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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/39903?offset=190</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34391/taxoblast-taxoblast-is-a-pipeline-to-identify-contamination-in-genomic-sequence</guid>
	<pubDate>Thu, 23 Nov 2017 08:37:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34391/taxoblast-taxoblast-is-a-pipeline-to-identify-contamination-in-genomic-sequence</link>
	<title><![CDATA[Taxoblast : Taxoblast is a pipeline to identify contamination in genomic sequence]]></title>
	<description><![CDATA[<p><span>Modern genome sequencing strategies are highly sensitive to contamination making the detection of foreign DNA sequences an important part of analysis pipelines. Here we use Taxoblast, a simple pipeline with a graphical user interface, for the post-assembly detection of contaminating sequences in the published genome of the kelp&nbsp;</span><em>Saccharina japonica</em><span>. Analyses were based on multiple blastn searches with short sequence fragments. They revealed a number of probable bacterial contaminations as well as hybrid scaffolds that contain both bacterial and algal sequences. This or similar types of analysis, in combination with manual curation, may thus constitute a useful complement to standard bioinformatics analyses prior to submission of genomic data to public repositories. Our analysis pipeline is open-source and freely available at&nbsp;</span><a href="http://sdittami.altervista.org/taxoblast" title="">http://sdittami.altervista.org/taxoblast</a><span>&nbsp;and via SourceForge (</span><a href="https://sourceforge.net/projects/taxoblast" title="">https://sourceforge.net/projects/taxoblast</a><span>).</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/taxoblast/files/" rel="nofollow">https://sourceforge.net/projects/taxoblast/files/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38067/metaplotr-a-perlr-pipeline-for-plotting-metagenes-of-nucleotide-modifications-and-other-transcriptomic-sites</guid>
	<pubDate>Mon, 05 Nov 2018 08:12:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38067/metaplotr-a-perlr-pipeline-for-plotting-metagenes-of-nucleotide-modifications-and-other-transcriptomic-sites</link>
	<title><![CDATA[MetaPlotR: a Perl/R pipeline for plotting metagenes of nucleotide modifications and other transcriptomic sites]]></title>
	<description><![CDATA[<p><span>An increasing number of studies are mapping protein binding and nucleotide modifications sites throughout the transcriptome. Often, these sites cluster in certain regions of the transcript, giving clues to their function. Hence, it is informative to summarize where in the transcript these sites occur. A metagene is a simple and effective tool for visualizing the distribution of sites along a simplified transcript model. In this work, we introduce MetaPlotR, a Perl/R pipeline for creating metagene plots.</span></p><p>Address of the bookmark: <a href="https://github.com/olarerin/metaPlotR" rel="nofollow">https://github.com/olarerin/metaPlotR</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39843/dnapipete-a-pipeline-designed-to-find-annotate-and-quantify-transposable-elements</guid>
	<pubDate>Mon, 12 Aug 2019 21:56:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39843/dnapipete-a-pipeline-designed-to-find-annotate-and-quantify-transposable-elements</link>
	<title><![CDATA[dnaPipeTE: a pipeline designed to find, annotate and quantify Transposable Elements]]></title>
	<description><![CDATA[<p><span>dnaPipeTE (for de-novo assembly &amp; annotation Pipeline for Transposable Elements), is a pipeline designed to find, annotate and quantify Transposable Elements in small samples of NGS datasets. It is very useful to quantify the proportion of TEs in newly sequenced genomes since it does not require genome assembly and works on small datasets (&lt; 1X).</span></p>
<p><span><a href="https://github.com/clemgoub/dnaPipeTE/wiki/dnaPipeTE-WIKI-home">https://github.com/clemgoub/dnaPipeTE/wiki/dnaPipeTE-WIKI-home</a></span></p><p>Address of the bookmark: <a href="https://github.com/clemgoub/dnaPipeTE" rel="nofollow">https://github.com/clemgoub/dnaPipeTE</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40611/deepvariant-an-analysis-pipeline-that-uses-a-deep-neural-network-to-call-genetic-variants-from-next-generation-dna-sequencing-data</guid>
	<pubDate>Sat, 25 Jan 2020 13:28:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40611/deepvariant-an-analysis-pipeline-that-uses-a-deep-neural-network-to-call-genetic-variants-from-next-generation-dna-sequencing-data</link>
