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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/40598?offset=730</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40516/nextdenovo-string-graph-based-de-novo-assembler-for-tgs-long-reads</guid>
	<pubDate>Sun, 05 Jan 2020 04:08:29 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40516/nextdenovo-string-graph-based-de-novo-assembler-for-tgs-long-reads</link>
	<title><![CDATA[NextDenovo: string graph-based de novo assembler for TGS long reads]]></title>
	<description><![CDATA[<p>NextDenovo is a string graph-based<span>&nbsp;</span><em>de novo</em><span>&nbsp;</span>assembler for TGS long reads. It uses a "correct-then-assemble" strategy similar to canu, but requires significantly less computing resources and storages. After assembly, the per-base error rate is about 97-98%, to further improve single base accuracy, please use<span>&nbsp;</span><a href="https://github.com/Nextomics/NextPolish">NextPolish</a>.</p>
<p>NextDenovo contains two core modules: NextCorrect and NextGraph. NextCorrect can be used to correct TGS long reads with approximately 15% sequencing errors, and NextGraph can be used to construct a string graph with corrected reads. It also contains a modified version of<span>&nbsp;</span><a href="https://github.com/lh3/minimap2">minimap2</a><span>&nbsp;</span>for adapting input and output and producing more sensitive and accurate dovetail overlaps, and some useful utilities (see<span>&nbsp;</span><a href="https://github.com/Nextomics/NextDenovo/blob/master/doc/UTILITY.md">here</a><span>&nbsp;</span>for more details).</p><p>Address of the bookmark: <a href="https://github.com/Nextomics/NextDenovo" rel="nofollow">https://github.com/Nextomics/NextDenovo</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40946/free-genomics-data</guid>
	<pubDate>Fri, 07 Feb 2020 14:08:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40946/free-genomics-data</link>
	<title><![CDATA[Free Genomics data !]]></title>
	<description><![CDATA[<p><span>The specimens were collected by the Oxford Wytham Woods and Edinburgh Lohse lab teams. DNA extraction and sequencing was carried out by the Sanger Institute Scientific Operations teams. Assemblies were carried out by the Tree of Life team (Shane McCarthy) and colleagues in Pacific Biosciences (Jonas Korlach).</span></p>
<p><a href="https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/">https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/</a></p><p>Address of the bookmark: <a href="https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/" rel="nofollow">https://www.darwintreeoflife.org/an-initial-set-of-raw-genome-assemblies-from-the-darwin-tree-of-life-project/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/43732/spades-tutorial-pdf</guid>
	<pubDate>Tue, 01 Feb 2022 04:56:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/file/view/43732/spades-tutorial-pdf</link>
	<title><![CDATA[Spades tutorial PDF]]></title>
	<description><![CDATA[<p>SPAdes&mdash;St. Petersburg genome Assembler&mdash;was originally developed for de novo assembly of genome sequencing data produced for cultivated microbial isolates and for single-cell genomic DNA sequencing. With time, the functionality of SPAdes was extended to enable assembly of IonTorrent data, as well as hybrid assembly from short and long reads (PacBio and Oxford Nanopore). In this article we present protocols for five different assembly pipelines that comprise the SPAdes package and that are used for assembly of metagenomes and transcriptomes as well as assembly of putative plasmids and biosynthetic gene clusters from whole-genome sequencing and metagenomic datasets.&nbsp;</p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/43732" length="268093" type="application/pdf" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44529/contigextender-a-new-approach-to-improving-de-novo-sequence-assembly-for-viral-metagenomics-data</guid>
	<pubDate>Wed, 08 May 2024 07:32:45 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44529/contigextender-a-new-approach-to-improving-de-novo-sequence-assembly-for-viral-metagenomics-data</link>
	<title><![CDATA[ContigExtender: a new approach to improving de novo sequence assembly for viral metagenomics data]]></title>
	<description><![CDATA[<p dir="auto">ContigExtender, was developed to extend contigs, complementing de novo assembly. ContigExtender employs a novel recursive Overlap Layout Candidates (r-OLC) strategy that explores multiple extending paths to achieve longer and highly accurate contigs. ContigExtender is effective for extending contigs significantly in in silico synthesized and real metagenomics datasets.</p>
<p dir="auto">More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953547/</p>
<p dir="auto"><a href="https://camo.githubusercontent.com/72dc78177cd84dd0c667a2922a9fd984fb548b5ec94b11f9a547211a4adba3b1/68747470733a2f2f692e696d6775722e636f6d2f7734516944496a2e706e67" target="_blank"><img src="https://camo.githubusercontent.com/72dc78177cd84dd0c667a2922a9fd984fb548b5ec94b11f9a547211a4adba3b1/68747470733a2f2f692e696d6775722e636f6d2f7734516944496a2e706e67" alt="extension process" title="extension process" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/dengzac/contig-extender" rel="nofollow">https://github.com/dengzac/contig-extender</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44513/mike-an-ultrafast-assembly-and-alignment-free-approach-for-phylogenetic-tree-construction</guid>
	<pubDate>Mon, 08 Apr 2024 06:19:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44513/mike-an-ultrafast-assembly-and-alignment-free-approach-for-phylogenetic-tree-construction</link>
	<title><![CDATA[MIKE: an ultrafast, assembly-, and alignment-free approach for phylogenetic tree construction]]></title>
