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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/33479?offset=10</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27328/platanus</guid>
	<pubDate>Fri, 13 May 2016 05:12:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27328/platanus</link>
	<title><![CDATA[Platanus]]></title>
	<description><![CDATA[<p>Platanus is a novel <em>de novo</em> sequence assembler that can reconstruct genomic sequences of<br> highly heterozygous diploids from massively parallel shotgun sequencing data.</p>
<p>The latest version is <a href="http://platanus.bio.titech.ac.jp/platanus/?page_id=14">1.2.4</a>.</p>
<p>To cite Platanus, please use the following:</p>
<p>Kajitani R, Toshimoto K, Noguchi H, Toyoda A, Ogura Y, Okuno M, Yabana M, Harada M, Nagayasu E, Maruyama H, Kohara Y, Fujiyama A, Hayashi T, Itoh T, &ldquo;Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads&rdquo;.&nbsp;Genome Res. 2014 Aug;24(8):1384-95. doi: 10.1101/gr.170720.113. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/24755901">abstract</a> |<a href="http://genome.cshlp.org/content/24/8/1384.long"> full text</a>]</p><p>Address of the bookmark: <a href="http://platanus.bio.titech.ac.jp/" rel="nofollow">http://platanus.bio.titech.ac.jp/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</guid>
	<pubDate>Tue, 14 Jun 2016 10:28:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</link>
	<title><![CDATA[Blobsplorer]]></title>
	<description><![CDATA[<p>Blobsplorer is a tool for interactive visualization of assembled DNA sequence data ("contigs") derived from (often unintentionally) mixed-species pools. It allows the simultaneous display of GC content, coverage, and taxonomic annotation for collections of contigs with a view to separating out those belonging to different taxa.</p>
<p>Blobsplorer is unlikely to be of use on its own as it requires contig data to be supplied in a format that involves considerable preprocessing (see below for a description). The easiest way to use Blobsplorer is as part of a workflow using scripts from <a href="https://github.com/blaxterlab/blobology">here</a>.</p><p>Address of the bookmark: <a href="http://nematodes.org/martin/blobsplorer/blobsplorer.html" rel="nofollow">http://nematodes.org/martin/blobsplorer/blobsplorer.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30111/eager</guid>
	<pubDate>Sat, 10 Dec 2016 18:07:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30111/eager</link>
	<title><![CDATA[EAGER]]></title>
	<description><![CDATA[<p><span>The automated reconstruction of genome sequences in ancient genome analysis is a multifaceted process.</span></p>
<p><span>EAGER encompasses both state-of-the-art tools for each step as well as new complementary tools tailored for ancient DNA data within a single integrated solution in an easily accessible format.</span></p>
<p>https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-0918-z</p><p>Address of the bookmark: <a href="https://github.com/apeltzer/EAGER-GUI" rel="nofollow">https://github.com/apeltzer/EAGER-GUI</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33789/i-pv-interactive-protein-sequence-visualization</guid>
	<pubDate>Mon, 03 Jul 2017 07:52:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33789/i-pv-interactive-protein-sequence-visualization</link>
	<title><![CDATA[I-PV: Interactive Protein Sequence Visualization]]></title>
	<description><![CDATA[<p><span>I-PV is a interactive data visualization software designed for inspection of protein sequences and mutation information. It is mainly used for Genetics and Bioinformatics. So what exactly makes it standout?</span></p>
<p><span>http://i-pv.org/ipv_rec</span></p><p>Address of the bookmark: <a href="http://i-pv.org/" rel="nofollow">http://i-pv.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36893/beap-blast-extension-and-assembly-program</guid>
	<pubDate>Mon, 11 Jun 2018 04:52:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36893/beap-blast-extension-and-assembly-program</link>
	<title><![CDATA[BEAP: Blast Extension and Assembly Program]]></title>
	<description><![CDATA[The Blast Extension and Assembly Program (BEAP) is a computer program that uses a short starting DNA fragment, often a EST or partial gene segment, as "primer", to recursively blast nucleotide databases in an attempt to obtain all sequences that overlaps, directly or indirectly, with the "primer" therefore help to "extend" the length of the original sequence for constructing a "full length" sequence for functional analysis, or at least to obtain neighboring regions of the segment for SNP discovery and linkage disequilibrium analysis. The confidence of assembling the resulting sequences is achieved by using a known genome, such as human genome, as a reference.
