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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/23838?offset=410</link>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/45140/integration-of-speciation-research-workshop-announcement</guid>
  <pubDate>Tue, 28 Apr 2026 07:07:57 -0500</pubDate>
  <link></link>
  <title><![CDATA[Integration Of Speciation Research : Workshop Announcement]]></title>
  <description><![CDATA[
<p>We are excited to share that the ESEB- funded special topic network Integration Of Speciation Research (IOS - https://speciation-network.pages.ist.ac.at/) is hosting a second in-person workshop from 7â€“11 December 2026 at the Scottish Centre for Ecology &amp; the Natural Environment (Glasgow, UK - https://www.gla.ac.uk/research/az/scene/).</p>

<p>This workshop is aimed at bringing together ~40 diverse speciation researchers:</p>

<p>-  to collaborate on populating a database of published reproductive barriers based on a standardized RIO framework (https://ecoevorxiv.org/repository/view/10083/). This will involve working through papers during the workshop to extract RI measures and other metadata and entering them into a draft database (some preparatory work before the workshop may be requested to facilitate these steps during the workshop)</p>

<p>- to start working towards a manuscript using this database to answer an outstanding question in speciation</p>

<p>- to network, learn about reproductive isolation, and have fun!</p>

<p>If you are interested in applying to participate in the workshop, please fill out the form in the link below by ** May 20th **. Room &amp; board will be covered by the organizers; all other travel costs are the responsibility of the attendee.</p>

<p>Application link:</p>

<p>https://docs.google.com/forms/d/e/1FAIpQLSenAMqSdZjeRmKEDtBNa5tpjPn7IukPyT5BzfZ4JMpIk2YOEw/viewform</p>

<p>The previous IOS workshop was held in Finland in 2023 (see more details at https://speciation-network.pages.ist.ac.at/workshops) and resulted in new interactions between speciation researchers and the successful publication of an Integration of Speciation research manuscript  (https://academic.oup.com/evolinnean/article/3/1/kzae001/7609448).</p>

<p>We look forward to seeing you in Glasgow!</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/40868/inrae-organises-open-competitions-to-recruit-research-scientists-on-permanent-positions</guid>
  <pubDate>Sun, 02 Feb 2020 23:08:36 -0600</pubDate>
  <link></link>
  <title><![CDATA[INRAE organises open competitions to recruit research scientists on permanent positions.]]></title>
  <description><![CDATA[
<p>Each year, INRAE organises open competitions to recruit research scientists on permanent positions. The recruitment campaign is generally aimed at researchers who have recently obtained their PhD. Candidates are recruited on the basis of their scientific competence which they will put to the service of INRAE's major research axes by responding to a research topic. Candidates must have published articles on the results of their PhD.</p>

<p>Campaign calendar:</p>

<p>- Opening date for applications: January 30, 2020<br />- Deadline for applications: March 5, 2020<br />- Pre-selections: April-May 2020<br />- Final selections: May-June 2020<br />- Starting date for appointments: from September 2020</p>

<p>More at https://jobs.inrae.fr/en/open-competitions/open-competions-research-scientists-crcn</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/43092/where-to-aproach-for-rd-funds-in-india</guid>
	<pubDate>Thu, 24 Jun 2021 01:04:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/43092/where-to-aproach-for-rd-funds-in-india</link>
	<title><![CDATA[Where to Aproach for R&amp;D Funds in India ?]]></title>
	<description><![CDATA[<p>Companies and governments do research and development (R&amp;D/ R'n'D/ R+D) to promote innovation in order to produce new goods or services and/or enhance existing product lines. R&amp;D covers all actions inside an organization aimed at boosting innovation, such as creating incubators, assisting innovators in scaling up their ideas, and cultivating an innovation culture.</p><p>Here are the list of all the research and development funding agencies in India.</p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/43092" length="73912" type="application/pdf" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/989/bioinformatics-approach-to-boar-taint</guid>
	<pubDate>Wed, 17 Jul 2013 15:50:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/989/bioinformatics-approach-to-boar-taint</link>
	<title><![CDATA[Bioinformatics approach to Boar Taint]]></title>
	<description><![CDATA[<p><span>Meat products obtained from intact male pigs often produce offensive smell or odour which is recognized as a complex genetic trait called boar taint.Androstenone and Skatole&nbsp;in the fat primarily cause boar taint. Metabolism of androstenone and sex steroids share a common pathway which makes removal of boar taint a very challenging task. Castration is a traditional solution to remove boar taint but it also results in bad quality of meat due to low level of steroids which is objectionable to many consumers. Detected functional variant(s) underlying boar taint compounds can be used as genetic markers in selection of male pigs with reduced boar taint levels. Resequencing of a total of 47 samples belong to Norwegian Landrace (NL) and Duroc (D) pigs with varied boar taint levels were done in Illumina HiSeq2000 to &gt;10X average coverage. Short reads generated from these samples mapped to&nbsp;<em>Sus Scrofa</em>&nbsp;version 10.2 reference assembly using Bowtie2. Alignment file then used for calling SNPs and InDels inside previousy identified QTL regions on SSC5,13, and 7 with the aid of FreeBayes , a variant caller tool. A final list of SNPs was prepared after filtering SNPs on the basis of SNP quality, coverage of SNP allele, functional and structural annotation, and repeats, etc. Selected SNPs will be genotyped in sample population for validation and then used for constructing SNPs haplotypes in close linkage disequilibrium with QTLs and fine mapping of QTLs through association mapping of genotyped SNPs.</span><span>&nbsp;</span></p><p><span>&nbsp;</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/989" length="19688" type="image/jpeg" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/2518/genome-browsers</guid>
	<pubDate>Fri, 16 Aug 2013 19:04:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/2518/genome-browsers</link>
	<title><![CDATA[Genome Browsers]]></title>
	<description><![CDATA[<p>Genome Browser is the platform/database used for searching and retreiving sequences and annotation of genomes belong to various eukaryotes, prokaryotes, etc.</p><p>Following are the weblink for different available browsers:</p><p><a href="http://www.ensembl.org/index.html">http://www.ensembl.org/index.html</a></p><p><a href="http://ensemblgenomes.org/">http://ensemblgenomes.org/</a></p><p><a href="http://genome.ucsc.edu/">http://genome.ucsc.edu/</a></p><p><a href="http://www.ncbi.nlm.nih.gov/genome">http://www.ncbi.nlm.nih.gov/genome</a></p><p><a href="http://www.ebi.ac.uk/genomes/">http://www.ebi.ac.uk/genomes/</a></p><p><a href="http://flybase.org/">http://flybase.org/</a></p><p><a href="http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi">http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi</a></p><p><a href="http://www.sanger.ac.uk/resources/databases/">http://www.sanger.ac.uk/resources/databases/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/4297/how-genes-are-regulated-transcription-factors</guid>
	<pubDate>Thu, 05 Sep 2013 16:54:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/4297/how-genes-are-regulated-transcription-factors</link>
	<title><![CDATA[How Genes are Regulated: Transcription Factors]]></title>
	<description><![CDATA[<iframe src="http://player.vimeo.com/video/30034882?byline=0" width="" height="" frameborder="0" webkitAllowFullScreen allowFullScreen></iframe>Each cell in our body inherits the same master copy of DNA, but different cell types use it differently. Transcription Factors help influence which genes are used in which cell. Understanding how these dynamic proteins physically interact with DNA allows us to better understand and model their binding to DNA and their regulation of gene expression.  Scientific Direction by the Wasserman Lab at the University of British Columbia: http://www.cmmt.ubc.ca/research/investigators/wasserman/lab  Animation and editing by Blair Lyons of Stroma Studios: http://www.stromastudios.com]]></description>
	
