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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38310?offset=80</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/43728/short-read-assembly-using-spades</guid>
	<pubDate>Mon, 31 Jan 2022 07:18:16 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/43728/short-read-assembly-using-spades</link>
	<title><![CDATA[Short-read assembly using Spades !]]></title>
	<description><![CDATA[<h2 id="short-read-assembly-a-comparison">If we only had Illumina reads, we could also assemble these using the tool Spades.</h2><p>You can try this here, or try it later on your own data.</p><h2 id="get-data">Get data</h2><p>We will use the same Illumina data as we used above:</p><ul>
<li>illumina_R1.fastq.gz: the Illumina forward reads</li>
<li>illumina_R2.fastq.gz: the Illumina reverse reads</li>
</ul><h2 id="assemble">Assemble</h2><p>Run Spades:</p><div><pre>spades.py -1 illumina_R1.fastq.gz -2 illumina_R2.fastq.gz --careful --cov-cutoff auto -o spades_assembly_all_illumina
</pre></div><ul>
<li><code>-1</code>&nbsp;is input file of forward reads</li>
<li><code>-2</code>&nbsp;is input file of reverse reads</li>
<li><code>--careful</code>&nbsp;minimizes mismatches and short indels</li>
<li><code>--cov-cutoff auto</code>&nbsp;computes the coverage threshold (rather than the default setting, &ldquo;off&rdquo;)</li>
<li><code>-o</code>&nbsp;is the output directory</li>
</ul><h2 id="results">Results</h2><p>Move into the output directory and look at the contigs:</p><div><pre>infoseq contigs.fasta</pre></div>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36384/binding-site-prediction-in-protein</guid>
	<pubDate>Wed, 25 Apr 2018 04:35:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36384/binding-site-prediction-in-protein</link>
	<title><![CDATA[Binding Site Prediction in Protein !]]></title>
	<description><![CDATA[<p><span>The interaction between proteins and other molecules is fundamental to all biological functions. In this section we include tools that can assist in prediction of interaction sites on protein surface and tools for predicting the structure of the intermolecular complex formed between two or more molecules (docking).</span></p><h4>Pockets Identification</h4><p><a href="http://sts.bioengr.uic.edu/castp/" target="_blank">CASTp</a></p><div style="text-align: justify;">Automatic Identification of pockets and cavities in proteins structure, and quantitation of their volumes using Delaunay triangulation. Available also as PyMOL plugin</div><p><a href="http://www.bioinformatics.leeds.ac.uk/pocketfinder/" target="_blank">Pocket-Finder</a></p><div style="text-align: justify;">Automatic identification of pockets and cavities in proteins structure, and quantitation of their volumes.</div><p><a href="http://gecco.org.chemie.uni-frankfurt.de/pocketpicker/index.html" target="_blank">PocketPicker</a></p><div style="text-align: justify;">Grid-based technique for the analysis of protein pockets. PocketPicker available as a plugin for&nbsp;<a href="https://bip.weizmann.ac.il/toolbox/structure/pymol.htm">PyMOL</a></div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;"><h4>Binding Site Prediction</h4>
<p><a href="http://consurf.tau.ac.il/" target="_blank">ConSurf</a></p>
</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">Identification of functional regions in proteins by surface-mapping of phylogenetic information</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;"><a href="http://www-cryst.bioc.cam.ac.uk/~crescendo/crescendo.php" target="_blank">CRESCENDO</a></div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">Identification protein interaction sites. It uses sequence conservation patterns in homologous proteins to distinguish between residues that are conserved due to structural restraints from those due to functional restraints.&nbsp;&nbsp;</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;"><strong>Ligand Binding Sites</strong></div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;"><a href="http://www.sbg.bio.ic.ac.uk/~3dligandsite/" target="_blank">3DLigandSite</a></div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">The server utilizes protein-structure prediction to provide structural models of the binding site. Ligands bound to structures are superimposed onto the model and use to predict the binding site.</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">F<a href="http://cssb.biology.gatech.edu/skolnick/files/FINDSITE/" target="_blank">INDSITE</a></div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">A threading-based method for ligand-binding site prediction and functional annotation based on binding-site similarity across superimposed groups of threading templates.</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">
<p><a href="http://scoppi.biotec.tu-dresden.de/pocket/" target="_blank">LIGSITE<sup>csc</sup></a></p>
<div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;">Prediction of binding site by pocket identification using the Connolly surface and degree of conservation</div>
<p><a href="http://metapocket.eml.org/" target="_blank"></a></p>
