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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/42319?offset=10</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/37198/understanding-blastn-output-format-6</guid>
	<pubDate>Wed, 27 Jun 2018 18:38:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/37198/understanding-blastn-output-format-6</link>
	<title><![CDATA[Understanding BLASTn output format 6 !]]></title>
	<description><![CDATA[<h3 id="sites-page-title-header" style="text-align: left;"><span>BLASTn output format 6</span></h3><div id="sites-canvas-main"><div id="sites-canvas-main-content"><div dir="ltr"><div><div><em>BLASTn</em> maps DNA against DNA, for example gene sequences against a reference genome<br /><br /><code><strong>blastn</strong>  -query <span>genes.ffn</span>  -subject <span>genome.fna</span>  -outfmt <strong>6</strong></code></div><h2>BLASTn tabular output format 6</h2>
<p><strong>Column headers:</strong><br /><code>qseqid sseqid pident length mismatch gapopen qstart qend sstart send evalue bitscore</code><br /></p>
<table border="1" cellspacing="0">
<tbody>
<tr>
<td> 1.</td>
<td> qseqid</td>
<td> query (e.g., gene) sequence id</td>
</tr>
<tr>
<td> 2.</td>
<td> sseqid</td>
<td> subject (e.g., reference genome) sequence id</td>
</tr>
<tr>
<td> 3.</td>
<td> pident</td>
<td> percentage of identical matches</td>
</tr>
<tr>
<td> 4.</td>
<td> length</td>
<td> alignment length</td>
</tr>
<tr>
<td> 5.</td>
<td> mismatch</td>
<td> number of mismatches</td>
</tr>
<tr>
<td> 6.</td>
<td> gapopen</td>
<td> number of gap openings</td>
</tr>
<tr>
<td> 7.</td>
<td> qstart</td>
<td> start of alignment in query</td>
</tr>
<tr>
<td> 8.</td>
<td> qend</td>
<td> end of alignment in query</td>
</tr>
<tr>
<td> 9.</td>
<td> sstart</td>
<td> start of alignment in subject</td>
</tr>
<tr>
<td> 10.</td>
<td> send</td>
<td> end of alignment in subject</td>
</tr>
<tr>
<td> 11.</td>
<td> evalue</td>
<td> <a href="http://www.metagenomics.wiki/tools/blast/evalue">expect value</a></td>
</tr>
<tr>
<td> 12.</td>
<td> bitscore</td>
<td> <a href="http://www.metagenomics.wiki/tools/blast/evalue"><strong>bit score</strong></a></td>
</tr>
</tbody>
</table>
<p><strong><br /></strong></p>
</div><h2><a name="TOC-Define-your-own-output-format" id="TOC-Define-your-own-output-format"></a>Define your own output format</h2><div><em>by adding the option -outfmt, as for example: </em><strong><br /></strong></div>
<p><code><strong>-outfmt</strong> <strong>"6</strong> <span>qseqid sseqid pident qlen length mismatch gapope evalue bitscore</span><strong>"</strong></code><br /><br /><em><strong>supported format specifiers are:</strong></em><br /><code>qseqid    </code>Query Seq-id<br /><code>qgi       </code>Query GI<br /><code>qacc      </code>Query accesion<br /><code>qaccver   </code>Query accesion.version<br /><code>qlen      </code>Query sequence length<br /><code>sseqid    </code>Subject Seq-id<br /><code>sallseqid </code>All subject Seq-id(s), separated by a ';'<br /><code>sgi       </code>Subject GI<br /><code>sallgi    </code>All subject GIs<br /><code>sacc      </code>Subject accession<br /><code>saccver   </code>Subject accession.version<br /><code>sallacc   </code>All subject accessions<br /><code>slen      </code>Subject sequence length<br /><code>qstart    </code>Start of alignment in query<br /><code>qend      </code>End of alignment in query<br /><code>sstart    </code>Start of alignment in subject<br /><code>send      </code>End of alignment in subject<br /><code>qseq      </code>Aligned part of query sequence<br /><code>sseq      </code>Aligned part of subject sequence<br /><code>evalue    </code>Expect value<br /><code>bitscore  </code>Bit score<br /><code>score     </code>Raw score<br /><code>length    </code>Alignment length<br /><code>pident    </code>Percentage of identical matches<br /><code>nident    </code>Number of identical matches<br /><code>mismatch  </code>Number of mismatches<br /><code>positive  </code>Number of positive-scoring matches<br /><code>gapopen   </code>Number of