-managing-biological-sequences-efficiently-using-the-r</link>
	<title><![CDATA[DECIPHER; a software toolset for deciphering and managing biological sequences efficiently using the R]]></title>
	<description><![CDATA[<p><span>DECIPHER is a software toolset that can be used for deciphering and managing biological sequences efficiently using the&nbsp;</span><a href="http://www.r-project.org/">R</a><span>&nbsp;programming language. The&nbsp;</span><a href="http://www.r-project.org/">R</a><span>&nbsp;package is distributed as platform independent source code under the&nbsp;</span><a href="http://www.gnu.org/copyleft/gpl.html">GPL version 3 license</a><span>. Some functionality of the program is accessible online through web tools.</span></p>
<p><span style="font-size: medium; text-align: justify;">&nbsp;</span></p><p>Address of the bookmark: <a href="http://www2.decipher.codes/" rel="nofollow">http://www2.decipher.codes/</a></p>]]></description>
	<dc:creator>BioStar</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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41493/coronavirus-resources</guid>
	<pubDate>Wed, 25 Mar 2020 17:11:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41493/coronavirus-resources</link>
	<title><![CDATA[Coronavirus Resources !]]></title>
	<description><![CDATA[<p><span>2019nCoVR features comprehensive integration of genomic and proteomic sequences as well as their metadata information from the GISAID, NCBI, NMDC and CNCB/NGDC. It also incorporates a wide range of relevant information including scientific literatures, news, and popular articles for science dissemination, and provides visualization functionalities for genome variation analysis results based on all collected 2019-nCoV strains.</span></p>
<p><span>Annotation</span></p>
<p><span><a href="https://bigd.big.ac.cn/ncov/variation/annotation">https://bigd.big.ac.cn/ncov/variation/annotation</a></span></p>
<p><span>Genome wharehouse&nbsp;</span></p>
<p><span><a href="https://bigd.big.ac.cn/gwh/browse/index">https://bigd.big.ac.cn/gwh/browse/index</a></span></p>
<p>Released Genome</p>
<p><a href="https://bigd.big.ac.cn/ncov/release_genome">https://bigd.big.ac.cn/ncov/release_genome</a></p>
<p>Download data&nbsp;</p>
<p><a href="ftp://download.big.ac.cn/Genome/Viruses/Coronaviridae/">ftp://download.big.ac.cn/Genome/Viruses/Coronaviridae/</a></p>
<p>Raw data</p>
<p><a href="https://bigd.big.ac.cn/gsa/browse/run/?tag=Coronaviridae">https://bigd.big.ac.cn/gsa/browse/run/?tag=Coronaviridae</a></p><p>Address of the bookmark: <a href="https://bigd.big.ac.cn/ncov/about" rel="nofollow">https://bigd.big.ac.cn/ncov/about</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

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