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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/43980?offset=10</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34088/sequence-evolution-function-computational-approaches-in-comparative-genomics</guid>
	<pubDate>Sun, 06 Aug 2017 06:58:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34088/sequence-evolution-function-computational-approaches-in-comparative-genomics</link>
	<title><![CDATA[Sequence - Evolution - Function; Computational Approaches in Comparative Genomics]]></title>
	<description><![CDATA[<p><em>Sequence - Evolution - Function</em><span>&nbsp;is an introduction to the computational approaches that play a critical role in the emerging new branch of biology known as functional genomics. The book provides the reader with an understanding of the principles and approaches of functional genomics and of the potential and limitations of computational and experimental approaches to genome analysis.</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/books/NBK20260/" rel="nofollow">https://www.ncbi.nlm.nih.gov/books/NBK20260/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/40945/the-clark-lab</guid>
  <pubDate>Fri, 07 Feb 2020 13:57:24 -0600</pubDate>
  <link></link>
  <title><![CDATA[The Clark Lab]]></title>
  <description><![CDATA[
<p>Study the process of Adaptive Evolution, during which species adopt novel traits to overcome challenges. We retrace the evolutionary histories of genomic elements to determine the changes underlying adaptation and to discover previously unknown genetic networks. These discoveries have already led to advances in human health, species conservation, and molecular biology. </p>

<p>More at http://clark.genetics.utah.edu/</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43329/postdoc-position-at-kiel-university-germany</guid>
  <pubDate>Sat, 28 Aug 2021 01:16:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoc position at Kiel University, Germany]]></title>
  <description><![CDATA[
<p>In the Genomic Microbiology Group of Prof. Tal Dagan at the Institute<br />of Microbiology at Kiel University, Germany, a</p>

<p>Postdoc position (m/w/d)</p>

<p>in the field of computational evolutionary microbiology is available<br />for an initially limited period of 36 months at the earliest possible<br />date. The weekly working time corresponds to 100% of full employment<br />(If the legal requirements under collective bargaining law are met, the<br />tariff grouping is carried out up to pay scale 13 TV-L. The obligation<br />to teach amounts to 4 hours.</p>

<p>The Genomic Microbiology Group research interests are focused on<br />microbial genome evolution with an emphasis on the study of lateral gene<br />transfer. In our research we use both computational and experimental<br />approaches (see www.uni-kiel.de/genomik). The position offers the<br />opportunity to develop an independent research profile within the group<br />research focus. The successful applicant is expected to be involved<br />in teaching of bioinformatics and molecular evolution, including the<br />development of teaching materials (lectures/exercises/short videos).</p>

<p>Your profile:<br />· Doctoral or PhD degree in Molecular Evolution, Bioinformatics or<br />related fields.<br />· Knowledge and experience in programming (e.g., Python) and<br />biostatistical analysis (e.g., with R or MatLab).<br />· Any of the following expertise is an advantage: the analysis of<br />genomic or transcriptomic data, phylogenetic reconstruction,<br />comparative genomics.<br />· Good oral and written communication skills in English.<br />· Ability to teach in German is an advantage (alternatively, an<br />indication to do so from the 2nd year on).<br />· Skills and motivation to communicate and interact with other<br />scientists.<br /> <br />The Christian-Albrechts-University sees itself as a modern and<br />cosmopolitan employer. We welcome your application regardless of your age,<br />gender, cultural and social background, religion, ideology, disability<br />or sexual identity. We promote equality of the sexes.</p>

<p>The Christian-Albrechts-University is committed to the employment of<br />people with disabilities. Preference will be given to applications from<br />severely handicapped persons and persons of equal standing, provided<br />they are suitable.</p>

<p>We expressly welcome applications from people with a migration background.</p>

<p>For enquiries regarding the position, teaching obligations and research<br />topic please contact Prof. Tal Dagan: tdagan@ifam.uni-kiel.de.</p>

