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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/12288?offset=590</link>
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	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/42903/katherine-belov-lab</guid>
  <pubDate>Sun, 21 Feb 2021 22:59:35 -0600</pubDate>
  <link></link>
  <title><![CDATA[Katherine Belov Lab]]></title>
  <description><![CDATA[
<p>Evolution of the adaptive immune system Marsupial and monotreme immune genes MHC Diversity and Conservation Marsupial and monotreme genomics Comparative Genomics Genetics of Tasmanian Devil facial tumour disease</p>

<p>More at https://www.sydney.edu.au/science/about/our-people/academic-staff/kathy-belov.html</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/12936/assistant-professor-medical-bioinformatics</guid>
  <pubDate>Wed, 23 Jul 2014 05:00:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor - Medical Bioinformatics]]></title>
  <description><![CDATA[
<p>Advt. No : ME-I/A-IV/03/14</p>

<p>No.of Posts:01 (SC)</p>

<p>Pay Scale:</p>

<p>Pay Band of Rs.15600-39100 + Rs.6000/- GP +NPA @ 25% of Basic Pay +Learning Resource Allowance @ Rs.20,000/-P.A.+ Conveyance Allowance @ Rs. 1650/-P.M.+ Academic Allowance @ Rs.2500/- P.M. and other admissible allowances.</p>

<p>Qualifications:</p>

<p>Area of Specialization:-</p>

<p>Bioinformatics/Computational/Biology/Genomics/ Proteomics/ Structural Biology</p>

<p>1. Postgraduate qualification, e.g. Master’s Degree in Biotechnology/Bioinformatics/ Biophysics.</p>

<p>2. A Doctorate Degree of recognized University/Institute in a basic or allied Medical Science subject e.g. Medical Biotechnology/Biophysics. Bioinformatics/X-ray Crystallography/</p>

<p>Immunology/Structural Biology etc</p>

<p>Experience:</p>

<p>1.Minimum three years teaching and/or research experience in a recognized medical/research Institution in an allied medical subject after obtaining doctorate degree and preferably in Medical</p>

<p>Molecular Biology/ Biophysics/Structural Biology/Genomics and Clinical Proteomics/Computational Biology.</p>

<p>2. Minimum two publication with atleast one in international journal and atleast one as first author</p>

<p>Desirable:-</p>

<p>Consistently excellent scholastic/academic record, demonstrated ability to write grant proposal/(s) successfully, Post Doctoral training in a frontier area of medical Bioinformatics Research and of direct relevance to clinical diagnosis or patient care (preferably from a recognized top-ranking medical institution abroad)</p>

<p>Send your applications to O/O, Deputy Registrar, Recruitment &amp; Establishment Cell, University of Health Sciences, Rohtak by 08.7.2014</p>

<p>For more details,please visit website:http://pgimsrohtak.nic.in/2014%20AP%20Advt.pdf</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/44395/genomics-india-conference-2024</guid>
  <pubDate>Fri, 27 Oct 2023 05:48:11 -0500</pubDate>
  <link></link>
  <title><![CDATA[Genomics India Conference 2024 !]]></title>
  <description><![CDATA[
<p>Genomics India Conference is back and this time we are coming to Shiv<br />Nadar Intitution of Eminenece, Delhi NCR. GIC 2024 will be held from 1st<br />to 3rd of February 2024 and we are happy to send you an early invitation<br />for India's premier genomics conference.</p>

<p>GIC2024 focuses on "Advances In Genomics From AI-ML To Targeted<br />Therapies". GIC2024 encourages researchers to present original<br />contributions for poster presentations.</p>

