<?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/43620?offset=440</link>
	<atom:link href="https://bioinformaticsonline.com/related/43620?offset=440" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2727/download-mutliple-fasta-file-from-ncbi-in-one-go</guid>
	<pubDate>Wed, 21 Aug 2013 08:13:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2727/download-mutliple-fasta-file-from-ncbi-in-one-go</link>
	<title><![CDATA[Download mutliple fasta file from NCBI in one GO!!]]></title>
	<description><![CDATA[<p>if you have less time, then use three ways mentioned in bookmark link to extract/download all fasta sequences in single click given that you already have a list of GIs or accession IDs .</p>
<p>Alternatively, use one liner perl script:</p>
<p>perl -ne 'if(/^&gt;(\S+)/){$c=$i{$1}}$c?print:chomp;$i{$_}=1 if @ARGV' GIs.txt &gt;sequence.fasta</p>
<p>where GIs.txt contains&nbsp;a list of GIs or accession IDs.</p>
<p>(from :<a href="http://edwards.sdsu.edu/labsite/index.php/robert?start=5">http://edwards.sdsu.edu/labsite/index.php/robert?start=5</a>)</p><p>Address of the bookmark: <a href="http://edwards.sdsu.edu/labsite/index.php/robert/380-ncbi-sequence-or-fasta-batch-download-using-entrez" rel="nofollow">http://edwards.sdsu.edu/labsite/index.php/robert/380-ncbi-sequence-or-fasta-batch-download-using-entrez</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/8417/conserved-domain-database-cdd-version-311-released</guid>
	<pubDate>Wed, 19 Feb 2014 15:02:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/8417/conserved-domain-database-cdd-version-311-released</link>
	<title><![CDATA[Conserved Domain Database (CDD) version 3.11 released]]></title>
	<description><![CDATA[<p>National Center for Biotechnology Information (NCBI) Conserved Domain Database (CDD) version 3.11 is now available with 596 new or updated NCBI-curated and 49,641 total domain models. The new version now contains the most recent Pfam release 27.</p><p><img src="http://www.ncbi.nlm.nih.gov/Structure/cdd/docs/images/np_081086_triangles_site_features_on_query_gi255958238_mouse_mutl1.png" alt="image" width="800" height="415" style="border: 0px; border: 0px;"></p><p>Updates to the Conserved Domain Database include:</p><ul>
<li>Position-specific score matrices (PSSMs) have been recomputed for many models in CDD, and frequency tables have been added to the PSSMs;</li>
</ul><ul>
<li>The search databases distributed as part of this release can now be used with the more recent versions of RPS-BLAST (BLAST release 2.2.28 and up) using composition-based scoring. This abolishes the need to mask out compositionally biased regions in query sequences;</li>
</ul><ul>
<li>Domain annotation displays in CD-Search, BATCH CD-Search, and other services now all use a uniform display style. A new display option in CD-Search and BATCH CD-Search provides “standard” results, in addition to “concise” and “full” results. “Standard” results will provide, for each region on the query sequence, the best0-scoring domain model (if any) from each of CDD’s database providers (Pfam, SMART, COG, TIGRFAMs, Protein Clusters, and the NCBI in-house curation project), but will suppress redundancy from within a single provider's results list.</li>
</ul><p>You can access CDD at the <a href="http://www.ncbi.nlm.nih.gov/cdd">Conserved Domains homepage</a> and find updated content on the <a href="ftp://ftp.ncbi.nih.gov/pub/mmdb/cdd">CDD FTP site</a>.</p><p>Reference:</p><p>NCBI Website</p>]]></description>
	<dc:creator>Shikha Logwani</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26375/ncbi-remap</guid>
	<pubDate>Thu, 11 Feb 2016 11:02:26 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26375/ncbi-remap</link>
	<title><![CDATA[NCBI Remap]]></title>
	<description><![CDATA[<p><span><span><strong>NCBI Remap</strong>. This tool is conceptually similar to liftOver in that in manages conversions between a pair of genome assemblies but it uses different methods to achieve these mappings. It is also available through a simple <a href="http://www.ncbi.nlm.nih.gov/genome/tools/remap">web interface</a> or you can use the <a href="http://www.ncbi.nlm.nih.gov/genome/tools/remap/docs/api">API for NCBI Remap</a>.</span></span></p>
<p><span><span>More at http://www.ncbi.nlm.nih.gov/genome/tools/remap</span></span></p>
