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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44525?offset=110</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38505/allhic-phasing-and-scaffolding-polyploid-genomes-based-on-hi-c-data</guid>
	<pubDate>Thu, 20 Dec 2018 12:03:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38505/allhic-phasing-and-scaffolding-polyploid-genomes-based-on-hi-c-data</link>
	<title><![CDATA[ALLHiC: Phasing and scaffolding polyploid genomes based on Hi-C data]]></title>
	<description><![CDATA[<p><span>The major problem of scaffolding polyploid genome is that Hi-C signals are frequently detected between allelic haplotypes and any existing stat of art Hi-C scaffolding program links the allelic haplotypes together. To solve the problem, we developed a new Hi-C scaffolding pipeline, called ALLHIC, specifically tailored to the polyploid genomes. ALLHIC pipeline contains a total of 5 steps:&nbsp;</span><em>prune</em><span>,&nbsp;</span><em>partition</em><span>,&nbsp;</span><em>rescue</em><span>,&nbsp;</span><em>optimize</em><span>&nbsp;and&nbsp;</span><em>build</em><span>.</span></p><p>Address of the bookmark: <a href="https://github.com/tangerzhang/ALLHiC/wiki" rel="nofollow">https://github.com/tangerzhang/ALLHiC/wiki</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</guid>
	<pubDate>Thu, 19 Dec 2019 07:33:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</link>
	<title><![CDATA[HaploTypo: a variant-calling pipeline for phased genomes]]></title>
	<description><![CDATA[<p>An increasing number of phased (i.e. with resolved haplotypes) reference genomes are available. However, most genetic variant calling tools do not explicitly account for haplotype structure. Here, we present HaploTypo, a pipeline tailored to resolve haplotypes in genetic variation analyses. HaploTypo infers the haplotype correspondence for each heterozygous variant called on a phased reference genome.</p>
<div>Availability and Implementation</div>
<p>HaploTypo is implemented in Python 2.7 and Python 3.5, and is freely available at&nbsp;<a href="https://github.com/gabaldonlab/haplotypo" target="">https://github.com/gabaldonlab/haplotypo</a>, and as a Docker image.</p><p>Address of the bookmark: <a href="https://github.com/gabaldonlab/haplotypo" rel="nofollow">https://github.com/gabaldonlab/haplotypo</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41592/refka-a-fast-and-efficient-long-read-genome-assembly-approach-for-large-and-complex-genomes</guid>
	<pubDate>Fri, 01 May 2020 03:00:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41592/refka-a-fast-and-efficient-long-read-genome-assembly-approach-for-large-and-complex-genomes</link>
	<title><![CDATA[RefKA: A fast and efficient long-read genome assembly approach for large and complex genomes]]></title>
	<description><![CDATA[<p><span>RefKA, a reference-based approach for long read genome assembly. This approach relies on breaking up a closely related reference genome into bins, aligning k-mers unique to each bin with PacBio reads, and then assembling each bin in parallel followed by a final bin-stitching step.</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/AppliedBioinformatics/RefKA" rel="nofollow">https://github.com/AppliedBioinformatics/RefKA</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</guid>
	<pubDate>Thu, 13 Aug 2020 10:06:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42038/pyparanoid-a-pipeline-for-rapid-identification-of-homologous-gene-families-in-a-set-of-genomes</link>
	<title><![CDATA[PyParanoid: a pipeline for rapid identification of homologous gene families in a set of genomes]]></title>
	<description><![CDATA[<p>PyParanoid is a pipeline for rapid identification of homologous gene families in a set of genomes - a central task of any comparative genomics analysis. The "gold standard" for identifying homologs is to use reciprocal best hits (RBHs) which depends on performing a all-vs-all sequence comparison, usually using BLAST, to determine homology. However, these methods are computationally expensive, requiring&nbsp;O(n2)&nbsp;resources to identify RBHs. This is problematic, as the modern deluge of sequencing data means that comparative genomics analyses could be performed on datasets of thousands of strains.</p><p>Address of the bookmark: <a href="https://github.com/ryanmelnyk/PyParanoid" rel="nofollow">https://github.com/ryanmelnyk/PyParanoid</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44313/orthovenn3-an-integrated-platform-for-exploring-and-visualizing-orthologous-data-across-genomes</guid>
	<pubDate>Tue, 02 May 2023 00:48:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44313/orthovenn3-an-integrated-platform-for-exploring-and-visualizing-orthologous-data-across-genomes</link>
	<title><![CDATA[OrthoVenn3: an integrated platform for exploring and visualizing orthologous data across genomes]]></title>
