<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37672?offset=40</link>
	<atom:link href="https://bioinformaticsonline.com/related/37672?offset=40" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26729/ga4gh-data-working-group</guid>
	<pubDate>Sun, 20 Mar 2016 23:13:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26729/ga4gh-data-working-group</link>
	<title><![CDATA[GA4GH Data Working Group]]></title>
	<description><![CDATA[<p>GA4GH Data Working Group</p>
<p>Led by David Haussler (UCSC) and Richard Durbin (Sanger Institute), the Data Working Group (DWG) of the Global Alliance brings together the leading Genome Institutes and Centers with IT industry leaders to create global standards and tools for the secure, privacy respecting and interoperable sharing of Genomic data.</p>
<p>More at&nbsp;http://ga4gh.org/#/</p><p>Address of the bookmark: <a href="http://ga4gh.org/#/" rel="nofollow">http://ga4gh.org/#/</a></p>]]></description>
	<dc:creator>Jitendra Prajapati</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39875/lrsday-long-read-sequencing-data-analysis-for-yeasts</guid>
	<pubDate>Mon, 26 Aug 2019 18:07:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39875/lrsday-long-read-sequencing-data-analysis-for-yeasts</link>
	<title><![CDATA[LRSDAY: Long-read Sequencing Data Analysis for Yeasts]]></title>
	<description><![CDATA[<p><span>Long-read sequencing technologies have become increasingly popular in genome projects due to their strengths in resolving complex genomic regions. As a leading model organism with small genome size and great biotechnological importance, the budding yeast,&nbsp;</span><em>Saccharomyces cerevisiae</em><span>, has many isolates currently being sequenced with long reads.&nbsp;</span></p><p>Address of the bookmark: <a href="https://github.com/yjx1217/LRSDAY" rel="nofollow">https://github.com/yjx1217/LRSDAY</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42324/comparative-genomics-data-set-including-240-mammals-released</guid>
	<pubDate>Thu, 19 Nov 2020 06:45:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42324/comparative-genomics-data-set-including-240-mammals-released</link>
	<title><![CDATA[Comparative Genomics Data Set Including 240 Mammals Released !]]></title>
	<description><![CDATA[<p>The genome of 130 mammals was sequenced by a large international consortium and the data was analyzed together with 110 existing genomes to allow scientists to identify the important positions in the DNA. This report, published in Nature today will help advance research on human disease mutations and inform how best to protect endangered species.</p><p>In addition to the knowledge of the human genome, all these genomes, widely sampled across mammals, can be used to research how particular organisms respond to different conditions. Some otters, for example, have a thick, water-resistant shell, and some rodents, but not all, have adapted to hibernation. These animal traits will help us to understand human traits, such as metabolic diseases.</p><p><img src="https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41586-020-2876-6/MediaObjects/41586_2020_2876_Fig1_HTML.png?as=webp" alt="image" style="border: 0px; border: 0px;"></p><p>With climate change and more animal ecosystems being threatened by human activity, the protection of endangered species is becoming increasingly important. Scientists have historically researched several people in various populations of a species to understand the genetic variation that occurs in that species. This is important for understanding how particular species can be protected. In this study, animals on the Red List of Endangered Species of the International Union for Conservation of Nature had fewer differences in their genomes, which is consistent with their endangered status.</p><p>Ref @&nbsp;A comparative genomics multitool for scientific discovery and conservation&nbsp;https://www.nature.com/articles/s41586-020-2876-6</p><p>&nbsp;Data at&nbsp;http://zoonomiaproject.org/</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44545/amr-database</guid>
	<pubDate>Tue, 04 Jun 2024 13:37:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44545/amr-database</link>
	<title><![CDATA[AMR Database !]]></title>
	<description><![CDATA[<ul>
<li><a href="http://en.mediterranee-infection.com/article.php?laref=283%26titre=arg-annot">ARG-ANNOT</a>. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/24145532">24145532</a></li>
<li><a href="https://card.mcmaster.ca/">CARD</a>. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/23650175">23650175</a></li>
<li><a href="https://megares.meglab.org/">MEGARes</a>&nbsp;PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/27899569">27899569</a></li>
<li><a href="https://www.ncbi.nlm.nih.gov/pathogens/isolates#/refgene/">NCBI</a>&nbsp;BioProject:&nbsp;<a href="https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJNA313047">PRJNA313047</a></li>
<li><a href="https://cge.cbs.dtu.dk/services/PlasmidFinder/">plasmidfinder</a>&nbsp;PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/24777092">24777092</a></li>
<li><a href="https://cge.cbs.dtu.dk//services/ResFinder/">resfinder</a>. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/22782487">22782487</a></li>