<p><span><span>API http://www.ncbi.nlm.nih.gov/genome/tools/remap/docs/api</span></span></p><p>Address of the bookmark: <a href="http://www.ncbi.nlm.nih.gov/genome/tools/remap" rel="nofollow">http://www.ncbi.nlm.nih.gov/genome/tools/remap</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29410/entrez-direct-e-utilities-on-the-unix-command-line</guid>
	<pubDate>Wed, 19 Oct 2016 08:06:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29410/entrez-direct-e-utilities-on-the-unix-command-line</link>
	<title><![CDATA[Entrez Direct: E-utilities on the UNIX Command Line]]></title>
	<description><![CDATA[<p>Entrez Direct (EDirect) is an advanced method for accessing the NCBI's suite of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. Functions take search terms from command-line arguments. Individual operations are combined to build multi-step queries. Record retrieval and formatting normally complete the process.</p>
<p>EDirect also provides an argument-driven function that simplifies the extraction of data from document summaries or other results that are returned in structured XML format. This can eliminate the need for writing custom software to answer ad hoc questions. Queries can move seamlessly between EDirect commands and UNIX utilities or scripts to perform actions that cannot be accomplished entirely within Entrez.</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/books/NBK179288/" rel="nofollow">https://www.ncbi.nlm.nih.gov/books/NBK179288/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41482/magic-blast</guid>
	<pubDate>Fri, 20 Mar 2020 15:18:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41482/magic-blast</link>
	<title><![CDATA[Magic-BLAST]]></title>
	<description><![CDATA[<p>Magic-BLAST is a tool for mapping large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome. Each alignment optimizes a composite score, taking into account simultaneously the two reads of a pair, and in case of RNA-seq, locating the candidate introns and adding up the score of all exons. This is very different from other versions of BLAST, where each exon is scored as a separate hit and read-pairing is ignored.</p><p>Address of the bookmark: <a href="https://ncbi.github.io/magicblast/" rel="nofollow">https://ncbi.github.io/magicblast/</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/44604/new-release-of-refseq</guid>
	<pubDate>Tue, 16 Jul 2024 10:09:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/44604/new-release-of-refseq</link>
	<title><![CDATA[New Release of RefSeq !]]></title>
	<description><![CDATA[<p>Check out RefSeq release 225, now available&nbsp;<a href="https://www.ncbi.nlm.nih.gov/refseq/?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=refseq-release-225-20240715">online</a>&nbsp;and from the&nbsp;<a href="https://ftp.ncbi.nlm.nih.gov/refseq/release/">FTP</a>&nbsp;site. You can access RefSeq data through&nbsp;<a href="https://www.ncbi.nlm.nih.gov/datasets/?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=refseq-release-225-20240715">NCBI Datasets</a>.</p><h5>What&rsquo;s included in this release?</h5><p>As of July 8, 2024, this full release incorporates genomic, transcript, and protein data containing:</p><ul>
<li><span>448,507,905 records</span></li>
<li><span>334,845,613 proteins</span></li>
<li><span>63,542,774 RNAs</span></li>
<li><span>Sequences from 152,668 organisms</span></li>
</ul><p>The release is provided in several directories as a complete dataset and also as divided by logical groupings.</p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/24264/cancer-research-database</guid>
	<pubDate>Tue, 01 Sep 2015 17:36:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/24264/cancer-research-database</link>
	<title><![CDATA[Cancer research database]]></title>
	<description><![CDATA[<p>Researchers in Andhra Pradesh have developed a database to identify genes that are common in tumours to provide their colleagues with easy access to insights into the genetic alterations in cancer.<br /> &nbsp;<br /> The database, hosted at the Sri Venkateswara University (SVU) in Tirupati, will integrate information on cancer genes and markers with experimental data.<br /> &nbsp;<br /> The <a href="http://cgmd.in/" target="_blank">Cancer Gene Markers Database</a> (CGMD) is meant to help scientists better understand tumour genes and markers at a molecular level by combining data with literature on treatment regimen and recent advances in cancer therapy.