	<description><![CDATA[<p><span>OrthoVenn3 is a powerful tool for comparative genomics analysis, used as a web server for full genome comparisons, annotation, and evolutionary analysis of orthologous clusters across multiple species. It has already been used by thousands of users from over 60 countries.</span></p><p>Address of the bookmark: <a href="https://orthovenn3.bioinfotoolkits.net/" rel="nofollow">https://orthovenn3.bioinfotoolkits.net/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44768/tritex-a-computational-pipeline-for-chromosome-scale-assembly-of-plant-genomes</guid>
	<pubDate>Fri, 14 Feb 2025 10:53:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44768/tritex-a-computational-pipeline-for-chromosome-scale-assembly-of-plant-genomes</link>
	<title><![CDATA[TRITEX, a computational pipeline for chromosome-scale assembly of plant genomes]]></title>
	<description><![CDATA[<p><span>This is the documentation of TRITEX, a computational pipeline for chromosome-scale assembly of plant genomes. It was developed in the research group Domestication Genomics at the Leibniz Institute of Plant Genetics and Crop Research (IPK) Gatersleben.</span></p><p>Address of the bookmark: <a href="https://tritexassembly.bitbucket.io/" rel="nofollow">https://tritexassembly.bitbucket.io/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</guid>
	<pubDate>Tue, 15 Jan 2019 09:39:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38692/geneck-gene-network-construction-kit-is-a-comprehensive-online-tool-kit-that-integrate-various-statistical-methods-to-construct-gene-networks</link>
	<title><![CDATA[GeNeCK (Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks]]></title>
	<description><![CDATA[<p><strong>GeNeCK</strong><span>&nbsp;(Gene Network Construction Kit) is a comprehensive online tool kit that integrate various statistical methods to construct gene networks based on gene expression data and optional hub gene information.</span></p>
<p><span><span>It efficiently constructs gene networks from expression data. It allows the user to use ten different network construction methods (such as partial correlation-, likelihood-, Bayesian- and mutual information-based methods) and integrates the resulting networks from multiple methods. Hub gene information, if available, can be incorporated to enhance performance.</span></span></p>
<p><span><span><span>GeNeCK is an efficient and easy-to-use web application for gene regulatory network construction. It can be accessed at&nbsp;</span><span><a href="http://lce.biohpc.swmed.edu/geneck" target="_blank"><span>http://lce.biohpc.swmed.edu/geneck</span></a></span></span></span></p><p>Address of the bookmark: <a href="http://lce.biohpc.swmed.edu/geneck/" rel="nofollow">http://lce.biohpc.swmed.edu/geneck/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29274/strudel</guid>
	<pubDate>Fri, 30 Sep 2016 09:47:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29274/strudel</link>
	<title><![CDATA[Strudel]]></title>
	<description><![CDATA[<p>Strudel is our graphical tool for visualizing genetic and physical maps of genomes for comparative purposes. The application aims to let the user examine their data at a variety of different levels of resolution, from entire maps to individual markers, and explore syntenic relationships between genomes. All browsing and interaction with Strudel happens in real-time &ndash; there is no need to wait while the maps are generated. It is built using Java 1.6 and ships with its own JRE, so there is no need for users to install or update Java.</p><p>Address of the bookmark: <a href="https://ics.hutton.ac.uk/strudel/" rel="nofollow">https://ics.hutton.ac.uk/strudel/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</guid>
	<pubDate>Thu, 22 Dec 2016 03:53:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</link>
	<title><![CDATA[MCscan]]></title>
	<description><![CDATA[<p><span>MCscan is a computer program that can simultaneously scan multiple genomes to identify homologous chromosomal regions and subsequently align these regions using genes as anchors. This is the toolset for generating the synteny correspondences in&nbsp;</span><a href="http://chibba.agtec.uga.edu/duplication">Plant Genome Duplication Database</a><span>. It is intended as an easy-to-use and quick way to identify conserved gene arrays both within the same genome and across different genomes.</span></p>
<p><span>More at&nbsp;http://chibba.agtec.uga.edu/duplication/mcscan/</span></p><p>Address of the bookmark: <a href="http://chibba.agtec.uga.edu/duplication/mcscan/" rel="nofollow">http://chibba.agtec.uga.edu/duplication/mcscan/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33720/deschrambler</guid>
	<pubDate>Thu, 29 Jun 2017 11:54:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33720/deschrambler</link>
	<title><![CDATA[DESCHRAMBLER]]></title>
	<description><![CDATA[<p>DESCHRAMBLER is shown to produce highly accurate reconstructions using data simulation and by benchmarking it against other reconstruction tools</p>
<p>You can find the detail of reconstructed data at http://bioinfo.konkuk.ac.kr/DESCHRAMBLER/</p><p>Address of the bookmark: <a href="https://github.com/jkimlab/DESCHRAMBLER" rel="nofollow">https://github.com/jkimlab/DESCHRAMBLER</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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