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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/34922?offset=70</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38475/purge-haplotigs-pipeline-to-help-with-curating-heterozygous-diploid-genome-assemblies</guid>
	<pubDate>Mon, 17 Dec 2018 03:17:20 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38475/purge-haplotigs-pipeline-to-help-with-curating-heterozygous-diploid-genome-assemblies</link>
	<title><![CDATA[Purge Haplotigs: Pipeline to help with curating heterozygous diploid genome assemblies]]></title>
	<description><![CDATA[<p>Some parts of a genome may have a very high degree of heterozygosity. This causes contigs for both haplotypes of that part of the genome to be assembled as separate primary contigs, rather than as a contig and an associated haplotig. This can be an issue for downstream analysis whether you're working on the haploid or phased-diploid assembly.</p>
<p><span>Identify pairs of contigs that are syntenic and move one of them to the haplotig 'pool'. The pipeline uses mapped read coverage and Minimap2 alignments to determine which contigs to keep for the haploid assembly. Dotplots are optionally produced for all flagged contig matches, juxtaposed with read-coverage, to help the user determine the proper assignment of any remaining ambiguous contigs. The pipeline will run on either a haploid assembly (i.e. Canu, FALCON or FALCON-Unzip primary contigs) or on a phased-diploid assembly (i.e. FALCON-Unzip primary contigs + haplotigs). Here are&nbsp;</span><a href="https://bitbucket.org/mroachawri/purge_haplotigs/wiki/Examples">two examples</a><span>&nbsp;of how Purge Haplotigs can improve a haploid and diploid assembly.</span></p><p>Address of the bookmark: <a href="https://bitbucket.org/mroachawri/purge_haplotigs" rel="nofollow">https://bitbucket.org/mroachawri/purge_haplotigs</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40814/accesssyri-finding-genomic-rearrangements-and-local-sequence-differences-from-whole-genome-assemblies</guid>
	<pubDate>Sat, 01 Feb 2020 13:38:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40814/accesssyri-finding-genomic-rearrangements-and-local-sequence-differences-from-whole-genome-assemblies</link>
	<title><![CDATA[AccessSyRI: finding genomic rearrangements and local sequence differences from whole-genome assemblies]]></title>
	<description><![CDATA[<p><span>Access</span><span>SyRI: finding genomic rearrangements and</span><span>local sequence differences from whole-</span><span>genome assemblies</span><span><br></span></p>
<p><span><span>SyRI, a pairwise whole-genome comparison tool for chromosome-level assemblies. SyRI starts by finding rearranged regions and then searches for differences in the sequences, which are distinguished for residing in syntenic or rearranged regions. This distinction is important as rearranged regions are inherited differently compared to syntenic regions.</span></span></p>
