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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36597?offset=220</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</guid>
	<pubDate>Wed, 27 Dec 2017 00:04:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34877/recovery-of-complete-genomes-from-metagenomes</link>
	<title><![CDATA[Recovery of complete genomes from metagenomes]]></title>
	<description><![CDATA[<p>This project contains scripts and tutorials on how to assemble individual microbial genomes from metagenomes, as described in:</p>
<p><strong>Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes</strong></p>
<p><a href="http://personprofil.aau.dk/120257">Mads Albertsen</a>,&nbsp;<a href="http://ecogenomic.org/users/phil-hugenholtz">Philip Hugenholtz</a>,&nbsp;<a href="http://ecogenomic.org/users/adam-skarshewski">Adam Skarshewski</a>,&nbsp;<a href="http://www.ecogenomic.org/users/gene-tyson">Gene W. Tyson</a>,&nbsp;<a href="http://personprofil.aau.dk/103057">K&aring;re L. Nielsen</a>&nbsp;and&nbsp;<a href="http://personprofil.aau.dk/105842">Per .H. Nielsen</a></p>
<p>Nature Biotechnology 2013, doi:&nbsp;<a href="http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.2579.html">10.1038/nbt.2579</a></p><p>Address of the bookmark: <a href="http://madsalbertsen.github.io/multi-metagenome/" rel="nofollow">http://madsalbertsen.github.io/multi-metagenome/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</guid>
	<pubDate>Mon, 14 May 2018 04:02:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36590/digest-in-silico-restriction-digest-of-complete-genomes</link>
	<title><![CDATA[Digest: In silico restriction digest of complete genomes]]></title>
	<description><![CDATA[<p><span>This tool allows to retrieve number of cleavages yielded by commercially available endonucleases in up-to-date sequenced prokaryotic genomes. When the number of fragments is bellow 50, Pulse Field gel Electrophoresis (PFGE) is simulated.</span></p>
<p>A tool for restriction digest of&nbsp;<a href="http://insilico.ehu.eus/restriction/long_seq/">long</a>user's sequences is available.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://insilico.ehu.es/digest/" rel="nofollow">http://insilico.ehu.es/digest/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</guid>
	<pubDate>Wed, 22 Aug 2018 03:21:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37572/gtdb-tk-a-toolkit-for-assigning-objective-taxonomic-classifications-to-bacterial-and-archaeal-genomes</link>
	<title><![CDATA[GTDB-Tk: A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes.]]></title>
	<description><![CDATA[<p>GTDB-Tk is a software toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. It is computationally efficient and designed to work with recent advances that allow hundreds or thousands of metagenome-assembled genomes (MAGs) to be obtained directly from environmental samples. It can also be applied to isolate and single-cell genomes. The GTDB-Tk is open source and released under the GNU General Public License (Version 3).</p>
<p>GTDB-Tk is&nbsp;<span>under active development and validation</span>. Please independently confirm the GTDB-Tk predictions by manually inspecting the tree and bringing any discrepencies to our attention. Notifications about GTDB-Tk releases will be available through the ACE Twitter account (<a href="https://twitter.com/ace_uq">https://twitter.com/ace_uq</a>).</p><p>Address of the bookmark: <a href="https://github.com/Ecogenomics/GTDBTk" rel="nofollow">https://github.com/Ecogenomics/GTDBTk</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39869/mfannot-a-program-for-the-annotation-of-mitochondrial-and-plastid-genomes</guid>
	<pubDate>Mon, 26 Aug 2019 11:47:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39869/mfannot-a-program-for-the-annotation-of-mitochondrial-and-plastid-genomes</link>
	<title><![CDATA[MFannot : a program for the annotation of mitochondrial and plastid genomes]]></title>
	<description><![CDATA[<p><span>MFannot is a program for the annotation of mitochondrial and plastid genomes</span></p>
<p>MFannot is a program for the annotation of mitochondrial and plastid genomes. It is a PERL wrapper around a set of diverse, external independent tools.</p>
<p>It makes intense use of RNA/intron detection tools including&nbsp;<a href="http://hmmer.org/">HMMER</a>,&nbsp;<a href="https://github.com/nathanweeks/exonerate">Exonerate</a>,&nbsp;<a href="https://bioinformatics.ca/links_directory/tool/9822/erpin">Erpin</a>&nbsp;and others.</p>
<p><a href="http://megasun.bch.umontreal.ca/cgi-bin/mfannot/mfannotInterface.pl">http://megasun.bch.umontreal.ca/cgi-bin/mfannot/mfannotInterface.pl</a></p><p>Address of the bookmark: <a href="https://github.com/BFL-lab/Mfannot" rel="nofollow">https://github.com/BFL-lab/Mfannot</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41686/catbat-tool-for-taxonomic-classification-of-contigs-and-metagenome-assembled-genomes-mags</guid>
	<pubDate>Mon, 18 May 2020 10:53:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41686/catbat-tool-for-taxonomic-classification-of-contigs-and-metagenome-assembled-genomes-mags</link>
	<title><![CDATA[CAT/BAT: tool for taxonomic classification of contigs and metagenome-assembled genomes (MAGs)]]></title>
	<description><![CDATA[<p>Contig Annotation Tool (CAT) and Bin Annotation Tool (BAT) are pipelines for the taxonomic classification of long DNA sequences and metagenome assembled genomes (MAGs/bins) of both known and (highly) unknown microorganisms, as generated by contemporary metagenomics studies. The core algorithm of both programs involves gene calling, mapping of predicted ORFs against the nr protein database, and voting-based classification of the entire contig / MAG based on classification of the individual ORFs. CAT and BAT can be run from intermediate steps if files are formated appropriately (see <a href="https://github.com/dutilh/CAT#usage">Usage</a>).</p><p>Address of the bookmark: <a href="https://github.com/dutilh/CAT" rel="nofollow">https://github.com/dutilh/CAT</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42357/irscope-an-online-program-to-visualize-the-junction-sites-of-chloroplast-genomes</guid>