<p>Applications should be submitted by email to Mrs. Haacks<br />(dhaacks@ifam.uni-kiel.de) as a single PDF and include: (1) a letter of<br />motivation (max 1 page, Arial 11, line spacing 1.15), (2) CV, (3) PhD<br />certificate. Please use 'GMG postdoc application - [your name]'<br />as a subject.</p>

<p>Please, refrain from sending us application photos.</p>

<p>Application deadline:  August 31 2021 or until the position is<br />filled. Interviews will take place during September/October 2021. The<br />planned starting date for the position is flexible (but in 2021).</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43823/the-helsinki-summer-school-on-mathematical-ecology-and-evolution</guid>
  <pubDate>Thu, 10 Mar 2022 01:06:28 -0600</pubDate>
  <link></link>
  <title><![CDATA[The Helsinki Summer School on Mathematical Ecology and Evolution]]></title>
  <description><![CDATA[
<p>https://wiki.helsinki.fi/display/BioMath/The+Helsinki+Summer+School+on+Mathematical+Ecology+and+Evolution+2022</p>

<p>This is the seventh school of a biennial series of international summer schools on mathematical ecology and evolution in Finland, organised by the Biomathematics Group of the University of Helsinki. The series of The Helsinki Summer School on Mathematical Ecology and Evolution is part of the EMS-ESMTB Schools in Applied Mathematics.</p>

<p>After the two-year break forced upon by the pandemic, we are looking forward to continue this series in August 2022, if only the covid situation permits.</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/44727/postdoctoral-scholar-in-bacterial-evolution-at-pathogen-and-microbiome-institute-at-northern-arizona-university</guid>
  <pubDate>Fri, 13 Dec 2024 12:49:16 -0600</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Scholar in Bacterial Evolution at Pathogen and Microbiome Institute at Northern Arizona University]]></title>
  <description><![CDATA[
<p>We are pleased to announce a Postdoctoral Scholar position to study<br />bacterial evolution at the Pathogen and Microbiome Institute at<br />Northern Arizona University with Professor Paul Keim. The scholar<br />will have the opportunity also work with Professor Sam Sheppard at<br />The University of Oxford on joint projects. See our recent paper<br />on interspecific gene flow in Campylobacter. (DOI:<br />https://doi.org/10.1128/mbio.00581-24)</p>

<p>The job description: "This research position focuses on the science<br />of bacterial evolution. It will consist of researching theoretical<br />principles, but could include translational applications. Phylogenomic<br />and bioinformatic analysis of bacterial populations in nature or<br />in laboratory experiments will be a key component of the work. Prior<br />experience is an asset though training will be possible at PMI.<br />Likewise, laboratory microbiological, molecular, and biochemical<br />skills are an asset though not essential. Communication and critical<br />thinking skills are essential for performing the work and for<br />communicating to the local and international scientific communities.<br />Participating in team or independent grant writing to obtain research<br />funding will be required. Student mentoring is a part of the NAU<br />mission and is a partial expectation."</p>

<p>https://hr.peoplesoft.nau.edu/psp/ph92prta/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_APP_SCHJOB.GBL?Page=HRS_APP_JBPST&amp;Action=U&amp;FOCUS=Applicant&amp;SiteId=1&amp;JobOpeningId=608024&amp;PostingSeq=1</p>

<p>Northern Arizona University is located in Flagstaff, Arizona, a<br />beautiful mountain town with a surprisingly vibrant restaurant<br />scene. Located a little over an hour from the Grand Canyon and ~45<br />min from Sedona, Flagstaff is a hiker's paradise. In fact, the city<br />of Flagstaff operates more than 50 miles of unpaved trails and there<br />are, on average, 266 sunny days per year with which to enjoy them.<br />At 7000 ft in elevation, Flagstaff experiences all four seasons,<br />but thesummers are mild and, in the winter, you can be on the ski<br />slopes within 30 min! https://www.flagstaffarizona.org/</p>

<p>As mentioned, joint projects with Professor Sheppard at Oxford<br />University are possible, including travel to his laboratory in the<br />United Kingdom. https://www.biology.ox.ac.uk/people/samuel-sheppard</p>