	<title><![CDATA[DeepVariant : an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.]]></title>
	<description><![CDATA[<p><span>DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.</span></p>
<p><span><span>DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data. DeepVariant relies on&nbsp;</span><a href="https://github.com/google/nucleus">Nucleus</a><span>, a library of Python and C++ code for reading and writing data in common genomics file formats (like SAM and VCF) designed for painless integration with the&nbsp;</span><a href="https://www.tensorflow.org/">TensorFlow</a><span>&nbsp;machine learning framework.</span></span></p>
<p><span><a href="https://ai.googleblog.com/2017/12/deepvariant-highly-accurate-genomes.html">https://ai.googleblog.com/2017/12/deepvariant-highly-accurate-genomes.html</a></span></p>
<p><span><a href="https://www.biorxiv.org/content/10.1101/092890v6">https://www.biorxiv.org/content/10.1101/092890v6</a></span></p>
<p><span><img src="https://4.bp.blogspot.com/-2KlXZO60sWE/WiGc8qlZfxI/AAAAAAAACOs/s1pNiKI8jsAvJLr1E_po5udDO8eObm_awCLcBGAs/s640/image3.png" width="640" height="427" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/google/deepvariant" rel="nofollow">https://github.com/google/deepvariant</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41998/wgddetector-a-pipeline-for-detecting-whole-genome-duplication-events-using-the-genome-or-transcriptome-annotations</guid>
	<pubDate>Thu, 23 Jul 2020 05:52:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41998/wgddetector-a-pipeline-for-detecting-whole-genome-duplication-events-using-the-genome-or-transcriptome-annotations</link>
	<title><![CDATA[WGDdetector: a pipeline for detecting whole genome duplication events using the genome or transcriptome annotations]]></title>
	<description><![CDATA[<p><span>WGDdetector pipeline that integrates all analyses including gene family constructing, dS estimating and phasing, and outputting the dS values of each paralogs pairs processed with only one command. We further chose four species (</span><em>Arabidopsis thaliana</em><span>,<span>&nbsp;</span></span><em>Juglans regia</em><span>,<span>&nbsp;</span></span><em>Populus trichocarpa</em><span><span>&nbsp;</span>and<span>&nbsp;</span></span><em>Xenopus laevis</em><span>) representing herb, wood and animal, to test its practicability. Our final results showed a high degree of accuracy with the previous studies using both genome and transcriptome data.</span></p>
<p><span>More at <a href="https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-019-2670-3">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-019-2670-3</a></span></p><p>Address of the bookmark: <a href="https://github.com/yongzhiyang2012/wgddetector" rel="nofollow">https://github.com/yongzhiyang2012/wgddetector</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42941/csa-a-high-throughput-chromosome-scale-assembly-pipeline-for-vertebrate-genomes</guid>
	<pubDate>Wed, 10 Mar 2021 06:13:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42941/csa-a-high-throughput-chromosome-scale-assembly-pipeline-for-vertebrate-genomes</link>
	<title><![CDATA[CSA: A high-throughput chromosome-scale assembly pipeline for vertebrate genomes]]></title>
	<description><![CDATA[<p>The pipeline can use information from scaffolded assemblies (for example from HiC or 10X Genomics), or even from diverged (~65-100 Mya) reference genomes for ordering the contigs and thus support the assembly process. This typically results in improved contig N50 when compared to current state of the art methods.</p>
<p><img src="https://github.com/HMPNK/CSA2.6/raw/master/Fig1.png" alt="image" style="border: 0px;"></p>
<p>For smaller vertebrate genomes (~1 Gbp) chromosome scale assemblies can be achieved within 12h on high-end Desktop computers (Intel i7, 12 CPU threads, 128 GB RAM). Larger mammalian genomes (~3Gbp) can be processed within 15-18 h on server equipment (Xeon, 96 CPU threads, 1TB RAM).</p><p>Address of the bookmark: <a href="https://github.com/HMPNK/CSA2.6" rel="nofollow">https://github.com/HMPNK/CSA2.6</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43384/lncpipea-nextflow-based-pipeline-for-comprehensive-analyses-of-long-non-coding-rnas-from-rna-seq-datasets</guid>
	<pubDate>Fri, 17 Sep 2021 01:57:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43384/lncpipea-nextflow-based-pipeline-for-comprehensive-analyses-of-long-non-coding-rnas-from-rna-seq-datasets</link>