</div><div style="text-align: justify;">&nbsp;</div><div style="text-align: justify;"><a href="http://metapocket.eml.org/" target="_blank">metaPocket</a>A meta server for ligand-binding site prediction. metaPocket use&nbsp;<a href="https://bip.weizmann.ac.il/toolbox/structure/binding.htm#ligsite">LIGSITE<sup>csc</sup></a>,&nbsp;<a href="https://bip.weizmann.ac.il/toolbox/structure/binding.htm#pass">PASS</a>,&nbsp;<a href="https://bip.weizmann.ac.il/toolbox/structure/binding.htm#qsite">Q-SiteFinder</a>&nbsp;and&nbsp;<a href="http://www.biochem.ucl.ac.uk/~roman/surfnet/surfnet.html" target="_blank">SURFNET</a></div>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43445/parebrick-parallel-rearrangements-and-breaks-identification-toolkit</guid>
	<pubDate>Fri, 08 Oct 2021 10:20:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43445/parebrick-parallel-rearrangements-and-breaks-identification-toolkit</link>
	<title><![CDATA[PaReBrick: PArallel REarrangements and BReaks identification toolkit]]></title>
	<description><![CDATA[<p><span>PaReBrick. The tool takes a collection of strains represented as a sequence of oriented synteny blocks and a phylogenetic tree as input data. It identifies rearrangements, tests them for consistency with a tree, and sorts the events by their parallelism score. The tool provides diagrams of the neighbors for each block of interest, allowing the detection of horizontally transferred blocks or their extra copies and the inversions in which copied blocks are involved.We demonstrated PaReBrick&rsquo;s efficiency and accuracy and showed its potential to detect genome rearrangements responsible for pathogenicity and adaptation in bacterial genomes</span></p>
<p>More at&nbsp;https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btab691/6380551</p>
<p><img src="https://github.com/ctlab/parallel-rearrangements/raw/master/figs/pipeline.svg" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/ctlab/parallel-rearrangements" rel="nofollow">https://github.com/ctlab/parallel-rearrangements</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34324/orthognc-a-software-for-accurate-identification-of-orthologs-based-on-gene-neighborhood-conservation</guid>
	<pubDate>Tue, 14 Nov 2017 09:30:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34324/orthognc-a-software-for-accurate-identification-of-orthologs-based-on-gene-neighborhood-conservation</link>
	<title><![CDATA[OrthoGNC: A Software for Accurate Identification of Orthologs Based on Gene Neighborhood Conservation]]></title>
	<description><![CDATA[<div>
<p id="sp0005">Orthology relations can be used to transfer annotations from one gene (or protein) to another. Hence, detecting orthology relations has become an important task in the post-genomic era. Various genomic events, such as duplication and horizontal gene transfer, can cause erroneous assignment of orthology relations. In closely-related species, gene neighborhood information can be used to resolve many ambiguities in orthology inference. Here we present OrthoGNC, a software for accurately predicting pairwise orthology relations based on gene neighborhood conservation. Analyses on simulated and real data reveal the high accuracy of OrthoGNC. In addition to orthology detection, OrthoGNC can be employed to investigate the conservation of genomic context among potential orthologs detected by other methods. OrthoGNC is freely available online at http://bs.ipm.ir/softwares/orthognc and http://tinyurl.com/orthoGNC.</p>
<p>http://www.comp.nus.edu.sg/~wongls/projects/orthoGNC/</p>
</div><p>Address of the bookmark: <a href="http://www.sciencedirect.com/science/article/pii/S1672022917301663" rel="nofollow">http://www.sciencedirect.com/science/article/pii/S1672022917301663</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32905/bigmac-breaking-inaccurate-genomes-and-merging-assembled-contigs-for-long-read-metagenomic-assembly</guid>
	<pubDate>Mon, 22 May 2017 05:43:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32905/bigmac-breaking-inaccurate-genomes-and-merging-assembled-contigs-for-long-read-metagenomic-assembly</link>
	<title><![CDATA[BIGMAC : breaking inaccurate genomes and merging assembled contigs for long read metagenomic assembly]]></title>
	<description><![CDATA[<p>This tool is for users to upgrade their metagenomics assemblies using long reads. This includes fixing mis-assemblies and scaffolding/gap-filling. If you encounter any issues, please contact me at&nbsp;<a href="mailto:kklam@eecs.berkeley.edu">kklam@eecs.berkeley.edu</a>. My name is Ka-Kit Lam.</p>
<p>https://github.com/kakitone/MetaFinisherSC</p>
<p>https://github.com/kakitone/BIGMAC</p><p>Address of the bookmark: <a href="https://github.com/kakitone/BIGMAC" rel="nofollow">https://github.com/kakitone/BIGMAC</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35057/ectools-long-read-correction-and-other-correction-tools</guid>
	<pubDate>Fri, 05 Jan 2018 04:02:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35057/ectools-long-read-correction-and-other-correction-tools</link>
	<title><![CDATA[ECTOOLS: Long Read Correction and other Correction tools]]></title>
	<description><![CDATA[<p>Long Read Correction and other Correction tools</p>
<p>This package is a loose collection of scripts. To run the correction<br>routine see the section below. Descriptions of the other scripts<br>are at the bottom of this file.</p>
