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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/33479?offset=40</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41689/medaka-sequence-correction-provided-by-ont-research</guid>
	<pubDate>Mon, 18 May 2020 16:28:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41689/medaka-sequence-correction-provided-by-ont-research</link>
	<title><![CDATA[medaka: Sequence correction provided by ONT Research]]></title>
	<description><![CDATA[<p><code>medaka</code><span>&nbsp;is a tool to create a consensus sequence from nanopore sequencing data. This task is performed using neural networks applied from a pileup of individual sequencing reads against a draft assembly. It outperforms graph-based methods operating on basecalled data, and can be competitive with state-of-the-art signal-based methods, whilst being much faster.</span></p><p>Address of the bookmark: <a href="https://github.com/nanoporetech/medaka" rel="nofollow">https://github.com/nanoporetech/medaka</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43995/tools-for-sequence-translation</guid>
	<pubDate>Tue, 08 Nov 2022 03:37:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43995/tools-for-sequence-translation</link>
	<title><![CDATA[Tools for Sequence translation !]]></title>
	<description><![CDATA[<p><span>BOrf</span>&nbsp;-&nbsp;<a href="https://github.com/betsig/borf" target="_blank">https://github.com/betsig/borf</a></p><p><span>CodAn</span>&nbsp;-&nbsp;<a href="https://github.com/pedronachtigall/CodAn" target="_blank">https://github.com/pedronachtigall/CodAn</a></p><p><span>EMBOSS-Sixpack</span>&nbsp;-&nbsp;<a href="https://www.ebi.ac.uk/Tools/st/emboss_sixpack/" target="_blank">https://www.ebi.ac.uk/Tools/st/emboss_sixpack/</a></p><p><span>esl-translate</span>&nbsp;-&nbsp;<a href="http://hmmer.org/" target="_blank">http://hmmer.org/</a>,&nbsp;<a href="https://github.com/EddyRivasLab/easel" target="_blank">https://github.com/EddyRivasLab/easel</a></p><p><span>GeneMarkS-T</span>&nbsp;-&nbsp;<a href="http://exon.gatech.edu/GeneMark/license_download.cgi" target="_blank">http://exon.gatech.edu/GeneMark/license_download.cgi</a></p><p><span>ORFfinder</span>&nbsp;-&nbsp;<a href="https://www.ncbi.nlm.nih.gov/orffinder/" target="_blank">https://www.ncbi.nlm.nih.gov/orffinder/</a>&nbsp;(web server)</p><p><span>PLASS</span>&nbsp;-&nbsp;<a href="https://github.com/soedinglab/plass" target="_blank">https://github.com/soedinglab/plass</a></p><p><span>Prodigal</span>&nbsp;-&nbsp;<a href="https://github.com/hyattpd/Prodigal" target="_blank">https://github.com/hyattpd/Prodigal</a></p><p><span>TransDecoder</span>&nbsp;-&nbsp;<a href="https://github.com/TransDecoder/TransDecoder" target="_blank">https://github.com/TransDecoder/TransDecoder</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/fun/view/4196/chemical-elements-of-bioinformatics</guid>
	<pubDate>Tue, 03 Sep 2013 16:35:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/fun/view/4196/chemical-elements-of-bioinformatics</link>
	<title><![CDATA[Chemical Elements of Bioinformatics]]></title>
	<description><![CDATA[<p>You must be familiar with periodic table and colour pattern, but this time you are going to amaze by new elements table by Eagle genomics. Just check it out and have fun :)</p><p><a href="http://elements.eaglegenomics.com/">http://elements.eaglegenomics.com/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33942/mulan-multiple-sequence-local-alignment-and-conservation-visualization-tool</guid>
	<pubDate>Thu, 20 Jul 2017 08:02:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33942/mulan-multiple-sequence-local-alignment-and-conservation-visualization-tool</link>
	<title><![CDATA[Mulan: MUltiple sequence Local AligNment and conservation visualization tool]]></title>
