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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/40792?offset=330</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33482/tardis-toolkit-for-automated-and-rapid-discovery-of-structural-variants</guid>
	<pubDate>Fri, 09 Jun 2017 04:43:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33482/tardis-toolkit-for-automated-and-rapid-discovery-of-structural-variants</link>
	<title><![CDATA[TARDIS: Toolkit for automated and rapid discovery of structural variants]]></title>
	<description><![CDATA[<p>tardis</p>
<p>Toolkit for Automated and Rapid DIscovery of Structural variants</p>
<p>Requirements</p>
<p>zlib (http://www.zlib.net)<br>mrfast (https://github.com/BilkentCompGen/mrfast)<br>htslib (included as submodule; http://htslib.org/)<br>Fetching tardis</p>
<p>git clone https://github.com/BilkentCompGen/tardis.git --recursive</p>
<p>&nbsp;</p>
<p>https://github.com/BilkentCompGen/tardis</p><p>Address of the bookmark: <a href="https://github.com/BilkentCompGen/tardis" rel="nofollow">https://github.com/BilkentCompGen/tardis</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35907/alienness-rapid-detection-of-candidate-horizontal-gene-transfers-across-the-tree-of-life</guid>
	<pubDate>Mon, 12 Mar 2018 09:24:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35907/alienness-rapid-detection-of-candidate-horizontal-gene-transfers-across-the-tree-of-life</link>
	<title><![CDATA[alienness : Rapid Detection of Candidate Horizontal Gene Transfers across the Tree of Life]]></title>
	<description><![CDATA[<p><span>Horizontal gene transfer (HGT) is the transmission of genes between organisms by other means than parental to offspring inheritance. While it is prevalent in prokaryotes, HGT is less frequent in eukaryotes and particularly in Metazoa. Here, we propose Alienness, a taxonomy-aware web application available at&nbsp;</span>http://alienness.sophia.inra.fr</p>
<p>http://www.mdpi.com/2073-4425/8/10/248</p><p>Address of the bookmark: <a href="http://alienness.sophia.inra.fr/cgi/index.cgi" rel="nofollow">http://alienness.sophia.inra.fr/cgi/index.cgi</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42530/shovill-assemble-bacterial-isolate-genomes-from-illumina-paired-end-reads</guid>
	<pubDate>Sat, 02 Jan 2021 07:05:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42530/shovill-assemble-bacterial-isolate-genomes-from-illumina-paired-end-reads</link>
	<title><![CDATA[shovill: Assemble bacterial isolate genomes from Illumina paired-end reads]]></title>
	<description><![CDATA[<p><span>Shovill is a pipeline which uses SPAdes at its core, but alters the steps before and after the primary assembly step to get similar results in less time. Shovill also supports other assemblers like SKESA, Velvet and Megahit, so you can take advantage of the pre- and post-processing the Shovill provides with those too.</span></p><p>Address of the bookmark: <a href="https://github.com/tseemann/shovill" rel="nofollow">https://github.com/tseemann/shovill</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36758/pbalign-maps-pacbio-reads-to-reference-sequences-and-saves-alignments-to-a-bam-file</guid>
	<pubDate>Thu, 24 May 2018 10:06:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36758/pbalign-maps-pacbio-reads-to-reference-sequences-and-saves-alignments-to-a-bam-file</link>
	<title><![CDATA[pbalign: maps PacBio reads to reference sequences and saves alignments to a BAM file]]></title>
	<description><![CDATA[pbalign aligns PacBio reads to reference sequences, filters aligned reads according to user-specific filtering criteria, and converts the output to either the SAM format or PacBio Compare HDF5 (e.g., .cmp.h5) format. The output Compare HDF5 file will be compatible with Quiver if --forQuiver option is specified.<p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/pbalign" rel="nofollow">https://github.com/PacificBiosciences/pbalign</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38299/deepbinner-a-signal-level-demultiplexer-for-oxford-nanopore-reads</guid>
	<pubDate>Tue, 27 Nov 2018 03:38:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38299/deepbinner-a-signal-level-demultiplexer-for-oxford-nanopore-reads</link>
	<title><![CDATA[Deepbinner: a signal-level demultiplexer for Oxford Nanopore reads]]></title>