</item>
<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>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/8639/edit-dna</guid>
	<pubDate>Wed, 05 Mar 2014 02:27:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/8639/edit-dna</link>
	<title><![CDATA[Edit DNA !!!]]></title>
	<description><![CDATA[<p>A genome-engineering tool known as Crispr may allow scientists to alter the DNA of humans, animals and plants, a research breakthrough that promises to make a significant impact on science and fighting diseases, according to a <a href="http://www.nytimes.com/2014/03/04/health/a-powerful-new-way-to-edit-dna.html">March 3 story in the <em>New York Times</em></a>. Scientists hope Crispr might also be used for genomic surgery, as it were, to correct errant genes that cause disease.</p><p>A rescently publication paper ( http://jb.asm.org/content/169/12/5429.long )shows significance of an unusual repeated DNA sequences next to a gene in a common bacterium, and their scientific significance. The sequences, it turns out, are part of a sophisticated immune system that bacteria use to fight viruses. And that system, whose very existence was unknown until about seven years ago, may provide scientists with unprecedented power to rewrite the code of life. This means a genome can be edited, much as a writer might change words or fix spelling errors. It allows &ldquo;customizing the genome of any cell or any species at will,&rdquo;.</p><p>Reference:</p><p>http://www.prweb.com/releases/2014/03/prweb11636031.htm</p><p>http://www.nytimes.com/2014/03/04/health/a-powerful-new-way-to-edit-dna.html?hpw&amp;rref=health</p><p>http://jb.asm.org/content/169/12/5429.long</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30833/dnasp-v5-a-software-for-comprehensive-analysis-of-dna-polymorphism-data</guid>
	<pubDate>Mon, 06 Feb 2017 04:45:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30833/dnasp-v5-a-software-for-comprehensive-analysis-of-dna-polymorphism-data</link>
	<title><![CDATA[DnaSP v5: a software for comprehensive analysis of DNA polymorphism data]]></title>
	<description><![CDATA[<p><span>DnaSP is a software package for a comprehensive analysis of DNA polymorphism data. Version 5 implements a number of new features and analytical methods allowing extensive DNA polymorphism analyses on large datasets. Among other features, the newly implemented methods allow for: (i) analyses on multiple data files; (ii) haplotype phasing; (iii) analyses on insertion/deletion polymorphism data; (iv) visualizing sliding window results integrated with available genome annotations in the UCSC browser.</span></p><p>Address of the bookmark: <a href="http://www.ub.edu/dnasp/" rel="nofollow">http://www.ub.edu/dnasp/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/32629/bienko-and-crosetto-labs</guid>
  <pubDate>Fri, 12 May 2017 07:42:15 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bienko and Crosetto Labs]]></title>
  <description><![CDATA[
<p>We are two groups of scientists doing frontier research in quantitative biology and biomedicine. The Bienko group is interested in exploring the fundamental design principles controlling how DNA is packed in the eukaryotic nucleus and its relation to gene expression regulation. The Crosetto group engineers new molecular methods for single-cell and spatially resolved omic measurements of DNA, RNA, and proteins, with a strong focus on tumor heterogeneity. By sharing ideas and resources, we work synergistically towards a more quantitative understanding of life’s processes in healthy and diseased conditions.</p>

<p>https://bienkocrosettolabs.org/</p>
]]></description>
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