	<description><![CDATA[<p><span>Mulan performs multiple (2 or more) sequence alignments with an efficient and rapid "full local" alignment strategy that ensures a recapitulation of evolutionary sequence rearrangements (such as inversions and reshuffling) in any of the species. It combines&nbsp;</span><a href="http://www.bx.psu.edu/miller_lab/" target="_new"><em>refine</em>&nbsp;and&nbsp;<em>tba</em></a><span>&nbsp;tools to align either "draft" or "finished" quality sequences. Mulan provides a dynamic graphical interface to align and visualize conservation profiles for evolutionarily distant and closely related species.</span><br><span></span></p>
<p><span>Input formats, automated data upload from the&nbsp;</span><a href="http://genome.ucsc.edu/" target="_new">UCSC Genome Browser</a><span>, gene annotation, annotation of repetitive elements, and progress report were previously described in the&nbsp;</span><a href="https://zpicture.dcode.org/zpInstructions.html" target="_zp">zPicture instructions</a><span>&nbsp;and we refer the users to these materials for more details. This introduction is mainly focused on some novel features unique to the Mulan.</span><span><br></span></p><p>Address of the bookmark: <a href="https://mulan.dcode.org/mulanInstructions.php" rel="nofollow">https://mulan.dcode.org/mulanInstructions.php</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34493/plast-a-fast-accurate-and-ngs-scalable-bank-to-bank-sequence-similarity-search-tool</guid>
	<pubDate>Fri, 01 Dec 2017 04:10:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34493/plast-a-fast-accurate-and-ngs-scalable-bank-to-bank-sequence-similarity-search-tool</link>
	<title><![CDATA[PLAST: A fast, accurate and NGS scalable bank-to-bank sequence similarity search tool]]></title>
	<description><![CDATA[<p><strong>PLAST is a fast, accurate and NGS scalable bank-to-bank sequence similarity search tool providing significant accelerations of seeds-based heuristic comparison methods, such as the Blast suite of algorithms.</strong></p>
<p><strong>Relying on unique software architecture, PLAST takes full advantage of recent multi-core personal computers without requiring any additional hardware devices.</strong></p>
<p>PLAST stands for&nbsp;<em>Parallel Local Sequence Alignment Search Tool&nbsp;</em>and is was&nbsp;<a href="http://www.biomedcentral.com/1471-2105/10/329" target="_blank">published in BMC Bioinformatics.</a></p>
<p>PLAST is a general purpose sequence comparison tool providing the following benefits:</p>
<ul>
<li>PLAST is a high-performance sequence comparison tool designed to compare two sets of sequences (query vs. reference),</li>
<li>Reduces the processing time of sequences comparisons while providing highest quality results,</li>
<li>Contains a fully integrated data filtering engine capable of selecting relevant hits with user-defined criteria (E-Value, identity, coverage, alignment length, etc.),</li>
<li>Does not require any additional hardware, since it is a software solution. It is easy to install, cost-effective, takes full advantage of multi-core processors and uses a small RAM footprint,</li>
<li>Ready to be used on desktop computer, cluster, cloud as well as within distributed system running Hadoop.</li>
</ul>
<p>https://plast.inria.fr/</p><p>Address of the bookmark: <a href="https://plast.inria.fr/" rel="nofollow">https://plast.inria.fr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36711/ancestral-sequence-reconstruction-steps</guid>
	<pubDate>Fri, 18 May 2018 08:28:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36711/ancestral-sequence-reconstruction-steps</link>
	<title><![CDATA[Ancestral sequence reconstruction steps !]]></title>