	<description><![CDATA[<p><span>MIKE (MinHash-based&nbsp;</span><em>k</em><span>-mer algorithm). This algorithm is designed for the swift calculation of the Jaccard coefficient directly from raw sequencing reads and enables the construction of phylogenetic trees based on the resultant Jaccard coefficient. Simulation results highlight the superior speed of MIKE compared to existing state-of-the-art methods. We used MIKE to reconstruct a phylogenetic tree, incorporating 238 yeast, 303&nbsp;</span><em>Zea</em><span>, 141&nbsp;</span><em>Ficus</em><span>, 67&nbsp;</span><em>Oryza</em><span>, and 43&nbsp;</span><em>Saccharum spontaneum</em><span>&nbsp;samples. MIKE demonstrated accurate performance across varying evolutionary scales, reproductive modes, and ploidy levels, proving itself as a powerful tool for phylogenetic tree construction.</span></p><p>Address of the bookmark: <a href="https://github.com/Argonum-Clever2/mike" rel="nofollow">https://github.com/Argonum-Clever2/mike</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28805/bambus</guid>
	<pubDate>Tue, 16 Aug 2016 08:09:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28805/bambus</link>
	<title><![CDATA[Bambus]]></title>
	<description><![CDATA[<div>
<div>
<div>
<p>Bambus 2.0, the second generation Bambus scaffolder available as an open source package. While most other scaffolders are closely tied to a specific assembly program, Bambus accepts the output from most current assemblers and provides the user with great flexibility in choosing the scaffolding parameters. In particular, Bambus is able to accept contig linking data other than specified by mate-pairs. Such sources of information include alignment to a reference genome (Bambus can directly use the output of MUMmer), physical mapping data, or information about gene synteny.</p>
</div>
</div>
</div>
<div>
<div>Home Page:&nbsp;</div>
<div>
<div><a href="http://sourceforge.net/apps/mediawiki/amos/index.php?title=Bambus2">http://sourceforge.net/apps/mediawiki/amos/index.php?title=Bambus2</a></div>
</div>
</div><p>Address of the bookmark: <a href="https://www.cbcb.umd.edu/software/bambus2" rel="nofollow">https://www.cbcb.umd.edu/software/bambus2</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/38804/grabb-selective-assembly-of-genomic-regions-a-new-niche-for-genomic-research</guid>
	<pubDate>Sat, 26 Jan 2019 18:58:16 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38804/grabb-selective-assembly-of-genomic-regions-a-new-niche-for-genomic-research</link>
	<title><![CDATA[GRAbB: Selective Assembly of Genomic Regions, a New Niche for Genomic Research]]></title>
	<description><![CDATA[<p><span>GRAbB is shown to be more efficient than MITObim in terms of speed, memory and disk usage. The other functionalities (handling multiple targets simultaneously and extracting homologous regions) of the new program are not matched by other programs. The program is available with explanatory documentation at&nbsp;</span><a href="https://github.com/b-brankovics/grabb">https://github.com/b-brankovics/grabb</a><span>. GRAbB has been tested on Ubuntu (12.04 and 14.04), Fedora (23), CentOS (7.1.1503) and Mac OS X (10.7). Furthermore, GRAbB is available as a docker repository: brankovics/grabb (</span><a href="https://hub.docker.com/r/brankovics/grabb/">https://hub.docker.com/r/brankovics/grabb/</a><span>).</span></p><p>Address of the bookmark: <a href="https://github.com/b-brankovics/grabb" rel="nofollow">https://github.com/b-brankovics/grabb</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40940/consed-a-finishing-package-bam-file-viewer-assembly-editor-autofinish-autoreport-autoedit-and-align-reads-to-reference-sequence</guid>
	<pubDate>Fri, 07 Feb 2020 07:16:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40940/consed-a-finishing-package-bam-file-viewer-assembly-editor-autofinish-autoreport-autoedit-and-align-reads-to-reference-sequence</link>
	<title><![CDATA[Consed--A Finishing Package (BAM File Viewer, Assembly Editor, Autofinish, Autoreport, Autoedit, and Align Reads To Reference Sequence)]]></title>
	<description><![CDATA[<ul>
<li>Supports Illumina, 454, other Next-Gen and Sanger Reads and allows mixtures of these read types</li>
<li>Consed includes BamScape which can view bam files with unlimited numbers of reads. BamScape can bring up consed to edit reads and the reference sequence in targeted regions.</li>
<li>Consed is compatible with Newbler, Cross_match, Phrap, MIRA, Velvet and PCAP output.</li>
<li>Quickly takes the user to each variant site for viewing (also available as an automated report)</li>
<li>Overview of assembly can help detect and fix misassemblies</li>
<li>Editing time reduced by the program's ability to pin-point problem areas</li>
<li>Editing is guided by error probabilities</li>
</ul><p>Address of the bookmark: <a href="http://www.phrap.org/consed/consed.html" rel="nofollow">http://www.phrap.org/consed/consed.html</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44474/claw-chloroplast-long-read-assembly-workflow</guid>
	<pubDate>Wed, 21 Feb 2024 12:37:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44474/claw-chloroplast-long-read-assembly-workflow</link>
	<title><![CDATA[CLAW: Chloroplast Long-read Assembly Workflow]]></title>
	<description><![CDATA[<p dir="auto">CLAW (Chloroplast Long-read Assembly Workflow) is an mostly-automated Snakemake-based workflow for the assembly of chloroplast genomes. CLAW uses chloroplast long-reads, which are baited out of larger read libraries (e.g., an Oxford Nanopore Technologies MinION read library derived from photosynthetic tissue), for assembly with Flye and/or Unicycler. CLAW was designed with the novice bioinformatician in mind - it is easy to install and easy to use, requiring only minimal user input.</p><p>Address of the bookmark: <a href="https://github.com/aaronphillips7493/CLAW" rel="nofollow">https://github.com/aaronphillips7493/CLAW</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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