<li><a href="http://www.mgc.ac.cn/VFs/">VFDB</a>. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/26578559">26578559</a></li>
<li><a href="https://github.com/katholt/srst2">SRST2</a>'s version of ARG-ANNOT. PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/25422674">25422674</a>.</li>
<li><a href="https://cge.cbs.dtu.dk/services/VirulenceFinder/">VirulenceFinder</a>&nbsp;PMID:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/24574290">24574290</a>.</li>
</ul><p>Address of the bookmark: <a href="https://github.com/sanger-pathogens/ariba/wiki/Task%3A-getref" rel="nofollow">https://github.com/sanger-pathogens/ariba/wiki/Task%3A-getref</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44852/what-is-data-science-%E2%80%94-a-bioinformatics-perspective</guid>
	<pubDate>Mon, 16 Jun 2025 01:44:34 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44852/what-is-data-science-%E2%80%94-a-bioinformatics-perspective</link>
	<title><![CDATA[What is Data Science? — A Bioinformatics Perspective]]></title>
	<description><![CDATA[<p>In today&rsquo;s era of big biology, we&rsquo;re generating more data than ever before&mdash;genomes, transcriptomes, proteomes, metabolomes, microbiomes&hellip; you name it. But raw biological data doesn&rsquo;t speak for itself. Making sense of it requires more than traditional biology. This is where data science steps in.</p><p><strong>So, What Is Data Science?</strong><br />At its core, data science is the interdisciplinary field that extracts knowledge and insights from data using programming, statistics, and domain expertise. In bioinformatics, data science enables us to turn gigabytes of sequence data into biological meaning.</p><p>Imagine trying to understand gene regulation in cancer by analyzing thousands of RNA-seq samples, or predicting antibiotic resistance from bacterial genomes&mdash;these challenges are not solvable through wet lab experiments alone. They require data-driven thinking.</p><p><strong>Data Science Meets Bioinformatics</strong><br />Bioinformatics is inherently a data science domain. From genomics to systems biology, every field in modern biology relies on data science techniques to:</p><p>Clean and process massive datasets</p><p>Discover patterns in high-dimensional data</p><p>Build predictive models (e.g., for disease classification)</p><p>Visualize complex biological networks and trends</p><p>Integrate diverse data types (e.g., transcriptomic + epigenomic data)</p><p><strong>The Bioinformatics Toolkit</strong><br />Here&rsquo;s what data science typically looks like in bioinformatics:</p><p>Task Data Science Role<br />Sequence alignment Efficient algorithms, indexing, parallel processing<br />Gene expression analysis Statistical modeling (e.g., DESeq2, limma)<br />Variant calling Data filtering, probabilistic models<br />Clustering of cells in single-cell data Unsupervised learning<br />Protein structure prediction Deep learning models (e.g., AlphaFold)<br />Metagenomics Data integration, classification, dimensionality reduction</p><p>Common tools include Python, R, Bioconductor, scikit-learn, Pandas, Seurat, and TensorFlow&mdash;often working together in reproducible workflows.</p><p><strong>It's Not Just About Coding</strong><br />A common misconception is that bioinformatics is just programming or scripting. But being a data scientist in bioinformatics also means:</p><p>Understanding experimental design</p><p>Asking biologically meaningful questions</p><p>Choosing the right statistical or machine learning models</p><p>Communicating findings effectively (e.g., plots, dashboards, papers)</p><p>In other words, data science in bioinformatics is where biology, statistics, and computer science converge.</p><p><strong>Why It Matters</strong><br />The real power of data science in bioinformatics is its ability to scale discovery.</p><p>Instead of studying one gene, we can study thousands.</p><p>Instead of analyzing one species, we can explore entire ecosystems.</p><p>Instead of waiting months for lab results, we can generate hypotheses in days.</p><p>From personalized medicine and cancer diagnostics to agricultural genomics and pandemic surveillance, data science is at the heart of the bioinformatics revolution.</p><p><strong>Final Thoughts</strong><br />If you&rsquo;re a biologist who&rsquo;s curious about code, or a data enthusiast fascinated by life sciences, bioinformatics is your playground&mdash;and data science is your toolkit.</p><p>In bioinformatics, data science isn&rsquo;t just useful. It&rsquo;s essential.</p><p>&nbsp;</p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/16686/sequence-viewer-download-transcripts-exons-and-proteins</guid>
	<pubDate>Mon, 15 Sep 2014 17:30:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/16686/sequence-viewer-download-transcripts-exons-and-proteins</link>
	<title><![CDATA[Sequence Viewer: Download Transcripts, Exons and Proteins]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/ZWnLyYKozaI" frameborder="0" allowfullscreen></iframe>How to download FASTA sequence for certain gene features while in the NCBI's Sequence Viewer.

