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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/43714?offset=240</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45303/the-tree-that-learned-to-read-genomes</guid>
	<pubDate>Fri, 11 Sep 2026 00:51:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45303/the-tree-that-learned-to-read-genomes</link>
	<title><![CDATA[The Tree That Learned to Read Genomes]]></title>
	<description><![CDATA[<p>Imagine trying to reconstruct a family tree when many family photographs are missing, some names are unclear, and different relatives remember the past differently. This is similar to the challenge scientists face when trying to understand how organisms are related. Their family records are genomes, and the family tree is a phylogenetic tree. With modern sequencing technologies, scientists now have access to thousands of genomes, but comparing them can be difficult, especially when genomes are incomplete or poorly annotated.</p><p>A recent study by Webster and Chapman introduces Buscogeny (https://github.com/Jwebster89/Buscogeny), an open-source bioinformatics pipeline designed to make this process easier. The tool uses BUSCO (Benchmarking Universal Single-Copy Orthologs), which identifies conserved genes that are expected to occur as single copies in particular groups of organisms. These genes act like evolutionary landmarks, allowing researchers to compare genomes and investigate their relationships.</p><p>Buscogeny brings several steps of phylogenomic analysis into one workflow. It identifies BUSCO genes, extracts and aligns their sequences, removes unreliable regions, combines information from multiple genes, and uses the resulting data to construct a phylogenetic tree. It also provides quality-control information, helping researchers identify genomes that may be too incomplete for reliable analysis.</p><p>The authors demonstrate the usefulness of Buscogeny with bacterial and fungal genomes, including Alternaria. This is particularly valuable because fungal genomes can vary greatly in quality and annotation. Ultimately, Buscogeny helps transform massive amounts of genomic data into an understandable evolutionary story. Each DNA sequence becomes a clue, each conserved gene becomes a landmark, and together these clues reveal a picture of how life is connected.</p><p>More at&nbsp;https://link.springer.com/article/10.1007/s10123-025-00752-6?</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4585/new-vaccine-clears-aids-causing-virus-in-monkeys</guid>
	<pubDate>Tue, 17 Sep 2013 10:57:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4585/new-vaccine-clears-aids-causing-virus-in-monkeys</link>
	<title><![CDATA[New Vaccine Clears AIDS-Causing Virus in Monkeys]]></title>
	<description><![CDATA[<p>A newly developed vaccine has the ability to completely kill simian immunodeficiency virus (SIV) in non-human primates, according to scientists at Oregon Health &amp; Science University&rsquo;s Vaccine and Gene Therapy Institute.</p><p>The new approach involves the use of cytomegalovirus, or CMV, a common virus already carried by a large percentage of the population. Dr Picker and his colleagues discovered that pairing CMV with SIV had a unique effect.</p><p>Research finding provide compelling evidence for progressive clearance of a pathogenic lentiviral infection, and suggest that some lentiviral reservoirs may be susceptible to the continuous effector memory T-cell-mediated immune surveillance elicited and maintained by cytomegalovirus vectors.</p><p>Reference:</p><p>http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12519.html</p><p>http://www.bbc.co.uk/news/science-environment-24051860</p><p>Image Source: ucsf.edu</p><p><img src="http://www.cgl.ucsf.edu/chimera/data/hiv09/images/siv-tomography.png" width="749" height="719" alt="image" style="border: 0px;"></p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/11592/xampp-starting-apache-fail-ubuntu</guid>