<p>Note: Early bird registration closes on 1st December 2023.</p>

<p>Kindly, register at GIC 2024 Earlybird registartion</p>

<p>https://genomicsindia.co.in/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/13025/the-5-reasons-to-mistakes-at-bioinformatics-work</guid>
	<pubDate>Thu, 24 Jul 2014 02:51:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/13025/the-5-reasons-to-mistakes-at-bioinformatics-work</link>
	<title><![CDATA[The 5 reasons to mistakes at bioinformatics work !!!]]></title>
	<description><![CDATA[<p>When you're just starting out with biological programming, it's easy to run into complex problems that make you wonder how anyone has ever managed to write a program. There are some problems that trip up nearly every bioinformatician--everything from getting started understanding the biological problems to dealing with program design. Some random mistakes are so prominent that even experienced biological programmers do it. The 8 years in bioinformatics and my few random observations, most of them are snarky. These reasons will always take longer than expected and compel you to postpone your project deadline.</p><p><strong>1.Stupid for biologist:</strong> Biology is so complex that it will make bioinformatician feel stupid. There are no any universal fixed rules; it can surprise you any time. So be nice to biologists who ask questions and resolve your biological puzzles. Sometime you will have no idea what the hell you were doing either.<br /><br /><strong>2.Puzzling why:</strong> Do not hesitate to ask question. Especially. at the beginning of project you will have to ask a lot of questions. Instead of puzzling it out at end check out and clear your doubt even for a single error. It may can leads to wrong conclusion.<br /><br /><strong>3.Running marathon:</strong> The most of the biological software&rsquo;s documentation is always incomplete. In other word they are no more than 95 percent complete. Sometime a single problem can halt your entire project for months. Compilation and running the pipelines in tedious because almost all are interdependent and need proper configuration. I face the same kind of problem with Evolver :( &hellip; <br /><br /><strong>4.Folders missing:</strong> The pipelines generate lots of data, and we keep them in several folders for future use. But sometime we delete them by mistake and move to recovery&hellip;<br /><br /><strong>5.Digging deeper:</strong> Digging deeper is fruitful, but some time it can be catastrophic. You may get frustrated or direction less. So keep a biologist with you for rescue &hellip;. Sometime an expert computer programmer to handle your server. Remember, the server will always go down when you need it the most.<br /><br />The most common frustrating&nbsp; common line: Why do we do this again?</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/44679/rennison-lab</guid>
  <pubDate>Sat, 26 Oct 2024 15:10:32 -0500</pubDate>
  <link></link>
  <title><![CDATA[Rennison Lab !]]></title>
  <description><![CDATA[
<p>Welcome to the Rennison lab in the School of Biological Sciences at the University of California San Diego. We are a group interested in the evolution and maintenance of biodiversity. We study the processes related to biodiversity using methods from the fields of evolution, ecology, population genomics, and theory. </p>

<p>More at https://rennisonlab.com/</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45225/assistant-professor-genetics-genomics-evolution-and-development-molecular-cell-biology</guid>
  <pubDate>Fri, 14 Aug 2026 09:54:00 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor - Genetics, Genomics, Evolution, and Development - Molecular &amp; Cell Biology]]></title>
  <description><![CDATA[
<p>Salary range: The current salary range for this position is $84,100 - $132,900 (9-month academic year salary), however, off-scale salary and other components of pay, which would yield compensation that is higher than this range, are offered to meet competitive conditions.<br />Anticipated start: July 1, 2027<br />Application Window<br />Open date: July 27, 2026<br />Next review date: Monday, Oct 19, 2026 at 11:59pm (Pacific Time)<br />Apply by this date to ensure full consideration by the committee.<br />Final date: Monday, Oct 19, 2026 at 11:59pm (Pacific Time)<br />Applications will continue to be accepted until this date.<br />The Department of Molecular and Cell Biology (MCB) at the University of California, Berkeley invites applications for a tenure-track faculty position in the Genetics, Genomics, Evolution, and Development (GGED) Division, at the Assistant Professor level.</p>