gap openings<br /><code>gaps      </code>Total number of gaps<br /><code>ppos      </code>Percentage of positive-scoring matches<br /><code>frames    </code>Query and subject frames separated by a '/'<br /><code>qframe    </code>Query frame<br /><code>sframe    </code>Subject frame<br /><code>btop      </code>Blast traceback operations (BTOP)<br /><code>staxids   </code>Subject Taxonomy ID(s), separated by a ';'<br /><code>sscinames </code>Subject Scientific Name(s), separated by a ';'<br /><code>scomnames </code>Subject Common Name(s), separated by a ';'<br /><code>sblastnames </code>Subject Blast Name(s), separated by a ';'   (in alphabetical order)<br /><code>sskingdoms  </code>Subject Super Kingdom(s), separated by a ';'     (in alphabetical order) <br /><code>stitle      </code>Subject Title<br /><code>salltitles  </code>All Subject Title(s), separated by a '&lt;&gt;'<br /><code>sstrand   </code>Subject Strand<br /><code>qcovs     </code>Query Coverage Per Subject<br /><code>qcovhsp   </code>Query Coverage Per HSP<br /><strong><br /><em>default values are:</em></strong><br /><code><code>-outfmt "</code>6 qseqid sseqid pident length mismatch gapopen qstart qend sstart send evalue bitscore"</code></p>
</div></div></div>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43424/rest-api</guid>
	<pubDate>Mon, 04 Oct 2021 12:46:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43424/rest-api</link>
	<title><![CDATA[REST API]]></title>
	<description><![CDATA[<h3 id="PSIBLASTHelpandDocumentation-RESTAPI">REST API</h3><p>The&nbsp;<a href="https://www.ebi.ac.uk/seqdb/confluence/pages/viewpage.action?pageId=68165098">Representational State Transfer (REST)</a>&nbsp;sample clients are provided for a number of programming languages. For details of how to use these clients,&nbsp;<a href="https://github.com/ebi-wp/webservice-clients">download</a>&nbsp;the client and run the program without any arguments.</p><div><table><colgroup><col><col><col></colgroup>
<thead>
<tr><th scope="col">
<div>Language</div>
</th><th scope="col">
<div>Download</div>
</th><th scope="col">
<div>Requirements</div>
</th></tr>
</thead>
<tbody>
<tr><th>Perl</th>
<td><a href="https://raw.githubusercontent.com/ebi-wp/webservice-clients/master/perl/psiblast.pl">psiblast.pl</a></td>
<td><a href="http://search.cpan.org/perldoc?LWP">LWP</a>&nbsp;and&nbsp;<a href="http://search.cpan.org/perldoc?XML::Simple">XML::Simple</a></td>
</tr>
<tr><th colspan="1">
<h4 id="PSIBLASTHelpandDocumentation-Python">Python</h4>
</th>
<td colspan="1">
<p><a href="https://raw.githubusercontent.com/ebi-wp/webservice-clients/master/python/psiblast.py">psiblast.py</a></p>
</td>
<td colspan="1"><a href="https://pypi.python.org/pypi/xmltramp2/3.0.10" title="https://pypi.python.org/pypi/xmltramp2/3.0.10">xmltramp2</a></td>
</tr>
</tbody>
</table></div><p>For details see&nbsp;<a href="https://www.ebi.ac.uk/seqdb/confluence/display/JDSAT/Environment+setup+for+REST+Web+Services">Environment setup for REST Web Services</a>&nbsp;and&nbsp;<a href="https://www.ebi.ac.uk/seqdb/confluence/display/JDSAT/Examples+for+Perl+REST+Web+Services+Clients">Examples for Perl REST Web Services Clients</a>&nbsp;pages.</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38449/koala-keggs-internal-annotation-tool-for-k-number-assignment-of-kegg-genes-using-ssearch-computation</guid>
	<pubDate>Wed, 12 Dec 2018 09:16:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38449/koala-keggs-internal-annotation-tool-for-k-number-assignment-of-kegg-genes-using-ssearch-computation</link>
	<title><![CDATA[KOALA: KEGG&#039;s internal annotation tool for K number assignment of KEGG GENES using SSEARCH computation]]></title>