	<pubDate>Wed, 25 Nov 2020 19:44:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42357/irscope-an-online-program-to-visualize-the-junction-sites-of-chloroplast-genomes</link>
	<title><![CDATA[IRscope: an online program to visualize the junction sites of chloroplast genomes]]></title>
	<description><![CDATA[<p><span>eMPRess, a software program for phylogenetic tree reconciliation under the duplication-transfer-loss model that systematically addresses the problems of choosing event costs and selecting representative solutions, enabling users to make more robust inferences.</span></p><p>Address of the bookmark: <a href="https://sites.google.com/g.hmc.edu/empress/home" rel="nofollow">https://sites.google.com/g.hmc.edu/empress/home</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44561/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</guid>
	<pubDate>Sat, 08 Jun 2024 16:25:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44561/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</link>
	<title><![CDATA[Bactopia: a flexible pipeline for complete analysis of bacterial genomes]]></title>
	<description><![CDATA[<p>Bactopia is a flexible pipeline for complete analysis of bacterial genomes. The goal of Bactopia is process your data with a broad set of tools, so that you can get to the fun part of analyses quicker!</p>
<p>Bactopia was inspired by&nbsp;<a href="https://staphopia.github.io/">Staphopia</a>, a workflow we (Tim Read and myself) released that is targeted towards&nbsp;<em>Staphylococcus aureus</em>&nbsp;genomes. Using what we learned from Staphopia and user feedback, Bactopia was developed from scratch with usability, portability, and speed in mind from the start.</p>
<p>Bactopia uses&nbsp;<a href="https://www.nextflow.io/">Nextflow</a>&nbsp;to manage the workflow, allowing for support of many types of environments (e.g. cluster or cloud). Bactopia allows for the usage of many public datasets as well as your own datasets to further enhance the analysis of your sequencing. Bactopia only uses software packages available from&nbsp;<a href="https://bioconda.github.io/">Bioconda</a>&nbsp;and&nbsp;<a href="https://conda-forge.org/">Conda-Forge</a>&nbsp;to make installation as simple as possible for&nbsp;<em>all</em>&nbsp;users.</p>
<p>To highlight the use of&nbsp;<a href="https://bactopia.github.io/latest/full-guide/">Bactopia</a>&nbsp;and&nbsp;<a href="https://bactopia.github.io/latest/bactopia-tools/">Bactopia Tools</a>, we performed an analysis of 1,664 public&nbsp;<em>Lactobacillus</em>&nbsp;genomes, focusing on&nbsp;<em>Lactobacillus crispatus</em>, a species that is a common part of the human vaginal microbiome. The results from this analysis are published in mSystems under the title:&nbsp;<em><a href="https://doi.org/10.1128/mSystems.00190-20">Bactopia: a flexible pipeline for complete analysis of bacterial genomes</a></em></p>
<p><a href="https://bactopia.github.io/latest/assets/bactopia-workflow.png"><img src="https://bactopia.github.io/latest/assets/bactopia-workflow.png" alt="Bactopia Workflow" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://bactopia.github.io/latest/" rel="nofollow">https://bactopia.github.io/latest/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34702/run-miniasm-assembler-on-nanopore-reads</guid>
	<pubDate>Mon, 18 Dec 2017 04:07:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34702/run-miniasm-assembler-on-nanopore-reads</link>
	<title><![CDATA[Run miniasm assembler on nanopore reads !]]></title>
	<description><![CDATA[<p>Miniasm is a very fast OLC-based&nbsp;<em>de novo</em>&nbsp;assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by&nbsp;<a href="https://github.com/lh3/minimap">minimap</a>) as input and outputs an assembly graph in the&nbsp;<a href="https://github.com/pmelsted/GFA-spec/blob/master/GFA-spec.md">GFA</a>&nbsp;format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final&nbsp;<a href="http://wgs-assembler.sourceforge.net/wiki/index.php/Celera_Assembler_Terminology">unitig</a>&nbsp;sequences. Thus the per-base error rate is similar to the raw input reads.</p><p>Find the detail of the reads repeats:</p><blockquote><p>fq2fa ONT_A.fastq ONT_A.fasta&nbsp;<br /><br />minimap2 -xava-ont ONT_A.fasta ONT_A.fasta -t10 -X &gt; AONT.paf&nbsp;<br /><br />awk '{if($1==$6){print}}' AONT.paf &gt; AONTself.paf&nbsp;<br /><br />awk '$5=="-"' AONTself.paf | awk '{print $1}'| sort|uniq &gt; invertedrepeat.list</p></blockquote><p>Generated a few palindrome and repeats plots (highlighting only repeats largest than 10, 20 and 30 kb)</p><blockquote><p>minidot -f 5 -m 30000 AONTself.paf &gt; AONTself30000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself30000.eps &gt; AONTself30000final.eps&nbsp;<br /><br />minidot -f 5 -m 20000 AONTself.paf &gt; AONTself20000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself20000.eps &gt; AONTself20000final.eps&nbsp;<br /><br />minidot -f 5 -m 10000 AONTself.paf &gt; AONTself10000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself10000.eps &gt; AONTself10000final.eps&nbsp;</p></blockquote><p>Assemble with miniasm:</p><blockquote><p>miniasm -f ONT_A.fasta AONT.paf &gt; AONT.gfa&nbsp;</p><p>grep '^S' AONT.gfa |awk '{print "&gt;"$2"\n"$3}' &gt; AONT_miniasm.fasta&nbsp;<br /><br />minimap2 -xasm10 AONT_miniasm.fasta AONT_miniasm.fasta -t1 -X &gt; AONT_miniasm.paf&nbsp;<br /><br />awk '{if($1==$6){print}}' AONT_miniasm.paf &gt; AONT_miniasm_self.paf&nbsp;<br /><br />minidot -f 5 -m 10000 AONT_miniasm_self.paf &gt; AONT_miniasm_self10000.eps&nbsp;</p></blockquote><p>Njoy the assembly !</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36630/frequent-paired-end-reads-pe-2x100-mapping-command-lines</guid>
	<pubDate>Tue, 15 May 2018 08:59:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36630/frequent-paired-end-reads-pe-2x100-mapping-command-lines</link>
	<title><![CDATA[Frequent Paired-end reads (PE 2x100) mapping command lines]]></title>
	<description><![CDATA[
<p>bowtie2 -x hs37m -X 650 -q -1 r1.fq -2 r2.fq -S r12.bowtie2.sam  </p>