Sequence Viewer homepage:
www.ncbi.nlm.nih.gov/projects/sviewer/

Sequence Viewer playlist:
https://www.youtube.com/playlist?list=PL76D7EE6A6A8AC1C3]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27328/platanus</guid>
	<pubDate>Fri, 13 May 2016 05:12:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27328/platanus</link>
	<title><![CDATA[Platanus]]></title>
	<description><![CDATA[<p>Platanus is a novel <em>de novo</em> sequence assembler that can reconstruct genomic sequences of<br> highly heterozygous diploids from massively parallel shotgun sequencing data.</p>
<p>The latest version is <a href="http://platanus.bio.titech.ac.jp/platanus/?page_id=14">1.2.4</a>.</p>
<p>To cite Platanus, please use the following:</p>
<p>Kajitani R, Toshimoto K, Noguchi H, Toyoda A, Ogura Y, Okuno M, Yabana M, Harada M, Nagayasu E, Maruyama H, Kohara Y, Fujiyama A, Hayashi T, Itoh T, &ldquo;Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads&rdquo;.&nbsp;Genome Res. 2014 Aug;24(8):1384-95. doi: 10.1101/gr.170720.113. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/24755901">abstract</a> |<a href="http://genome.cshlp.org/content/24/8/1384.long"> full text</a>]</p><p>Address of the bookmark: <a href="http://platanus.bio.titech.ac.jp/" rel="nofollow">http://platanus.bio.titech.ac.jp/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</guid>
	<pubDate>Tue, 14 Jun 2016 10:28:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</link>
	<title><![CDATA[Blobsplorer]]></title>
	<description><![CDATA[<p>Blobsplorer is a tool for interactive visualization of assembled DNA sequence data ("contigs") derived from (often unintentionally) mixed-species pools. It allows the simultaneous display of GC content, coverage, and taxonomic annotation for collections of contigs with a view to separating out those belonging to different taxa.</p>
<p>Blobsplorer is unlikely to be of use on its own as it requires contig data to be supplied in a format that involves considerable preprocessing (see below for a description). The easiest way to use Blobsplorer is as part of a workflow using scripts from <a href="https://github.com/blaxterlab/blobology">here</a>.</p><p>Address of the bookmark: <a href="http://nematodes.org/martin/blobsplorer/blobsplorer.html" rel="nofollow">http://nematodes.org/martin/blobsplorer/blobsplorer.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30111/eager</guid>
	<pubDate>Sat, 10 Dec 2016 18:07:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30111/eager</link>
	<title><![CDATA[EAGER]]></title>
	<description><![CDATA[<p><span>The automated reconstruction of genome sequences in ancient genome analysis is a multifaceted process.</span></p>
<p><span>EAGER encompasses both state-of-the-art tools for each step as well as new complementary tools tailored for ancient DNA data within a single integrated solution in an easily accessible format.</span></p>
<p>https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-0918-z</p><p>Address of the bookmark: <a href="https://github.com/apeltzer/EAGER-GUI" rel="nofollow">https://github.com/apeltzer/EAGER-GUI</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33479/novelseq-novel-sequence-insertion-detection</guid>
	<pubDate>Fri, 09 Jun 2017 04:31:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33479/novelseq-novel-sequence-insertion-detection</link>
	<title><![CDATA[NovelSeq: Novel Sequence Insertion Detection]]></title>
	<description><![CDATA[<p><span>The NovelSeq framework is designed to detect novel sequence insertions using high throughput paired-end whole genome sequencing data.</span></p>
<p>http://novelseq.sourceforge.net/Home</p>
<p>Paper at&nbsp;https://www.ncbi.nlm.nih.gov/pubmed/20385726</p><p>Address of the bookmark: <a href="http://novelseq.sourceforge.net/Home" rel="nofollow">http://novelseq.sourceforge.net/Home</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

</channel>
</rss>