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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37820?offset=130</link>
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	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38053/swgis-v20-a-seqword-genomic-island-sniffer</guid>
	<pubDate>Thu, 01 Nov 2018 12:35:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38053/swgis-v20-a-seqword-genomic-island-sniffer</link>
	<title><![CDATA[swgis v2.0 : a seqword genomic island sniffer]]></title>
	<description><![CDATA[<p><strong>swgis v2.0</strong>&nbsp;is the modified version of the seqword genomic island sniffer. this version is specifically optimized for predicting genomic islands in eukaryotic genomes. swgis v2.0 was tested on several eukaryotic species of different lineages. all identified genomic islands were deposited in the&nbsp;<a href="http://eugi.bi.up.ac.za/" title="Go to EuGI database">eugi database</a>.</p>
<p><a href="http://eugi.bi.up.ac.za/download_swgis/swgisv2.0.zip" title="Download SWGIS v2.0">download swgis v2.0</a></p><p>Address of the bookmark: <a href="http://eugi.bi.up.ac.za/eugi_download_swgis.php" rel="nofollow">http://eugi.bi.up.ac.za/eugi_download_swgis.php</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/38682/bourque-lab</guid>
  <pubDate>Mon, 14 Jan 2019 15:39:25 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bourque Lab]]></title>
  <description><![CDATA[
<p>The goal of the lab is to understand mammalian genomes using comparative genomic and epigenomic analyses. Areas of interest include: the evolution of regulatory sequences, the role of transposable elements in gene regulation and the impact of genome rearrangements in evolution and cancer.</p>

<p>As a computational genomicists our work involves examining billions of DNA base pairs and interpreting how variation impacts basic biology and disease. We develop computational methods and resources for the functional annotation of genomes with a special emphasis on sequencing-based assays (e.g. ChIP-seq, RNA-Seq, exome- and whole-genome sequencing, single-cell analysis).</p>

<p>http://www.computationalgenomics.ca</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44589/sourmash-quickly-search-compare-and-analyze-genomic-and-metagenomic-data-sets</guid>
	<pubDate>Sat, 06 Jul 2024 04:24:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44589/sourmash-quickly-search-compare-and-analyze-genomic-and-metagenomic-data-sets</link>
	<title><![CDATA[sourmash: Quickly search, compare, and analyze genomic and metagenomic data sets.]]></title>
	<description><![CDATA[<p dir="auto">sourmash is a k-mer analysis multitool, and we aim to provide stable, robust programmatic and command-line APIs for a variety of sequence comparisons. Some of our special sauce includes:</p>
<ul dir="auto">
<li><code>FracMinHash</code>&nbsp;sketching, which enables accurate comparisons (including ANI) between data sets of different sizes</li>
<li><code>sourmash gather</code>, a combinatorial k-mer approach for more accurate metagenomic profiling</li>
</ul>
<p dir="auto">Please see the&nbsp;<a href="https://sourmash.readthedocs.io/en/latest/publications.html#sourmash-fundamentals">sourmash publications</a>&nbsp;for details.</p>
<p dir="auto">The name is a riff off of&nbsp;<a href="https://github.com/marbl/Mash">Mash</a>, combined with @ctb's love of whiskey. (<a href="https://en.wikipedia.org/wiki/Sour_mash">Sour mash</a>&nbsp;is used in making whiskey.)</p>
<p dir="auto">Maintainers:&nbsp;<a href="mailto:titus@idyll.org">C. Titus Brown</a>&nbsp;(<a href="http://github.com/ctb">@ctb</a>),&nbsp;<a href="mailto:luiz@sourmash.bio">Luiz C. Irber, Jr</a>&nbsp;(<a href="http://github.com/luizirber">@luizirber</a>), and&nbsp;<a href="mailto:tessa@sourmash.bio">N. Tessa Pierce-Ward</a>&nbsp;(<a href="http://github.com/bluegenes">@bluegenes</a>).</p>
<p dir="auto">sourmash was initially developed by the&nbsp;<a href="http://ivory.idyll.org/lab/">Lab for Data-Intensive Biology</a>&nbsp;at the&nbsp;<a href="http://www.vetmed.ucdavis.edu/">UC Davis School of Veterinary Medicine</a>, and now includes contributions from the global research and developer community.</p><p>Address of the bookmark: <a href="https://github.com/sourmash-bio/sourmash" rel="nofollow">https://github.com/sourmash-bio/sourmash</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44894/dna2bit-an-ultra-fast-and-accurate-genomic-distance-estimation-software</guid>
	<pubDate>Sun, 31 Aug 2025 06:24:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44894/dna2bit-an-ultra-fast-and-accurate-genomic-distance-estimation-software</link>
	<title><![CDATA[dna2bit: an ultra-fast and accurate genomic distance estimation software]]></title>
	<description><![CDATA[<p><span>dna2bit is a software tool developed in C++11, leveraging the capabilities of OpenMP for parallel computing and the popcount technique for efficient bit manipulation. It has been thoroughly tested using the g++ and clang compilers on both Linux and MacOS platforms.</span></p><p>Address of the bookmark: <a href="https://github.com/lijuzeng/dna2bit" rel="nofollow">https://github.com/lijuzeng/dna2bit</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</guid>
	<pubDate>Thu, 13 Aug 2020 10:06:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</link>
	<title><![CDATA[PyParanoid: a pipeline for rapid identification of homologous gene families in a set of genomes]]></title>
	<description><![CDATA[<p>PyParanoid is a pipeline for rapid identification of homologous gene families in a set of genomes - a central task of any comparative genomics analysis. The "gold standard" for identifying homologs is to use reciprocal best hits (RBHs) which depends on performing a all-vs-all sequence comparison, usually using BLAST, to determine homology. However, these methods are computationally expensive, requiring&nbsp;O(n2)&nbsp;resources to identify RBHs. This is problematic, as the modern deluge of sequencing data means that comparative genomics analyses could be performed on datasets of thousands of strains.</p><p>Address of the bookmark: <a href="https://github.com/ryanmelnyk/PyParanoid" rel="nofollow">https://github.com/ryanmelnyk/PyParanoid</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45212/assistant-professor-in-rapid-marine-adaptation-uvienna</guid>
  <pubDate>Mon, 03 Aug 2026 06:52:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor in Rapid Marine Adaptation @ UVienna]]></title>
  <description><![CDATA[
<p>The University of Vienna invites applications for a Tenure Track Professorship in the field of Rapid Marine Adaptation. We seek a scientist with an outstanding record in marine evolutionary genomics who investigates rapid evolutionary responsesâ€”such as evolutionary rescueâ€”through field studies and/or experimental evolution in the laboratory. Preferred model systems should be eukaryotic marine organisms that have vital roles in oceanic or coastal ecosystems. The successful candidate will cooperate with physiologists, ecologists, biochemists, systems biologists and evolutionary biologists in Vienna to link genomic targets of selection to organismal phenotypes and local environmental conditions. This integrative work will advance mechanistic understanding and predictive modeling of rapid adaptation to climate change in marine environments and inform effective marine conservation strategies across Europe.<br />For more information see: https://jobs.univie.ac.at/job/Tenure-Track-Professorship-in-Rapid-Marine-Adaptation/1417563233/</p>
]]></description>
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<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>
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	<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>
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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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	<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>
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