<p>bwa aln hs37m.fa r1.fq &gt; r1.sai &amp;&amp; bwa aln hs37m.fa r2.fq &gt; r2.sai \  <br />    &amp;&amp; bwa sampe hs37m r1.sai r2.sai r1.fq r2.fq &gt; r12.bwa.sam  </p>

<p>bwa bwasw ../index/bwa/hs37m.fa r12.fq &gt; r12.bwasw.sam  </p>

<p>gsnap -A sam -d hs37m r1.fq r2.fq &gt; r12.gsnap.sam  </p>

<p>novoalign -r Random -o SAM -f r1.fq r2.fq -i 500 50 -d hs37m-k14s3.novo &gt; r12.novo.sam  </p>

<p>smalt map -f samsoft -i 650 -o r12.smalt-k20s13.sam hs37m-k20s13 r1.fq r2.fq  </p>

<p>stampy.py -g hs37m -h hs37m -o r12.stampy.sam -M r1.fq,r2.fq  </p>

<p>soap -D hs37m.fa.index -a r1.fq -b r2.fq -l 32 -g 3 -u dummy -2 dummy -o r12.soap</p>
]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36812/porechop-tool-for-finding-and-removing-adapters-from-oxford-nanopore-reads</guid>
	<pubDate>Tue, 29 May 2018 07:33:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36812/porechop-tool-for-finding-and-removing-adapters-from-oxford-nanopore-reads</link>
	<title><![CDATA[Porechop:  tool for finding and removing adapters from Oxford Nanopore reads]]></title>
	<description><![CDATA[<p>Porechop is a tool for finding and removing adapters from <a href="https://nanoporetech.com/">Oxford Nanopore</a> reads. Adapters on the ends of reads are trimmed off, and when a read has an adapter in its middle, it is treated as chimeric and chopped into separate reads. Porechop performs thorough alignments to effectively find adapters, even at low sequence identity.</p>
<p>Porechop also supports demultiplexing of Nanopore reads that were barcoded with the <a href="https://store.nanoporetech.com/native-barcoding-kit-1d.html">Native Barcoding Kit</a>, <a href="https://store.nanoporetech.com/pcr-barcoding-kit-96.html">PCR Barcoding Kit</a> or <a href="https://store.nanoporetech.com/rapid-barcoding-sequencing-kit.html">Rapid Barcoding Kit</a>.</p><p>Address of the bookmark: <a href="https://github.com/rrwick/Porechop" rel="nofollow">https://github.com/rrwick/Porechop</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

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