	<pubDate>Sat, 07 Jun 2014 05:52:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/11592/xampp-starting-apache-fail-ubuntu</link>
	<title><![CDATA[XAMPP: Starting Apache fail Ubuntu]]></title>
	<description><![CDATA[<p>Once you install XAMMP on linux, the most common problem you face is Apache failure. To fix the issues please use following command to first stop and then again start it.</p><p>sudo /etc/init.d/apache2 stop</p><p>sudo /etc/init.d/mysql stop</p><p>sudo /etc/init.d/proftpd stop</p><p>sudo /opt/lampp/lampp start</p><p>&nbsp;</p><p><strong>PhpMyAdmin &ldquo;Wrong permissions on configuration file, should not be world writable!&rdquo;</strong></p><p>Once the Xammp is installed, it might be possible to set up the configuration file in writable mode. Try the following steps:</p><p>Just chmod 0755 the file</p><pre>sudo chmod 0755 config.inc.php</pre>]]></description>
	<dc:creator>Ram Yash Pal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38556/reactome-pathway-database</guid>
	<pubDate>Mon, 31 Dec 2018 02:41:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38556/reactome-pathway-database</link>
	<title><![CDATA[Reactome Pathway Database]]></title>
	<description><![CDATA[<p><span>REACTOME is an open-source, open access, manually curated and peer-reviewed pathway database. Our goal is to provide intuitive bioinformatics tools for the visualization, interpretation and analysis of pathway knowledge to support basic and clinical research, genome analysis, modeling, systems biology and education. Founded in 2003, the Reactome project is led by Lincoln Stein of&nbsp;</span><a href="http://oicr.on.ca/">OICR</a><span>, Peter D&rsquo;Eustachio of&nbsp;</span><a href="http://nyulangone.org/">NYULMC</a><span>, Henning Hermjakob of&nbsp;</span><a href="http://www.ebi.ac.uk/">EMBL-EBI</a><span>, and Guanming Wu of&nbsp;</span><a href="http://www.ohsu.edu/">OHSU</a><span>.</span></p><p>Address of the bookmark: <a href="https://reactome.org/" rel="nofollow">https://reactome.org/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44718/mycology-research-resources-for-bioinformaticians-unlocking-the-fungal-kingdom</guid>
	<pubDate>Fri, 13 Dec 2024 11:21:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44718/mycology-research-resources-for-bioinformaticians-unlocking-the-fungal-kingdom</link>
	<title><![CDATA[Mycology Research Resources for Bioinformaticians: Unlocking the Fungal Kingdom]]></title>
	<description><![CDATA[<p>Mycology, the study of fungi, is a field that bridges ecology, medicine, and biotechnology. With advancements in bioinformatics, researchers now have unprecedented opportunities to explore the fungal kingdom at molecular, genetic, and ecological levels. From understanding pathogenic fungi to harnessing fungal enzymes for industrial applications, the potential is vast.</p><p>To fully leverage these opportunities, bioinformaticians require specialized tools and databases. This blog highlights essential resources for mycology research, focusing on databases, tools, and platforms tailored for fungal biology.</p><h4><strong>1. Fungal Databases</strong></h4><h5><strong>1.1. MycoCosm</strong></h5><p><strong>Website</strong>: <a target="_new">MycoCosm</a><br />Developed by the DOE Joint Genome Institute, MycoCosm is a comprehensive portal for fungal genomics. It offers genomic and transcriptomic data for a wide range of fungi, including saprobes, pathogens, and symbionts.</p><ul>
<li><strong>Key Features</strong>: Genome browsers, comparative genomics tools, and functional annotations.</li>
<li><strong>Best For</strong>: Large-scale studies on fungal evolution and ecology.</li>
</ul><h5><strong>1.2. FungiDB</strong></h5><p><strong>Website</strong>: <a href="https://fungidb.org/" target="_new">FungiDB</a><br />FungiDB is an integrated genomic resource for fungal pathogens and non-pathogens. It provides access to genome sequences, transcriptomic data, and functional annotations.</p><ul>