	<description><![CDATA[<p>KOALA (KEGG Orthology And Links Annotation) is KEGG's internal annotation tool for&nbsp;<a href="https://www.kegg.jp/kegg/ko.html">K number</a>&nbsp;assignment of KEGG GENES using SSEARCH computation. BlastKOALA and GhostKOALA assign K numbers to the user's sequence data by&nbsp;<a href="http://www.ncbi.nlm.nih.gov/blast/">BLAST</a>&nbsp;and&nbsp;<a href="http://www.bi.cs.titech.ac.jp/ghostx/">GHOSTX</a>&nbsp;searches, respectively, against a nonredundant set of KEGG GENES. Annotate Sequence in KEGG Mapper and Pathogen Checker in KEGG Pathogen are special interfaces to the BlastKOALA server and can be executed in an interactive mode. &nbsp;&nbsp; See&nbsp;<a href="https://www.kegg.jp/blastkoala/help_blastkoala.html" target="_blastkoala">Step-by-step Instructions</a>.</p>
<div>Reference: Kanehisa, M., Sato, Y., and Morishima, K. (2016) BlastKOALA and GhostKOALA: KEGG tools for functional characterization of genome and metagenome sequences. J. Mol. Biol. 428, 726-731. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/26585406">pubmed</a>] [<a href="https://doi.org/10.1016/j.jmb.2015.11.006">pdf</a>]</div><p>Address of the bookmark: <a href="https://www.kegg.jp/blastkoala/" rel="nofollow">https://www.kegg.jp/blastkoala/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41901/far-manager-commands-and-links</guid>
	<pubDate>Tue, 23 Jun 2020 06:24:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41901/far-manager-commands-and-links</link>
	<title><![CDATA[Far Manager Commands and Links !]]></title>
	<description><![CDATA[<p>Far Manager is a program for managing files and archives in&nbsp;<acronym title="2000/XP/2003/Vista/2008/7">Windows operating systems</acronym>. Far Manager works in text mode and provides a simple and intuitive interface for performing most of the necessary actions:</p>
<ul>
<li>viewing files and directories;</li>
<li>editing, copying and renaming files;</li>
<li>and many other actions.</li>
</ul>
<p><a href="https://www.farmanager.com/">https://www.farmanager.com/</a></p>
<p>Basic instruction at</p>
<p><a href="https://conemu.github.io/en/FarManager.html">https://conemu.github.io/en/FarManager.html</a></p>
<p>Plugins at&nbsp;</p>
<p><a href="https://plugring.farmanager.com/">https://plugring.farmanager.com/</a></p><p>Address of the bookmark: <a href="https://www.farmanager.com/" rel="nofollow">https://www.farmanager.com/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/44364/genbank-release-2570-is-now-available</guid>
	<pubDate>Wed, 23 Aug 2023 00:23:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/44364/genbank-release-2570-is-now-available</link>
	<title><![CDATA[GenBank release 257.0 is now available!]]></title>
	<description><![CDATA[<p><span>GenBank release 257.0 is now available! This release has 25.10 trillion bases and 3.69 billion records. Learn more:&nbsp;https://ncbiinsights.ncbi.nlm.nih.gov/2023/08/21/genbank-release-257/</span><a href="https://ow.ly/zHbV50PBE5o"><br /></a></p><p><a href="https://www.ncbi.nlm.nih.gov/genbank/?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=genbank-release-20230821">GenBank</a>&nbsp;release 257.0 (8/15/2023) is now available on the&nbsp;<a href="https://ftp.ncbi.nlm.nih.gov/genbank/">NCBI FTP site</a>. This release has 25.10 trillion bases and 3.69 billion records.</p><p><strong>The current release has:</strong></p><ul>
<li>246,119,175 traditional records containing 2,112,058,517,945 base pairs of sequence data</li>
<li>2,631,493,489 WGS records containing 22,294,446,104,543 base pairs of sequence data</li>
<li>686,271,945 bulk-oriented TSA records containing 646,176,166,908 base pairs of sequence data</li>
<li>124,421,006 bulk-oriented TLS records containing 48,289,699,026 base pairs of sequence data</li>
</ul>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/4413/demo-4-using-blastblat-in-ensembl</guid>
	<pubDate>Tue, 10 Sep 2013 11:54:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/4413/demo-4-using-blastblat-in-ensembl</link>
	<title><![CDATA[Demo 4: Using BLAST/BLAT in Ensembl]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/PFCv3-ujrqk" frameborder="0" allowfullscreen></iframe>We demonstrate the BLAST/BLAT tool in Ensembl.  Search for a sequence in Ensembl, and identify hits to the genome, or to genes, with this tool.]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</guid>