	<title><![CDATA[LncPipe:A Nextflow-based pipeline for comprehensive analyses of long non-coding RNAs from RNA-seq datasets]]></title>
	<description><![CDATA[<p><span>The pipeline was developed based on a popular workflow framework&nbsp;</span><a href="https://github.com/nextflow-io/nextflow">Nextflow</a><span>, composed of four core procedures including reads alignment, assembly, identification and quantification. It contains various unique features such as well-designed lncRNAs annotation strategy, optimized calculating efficiency, diversified classification and interactive analysis report.&nbsp;</span><a href="https://github.com/likelet/LncPipe">LncPipe</a><span>&nbsp;allows users additional control in interuppting the pipeline, resetting parameters from command line, modifying main script directly and resume analysis from previous checkpoint.</span></p>
<p>Ref&nbsp;https://www.lncrnablog.com/lncpipe-a-nextflow-based-pipeline-for-identification-and-analysis-of-long-non-coding-rnas-from-rna-seq-data/</p>
<p><img src="https://ars.els-cdn.com/content/image/1-s2.0-S1673852718301176-gr1.jpg" alt="image" style="border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/likelet/LncPipe" rel="nofollow">https://github.com/likelet/LncPipe</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44597/imagine-in-silico-metagenomics-pipeline</guid>
	<pubDate>Sat, 06 Jul 2024 04:32:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44597/imagine-in-silico-metagenomics-pipeline</link>
	<title><![CDATA[iMAGine - in silico MetAGenomics pipeline]]></title>
	<description><![CDATA[<p dir="auto"><span>iMAGine</span>&nbsp;is a metagenomic workflow which includes filtering, assembling, and binning.</p>
<p dir="auto">This workflow includes the following tools which are needed to be installed in the system.</p>
<ol dir="auto">
<li><a href="https://github.com/OpenGene/fastp">fastp</a></li>
<li><a href="https://github.com/ablab/spades">spades assembler</a></li>
<li><a href="https://github.com/ablab/quast">QUAST</a></li>
<li><a href="https://github.com/lh3/bwa">bwa</a></li>
<li><a href="https://github.com/samtools/samtools">samtools</a></li>
<li><a href="https://bitbucket.org/berkeleylab/metabat/src/master/">metabat2</a></li>
<li><a href="https://github.com/Ecogenomics/CheckM">CheckM</a></li>
</ol><p>Address of the bookmark: <a href="https://github.com/avishekdutta14/iMAGine" rel="nofollow">https://github.com/avishekdutta14/iMAGine</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27035/spades</guid>
	<pubDate>Tue, 19 Apr 2016 08:37:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27035/spades</link>
	<title><![CDATA[SPAdes]]></title>
	<description><![CDATA[<p>SPAdes &ndash; St. Petersburg genome assembler &ndash; is intended for both standard isolates and single-cell MDA bacteria assemblies. This manual will help you to install and run SPAdes. SPAdes version 3.7.1 was released under GPLv2 on March 8, 2016 and can be downloaded from <a href="http://bioinf.spbau.ru/en/spades" target="_blank">http://bioinf.spbau.ru/en/spades</a>.</p>
<p>Manual at http://spades.bioinf.spbau.ru/release3.7.1/manual.html</p><p>Address of the bookmark: <a href="http://bioinf.spbau.ru/spades" rel="nofollow">http://bioinf.spbau.ru/spades</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33859/disco-multi-threaded-and-multiprocess-distributed-memory-overlap-layout-consensus-olc-metagenome-assembler</guid>
	<pubDate>Mon, 10 Jul 2017 10:09:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33859/disco-multi-threaded-and-multiprocess-distributed-memory-overlap-layout-consensus-olc-metagenome-assembler</link>
	<title><![CDATA[DISCO : multi threaded and multiprocess distributed memory overlap-layout-consensus (OLC) metagenome assembler]]></title>
	<description><![CDATA[<p><span>DISCO is a multi threaded and multiprocess distributed memory overlap-layout-consensus (OLC) metagenome assembler. Disco was developed as a&nbsp;scalable assembler to assemble large metagenomes from billions of Illumina sequencing reads of complex microbial communities. Disco was parallelized for computer clusters in a hybrid architecture that integrated shared-memory multi-threading, point-to-point message passing, and remote direct memory access. The assembly and scaffolding were performed using an iterative overlap graph approach.</span></p><p>Address of the bookmark: <a href="http://disco.omicsbio.org/" rel="nofollow">http://disco.omicsbio.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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