	<description><![CDATA[<div><strong>Ancestral sequence reconstruction</strong>&nbsp;(<strong>ASR</strong>) &ndash; also known as&nbsp;<strong>ancestral gene</strong>/<strong>sequence reconstruction</strong>/<strong>resurrection</strong>&nbsp;&ndash; is a technique used in the study of&nbsp;molecular evolution. The method consists of the synthesis of an ancestral&nbsp;gene&nbsp;and expression of the corresponding ancestral&nbsp;protein.&nbsp;<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-thornton-1"></a>The idea of protein 'resurrection' was suggested in 1963 by Pauling and Zuckerkandl.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-2"></a>&nbsp;Some early efforts were made in the eighties-nineties, led by the laboratory of&nbsp;Steven A. Benner, showing the potential of this technique &ndash; one that only started to be fulfilled in the post-genomic era.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-3"></a>&nbsp;Thanks to the improvement of algorithms and of better sequencing and synthesis techniques, the method was developed further in the early 2000s to allow the resurrection of a greater variety of and much more ancient genes.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-4"></a>&nbsp;Over the last decade, ancestral protein resurrection has developed as a strategy to reveal the mechanisms and dynamics of protein evolution.&nbsp;</div><div>&nbsp;</div><div>BEAST is the best way to predict the ancestral structure. but, I suggest following steps?</div><div>&nbsp;</div><div>1- Alignments "Mafft -&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fmafft.cbrc.jp%2Falignment%2Fsoftware%2Fsource.html" target="_blank">http://mafft.cbrc.jp/alignment/software/source.html</a>"</div><div>mafft --maxiterate 1000 --reorder --thread 24 --genafpair Dataset.fasta &gt; Dataset_Alig.fasta</div><div>&nbsp;</div><div>2- Your dataset has a good phylogenetic signal, is possible to perform with Tree-Puzzle "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.tree-puzzle.de" target="_blank">http://www.tree-puzzle.de</a>";</div><div>&nbsp;</div><div id="yui_3_14_1_1_1526649596608_1443">3 - This dataset which the saturation index, I perform with "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fdambe.bio.uottawa.ca%2Fdambe.asp" target="_blank">http://dambe.bio.uottawa.ca/dambe.asp</a>";</div><div>&nbsp;</div><div>4- Has evidence of possible recombination in your dataset, the evaluate if this presence or absence, because this may to influence the grouping of clades, I perform with</div><div>---recombination</div><div>&nbsp;</div><div>4.1- Phi-test, implemented in SplitTree4"<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.splitstree.org" target="_blank">http://www.splitstree.org</a>", (.nex file)</div><div>&nbsp;</div><div>4.2- GARD deployed in webserver in the DataMonkey "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.datamonkey.org%2F" target="_blank">http://www.datamonkey.org/</a>" - turning to the amino acid seaview -&gt; view proteins -&gt; save as ...) Ideally do a tree-based groups.</div><div>&nbsp;</div><div>4.3- RDP4 for download and installation on Windows in "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fweb.cbio.uct.ac.za%2F~darren%2Frdp.html" target="_blank">http://web.cbio.uct.ac.za/~darren/rdp.html</a>"</div><div>&nbsp;</div><div>4.4- Hyphy (Mac, Windows, Linux) in "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fhyphy.org%2Fw%2Findex.php%2FDownload" target="_blank">http://hyphy.org/w/index.php/Download</a>"</div><div>&nbsp;</div><div>4.5- Path-o-Gen (temporal structure of a tree input file -&gt; arquivo.tre)</div><div>These steps above, I call of pre-processing to inferences phylogenetic...</div><div>&nbsp;</div><div>5- Perform phylogenetic tree, used Bayesian Inference with Molecular Clock, but is necessary Clock Testing:</div><div>&nbsp;</div><div>- This step is performed with program Beast (Beauti, Beast and TreeAnnotator), and Tracer_v1.5 more FigTree to inspection.</div><div>&nbsp;</div><div>- Tutorials:&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fbeast.bio.ed.ac.uk%2Ftutorials" target="_blank">http://beast.bio.ed.ac.uk/tutorials</a></div><div>- Downloads:&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fbeast.bio.ed.ac.uk%2Fdownloads" target="_blank">http://beast.bio.ed.ac.uk/downloads</a></div>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37962/wtdbg2-a-de-novo-sequence-assembler-for-long-noisy-reads-produced-by-pacbio-or-oxford-nanopore</guid>