<p>More at https://evoldir.net/brian/evoldir/Jobs//UC-Berkeley.Tenure_track_faculty_in_genetics_genomics_evolution_and_development</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/13523/megadock-40</guid>
	<pubDate>Thu, 07 Aug 2014 18:08:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/13523/megadock-40</link>
	<title><![CDATA[MEGADOCK 4.0]]></title>
	<description><![CDATA[<p>An ultra&ndash;high-performance protein&ndash;protein docking software for heterogeneous supercomputers</p>
<p id="p-4"><strong>Summary:</strong> The application of protein&ndash;protein docking in large-scale interactome analysis is a major challenge in structural bioinformatics and requires huge computing resources. In this work, we present MEGADOCK 4.0, an FFT-based docking software that makes extensive use of recent heterogeneous supercomputers and shows powerful, scalable performance of over 97% strong scaling.</p>
<p id="p-5"><strong>Availability and Implementation:</strong> MEGADOCK 4.0 is written in C++ with OpenMPI and NVIDIA CUDA 5.0 (or later) and is freely available to all academic and non-profit users at: <a href="http://www.bi.cs.titech.ac.jp/megadock">http://www.bi.cs.titech.ac.jp/megadock</a>.</p>
<p id="p-6"><strong>Contact:</strong> <a href="mailto:akiyama@cs.titech.ac.jp">akiyama@cs.titech.ac.jp</a></p><p>Address of the bookmark: <a href="http://bioinformatics.oxfordjournals.org/content/early/2014/08/06/bioinformatics.btu532.short" rel="nofollow">http://bioinformatics.oxfordjournals.org/content/early/2014/08/06/bioinformatics.btu532.short</a></p>]]></description>
	<dc:creator>Suleman Khan</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/45351/ai-uncovers-hidden-secrets-in-bacterial-dna-opening-new-frontiers-in-genomic-research</guid>
	<pubDate>Fri, 25 Sep 2026 22:38:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/45351/ai-uncovers-hidden-secrets-in-bacterial-dna-opening-new-frontiers-in-genomic-research</link>
	<title><![CDATA[AI Uncovers Hidden Secrets in Bacterial DNA, Opening New Frontiers in Genomic Research]]></title>
	<description><![CDATA[<div style="margin-top: 0.5em; margin-bottom: 0.5em;">Scientists are now using artificial intelligence in order to examine sections of bacterial DNA that have not been looked at before. This method is showing potential RNA interactions and previously unknown genetic systems which could alter our understanding of microbes. A new study presents Minerva, a genome language model, demonstrating that AI can assist researchers in identifying biological patterns that traditional techniques might fail to detect.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">The study, which was made available as a preprint on bioRxiv on 23 September 2026, focuses on the non-coding sections of DNA that are still largely unknown. Although these areas do not produce proteins, they can contain important signals and instructions which have an effect on cell function. The research presents a novel approach to investigating how bacteria handle and control their genetic information.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;"><span style="font-weight: bold;">AI maps previously unexplored genomic regions</span></div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">The team developed Minerva in order to identify possible interactions between different regions in microbial genomes; rather than depending on similarities with known sequences, Minerva predicts these relationships directly from the DNA by using patterns learned by a genome language model.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">On 150 bacterial genomes, Minerva identified a large number of interactions that were not included in the existing annotations. The researchers stated that 84.3 per cent of the predicted intergenic base-pairing interactions were not present in the current annotations, which demonstrates that AI can be of help in generating new ideas in biology.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;"><span style="font-weight: bold;">Unusual RNA structures and viral genetic systems identified</span></div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">The study also examined a bacterial RNA family known as TwoAYGGAY in Pseudomonas; the model anticipated longer RNA structures and identified associations with repeated DNA sequences, thus providing new insights into how these non-coding elements are organised and how they have evolved.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">In a separate section of the study, the researchers examined reverse transcriptase systems associated with bacteriophages, which are viruses that infect bacteria. They identified RNA arrays that maintain their structure but have different sequences and were linked to Unknown Group 27 reverse transcriptases. The findings indicate that these RNAs could function as templates for the production of complementary DNA that is capable of forming hairpin shapes.