<br /> <br /> The database is free to access, and already includes 309 genes and 206 markers that correspond to 40 different human cancers. Accompanying literature comes from databases such as the United States&rsquo; <a href="http://www.ncbi.nlm.nih.gov/" target="_blank">National Center for Biotechnology Information</a> and the <a href="http://www.genome.jp/kegg/" target="_blank">Kyoto Encyclopedia of Genes and Genomes</a>. It also includes experimental data from <a href="http://www.ncbi.nlm.nih.gov/pubmed" target="_blank">PubMed</a>.<br /> <br /> In a paper <a href="http://dx.doi.org/10.1038/srep12035" target="_blank">published</a> last month in <em>Nature Scientific Reports</em>, the researchers from SVU&rsquo;s department of animal biotechnology, describes the need for a database for different genes and markers along with their molecular characteristics and pathway associations.</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30168/gene-synteny-database</guid>
	<pubDate>Fri, 16 Dec 2016 11:09:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30168/gene-synteny-database</link>
	<title><![CDATA[Gene Synteny Database]]></title>
	<description><![CDATA[<p>Comparative genomics remains a pivotal strategy to study the evolution of gene organization, and this primacy is reinforced by the growing number of full genome sequences available in public repositories. Despite this growth, bioinformatic tools available to visualize and compare genomes and to infer evolutionary events remain restricted to two or three genomes at a time, thus limiting the breadth and the nature of the question that can be investigated. Here we present Genomicus, a new synteny browser that can represent and compare unlimited numbers of genomes in a broad phylogenetic view. In addition, Genomicus includes reconstructed ancestral gene organization, thus greatly facilitating the interpretation of the data.</p>
<p><strong>Availability:</strong>&nbsp;Genomicus is freely available for online use at&nbsp;<a href="http://www.dyogen.ens.fr/genomicus" target="pmc_ext">http://www.dyogen.ens.fr/genomicus</a>&nbsp;while data can be downloaded at&nbsp;<a href="ftp://ftp.biologie.ens.fr/pub/dyogen/genomicus" target="pmc_ext">ftp://ftp.biologie.ens.fr/pub/dyogen/genomicus</a></p>
<p><strong>Contact:</strong>&nbsp;<a href="mailto:dev@null">rf.sne.eigoloib@crh</a></p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853686/" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853686/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/40589/new-layout-for-blast-ftp-database-site</guid>
	<pubDate>Tue, 21 Jan 2020 11:57:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/40589/new-layout-for-blast-ftp-database-site</link>
	<title><![CDATA[New Layout for BLAST ftp Database Site]]></title>
	<description><![CDATA[<p>As announced previously, the new default database version for&nbsp;<a href="https://ncbiinsights.ncbi.nlm.nih.gov/2019/12/18/blast-2-10-0/" target="_blank" title="Follow link">BLAST+</a>&nbsp;is&nbsp;<a href="https://ncbiinsights.ncbi.nlm.nih.gov/2019/09/30/protein-blastdbs-accession-based/" target="_blank" title="Follow link">dbV5</a>.&nbsp; To complete this transition, the&nbsp;<a href="ftp://ftp.ncbi.nlm.nih.gov/blast/db/" target="_blank" title="Follow link">ftp database site</a>&nbsp;will be updated to support this change.&nbsp; We expect this change to happen around February 4<sup>th</sup>, please adjust your scripts or procedures accordingly.</p><p>Here is a list of what is changing:</p><ol>
<li>All databases at the root level will be dbV5.</li>
<li>The dbV5 file naming, &nbsp;&ldquo;_v5&rdquo; will be removed. Databases with &nbsp;no &ldquo;_vX&rdquo; descriptor will be dbV5.</li>
<li>dbV4 tarballs will be renamed with "_v4", files included in tarball will not be renamed.</li>
<li>dbV4 databases will be moved to a v4 subdirectory.</li>
<li>As of 1/13/20 the Cloud directory will be frozen with no more new entries.</li>
<li>The will be no more updates to dbV4 databases.</li>
<li>The FASTA directory will contain nr, nt, swissprot, and pdbaa files.</li>
</ol><p>If you have any questions or concerns, please contact&nbsp;<a href="mailto:blast-help@ncbi.nlm.nih.gov" target="_blank" title="Follow link">blast-help@ncbi.nlm.nih.gov</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<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>
</item>

</channel>
</rss>