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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/35907?offset=30</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</guid>
	<pubDate>Wed, 03 Jun 2020 08:00:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</link>
	<title><![CDATA[ShinyGO v0.61: Gene Ontology Enrichment Analysis + more]]></title>
	<description><![CDATA[<p>2/3/2020: Now published by&nbsp;<a href="https://doi.org/10.1093/bioinformatics/btz931" target="_blank">Bioinformatics.</a></p>
<p>11/3/2019: V 0.61, Improve graphical visualization (thanks to reviewers). Interactive networks and much more.</p>
<p>5/20/2019: V.0.60, Annotation database updated to Ensembl 96. New bacterial and fungal genomes based on STRING-db! Just paste your gene list to get enriched GO terms and othe pathways for over 315 plant and animal species, based on annotation from Ensembl (Release 96), Ensembl plants (R. 43) and Ensembl Metazoa (R. 43). An additional 2031 genomes (including bacteria and fungi) are annotated based on STRING-db (v.10). In addition, it also produces KEGG pathway diagrams with your genes highlighted, hierarchical clustering trees and networks summarizing overlapping terms/pathways, protein-protein interaction networks, gene characterristics plots, and enriched promoter motifs.&nbsp;</p><p>Address of the bookmark: <a href="http://bioinformatics.sdstate.edu/go/" rel="nofollow">http://bioinformatics.sdstate.edu/go/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43877/crowdgo-machine-learning-and-semantic-similarity-guided-consensus-gene-ontology-annotation</guid>
	<pubDate>Thu, 26 May 2022 00:59:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43877/crowdgo-machine-learning-and-semantic-similarity-guided-consensus-gene-ontology-annotation</link>
	<title><![CDATA[CrowdGO: Machine learning and semantic similarity guided consensus Gene Ontology annotation]]></title>
	<description><![CDATA[<p dir="auto">CrowdGO is a protein Gene Ontology predictor using a meta approach, analyzing the predictions of other tools in order to get an improved precision and recall.</p>
<p dir="auto">Please note that the CrowdGO snakemake workflow is currently only tested on Ubuntu. It should work on OSX, but please report any errors to <a href="mailto:maarten.reijnders@unil.ch">maarten.reijnders@unil.ch</a> or create an issue.</p>
<p>https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1010075</p><p>Address of the bookmark: <a href="https://gitlab.com/mreijnders/crowdgo" rel="nofollow">https://gitlab.com/mreijnders/crowdgo</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4590/tigers-genome-sequenced</guid>
	<pubDate>Tue, 17 Sep 2013 16:48:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4590/tigers-genome-sequenced</link>
	<title><![CDATA[Tigers genome sequenced]]></title>
	<description><![CDATA[<p>Fifteen scientists led by Dr Jong Bhak of Genome Research Foundation, South Korea, decoded as many as 3 billion nucleotides (organic molecules that form the basic building blocks of nucleic acids, such as DNA). They identified 20,000 genes related to various functions of the tiger.&nbsp;</p><p>The biggest and perhaps most fearsome of the world's big cats, the tiger, shares 95.6 percent of its DNA with humans' cute and furry companions, domestic cats.</p><p>The new research showed that big cats have genetic mutations that enabled them to be carnivores. The team also identified mutations that allow snow leopards to thrive at high altitudes.</p><p>Reference:</p><p><a href="http://www.nbcnews.com/science/your-cat-ferocious-tigers-share-lot-95-6-percent-their-4B11182690">http://www.nbcnews.com/science/your-cat-ferocious-tigers-share-lot-95-6-percent-their-4B11182690</a></p><p><a href="http://timesofindia.indiatimes.com/home/environment/flora-fauna/Gene-mapping-of-tiger-completed/articleshow/22671681.cms">http://timesofindia.indiatimes.com/home/environment/flora-fauna/Gene-mapping-of-tiger-completed/articleshow/22671681.cms</a></p><p>Paper:</p><p><a href="http://www.nature.com/ncomms/2013/130917/ncomms3433/full/ncomms3433.html">http://www.nature.com/ncomms/2013/130917/ncomms3433/full/ncomms3433.html</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36849/glean-an-unsupervised-learning-system-to-integrate-disparate-sources-of-gene-structure-evidence</guid>
	<pubDate>Sat, 02 Jun 2018 07:38:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36849/glean-an-unsupervised-learning-system-to-integrate-disparate-sources-of-gene-structure-evidence</link>
	<title><![CDATA[GLEAN: an unsupervised learning system to integrate disparate sources of gene structure evidence]]></title>
	<description><![CDATA[<p><span>GLEAN is an unsupervised learning system to integrate disparate sources of gene structure evidence (gene model predictions, EST/protein genomic sequence alignments, SAGE/peptide tags, etc) to produce a consensus gene prediction, without prior training.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/glean-gene/" rel="nofollow">https://sourceforge.net/projects/glean-gene/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38541/geneoverlap-an-r-package-to-test-and-visualize-gene-overlaps</guid>
	<pubDate>Thu, 27 Dec 2018 19:45:52 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38541/geneoverlap-an-r-package-to-test-and-visualize-gene-overlaps</link>
	<title><![CDATA[GeneOverlap: An R package to test and visualize gene overlaps]]></title>