<li><strong>Key Features</strong>: Advanced search options, BLAST, and pathway analysis tools.</li>
<li><strong>Best For</strong>: Studying fungal pathogenesis and host-pathogen interactions.</li>
</ul><h5><strong>1.3. Index Fungorum</strong></h5><p><strong>Website</strong>: <a href="http://www.indexfungorum.org/" target="_new">Index Fungorum</a><br />This nomenclatural database provides information on the scientific names of fungi. It&rsquo;s an essential resource for taxonomists and researchers focused on fungal biodiversity.</p><ul>
<li><strong>Key Features</strong>: Taxonomic hierarchy and synonymy tracking.</li>
<li><strong>Best For</strong>: Identifying and classifying fungal species.</li>
</ul><h5><strong>1.4. UNITE</strong></h5><p><strong>Website</strong>: <a target="_new">UNITE</a><br />UNITE is a specialized database for fungal ITS (Internal Transcribed Spacer) sequences, often used in fungal identification and phylogenetics.</p><ul>
<li><strong>Key Features</strong>: Curated reference datasets and community annotations.</li>
<li><strong>Best For</strong>: Environmental mycology and microbial ecology studies.</li>
</ul><h4><strong>2. Analytical Tools</strong></h4><h5><strong>2.1. Funannotate</strong></h5><p><strong>Repository</strong>: <a href="https://github.com/nextgenusfs/funannotate" target="_new">GitHub - Funannotate</a><br />Funannotate is a genome annotation tool designed for fungi. It supports tasks like gene prediction, functional annotation, and orthology analysis.</p><ul>
<li><strong>Best For</strong>: Annotating newly sequenced fungal genomes.</li>
</ul><h5><strong>2.2. BUSCO (Benchmarking Universal Single-Copy Orthologs)</strong></h5><p><strong>Website</strong>: <a target="_new">BUSCO</a><br />BUSCO evaluates genome assembly and annotation completeness using orthologs. It includes a fungal-specific dataset.</p><ul>
<li><strong>Best For</strong>: Assessing the quality of fungal genome assemblies.</li>
</ul><h5><strong>2.3. Pathogen-Host Interactions Database (PHI-base)</strong></h5><p><strong>Website</strong>: <a href="http://www.phi-base.org/" target="_new">PHI-base</a><br />PHI-base is a manually curated resource containing information on pathogen-host interactions, including fungal pathogens.</p><ul>
<li><strong>Best For</strong>: Exploring virulence factors and host-pathogen relationships.</li>
</ul><h4><strong>3. Visualization Platforms</strong></h4><h5><strong>3.1. Cytoscape</strong></h5><p><strong>Website</strong>: <a href="https://cytoscape.org/" target="_new">Cytoscape</a><br />A powerful tool for visualizing molecular interaction networks, Cytoscape can be used to study protein-protein interactions, gene networks, and metabolic pathways in fungi.</p><ul>
<li><strong>Best For</strong>: Network biology and functional genomics.</li>
</ul><h5><strong>3.2. iTOL (Interactive Tree of Life)</strong></h5><p><strong>Website</strong>: <a target="_new">iTOL</a><br />iTOL is an interactive tool for visualizing phylogenetic trees.</p><ul>
<li><strong>Best For</strong>: Displaying fungal phylogenies and comparing evolutionary relationships.</li>
</ul><h4><strong>4. Community Resources</strong></h4><h5><strong>4.1. Mycological Society of America (MSA)</strong></h5><p><strong>Website</strong>: <a href="https://msafungi.org/" target="_new">MSA</a><br />The MSA promotes fungal research and provides access to resources, conferences, and publications.</p><ul>
<li><strong>Best For</strong>: Networking with fungal researchers and accessing recent studies.</li>
</ul><h5><strong>4.2. OpenFungi</strong></h5><p><strong>Website</strong>: <a href="https://openfungi.org/" target="_new">OpenFungi</a><br />OpenFungi is an open-source initiative providing fungal genomic and transcriptomic datasets for research and education.</p><ul>
<li><strong>Best For</strong>: Sharing and accessing public fungal datasets.</li>