<p><span><a href="https://genomebiology.biomedcentral.com/articles/10.1186/s13059-019-1911-0">https://genomebiology.biomedcentral.com/articles/10.1186/s13059-019-1911-0</a></span></p><p>Address of the bookmark: <a href="https://github.com/schneebergerlab/syri" rel="nofollow">https://github.com/schneebergerlab/syri</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43364/ragtag-a-collection-of-software-tools-for-scaffolding-and-improving-modern-genome-assemblies</guid>
	<pubDate>Sat, 11 Sep 2021 00:28:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43364/ragtag-a-collection-of-software-tools-for-scaffolding-and-improving-modern-genome-assemblies</link>
	<title><![CDATA[RagTag: a collection of software tools for scaffolding and improving modern genome assemblies]]></title>
	<description><![CDATA[<p>RagTag is a collection of software tools for scaffolding and improving modern genome assemblies. Tasks include:</p>
<ul>
<li>Homology-based misassembly&nbsp;<a href="https://github.com/malonge/RagTag/wiki/correct">correction</a></li>
<li>Homology-based assembly&nbsp;<a href="https://github.com/malonge/RagTag/wiki/scaffold">scaffolding</a>&nbsp;and&nbsp;<a href="https://github.com/malonge/RagTag/wiki/patch">patching</a></li>
<li>Scaffold&nbsp;<a href="https://github.com/malonge/RagTag/wiki/merge">merging</a></li>
</ul><p>Address of the bookmark: <a href="https://github.com/malonge/RagTag" rel="nofollow">https://github.com/malonge/RagTag</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/42402/two-postdoc-positions-to-study-multiscale-genome-evolution-and-cephalopod-gene-regulation-university-of-vienna-austria</guid>
  <pubDate>Thu, 17 Dec 2020 11:45:16 -0600</pubDate>
  <link></link>
  <title><![CDATA[Two postdoc positions to study multiscale genome evolution and cephalopod gene regulation (University of Vienna, Austria)]]></title>
  <description><![CDATA[
<p>Vienna Biocenter are seeking two postdoctoral researchers to join our team and work on the ERC funded project "METASCALE: Modes of genome evolution during major metazoan transitions". The task of both positions will be to study co-evolutionary trends within animal genomes and their association with the emergence of new gene regulation. Our group employs methods of comparative and regulatory genomics to study the regulatory impact of transitions in animal genome architecture. More recently, we have identified a major genome reorganization in the "smart" coleoid cephalopod molluscs (squid, octopus, cuttlefish) that, together with other genomic changes, potentially comprises a unique path or mode of genome evolution among animals. We are thus interested in quantifying these modes of genome evolution across all available animal genomes and to test whether their shifts are associated with the emergence of novel regulation (e.g., in cephalopods). One of our main model species is the Hawaiian bobtail squid species Euprymna scolopes.  The tasks of the two candidates will be complimentary and highly collaborative with one position focusing on comparative genomics analyses across all metazoans and the other position on regulatory genomics in the squid. A solid background in in bioinformatics and comparative genomics is highly desired for the first position, whereas the second position will benefit from experience in molecular and regulatory genomics methods such as HiC, ATAC-seq, RNA-seq or single cell transcriptomics.</p>