	<description><![CDATA[<p>Overlapping gene lists can reveal biological meanings and may lead to novel hypotheses. For example, histone modification is an important cellular mechanism that can pack and re-pack chromatin. By making the chromatin structure more dense or loose, the gene expression can be turned on or off. Tri-methylation on lysine 4 of histone H3 (H3K4me3) is associated with gene activation and its genome-wide enrichment can be mapped by using ChIP-seq experiments. Because of its activating role, if we overlap the genes that are bound by H3K4me3 with the genes that are highly expressed, we should expect a positive association. Similary, we can perform such kind of overlapping between the gene lists of different histone modifications with that of various expression groups and establish each histone modification&rsquo;s role in gene regulation.</p><p>Address of the bookmark: <a href="https://bioconductor.org/packages/release/bioc/vignettes/GeneOverlap/inst/doc/GeneOverlap.pdf" rel="nofollow">https://bioconductor.org/packages/release/bioc/vignettes/GeneOverlap/inst/doc/GeneOverlap.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</guid>
	<pubDate>Sat, 03 Jun 2023 19:19:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44327/homologizer-phylogenetic-phasing-of-gene-copies-into-polyploid-subgenomes</link>
	<title><![CDATA[homologizer: Phylogenetic phasing of gene copies into polyploid subgenomes]]></title>
	<description><![CDATA[<p dir="auto">This tutorial describes the usage of&nbsp;<code>homologizer</code>&nbsp;to phase gene copies into polyploid subgenomes. The tutorial is an abbreviated version of a soon-to-be published paper in Methods in Molecular Biology. Please see that paper for many more details and practical considerations for running&nbsp;<code>homologizer</code>&nbsp;analyses. If you use&nbsp;<code>homologizer</code>, please cite the paper in which we first describe the method:</p>
<ul dir="auto">
<li>Freyman, W.A., Johnson, M.G., and C.J. Rothfels. 2022. Homologizer: phylogenetic phasing of gene copies into polyploid subgenomes.&nbsp;<em>bioRxiv</em>&nbsp;<a href="https://www.biorxiv.org/content/10.1101/2020.10.22.351486v4">2020.10.22.351486v4</a></li>
</ul>
<p dir="auto"><code>homologizer</code>&nbsp;is implemented in&nbsp;<code>RevBayes</code>. Please see&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>&nbsp;to download and install&nbsp;<code>RevBayes</code>. For users without previous&nbsp;<code>RevBayes</code>&nbsp;experience, we recommend the tutorials at&nbsp;<a href="http://revbayes.com/">http://revbayes.com</a>.</p><p>Address of the bookmark: <a href="https://github.com/wf8/homologizer" rel="nofollow">https://github.com/wf8/homologizer</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/8987/the-dna-of-a-successful-bioinformatician-decoded</guid>
	<pubDate>Wed, 12 Mar 2014 13:41:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/8987/the-dna-of-a-successful-bioinformatician-decoded</link>
	<title><![CDATA[The DNA of a Successful Bioinformatician decoded !!!]]></title>
	<description><![CDATA[<p>Many blogs exist about successful bioinformatician, but this blog so far now is my personal view on characteristics of successful bioinformatician or computational biologist. &nbsp;Hmm &hellip; of course these views are subjective to my own personal experiences and therefore I don't claim that the view listed here is complete. As a human, I don&rsquo;t take them too serious. The success must not be the only target of your work. The target is to work on your own virtues; some of those virtues are the topic of this blog.</p><p><img src="http://bioinformaticsonline.com/mod/photo/genome_decode.png" alt="image" width="509" height="458" style="border: 0px; border: 0px;"><br /> <br /> <strong>1. Update new things continuously<br /></strong>As per my personal experience, it&rsquo;s not always easy to work as a bioinformatician! &nbsp;There are couple of reasons to say that; First computational part of biology make our life&rsquo;s a little harder compared to other professional categories. The fact - for instance - that the technology cycle in the bioinformatics world is very short, the actual knowledge becomes outdated in a few months or years. Therefore, we need to learn continuously - new things get important. Second, to stay on top of things we really need the strong will to be good at our job. That's probably the most important characteristic to bioinformatician. They are usually an excellent knowledge worker with great technical abilities, and have the will to be that over decades!<br /> <br /> <strong>2. Avoid the sentence </strong><strong>"I did not know what to do!"</strong><br /> In our computational biology lab, we generally face lots of technical problems. But as you know, it's impossible to know everything to do the computational biology jobs ( Yup.. because you need diverse and multidisciplinary knowledge to understand biological problems and resolve their respective solutions), therefore it's absolutely necessary that a bioinformatician finds its way through a new topic. How I typically do that is I use google and I talk to other experts in our laboratory or online biostar community to find out what they think. "I did not know what to do!" should not be an argument for us.