<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37957?offset=470</link>
	<atom:link href="https://bioinformaticsonline.com/related/37957?offset=470" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34562/harvest-a-suite-of-core-genome-alignment-and-visualization-tools</guid>
	<pubDate>Fri, 08 Dec 2017 07:16:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34562/harvest-a-suite-of-core-genome-alignment-and-visualization-tools</link>
	<title><![CDATA[Harvest: a suite of core-genome alignment and visualization tools]]></title>
	<description><![CDATA[<p>Harvest is a suite of core-genome alignment and visualization tools for quickly analyzing thousands of intraspecific microbial genomes, including variant calls, recombination detection, and phylogenetic trees.</p>
<p><a href="https://harvest.readthedocs.io/en/latest/_images/screen.png"><img src="https://harvest.readthedocs.io/en/latest/_images/screen.png" alt="_images/screen.png" style="border: 0px;"></a><span></span></p>
<p><strong>Tools</strong></p>
<ul>
<li><a href="https://harvest.readthedocs.io/en/latest/content/parsnp.html">Parsnp</a>&nbsp;- Core-genome alignment and analysis</li>
<li><a href="https://harvest.readthedocs.io/en/latest/content/gingr.html">Gingr</a>&nbsp;- Interactive visualization of alignments, trees and variants</li>
<li><a href="https://harvest.readthedocs.io/en/latest/content/harvest-tools.html">HarvestTools</a>&nbsp;- Archiving and postprocessing</li>
<li></li>
</ul><p>Address of the bookmark: <a href="https://harvest.readthedocs.io/en/latest/" rel="nofollow">https://harvest.readthedocs.io/en/latest/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35252/hgt-finder-a-new-tool-for-horizontal-gene-transfer-finding-and-application-to-aspergillus-genomes</guid>
	<pubDate>Wed, 17 Jan 2018 05:03:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35252/hgt-finder-a-new-tool-for-horizontal-gene-transfer-finding-and-application-to-aspergillus-genomes</link>
	<title><![CDATA[HGT-Finder: A New Tool for Horizontal Gene Transfer Finding and Application to Aspergillus genomes]]></title>
	<description><![CDATA[<p><span>HGT-Finder: </span></p>
<p><span>(i) can be used for HGT detection in both prokaryotes and eukaryotes, </span></p>
<p><span>(ii) can report a statistical&nbsp;</span><em>P</em><span>&nbsp;value for each gene to indicate how likely it is to be horizontally transferred, and </span></p>
<p><span>(iii) is fully automated (requires minimal human intervention), as well as very easy to install and run.&nbsp;</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626719/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626719/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36736/checkmassessing-the-quality-of-microbial-genomes-recovered-from-isolates-single-cells-and-metagenomes</guid>
	<pubDate>Wed, 23 May 2018 04:39:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36736/checkmassessing-the-quality-of-microbial-genomes-recovered-from-isolates-single-cells-and-metagenomes</link>
	<title><![CDATA[CheckM:Assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes]]></title>
	<description><![CDATA[<p><span>CheckM provides a set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes. It provides robust estimates of genome completeness and contamination by using collocated sets of genes that are ubiquitous and single-copy within a phylogenetic lineage. Assessment of genome quality can also be examined using plots depicting key genomic characteristics (e.g., GC, coding density) which highlight sequences outside the expected distributions of a typical genome. CheckM also provides tools for identifying genome bins that are likely candidates for merging based on marker set compatibility, similarity in genomic characteristics, and proximity within a reference genome tree.</span></p><p>Address of the bookmark: <a href="http://ecogenomics.github.io/CheckM/" rel="nofollow">http://ecogenomics.github.io/CheckM/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37980/csbfinder-discovery-of-colinear-syntenic-blocks-across-thousands-of-prokaryotic-genomes</guid>
	<pubDate>Wed, 24 Oct 2018 22:12:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37980/csbfinder-discovery-of-colinear-syntenic-blocks-across-thousands-of-prokaryotic-genomes</link>
	<title><![CDATA[CSBFinder: Discovery of colinear syntenic blocks across thousands of prokaryotic genomes]]></title>
	<description><![CDATA[<p>CSBFinder is a standalone Desktop java application with a graphical user interface, that can also be executed via command line.</p>
<p>CSBFinder implements a novel methodology for the discovery, ranking, and taxonomic distribution analysis of colinear syntenic blocks (<span>CSBs</span>) - groups of genes that are consistently located close to each other, in the same order, across a wide range of taxa. CSBFinder incorporates an efficient algorithm that identifies CSBs in large genomic datasets. The discovered CSBs are ranked according to a probabilistic score and clustered to families according to their gene content similarity.</p><p>Address of the bookmark: <a href="https://github.com/dinasv/CSBFinder" rel="nofollow">https://github.com/dinasv/CSBFinder</a></p>]]></description>
	<dc:creator>Jit</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/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</guid>
	<pubDate>Mon, 17 Feb 2020 05:38:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</link>