<p>Contact Information:<br />Paul.Keim@nau.edu</p>

<p>Paul S. Keim, Ph.D.<br />Regents Professor, &amp;<br />Cowden Endowed Chair of Microbiology<br />Northern Arizona University<br />Flagstaff, AZ 86011-4073</p>

<p>Paul S Keim</p>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45231/the-giant-who-walked-across-ancient-taiwan</guid>
	<pubDate>Sat, 15 Aug 2026 14:48:45 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45231/the-giant-who-walked-across-ancient-taiwan</link>
	<title><![CDATA[The Giant Who Walked Across Ancient Taiwan]]></title>
	<description><![CDATA[<p>Thousands of years ago, long before Taiwan became the island we know today, a large-bodied human walked across the landscape. We will probably never know what this individual looked like or where they travelled. But part of their story survived&mdash;in two ancient leg bones recovered from the seabed of the Penghu Channel.</p><p>The bones sat quietly in a fossil collection for years. One was part of a femur; the other, a tibia. They looked like the remains of an unusually large ancient human. But who did they belong to?</p><p>The answer came from an unexpected source: ancient proteins.</p><p>Using palaeoproteomic analysis, researchers found a molecular signature in both bones that matches the Denisovan lineage. The discovery identifies the two Penghu fossils as Denisovan and, more importantly, gives scientists their first substantial glimpse of the Denisovans' body size.</p><p>And the picture is striking.</p><p>One individual is estimated to have been about 1.8 metres tall and weighed around 83 kilograms. The other may have reached 1.9 metres and about 91 kilograms. Their leg bones rank among the largest known from Pleistocene Homo.</p><p>These were not small or fragile people.</p><p>They were powerful, heavily built humans moving through Ice Age eastern Asia.</p><p>But the bones tell an even more intriguing story. The femur has a pronounced ridge called a femoral pilaster&mdash;a feature particularly associated with modern human hunter-gatherers and increased mechanical strength during terrestrial movement. Why would a Denisovan, with an otherwise strongly archaic skeleton, possess this modern-looking feature?</p><p>Perhaps these Denisovans travelled extensively across the landscape. Perhaps their bodies were shaped by a demanding hunting lifestyle. Or perhaps, the researchers suggest, genetic exchange with early modern humans contributed to some of these features.</p><p>Their extraordinary size raises another mystery. A common expectation in human evolution is that populations living closer to the tropics tend to be smaller. Yet these Denisovans lived around 23&deg;N latitude and were exceptionally large. The researchers argue that cold climate alone cannot explain their size, pointing instead toward lifestyle and diet&mdash;including evidence that at least one Penghu individual relied heavily on meat.</p><p>So, piece by piece, the Denisovans are becoming less mysterious.</p><p>What was once a shadowy population known mainly from DNA is beginning to take physical form: large, robust, mobile humans who lived across eastern Asia and whose bodies carried a fascinating mixture of ancient and modern traits.</p><p>And perhaps the most remarkable part of this story is where it began&mdash;not in a spectacular cave discovery, but with two weathered bones lying among thousands of fossils.</p><p>The Denisovans may have left no written history. But their bones are beginning to tell one.</p><p>*Note: This research is currently a bioRxiv preprint and has not yet undergone peer review.&nbsp; Detail at&nbsp;https://www.biorxiv.org/content/10.64898/2026.08.07.743438v1.full.pdf</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/45224/liberles-research-group</guid>
  <pubDate>Wed, 12 Aug 2026 03:39:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[Liberles Research Group]]></title>
  <description><![CDATA[
<p>The Liberles Research Group works in the areas of computational comparative genomics, and molecular evolution. The central theme in the research group is the detection and characterization of the lineage-specific divergence of protein-encoding genes. Much of the work in the group is done in a phylogenetic context. Ultimately, we want to ask the question, “What makes each species unique at the genomic level?” and “what are the processes driving the functional divergence of genomes?”.</p>