</ul><h4><strong>5. Genomics Workflows</strong></h4><h5><strong>5.1. Galaxy</strong></h5><p><strong>Website</strong>: <a href="https://usegalaxy.org/" target="_new">Galaxy Project</a><br />Galaxy offers a web-based platform for reproducible bioinformatics workflows, including tools for fungal genome and transcriptome analysis.</p><ul>
<li><strong>Best For</strong>: User-friendly analysis pipelines without requiring coding skills.</li>
</ul><h5><strong>5.2. Snakemake</strong></h5><p><strong>Repository</strong>: <a target="_new">Snakemake</a><br />A flexible pipeline management tool that supports fungal data processing and analysis.</p><ul>
<li><strong>Best For</strong>: Custom workflows for large-scale fungal datasets.</li>
</ul><h4><strong>Conclusion</strong></h4><p>Fungal research is a rapidly growing field with vast implications for medicine, agriculture, and industry. For bioinformaticians, the availability of specialized resources&mdash;databases, tools, and community platforms&mdash;opens doors to innovative discoveries. Whether you are investigating fungal genomics, studying host-pathogen interactions, or exploring fungal biodiversity, the resources outlined above will empower your research journey.</p><p>Dive into these resources and help unravel the mysteries of the fungal kingdom!</p>]]></description>
	<dc:creator>Neel</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/39826/data-scientist-mwd</guid>
  <pubDate>Wed, 07 Aug 2019 03:19:46 -0500</pubDate>
  <link></link>
  <title><![CDATA[Data Scientist (m/w/d)]]></title>
  <description><![CDATA[
<p>https://uk-erlangen.concludis.de/prj/shw/b8b26f24186191c7af8a25e2cc6115ca_0/27008/Data_Scientist_m_w_d.htm?b=0</p>

<p>Deadline: 30.09.2019</p>

<p>Requirement:<br />Microsoft SQL Server: Administration, Transact-SQL<br />Machine Learning<br />Know Deutsch und Englisch langauge</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/39865/blast-nr-version-5-database-nr-v5</guid>
	<pubDate>Fri, 23 Aug 2019 11:35:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/39865/blast-nr-version-5-database-nr-v5</link>
	<title><![CDATA[BLAST nr version 5 database, (nr_v5)]]></title>
	<description><![CDATA[<p>NCBI have made changes the nr version 5 database, (nr_v5), to facilitate better search results and improved performance by reducing the number of redundant titles in the nr_v5 database used by webBLAST, which is also available for&nbsp;BLAST+ users.</p><p><span style="text-decoration: underline;"></span></p><p>The changes in nr preserve the taxonomic diversity of the entries in the database while reducing the number of titles for identical sequences. GenPept accessions are still accessible via&nbsp;<a href="http://www.ncbi.nlm.nih.gov/protein/$GENBANK_ACCESSION" target="_blank">www.ncbi.nlm.nih.gov/protein/$GENBANK_ACCESSION</a>&nbsp;or the IPG website&nbsp;<a href="https://www.ncbi.nlm.nih.gov/ipg/" target="_blank">https://www.ncbi.nlm.nih.gov/ipg/</a>.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>The "Identical Proteins" link in the alignments section of the webBLAST results takes you to a full list of all accessions associated with a sequence.</p><p><span style="text-decoration: underline;"></span></p><p>For&nbsp;BLAST+ users downloading nr_v5: the database is now approximately 50% smaller, resulting in faster downloads and&nbsp;BLAST&nbsp;searches, and smaller disk space requirements. The database is downloadable at: &nbsp;<a href="ftp://ftp.ncbi.nlm.nih.gov/blast/db/v5/" target="_blank">ftp://ftp.ncbi.nlm.nih.gov/blast/db/v5/</a></p><p><span style="text-decoration: underline;"></span></p><p>For&nbsp;BLAST+ there is a cleanup script to help you manage the transition to this smaller database. The script removes unused database volumes:&nbsp;<a href="ftp://ftp.ncbi.nlm.nih.gov/blast/temp/cleanup-blastdb-volumes.py" target="_blank">ftp://ftp.ncbi.nlm.nih.gov/blast/temp/cleanup-blastdb-volumes.py</a></p><p><span style="text-decoration: underline;"></span></p><p>Here are the new rules on how we keep titles in nr_v5:</p><p><span style="text-decoration: underline;"></span></p><p>1.&nbsp;&nbsp;&nbsp; We keep all refseq, swissprot, pir and PDB titles.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>2.&nbsp; &nbsp;&nbsp;We keep any GenPept titles with a TAXID that has not already been seen in the record.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>3.&nbsp; &nbsp;&nbsp;We keep at least five GenPept titles regardless of whether the TAXIDS have been seen before or not in this record.</p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43011/deg-50-a-database-of-essential-genes-in-both-prokaryotes-and-eukaryotes</guid>