	<description><![CDATA[<p>Deepbinner is a tool for demultiplexing barcoded&nbsp;<a href="https://nanoporetech.com/">Oxford Nanopore</a>&nbsp;sequencing reads. It does this with a deep&nbsp;<a href="https://adeshpande3.github.io/adeshpande3.github.io/A-Beginner's-Guide-To-Understanding-Convolutional-Neural-Networks/">convolutional neural network</a>&nbsp;classifier, using many of the&nbsp;<a href="https://towardsdatascience.com/neural-network-architectures-156e5bad51ba">architectural advances</a>&nbsp;that have proven successful in image classification. Unlike other demultiplexers (e.g. Albacore and&nbsp;<a href="https://github.com/rrwick/Porechop">Porechop</a>), Deepbinner identifies barcodes from the raw signal (a.k.a. squiggle) which gives it greater sensitivity and fewer unclassified reads.</p>
<ul>
<li><span>Reasons to use Deepbinner</span>:
<ul>
<li>To minimise the number of unclassified reads (use Deepbinner by itself).</li>
<li>To minimise the number of misclassified reads (use Deepbinner in conjunction with Albacore demultiplexing).</li>
<li>You plan on running signal-level downstream analyses, like&nbsp;<a href="https://github.com/jts/nanopolish">Nanopolish</a>. Deepbinner can&nbsp;<a href="https://github.com/rrwick/Deepbinner#using-deepbinner-before-basecalling">demultiplex the fast5 files</a>which makes this easier.</li>
</ul>
</li>
<li><span>Reasons to&nbsp;<em>not</em>&nbsp;use Deepbinner</span>:
<ul>
<li>You only have basecalled reads not the raw fast5 files (which Deepbinner requires).</li>
<li>You have a small/slow computer. Deepbinner is more computationally intensive than&nbsp;<a href="https://github.com/rrwick/Porechop">Porechop</a>.</li>
<li>You used a sequencing/barcoding kit other than&nbsp;<a href="https://github.com/rrwick/Deepbinner/blob/master/models">the ones Deepbinner was trained on</a>.</li>
</ul>
</li>
</ul><p>Address of the bookmark: <a href="https://github.com/rrwick/Deepbinner" rel="nofollow">https://github.com/rrwick/Deepbinner</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40889/rcorrector-efficient-and-accurate-error-correction-for-illumina-rna-seq-reads</guid>
	<pubDate>Tue, 04 Feb 2020 23:23:16 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40889/rcorrector-efficient-and-accurate-error-correction-for-illumina-rna-seq-reads</link>
	<title><![CDATA[Rcorrector: efficient and accurate error correction for Illumina RNA-seq reads]]></title>
	<description><![CDATA[<p><span>Rcorrector has an accuracy higher than or comparable to existing methods, including the only other method (SEECER) designed for RNA-seq reads, and is more time and memory efficient. With a 5 GB memory footprint for 100 million reads, it can be run on virtually any desktop or server. The software is available free of charge under the GNU General Public License from&nbsp;</span><a href="https://github.com/mourisl/Rcorrector/" target="_blank">https://github.com/mourisl/Rcorrector/</a><span>.</span></p>
<pre><code>Usage: perl run_rcorrector.pl [OPTIONS]
OPTIONS:
	Required
	-s seq_files: comma separated files for single-end data sets
	-1 seq_files_left: comma separated files for the first mate in the paried-end data sets
	-2 seq_files_right: comma separated files for the second mate in the paired-end data sets
	-i seq_files_interleaved: comma sperated files for interleaved paired-end data sets
	Optional
	-k INT: kmer_length (&lt;=32, default: 23)
	-od STRING: output_file_directory (default: ./)
	-t INT: number of threads to use (default: 1)
	-trim : allow trimming (default: false)
	-maxcorK INT: the maximum number of correction within k-bp window (default: 4)
	-wk FLOAT: the proportion of kmers that are used to estimate weak kmer count threshold, lower for more divergent genome (default: 0.95)
	-ek INT: expected number of kmers; does not affect the correctness of program but affects the memory usage (default: 100000000)
	-stdout: output the corrected reads to stdout (default: not used)
	-verbose: output some correction information to stdout (default: not used)
	-stage INT: start from which stage (default: 0)
		0-start from begining(storing kmers in bloom filter) ;
		1-start from count kmers showed up in bloom filter;
		2-start from dumping kmer counts into a jf_dump file;
		3-start from error correction.</code></pre><p>Address of the bookmark: <a href="https://github.com/mourisl/Rcorrector/" rel="nofollow">https://github.com/mourisl/Rcorrector/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</guid>