	<pubDate>Fri, 19 Oct 2018 08:48:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37962/wtdbg2-a-de-novo-sequence-assembler-for-long-noisy-reads-produced-by-pacbio-or-oxford-nanopore</link>
	<title><![CDATA[Wtdbg2: a de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore]]></title>
	<description><![CDATA[<p><span>Wtdbg2 is a&nbsp;</span><em>de novo</em><span>&nbsp;sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies (ONT). It assembles raw reads without error correction and then builds the consensus from intermediate assembly output. Wtdbg2 is able to assemble the human and even the 32Gb&nbsp;</span><a href="https://www.nature.com/articles/nature25458">Axolotl</a><span>&nbsp;genome at a speed tens of times faster than&nbsp;</span><a href="https://github.com/marbl/canu">CANU</a><span>&nbsp;and&nbsp;</span><a href="https://github.com/PacificBiosciences/FALCON">FALCON</a><span>while producing contigs of comparable base accuracy.</span></p><p>Address of the bookmark: <a href="https://github.com/ruanjue/wtdbg2" rel="nofollow">https://github.com/ruanjue/wtdbg2</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39372/irnad-a-computational-tool-for-identifying-d-modification-sites-in-rna-sequence</guid>
	<pubDate>Thu, 16 May 2019 00:20:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39372/irnad-a-computational-tool-for-identifying-d-modification-sites-in-rna-sequence</link>
	<title><![CDATA[iRNAD: a computational tool for identifying D modification sites in RNA sequence]]></title>
	<description><![CDATA[<p><span>iRNAD, for identifying D modification sites in RNA sequence. In this predictor, the RNA samples derived from five species were encoded by nucleotide chemical property and nucleotide density. Support vector machine was utilized to perform the classification.&nbsp;</span></p>
<p><span><a href="http://lin-group.cn/server/iRNAD/">http://lin-group.cn/server/iRNAD/</a></span></p><p>Address of the bookmark: <a href="http://lin-group.cn/server/iRNAD/" rel="nofollow">http://lin-group.cn/server/iRNAD/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39881/apollo-a-sequence-annotation-editor</guid>
	<pubDate>Tue, 27 Aug 2019 08:08:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39881/apollo-a-sequence-annotation-editor</link>
	<title><![CDATA[Apollo: a sequence annotation editor]]></title>
	<description><![CDATA[<p><span>The well-established inaccuracy of purely computational methods for annotating genome sequences necessitates an interactive tool to allow biological experts to refine these approximations by viewing and independently evaluating the data supporting each annotation. Apollo was developed to meet this need, enabling curators to inspect genome annotations closely and edit them</span></p><p>Address of the bookmark: <a href="https://genomebiology.biomedcentral.com/articles/10.1186/gb-2002-3-12-research0082" rel="nofollow">https://genomebiology.biomedcentral.com/articles/10.1186/gb-2002-3-12-research0082</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40594/gfaviz-flexible-and-interactive-visualization-of-gfa-sequence-graphs</guid>
	<pubDate>Thu, 23 Jan 2020 07:33:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40594/gfaviz-flexible-and-interactive-visualization-of-gfa-sequence-graphs</link>
	<title><![CDATA[GfaViz: flexible and interactive visualization of GFA sequence graphs]]></title>
	<description><![CDATA[<p><span>GFA (Graphical Fragment Assembly) is an emerging standard format for representing sequence graphs. Although it was originally conceived as a format for sequence assembly (hence the name), and this remains its core application, it is more general, and able to represent many different types of sequence graphs, including scaffolding graphs, alignment graphs, variant graphs and splicing graphs.</span></p><p>Address of the bookmark: <a href="https://github.com/ggonnella/gfaviz" rel="nofollow">https://github.com/ggonnella/gfaviz</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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