	<pubDate>Tue, 30 Mar 2021 11:47:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43011/deg-50-a-database-of-essential-genes-in-both-prokaryotes-and-eukaryotes</link>
	<title><![CDATA[DEG 5.0: a database of essential genes in both prokaryotes and eukaryotes]]></title>
	<description><![CDATA[<p><span>Essential genes are those indispensable for the survival of an organism, and their functions are therefore considered a foundation of life. Determination of a minimal gene set needed to sustain a life form, a fundamental question in biology, plays a key role in the emerging field, synthetic biology. </span></p>
<p><span></span><span>DEG is freely available at the website&nbsp;</span><a href="http://tubic.tju.edu.cn/deg" target="_blank">http://tubic.tju.edu.cn/deg</a><span>&nbsp;or&nbsp;</span><a href="http://www.essentialgene.org/" target="_blank">http://www.essentialgene.org</a><span>.</span></p><p>Address of the bookmark: <a href="http://www.essentialgene.org/" rel="nofollow">http://www.essentialgene.org/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43685/chipbase-open-database-for-studying-the-transcription-factor-binding-sites-and-motifs</guid>
	<pubDate>Wed, 29 Dec 2021 05:36:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43685/chipbase-open-database-for-studying-the-transcription-factor-binding-sites-and-motifs</link>
	<title><![CDATA[ChIPBase: open database for studying the transcription factor binding sites and motifs]]></title>
	<description><![CDATA[<p>ChIPBase v2.0 is an open database for studying the transcription factor binding sites and motifs, and decoding the transcriptional regulatory networks of lncRNAs, miRNAs, other ncRNAs and protein-coding genes from ChIP-seq data. Our database currently contains ~10,200 curated peak datasets derived from ChIP-seq methods in 10 species.</p><p>Address of the bookmark: <a href="https://rna.sysu.edu.cn/chipbase/" rel="nofollow">https://rna.sysu.edu.cn/chipbase/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4288/new-born-babies-get-ready-to-know-their-whole-genome-soon</guid>
	<pubDate>Thu, 05 Sep 2013 07:24:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4288/new-born-babies-get-ready-to-know-their-whole-genome-soon</link>
	<title><![CDATA[New born babies get ready to know their whole genome soon!!!]]></title>
	<description><![CDATA[<p>USA launch a pilot projects to examine medical information of newborn baby, which are being funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and the National Human Genome Research Institute (NHGRI), both parts of the National Institutes of Health.</p><p>Awards of $5 million to four grantees have been made in fiscal year 2013 under the Genomic Sequencing and Newborn Screening Disorders research program. The program will be funded at $25 million over five years, as funds are made available.</p><p>"Hundreds of US babies will be pioneers in genomic medicine through a&nbsp;US$25-million programme to sequence their genomes&nbsp;soon after they are born."</p><p><strong>Source</strong>:</p><p><a href="http://blogs.nature.com/news/2013/09/scientists-to-sequence-hundreds-of-newborns-genomes.html">http://blogs.nature.com/news/2013/09/scientists-to-sequence-hundreds-of-newborns-genomes.html</a></p><p><a href="http://www.genome.gov/27554919">http://www.genome.gov/27554919</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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