	<pubDate>Mon, 17 Aug 2020 05:25:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins</link>
	<title><![CDATA[SqueezeMeta: a fully automated metagenomics pipeline, from reads to bins]]></title>
	<description><![CDATA[<p>SqueezeMeta is a full automatic pipeline for metagenomics/metatranscriptomics, covering all steps of the analysis. SqueezeMeta includes multi-metagenome support allowing the co-assembly of related metagenomes and the retrieval of individual genomes via binning procedures. Thus, SqueezeMeta features several unique characteristics:</p>
<ol>
<li>Co-assembly procedure with read mapping for estimation of the abundances of genes in each metagenome</li>
<li>Co-assembly of a large number of metagenomes via merging of individual metagenomes</li>
<li>Includes binning and bin checking, for retrieving individual genomes</li>
<li>The results are stored in a database, where they can be easily exported and shared, and can be inspected anywhere using a web interface.</li>
<li>Internal checks for the assembly and binning steps inform about the consistency of contigs and bins, allowing to spot potential chimeras.</li>
<li>Metatranscriptomic support via mapping of cDNA reads against reference metagenomes</li>
</ol><p>Address of the bookmark: <a href="https://github.com/jtamames/SqueezeMeta" rel="nofollow">https://github.com/jtamames/SqueezeMeta</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26453/stacks</guid>
	<pubDate>Wed, 24 Feb 2016 15:52:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26453/stacks</link>
	<title><![CDATA[Stacks]]></title>
	<description><![CDATA[<p>Stacks is a software pipeline for building loci from short-read sequences, such as those generated on the Illumina platform. Stacks was developed to work with restriction enzyme-based data, such as RAD-seq, for the purpose of building genetic maps and conducting population genomics and phylogeography.</p>
<p>More at http://catchenlab.life.illinois.edu/stacks/</p><p>Address of the bookmark: <a href="http://catchenlab.life.illinois.edu/stacks/" rel="nofollow">http://catchenlab.life.illinois.edu/stacks/</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</guid>
	<pubDate>Thu, 23 Jun 2016 07:26:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27973/wgsim</link>
	<title><![CDATA[WgSim]]></title>
	<description><![CDATA[<p>Reads simulator</p>
<p>Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simulate diploid genomes with SNPs and insertion/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution sequencing errors. It does not generate INDEL sequencing errors, but this can be partly compensated by simulating INDEL polymorphisms.<br><br>Wgsim outputs the simulated polymorphisms, and writes the true read coordinates as well as the number of polymorphisms and sequencing errors in read names. One can evaluate the accuracy of a mapper or a SNP caller with wgsim_eval.pl that comes with the package.<br><br></p><p>Address of the bookmark: <a href="https://github.com/lh3/wgsim" rel="nofollow">https://github.com/lh3/wgsim</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31714/krona</guid>
	<pubDate>Wed, 22 Mar 2017 04:47:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31714/krona</link>
	<title><![CDATA[Krona]]></title>
	<description><![CDATA[<p>Krona allows hierarchical data to be explored with zooming, multi-layered pie charts. Krona charts can be created using an <a href="https://github.com/marbl/Krona/wiki/ExcelTemplate">Excel template</a> or <a href="https://github.com/marbl/Krona/wiki/KronaTools">KronaTools</a>, which includes support for several bioinformatics tools and raw data formats. The interactive charts are self-contained and can be viewed with any modern web browser (see <a href="https://github.com/marbl/Krona/wiki/Browser%20support">Browser support</a>).</p>
<p><a href="http://marbl.github.io/Krona/img/screen_mgrast.png"><img src="https://camo.githubusercontent.com/27b71b1f1832523723c3d14dec764e7ad098438c/687474703a2f2f6d6172626c2e6769746875622e696f2f4b726f6e612f696d672f7468756d625f6d67726173742e706e67" width="210" height="167" alt="image" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/marbl/Krona/wiki" rel="nofollow">https://github.com/marbl/Krona/wiki</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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