 
https://www.animalgenome.org/tools/beap/<p>Address of the bookmark: <a href="https://www.animalgenome.org/tools/beap/" rel="nofollow">https://www.animalgenome.org/tools/beap/</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41405/sequence-tube-maps-displays-multiple-genomic-sequences-in-the-form-of-a-tube-map</guid>
	<pubDate>Wed, 11 Mar 2020 01:12:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41405/sequence-tube-maps-displays-multiple-genomic-sequences-in-the-form-of-a-tube-map</link>
	<title><![CDATA[Sequence Tube Maps: displays multiple genomic sequences in the form of a tube map]]></title>
	<description><![CDATA[<p>A JavaScript module for the visualization of genomic sequence graphs. It automatically generates a "tube map"-like visualization of sequence graphs which have been created with <a href="https://github.com/vgteam/vg">vg</a>. (<a href="https://github.com/vgteam/vg">https://github.com/vgteam/vg</a>)</p>
<h3>Link to working demo: <a href="https://vgteam.github.io/sequenceTubeMap/">https://vgteam.github.io/sequenceTubeMap/</a></h3>
<p><img src="https://raw.githubusercontent.com/vgteam/sequenceTubeMap/master/images/header.png" alt="image" style="border: 0px; border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/vgteam/sequenceTubeMap" rel="nofollow">https://github.com/vgteam/sequenceTubeMap</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43810/seqfu-a-suite-of-utilities-for-the-robust-and-reproducible-manipulation-of-sequence-files</guid>
	<pubDate>Tue, 01 Mar 2022 03:13:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43810/seqfu-a-suite-of-utilities-for-the-robust-and-reproducible-manipulation-of-sequence-files</link>
	<title><![CDATA[SeqFu: A Suite of Utilities for the Robust and Reproducible Manipulation of Sequence Files]]></title>
	<description><![CDATA[<p>A general-purpose program to manipulate and parse information from FASTA/FASTQ files, supporting gzipped input files. Includes functions to&nbsp;<em>interleave</em>&nbsp;and&nbsp;<em>de-interleave</em>&nbsp;FASTQ files, to&nbsp;<em>rename</em>&nbsp;sequences and to&nbsp;<em>count</em>&nbsp;and print&nbsp;<em>statistics</em>&nbsp;on sequence lengths. SeqFu is available for Linux and MacOS.</p>
<ul>
<li>A compiled program delivering high performance analyses</li>
<li>Supports FASTA/FASTQ files, also Gzip compressed</li>
<li>A growing collection of handy utilities, also for quick inspection of the datasets</li>
</ul>
<p>Can be easily&nbsp;<a href="https://telatin.github.io/seqfu2/installation">installed</a>&nbsp;via conda:</p>
<div>
<div>
<pre><code>conda <span>install</span> <span>-c</span> bioconda seqfu</code></pre>
</div>
</div><p>Address of the bookmark: <a href="https://telatin.github.io/seqfu2/" rel="nofollow">https://telatin.github.io/seqfu2/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44569/seqcat-sequence-conversion-and-analysis-toolbox</guid>
	<pubDate>Fri, 14 Jun 2024 14:36:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44569/seqcat-sequence-conversion-and-analysis-toolbox</link>
	<title><![CDATA[SeqCAT: Sequence Conversion and Analysis Toolbox]]></title>
	<description><![CDATA[<div>Your all-in-one solution for smooth conversion of sequence coordinates.</div>
<div>Designed for bioinformatics data analysis and daily laboratory work, SeqCAT simplifies sequence coordinate conversion. Extract gene and transcript information, manipulate sequences, and easily validate complex genetic events such as fusions with SeqCAT.</div>
<div>&nbsp;</div>
<div>More at&nbsp;https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkae422/7683049?login=false</div><p>Address of the bookmark: <a href="https://mtb.bioinf.med.uni-goettingen.de/SeqCAT/home" rel="nofollow">https://mtb.bioinf.med.uni-goettingen.de/SeqCAT/home</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33955/crocoblast-optimized-parallel-implementation-of-local-sequence-alignment-algorithms</guid>
	<pubDate>Tue, 25 Jul 2017 05:03:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33955/crocoblast-optimized-parallel-implementation-of-local-sequence-alignment-algorithms</link>
	<title><![CDATA[CrocoBLAST: Optimized parallel implementation of local sequence alignment algorithms]]></title>
	<description><![CDATA[<p><span>Local sequence alignment is a cornerstone of bioinformatics, allowing to compare the amino-acid sequences of different proteins, or the nucleotide sequences of different pieces of DNA. The Basic Local Alignment Search Tool (BLAST) has revolutionized the field of bioinformatics, and is currently implemented in all free and commercial bioinformatics packages. However, with the advent of Next Generation Sequencing (NGS) and the development of new sequencing techniques, the utility of traditional BLAST implementations is limited. CrocoBLAST combines the accuracy and general applicability of BLAST with computational efficiency, accessibility, and user experience, so that NGS data can be analyzed efficiently even when only modest computational resources are available.</span></p>
<p>https://webchem.ncbr.muni.cz/Platform/App/CrocoBLAST</p><p>Address of the bookmark: <a href="https://webchem.ncbr.muni.cz/Platform/App/CrocoBLAST" rel="nofollow">https://webchem.ncbr.muni.cz/Platform/App/CrocoBLAST</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34488/scripts-for-the-analysis-of-hgt-in-genome-sequence-data</guid>
	<pubDate>Wed, 29 Nov 2017 16:44:10 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34488/scripts-for-the-analysis-of-hgt-in-genome-sequence-data</link>
	<title><![CDATA[Scripts for the analysis of HGT in genome sequence data.]]></title>
	<description><![CDATA[<p><span>Scripts for the analysis of HGT in genome sequence data</span></p><p>Address of the bookmark: <a href="https://github.com/reubwn/hgt" rel="nofollow">https://github.com/reubwn/hgt</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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