<p>Contact: gurtowsk@cshl.edu</p>
<p>In short, the correction algorithm takes as input the unitigs from a short read assembly and uses them to correct long read data. More background information for the algorithm can be found:<br>http://schatzlab.cshl.edu/presentations/2013-06-18.PBUserMeeting.pdf</p><p>Address of the bookmark: <a href="https://github.com/jgurtowski/ectools" rel="nofollow">https://github.com/jgurtowski/ectools</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38304/lordfast-sensitive-and-fast-alignment-search-tool-for-long-noisy-read-sequencing-data</guid>
	<pubDate>Tue, 27 Nov 2018 04:43:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38304/lordfast-sensitive-and-fast-alignment-search-tool-for-long-noisy-read-sequencing-data</link>
	<title><![CDATA[lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data]]></title>
	<description><![CDATA[<p><span>lordFAST is a sensitive tool for mapping long reads with high error rates. lordFAST is specially designed for aligning reads from PacBio sequencing technology but provides the user the ability to change alignment parameters depending on the reads and application.</span></p>
<p>lordFAST, a novel long-read mapper that is specifically designed to align reads generated by PacBio and potentially other SMS technologies to a reference. lordFAST not only has higher sensitivity than the available alternatives, it is also among the fastest and has a very low memory footprint.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/vpc-ccg/lordfast" rel="nofollow">https://github.com/vpc-ccg/lordfast</a></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34394/tulip-the-uncorrected-long-read-itegration-pipeline</guid>
	<pubDate>Thu, 23 Nov 2017 09:30:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34394/tulip-the-uncorrected-long-read-itegration-pipeline</link>
	<title><![CDATA[TULIP - The Uncorrected Long read Itegration Pipeline]]></title>
	<description><![CDATA[<p>#Running TULIP (The Uncorrected Long-read Integration Process), version 0.4 late 2016 (European eel)</p>
<p>TULIP currently consists of to Perl scripts, tulipseed.perl and tulipbulb.perl. These are very much intended as prototypes, and additional components and/or implementations are likely to follow.&nbsp;<br>Tulipseed takes as input alignments files of long reads to sparse short seeds, and outputs a graph and scaffold structures. Tulipbulb adds long read sequencing data to these.</p>
<p>&nbsp;</p>
<p>https://github.com/Generade-nl/TULIP</p><p>Address of the bookmark: <a href="https://github.com/Generade-nl/TULIP" rel="nofollow">https://github.com/Generade-nl/TULIP</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36632/tulip-the-uncorrected-long-read-integration-pipeline</guid>
	<pubDate>Tue, 15 May 2018 09:06:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36632/tulip-the-uncorrected-long-read-integration-pipeline</link>
	<title><![CDATA[TULIP - The Uncorrected Long read Integration Pipeline]]></title>
	<description><![CDATA[TULIP currently consists of two Perl scripts, tulipseed.perl and tulipbulb.perl. These are very much intended as prototypes, and additional components and/or implementations are likely to follow.

Tulipseed takes as input alignments files of long reads to sparse short seeds, and outputs a graph and scaffold structures.<p>Address of the bookmark: <a href="https://github.com/Generade-nl/TULIP" rel="nofollow">https://github.com/Generade-nl/TULIP</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37473/lsc-a-long-read-error-correction-tool</guid>
	<pubDate>Thu, 02 Aug 2018 07:39:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37473/lsc-a-long-read-error-correction-tool</link>
	<title><![CDATA[LSC :a long read error correction tool]]></title>
	<description><![CDATA[<h2>Getting Started</h2>
<p>These simple steps will help you integrate LSC into your transcriptomics analysis pipeline.</p>
<ul>
<li>Read the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_requirements.asp">LSC_requirements</a>&nbsp;for running LSC.</li>
<li><a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_download.asp">Download</a>&nbsp;and set-up the LSC package.</li>
<li>Follow the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_tutorial.asp">tutorial</a>&nbsp;to see how LSC works on some example data.</li>
<li>Read the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_manual.asp">manual</a>&nbsp;if anything is unclear.</li>
<li>You're ready, Happy LSCing!</li>
</ul>
<h2>Latest publication</h2>
<p><span>Kin Fai Au, Jason Underwood, Lawrence Lee and Wing Hung Wong&nbsp;</span><br><strong>Improving PacBio Long Read Accuracy by Short Read Alignment&nbsp;</strong><span>[</span><a href="http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0046679">Manuscript</a><span>]&nbsp;</span><br><em>PLoS ONE</em><span>&nbsp;2012. 7(10): e46679. doi:10.1371/journal.pone.0046679</span></p><p>Address of the bookmark: <a href="https://www.healthcare.uiowa.edu/labs/au/LSC/" rel="nofollow">https://www.healthcare.uiowa.edu/labs/au/LSC/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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