<p>The postdocs will join an international group and network of researchers at the University of Vienna studying a diverse range of species and questions in molecular evolution, development, morphology and genomics. Our group is also part of the large evolVienna network of more than 50 evolutionary biology labs in Vienna, across several universities and research institutes. Our Faculty will be relocating to a new campus at the Vienna Biocenter in summer 2021 (https://biologiezentrum.univie.ac.at/en/). Vienna is a vibrant historic European capital with a high QOL. Information about postdoctoral salaries in Austria can be found on this webpage: https://www.fwf.ac.at/en/research-funding/personnel-costs/</p>

<p>Earliest start date will be after July 2021. Initial term of employment is for two years with the possibility of extension. Remote working, at least initially, is a possibility.</p>

<p>Requirements:<br />- PhD degree or equivalent by the start date <br />- Publishing record in peer-reviewed journals or evidence thereof <br />- At least 2 letters of support</p>

<p>Applications including a letter of motivation should be submitted via the Job Center to the University of Vienna (https://personalwesen.univie.ac.at/en/jobs-recruiting/job-center/,<br />job reference number 11615).</p>

<p>Application deadline: January 15th 2021.<br />Application link: https://univis.univie.ac.at/ebewerbung</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37579/cbs-comparative-microbial-genomics-group-biotools-download-page</guid>
	<pubDate>Wed, 22 Aug 2018 21:59:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37579/cbs-comparative-microbial-genomics-group-biotools-download-page</link>
	<title><![CDATA[CBS Comparative Microbial Genomics group - BioTools download page]]></title>
	<description><![CDATA[<div id="section2">
<p>he CMG-biotools system presents a stand-alone interface for comparative microbial genomics. The package is a customized operating system, based on Xubuntu 10.10, available through the open source Ubuntu project. The system can be installed on a virtual computer, allowing the user to run the system alongside any other operating system. Source codes for all programs are provided under GNU license, which makes it possible to transfer the programs to other systems if so desired. We here demonstrate the package by comparing and analyzing the diversity within the class&nbsp;<em>Negativicutes</em>, represented by 31 genomes including 10 genera. The analyses include 16S rRNA phylogeny, basic DNA and codon statistics, proteome comparisons using BLAST and graphical analyses of DNA structures.</p>
<p>&nbsp;Paper:&nbsp;http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0060120</p>
</div>
<div id="section3"><a name="" title="Conclusion"></a><span></span></div><p>Address of the bookmark: <a href="http://www.cbs.dtu.dk/biotools/CMGtools/" rel="nofollow">http://www.cbs.dtu.dk/biotools/CMGtools/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/42588/postdoc-in-genomics-of-pipefishes-and-seahorses-at-nsf-funded-postdoctoral-project-in-adam-jones-lab</guid>
  <pubDate>Thu, 07 Jan 2021 21:22:24 -0600</pubDate>
  <link></link>
  <title><![CDATA[Postdoc in Genomics of Pipefishes and Seahorses at NSF-funded postdoctoral project in Adam Jones' Lab]]></title>
  <description><![CDATA[
<p>An NSF-funded postdoctoral position is available in Adam Jones' Lab<br />at the University of Idaho to study the evolution and development of<br />the male's brood pouch in syngnathid fishes (seahorses, pipefishes<br />and seadragons). The project is being conducted in collaboration<br />with Dr. William Cresko's group at the University of Oregon. The<br />postdoc will be involved in studies of comparative genomics across<br />the family Syngnathidae, investigations of brood pouch morphology, and<br />characterization of the brood pouch microbiome. The position will be<br />funded for two years, with the possibility of a third year. The postdoc<br />will be based at the University of Idaho and will interact extensively<br />with the Cresko Lab at the University of Oregon.</p>

<p>The University of Idaho is in Moscow, a small college town located in<br />Northern Idaho on the Washington border. Moscow is widely considered to<br />be a great place to live, and it's known for a pleasant downtown, active<br />farmer's market, and nearby recreational opportunities. All of Moscow<br />is within biking or walking distance of the University of Idaho. For<br />more information about Moscow, see https://visitmoscowid.com/.</p>

<p>The University of Idaho has very strong faculty in evolution and<br />genomics in multiple departments and interdisciplinary programs. Of<br />particular note are the Bioinformatics and Computational Biology<br />Program (BCB: https://www.uidaho.edu/sci/bcb/people/faculty) and<br />the Institute for Bioinformatics and Evolutionary Studies (IBEST:<br />https://www.ibest.uidaho.edu/index.php). In addition, the University of<br />Idaho is only eight miles from Washington State University in Pullman, and<br />faculty from the two institutions interact and collaborate extensively.</p>

<p>Minimum qualifications include: a Ph.D. in biological sciences,<br />bioinformatics, or a related discipline; experience conducting research<br />in genomics or evolutionary biology, as evidenced by publications<br />in peer-reviewed journals; and evidence of strong written and oral<br />communication skills.  Experience analyzing next-generation sequence<br />data and familiarity with the genomics of marine fishes are desirable<br />but not required.</p>

<p>Apply at: https://uidaho.peopleadmin.com/postings/30003</p>

<p>Review of applications will begin January 15, 2021. The start date<br />is flexible.</p>

<p>The University of Idaho is an equal opportunity/Affirmative Action/equal<br />access employer.</p>

<p>Informal inquiries are encouraged and can be directed to Adam Jones<br />(adamjones@uidaho.edu).</p>