	<title><![CDATA[Chromonomer: a tool set for repairing and enhancing assembled genomes through integration of genetic maps and conserved synteny]]></title>
	<description><![CDATA[<p>Chromonomer is a program designed to integrate a genome assembly with a genetic map. Chromonomer tries very hard to identify and remove markers that are out of order in the genetic map, when considered against their local assembly order; and to identify scaffolds that have been incorrectly assembled according to the genetic map, and split those scaffolds.</p><p>Address of the bookmark: <a href="http://catchenlab.life.illinois.edu/chromonomer/" rel="nofollow">http://catchenlab.life.illinois.edu/chromonomer/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41918/phispy-phispy-identifies-prophages-in-bacterial-and-probably-archaeal-genomes</guid>
	<pubDate>Tue, 30 Jun 2020 21:36:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41918/phispy-phispy-identifies-prophages-in-bacterial-and-probably-archaeal-genomes</link>
	<title><![CDATA[PhiSpy: PhiSpy identifies prophages in Bacterial (and probably Archaeal) genomes]]></title>
	<description><![CDATA[<p>PhiSpy identifies prophages in Bacterial (and probably Archaeal) genomes. Given an annotated genome it will use several approaches to identify the most likely prophage regions.</p>
<p>Initial versions of PhiSpy were written by</p>
<p>Sajia Akhter (<a href="mailto:sajia@stanford.edu">sajia@stanford.edu</a>)&nbsp;<a href="http://edwards.sdsu.edu/research/">Edwards Bioinformatics Lab</a></p>
<p>Improvements, bug fixes, and other changes were made by</p>
<p>Katelyn McNair&nbsp;<a href="http://edwards.sdsu.edu/research/">Edwards Bioinformatics Lab</a>&nbsp;and Przemyslaw Decewicz&nbsp;<a href="http://ddlemb.com/">DEMB at the University of Warsaw</a></p><p>Address of the bookmark: <a href="https://github.com/linsalrob/PhiSpy" rel="nofollow">https://github.com/linsalrob/PhiSpy</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43090/loretta-a-user-friendly-tool-for-assembling-viral-genomes-from-pacbio-sequence-data</guid>
	<pubDate>Wed, 23 Jun 2021 07:54:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43090/loretta-a-user-friendly-tool-for-assembling-viral-genomes-from-pacbio-sequence-data</link>
	<title><![CDATA[LoReTTA, a user-friendly tool for assembling viral genomes from PacBio sequence data]]></title>
	<description><![CDATA[<p>LoReTTA (Long Read Template-Targeted Assembler), a tool designed for performing <em>de novo</em> assembly of long reads generated from viral genomes on the PacBio platform. LoReTTA exploits a reference genome to guide the assembly process, an approach that has been successful with short reads.</p>
<p>https://academic.oup.com/ve/article/7/1/veab042/6248116</p><p>Address of the bookmark: <a href="https://academic.oup.com/ve/article/7/1/veab042/6248116" rel="nofollow">https://academic.oup.com/ve/article/7/1/veab042/6248116</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</guid>
	<pubDate>Mon, 06 May 2024 06:21:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44525/synorth-exploring-the-evolution-of-synteny-and-long-range-regulatory-interactions-in-vertebrate-genomes</link>
	<title><![CDATA[Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes]]></title>
	<description><![CDATA[<p><span>Genomic regulatory blocks are chromosomal regions spanned by long clusters of highly conserved noncoding elements devoted to long-range regulation of developmental genes, often immobilizing other, unrelated genes into long-lasting syntenic arrangements. Synorth&nbsp;</span><a href="http://synorth.genereg.net/" target="_blank">http://synorth.genereg.net/</a><span>&nbsp;is a web resource for exploring and categorizing the syntenic relationships in genomic regulatory blocks across multiple genomes, tracing their evolutionary fate after teleost whole genome duplication at the level of genomic regulatory block loci, individual genes, and their phylogenetic context.</span></p>
<p><span>More at&nbsp;https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745767/</span></p><p>Address of the bookmark: <a href="http://synorth.genereg.net/" rel="nofollow">http://synorth.genereg.net/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33791/slactree-svg-large-annotated-circular-tree-drawing</guid>
	<pubDate>Mon, 03 Jul 2017 08:02:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33791/slactree-svg-large-annotated-circular-tree-drawing</link>
	<title><![CDATA[slacTree: SVG Large Annotated Circular Tree drawing]]></title>
	<description><![CDATA[<p>A simple, extensible, Perl script for producing figures of large phylogenetic trees.</p>
<ul>
<li>While there are many other tree drawing programs, slacTree was originally written in 2009 to fill a need for producing publication quality figures of circular trees with more than 1000 taxa with custom annotations</li>
<li>Because it is a single Perl script with very few dependencies, it is easy to run, and easy to further customize</li>
<li>SVG is used because it is a scalable format allowing for very small representations of entire trees or highly magnified regions with unlimited resolution</li>
<li>Circular and radial trees are more compact than linear representations</li>
<li></li>
</ul>
<h2>&nbsp;</h2><p>Address of the bookmark: <a href="https://github.com/mccrowjp/slacTree" rel="nofollow">https://github.com/mccrowjp/slacTree</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

</channel>
</rss>