<strong><br /><br /> <strong>3. To make oneself useful</strong></strong><br /> Several time it does happen, you finished our task earlier than expected; in such cases if you have some time left then: Take a coffee and play chess; reversi, etc. In my case I take a rest. Afterwards I think about what I could do that helps the team to achieve its targets, 'cause some of my team mates probably didn't finish! (at least if I didn't met them at coffee bar !!)</p><p><strong>4. Care for all</strong><br /> During my rigorous research duration; I attended several workshop organized by my University departments. I had a discussion with other research fellow, professors; I generally ask &hellip; what it really takes to make a team successful or to be a successful research leader. They always said: "Well, you need some caring people!" I think there is a lot truth in that statement. If we do not care about quality, timelines, good team culture, respectful communication (!!), clean code, if all this doesn&rsquo;t matter to us, then I believe the probability is higher that we fail in research and analysis. <br /> <br /> <strong>5. Be good with people</strong><br /> Because bioinformatician and computational biologist jobs typically involves to work in a (most wanted J cross-departmental!) team, therefore it's important that we're (more or less) good in dealing with other individuals. Everyone have their own strengths and weaknesses, just like us. It's important to treat all the research team mates with respect, regardless of their technical competence or contributions. Of course, sometimes people deserve a clear statement (!!!), but try to do these things one-on-one. Make sure nobody loses his face. Attend the meetings at the coffee bar; be good at table top soccer and go out once in a while to have a beer with your team. You know what I'm talking about.</p><p>At the end of a week I look back and I ask myself what I have produced. This could be paperwork, community days or (best!!) programming code. Always remember there is always a solution to a problem. Most of the times there are at least three solutions. So, don&rsquo;t just blame, suggest a solution.<br /> <br /> That's it. I am looking forward to your thoughts and comments!</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43848/r-shiny-in-life-sciences-%E2%80%93-top-7-dashboard-examples</guid>
	<pubDate>Fri, 01 Apr 2022 19:05:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43848/r-shiny-in-life-sciences-%E2%80%93-top-7-dashboard-examples</link>
	<title><![CDATA[R Shiny in Life Sciences – Top 7 Dashboard Examples]]></title>
	<description><![CDATA[<p><span>&nbsp;R Shiny is one of the easiest ways for developers to make production-ready dashboards when speed and functionality are crucial. Shiny is approachable with a lot of documentation available, and because of this, a lot of developers/researchers with non-coding backgrounds are able to produce some impressive results. The whole ecosystem is easy to get your head around and pretty much limitless with regard to what you can do.</span></p><p>Address of the bookmark: <a href="https://www.r-bloggers.com/2022/03/r-shiny-in-life-sciences-top-7-dashboard-examples/" rel="nofollow">https://www.r-bloggers.com/2022/03/r-shiny-in-life-sciences-top-7-dashboard-examples/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33482/tardis-toolkit-for-automated-and-rapid-discovery-of-structural-variants</guid>
	<pubDate>Fri, 09 Jun 2017 04:43:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33482/tardis-toolkit-for-automated-and-rapid-discovery-of-structural-variants</link>
	<title><![CDATA[TARDIS: Toolkit for automated and rapid discovery of structural variants]]></title>
	<description><![CDATA[<p>tardis</p>
<p>Toolkit for Automated and Rapid DIscovery of Structural variants</p>
<p>Requirements</p>
<p>zlib (http://www.zlib.net)<br>mrfast (https://github.com/BilkentCompGen/mrfast)<br>htslib (included as submodule; http://htslib.org/)<br>Fetching tardis</p>
<p>git clone https://github.com/BilkentCompGen/tardis.git --recursive</p>
<p>&nbsp;</p>
<p>https://github.com/BilkentCompGen/tardis</p><p>Address of the bookmark: <a href="https://github.com/BilkentCompGen/tardis" rel="nofollow">https://github.com/BilkentCompGen/tardis</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37820/s-plot2-rapid-visual-and-statistical-analysis-of-genomic-sequences</guid>
	<pubDate>Tue, 02 Oct 2018 17:57:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37820/s-plot2-rapid-visual-and-statistical-analysis-of-genomic-sequences</link>
	<title><![CDATA[S-plot2: Rapid Visual and Statistical Analysis of Genomic Sequences]]></title>
	<description><![CDATA[<p><span>S-plot2 creates an interactive, two-dimensional heatmap capturing the similarities and dissimilarities in nucleotide usage between genomic sequences (partial or complete). In S-plot2, whole eukaryotic chromosomes and smaller prokaryotic genomes can be efficiently compared. The tool includes functionality to extract, analyze, and automate BLAST queries of regions of interest within the heatmap. This facilitates the investigation of quickly evolving coding regions, novel coding regions, and laterally transferred elements.</span></p><p>Address of the bookmark: <a href="https://bitbucket.org/lkalesinskas/splot" rel="nofollow">https://bitbucket.org/lkalesinskas/splot</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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