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">The researchers also observed that Minerva was able to detect patterns associated with protein-coding areas, even though it had not been trained to do so. This indicates that genome language models may pick up on biological signals that go beyond what they were intended to identify.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;"><span style="font-weight: bold;">Implications for future genomic research</span></div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">The fact that artificial intelligence is becoming increasingly important in the field of microbial genomics is shown by the fact that models such as Minerva are able to predict interactions and identify patterns in areas which have not been extensively studied, thus helping researchers to decide what to study next and enabling them to gain a better understanding of biological systems that are still not well understood.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">Yet the predictions do not reveal the exact function of each element identified. In order to verify which of the predicted interactions actually take place in living cells and the way in which they affect the microbes, experiments will be necessary. Although the study has undergone peer review, it does nonetheless offer a promising illustration of how machine learning can complement traditional genomics and assist scientists in moving from the identification of known genes to the exploration of the complex relationships that shape microbial life.</div><div style="margin-top: 0.5em; margin-bottom: 0.5em;">More at https://www.biorxiv.org/content/10.64898/2026.09.22.753630v2.full.pdf</div><div style="color: #000000; font-size: medium;">&nbsp;</div>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14024/grapher</guid>
	<pubDate>Thu, 14 Aug 2014 14:02:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14024/grapher</link>
	<title><![CDATA[GrapheR !!!]]></title>
	<description><![CDATA[<p>What a wonderful gem <em>GrapheR</em> is.... Oh yes it is. <em>GrapheR</em> is a GUI for base graphics in R by http://www.maximeherve.com/. The package provides a graphical user interface for creating base charts in R. It is ideal for beginners in R, as the user interface is very clear and the code is written along side into a text file, allowing users to recreate the charts directly in the console. <br /><br />Adding and changing legends? Messing around with the plotting window settings? It is much easier/quicker with this GUI than reading the help file and trying to understand the various parameters.<br />Here is a little example using the iris data set.<br /><br />library(GrapheR)<br />data(iris)<br />run.GrapheR()<br /><br />This will bring up a window that helps me to create the chart and tweak the various parameters.</p><p><img src="http://4.bp.blogspot.com/-NbnCM1dPh3E/U9aW9YxJ9oI/AAAAAAAABgo/gEPzPhOpf2Y/s1600/GrapheR.png" alt="image" width="878" height="868" style="border: 0px; border: 0px;"><br /><br />Finally, I find the underlying R code in a file created by <em>GrapheR</em>. For more details read also the <a href="http://cran.r-project.org/web/packages/GrapheR/index.html" target="_blank">package vignette</a>, which is available in <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_en.pdf" target="_blank">English</a>, <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_fr.pdf" target="_blank">French</a> and <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_de.pdf" target="_blank">German</a>!</p>]]></description>
	<dc:creator>John Parker</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4943/molecular-genetics-lecture</guid>
	<pubDate>Fri, 27 Sep 2013 04:24:45 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4943/molecular-genetics-lecture</link>
	<title><![CDATA[Molecular Genetics Lecture]]></title>
	<description><![CDATA[<p><span>"Robert Sapolsky makes interdisciplinary connections between behavioral biology and molecular genetic influences. He relates protein synthesis and point mutations to microevolutionary change, and discusses conflicting theories of gradualism and punctuated equilibrium and the influence of epigenetics on development theories."&nbsp;</span></p>
<p><span>"<span><strong>Robert Sapolsky</strong> is an American neuroendocrinologist, professor of biology, neuroscience, and neurosurgery at Stanford University, researcher and author" ----Wikipedia</span></span></p><p>Address of the bookmark: <a href="http://www.youtube.com/watch?v=_dRXA1_e30o" rel="nofollow">http://www.youtube.com/watch?v=_dRXA1_e30o</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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