<p>"adamjones@uidaho.edu"</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43725/comparative-genomics-workshops</guid>
	<pubDate>Tue, 25 Jan 2022 20:39:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43725/comparative-genomics-workshops</link>
	<title><![CDATA[Comparative Genomics Workshops !]]></title>
	<description><![CDATA[<p><span>This meeting's objective was to obtain a big picture look at the current state of the field of comparative&nbsp;genomics with a focus on commonalities across genomic investigations into humans, model organisms&nbsp;(both traditional and non-traditional), agricultural species, wildlife species and microbes.</span></p>
<p>https://www.genome.gov/event-calendar/perspectives-in-comparative-genomics-and-evolution</p><p>Address of the bookmark: <a href="https://www.genome.gov/event-calendar/perspectives-in-comparative-genomics-and-evolution" rel="nofollow">https://www.genome.gov/event-calendar/perspectives-in-comparative-genomics-and-evolution</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44799/unlocking-evolutionary-secrets-a-dive-into-comparative-genomics-methods</guid>
	<pubDate>Tue, 20 May 2025 00:25:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44799/unlocking-evolutionary-secrets-a-dive-into-comparative-genomics-methods</link>
	<title><![CDATA[Unlocking Evolutionary Secrets: A Dive into Comparative Genomics Methods]]></title>
	<description><![CDATA[<p>Comparative genomics is the art and science of comparing genomes&mdash;across species, within species, or even among individuals&mdash;to unravel evolutionary relationships, functional elements, and genetic adaptations. As sequencing technologies have advanced and genome databases have expanded, comparative genomics has become a cornerstone of modern biology, shedding light on everything from antibiotic resistance in bacteria to human disease genetics.</p><p>In this post, we&rsquo;ll explore the core methods used in comparative genomics, the questions they help answer, and how they&rsquo;re shaping our understanding of life.</p><p><strong>1. Whole-Genome Alignment</strong><br />Whole-genome alignment involves mapping the entire genome of one species to another. Tools like MUMmer, MAUVE, and LASTZ perform large-scale sequence alignments to detect conserved regions, rearrangements, insertions, and deletions.</p><p>Use Case:<br />Comparing human and chimpanzee genomes to identify evolutionary conserved sequences (ECS) and regions of divergence.</p><p>Key Challenges:<br />Handling repetitive sequences and genome rearrangements.</p><p>Computational complexity in large genomes.</p><p><strong>2. Synteny and Collinearity Analysis</strong><br />Synteny refers to conserved blocks of gene order across species. Tools like MCScanX, SynMap, or CHITRA (for visualizing synteny interactively) detect these blocks to understand chromosomal evolution.</p><p>Use Case:<br />Studying ancient genome duplications in plants.</p><p>Investigating chromosomal rearrangements in cancer genomes.</p><p><strong>3. Ortholog and Paralog Detection</strong><br />Orthologs are genes in different species that evolved from a common ancestor, while paralogs are genes duplicated within a genome. Identifying them is crucial for functional annotation and evolutionary studies.</p><p>Popular Tools:<br />OrthoFinder, Orthologous MAtrix (OMA), InParanoid, and EggNOG.</p><p>Use Case:<br />Functional prediction of uncharacterized genes based on orthologs in model organisms.</p><p>Tracing gene family evolution.</p><p><strong>4. Phylogenomic Analysis</strong><br />Phylogenomic methods combine phylogenetics and genomics to infer evolutionary trees based on genome-wide data. These methods can handle dozens to hundreds of genomes, using concatenated alignments or gene trees.</p><p>Tools:<br />RAxML, IQ-TREE, ASTRAL, Phylip, BEAST.</p><p>Use Case:<br />Resolving the evolutionary relationships between microbial species.</p><p>Studying speciation events.</p><p><strong>5. Pan-Genome Analysis</strong><br />The pan-genome consists of the core genome (shared by all strains) and the accessory genome (strain-specific genes). This is especially popular in microbial genomics.</p><p>Tools:<br />Roary, Panaroo, BPGA, PGAP.</p><p>Use Case:<br />Understanding virulence factor diversity in E. coli.</p><p>Designing broad-spectrum vaccines.</p><p><strong>6. Comparative Transcriptomics</strong><br />Comparing transcriptomes across species or conditions reveals conserved and unique expression patterns. RNA-seq data can be mapped to reference genomes to identify orthologous expression profiles.