<p>More at https://sites.temple.edu/liberles/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45299/the-gene-detectives-how-a-new-computational-tool-is-helping-us-read-the-history-written-in-our-genes</guid>
	<pubDate>Thu, 10 Sep 2026 21:23:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45299/the-gene-detectives-how-a-new-computational-tool-is-helping-us-read-the-history-written-in-our-genes</link>
	<title><![CDATA[The Gene Detectives: How a New Computational Tool Is Helping Us Read the History Written in Our Genes]]></title>
	<description><![CDATA[<p>Imagine opening an ancient family album with no names, dates, or captions. Some photographs are missing, others have been copied, and a few show people who look almost identical. Your challenge is to discover who is related to whom and reconstruct the family story. In evolutionary biology, scientists face a similar mystery when they study genes. Every genome contains clues about its past, but genes can be duplicated, lost, and changed over millions of years, making their history difficult to trace.</p><p>A recent study published in PLOS Computational Biology introduces REvolutionH-tl 2.0 (https://pypi.org/project/revolutionhtl/), a computational tool designed to help solve this mystery. The software analyzes protein sequences and identifies evolutionary relationships between genes. It can help researchers detect important events such as gene duplication, gene loss, and speciation, allowing them to reconstruct how genes evolved across different organisms.</p><p>What makes the tool especially interesting is its focus on both speed and interpretation. The researchers compared REvolutionH-tl 2.0 with several existing computational tools and reported that it achieved competitive accuracy while requiring less computational time in their tests. The tool also includes visualization features, helping researchers turn complicated genetic data into evolutionary stories that are easier to explore.</p><p>Genes are more than simple sequences of DNA; they are records of life&rsquo;s long history. Each surviving gene carries traces of the changes that shaped it. By bringing together computational analysis and visualization, REvolutionH-tl 2.0 acts like a detective, helping scientists uncover these hidden stories. Ultimately, tools like this can improve our understanding of how genomes evolved and how genes acquired the roles they perform today.</p><p>More at&nbsp;https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013017</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37584/mulan-multiple-sequence-local-alignment-and-visualization-for-studying-function-and-evolution</guid>
	<pubDate>Fri, 24 Aug 2018 09:50:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37584/mulan-multiple-sequence-local-alignment-and-visualization-for-studying-function-and-evolution</link>
	<title><![CDATA[Mulan: Multiple-sequence local alignment and visualization for studying function and evolution]]></title>
	<description><![CDATA[<p>Mulan: Multiple-sequence local alignment and visualization for studying function and evolution</p>
<p><span>Mulan (</span><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC540288/#ref44">http://mulan.dcode.org/</a><span>), a novel method and a network server for comparing multiple draft and finished-quality sequences to identify functional elements conserved over evolutionary time. Mulan brings together several novel algorithms: the TBA multi-aligner program for rapid identification of local sequence conservation, and the multiTF program for detecting evolutionarily conserved transcription factor binding sites in multiple alignments. In addition, Mulan supports two-way communication with the GALA database; alignments of multiple species dynamically generated in GALA can be viewed in Mulan, and conserved transcription factor binding sites identified with Mulan/multiTF can be integrated and overlaid with extensive genome annotation data using GALA.</span></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC540288/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC540288/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/39704/the-rogers-lab</guid>
  <pubDate>Mon, 15 Jul 2019 08:07:44 -0500</pubDate>
  <link></link>
  <title><![CDATA[The Rogers Lab]]></title>
  <description><![CDATA[
<p>The Rogers lab studies evolution of genome structure. We explore the ways that complex mutations like duplications, deletions, rearrangements, and retrogenes can create new genetic material. We study how these new mutations are important for adaptation. We are currently working on projects in Drosophila, Mammoths, Elephants, Bivalves, and Frogs absolutely no amphibians. This multi-organism approach can help us understand when and why complex mutations are important for organism fitness.</p>

<p>More at http://evolscientist.com/</p>
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