</p><p>Use Case:<br />Comparing stress response in extremophiles and model species.</p><p>Studying conserved regulatory networks.</p><p><strong>7. Functional Element Comparison</strong><br />Beyond genes, comparative genomics also targets non-coding regions&mdash;enhancers, promoters, miRNAs. Conservation across species often implies functional importance.</p><p>Tools:<br />PhastCons, GERP, phyloP (based on multiple alignments).</p><p>Use Case:<br />Detecting conserved non-coding elements in vertebrates.</p><p>Studying regulatory divergence in human evolution.</p><p><strong>8. Horizontal Gene Transfer (HGT) Detection</strong><br />In microbes, genes often jump across species boundaries. Comparative genomics can detect HGT by identifying genes that defy the expected phylogenetic pattern.</p><p>Tools:<br />HGTector, DarkHorse, AlienHunter, SIGI-HMM.</p><p>Use Case:<br />Tracing antibiotic resistance genes.</p><p>Exploring microbial adaptability in extreme environments.</p><p><strong>Final Thoughts</strong><br />Comparative genomics is a powerful lens to observe the diversity and unity of life. With a broad toolkit&mdash;from aligners to orthology pipelines, phylogenetic engines to visualization tools&mdash;it allows scientists to ask big questions: How did genomes evolve? What makes species unique? Where do new genes come from?</p><p>Whether you're studying extremophiles, building better crops, or exploring human ancestry, comparative genomics offers the methods to connect the dots across the tree of life.</p><p>&nbsp;</p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40369/phyloxml-xml-for-evolutionary-biology-and-comparative-genomics</guid>
	<pubDate>Sun, 08 Dec 2019 09:41:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40369/phyloxml-xml-for-evolutionary-biology-and-comparative-genomics</link>
	<title><![CDATA[phyloXML: XML for evolutionary biology and comparative genomics]]></title>
	<description><![CDATA[<p><a href="http://www.biomedcentral.com/1471-2105/10/356/">phyloXML</a><span>&nbsp;(</span><a href="http://www.phyloxml.org/examples_syntax/phyloxml_syntax_example_1.html">example</a><span>) is an&nbsp;</span><a href="http://en.wikipedia.org/wiki/XML">XML</a><span>&nbsp;language designed to describe phylogenetic trees (or networks) and associated data. PhyloXML provides elements for commonly used features, such as taxonomic information, gene names and identifiers, branch lengths, support values, and gene duplication and speciation events. Using these standardized elements allows interoperability between various applications and databases. Furthermore, both due to extensible nature of XML itself and the provision of &lt;property&gt; elements by phyloXML, extensibility as well as domain specific applications are ensured. The structure of phyloXML is described by&nbsp;</span><a href="http://en.wikipedia.org/wiki/XML_Schema_%28W3C%29">XML Schema Definition (XSD)</a><span>&nbsp;language.</span></p>
<p><a href="http://www.phyloxml.org/archaeopteryx-js/adh.html">http://www.phyloxml.org/archaeopteryx-js/adh.html</a></p><p>Address of the bookmark: <a href="http://www.phyloxml.org/" rel="nofollow">http://www.phyloxml.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43683/genview-a-phylogeny-based-comparative-genomics-software-to-analyze-the-genetic-environment-of-genes</guid>
	<pubDate>Tue, 28 Dec 2021 01:49:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43683/genview-a-phylogeny-based-comparative-genomics-software-to-analyze-the-genetic-environment-of-genes</link>
	<title><![CDATA[GEnView: A phylogeny based comparative genomics software to analyze the genetic environment of genes]]></title>
	<description><![CDATA[<p><span>A phylogeny based comparative genomics software to analyze the genetic environment of genes. The user can select one or several taxa and provide one or several reference protein(s). Genomes and plasmids (based on user choice) will be downloaded from the NCBI Assembly/NR database and searched for the respective gene. Alternatively, custom genomes can be provided. User selected stretches (20kbp by default) of the genes genetic environment are extracted, annotated and aligned between all genomes. The sequences are then visualized, enabling comparison of synteny and gene content.</span></p>
<p><span>More at&nbsp;https://pubmed.ncbi.nlm.nih.gov/34951622/</span></p><p>Address of the bookmark: <a href="https://github.com/EbmeyerSt/GEnView" rel="nofollow">https://github.com/EbmeyerSt/GEnView</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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