	<pubDate>Fri, 01 Jul 2016 12:09:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</link>
	<title><![CDATA[Genome Workbench 2.10.7]]></title>
	<description><![CDATA[<p>Genome Workbench 2.10.7 is here! New features include added support for local custom BLAST databases and improvements to Tree View.</p><p>For the full list of features, improvements and fixes, see the release notes:<a href="https://ncbi.nlm.nih.gov/tools/gbench/releasenotes" target="_blank">https://ncbi.nlm.nih.gov/tools/gbench/releasenotes</a></p><p>New Features</p><ul>
<li>BLAST Tool: added support for local custom BLAST databases</li>
<li>Graphical Sequence View: added log scaling option for graph tracks</li>
<li>Generic Table View:&nbsp;<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial17">new tutorial</a>&nbsp;added</li>
</ul><p>Bug Fixes and Improvements</p><ul>
<li>Project Tree View: Genomic Collections/Assemblies now show accessions, not just names</li>
<li>Tree View: layout updated to better accommodate nodes of different sizes</li>
<li>Table Import Dialog (MacOS): fixed issue with table visibility</li>
<li>Fixed bug where different molecules IDs in GenBank could resolve to the same sequence</li>
<li>Graphical Sequence View: fixed issue where sequence track was not shown for some sequences</li>
<li>Graphical Sequence View: fixed protein coloration methods</li>
<li>Graphical Sequence View: improved rendering of Markers to better indicate boundaries and produce higher quality PDF images</li>
<li>Create Gene Model tool: fixed scenario when gene model tool failed with local sequences</li>
<li>Search View: ORF Finder &ndash; fixed incorrect protein lengths</li>
<li>Fixed bug with not opening project file (.gbp) on a click</li>
<li>Fixed issues in GVF import</li>
<li>Fixed BLAST Search tool against NCBI databases not working</li>
<li>Fixed tblastn (protein BLAST) not working in standalone mode</li>
<li>Fixed GTF export failure</li>
</ul>]]></description>
	<dc:creator>Gudiya Pal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32376/diamond</guid>
	<pubDate>Thu, 27 Apr 2017 04:21:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32376/diamond</link>
	<title><![CDATA[DIAMOND]]></title>
	<description><![CDATA[<p><span>DIAMOND is a sequence aligner for protein and translated DNA searches and functions as a drop-in replacement for the NCBI BLAST software tools. It is suitable for protein-protein search as well as DNA-protein search on short reads and longer sequences including contigs and assemblies, providing a speedup of BLAST ranging up to x20,000.</span></p>
<p><span>More at&nbsp;file:///home/urbe/Downloads/diamond_manual.pdf</span></p>
<p><span>http://www.nature.com/nmeth/journal/v12/n1/full/nmeth.3176.html</span></p><p>Address of the bookmark: <a href="https://github.com/bbuchfink/diamond" rel="nofollow">https://github.com/bbuchfink/diamond</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<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>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/44640/new-blast-core-nucleotide-database-core-nt</guid>
	<pubDate>Tue, 13 Aug 2024 07:12:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/44640/new-blast-core-nucleotide-database-core-nt</link>
	<title><![CDATA[New BLAST Core Nucleotide Database (core_nt)]]></title>
	<description><![CDATA[<p><span>The Core Nucleotide Database (core_nt) is now the default nucleotide BLAST database. Core_nt is also available on the command line. You get faster searches &amp; more focused results.</span></p><p><span><span>Core_nt contains the same eukaryotic transcript and gene-related sequences as nt. The core_nt database is nt without most eukaryotic chromosome sequences. Most nucleotide BLAST searches with core_nt will be similar to the nt database. However, core_nt is better than nt for accomplishing your most common BLAST search goals, such as identifying gene-related sequences like transcript sequences and complete bacterial chromosomes. This is because, in recent years, nt has acquired more low-relevance, non-annotated, and non-gene&nbsp;<span>content.&nbsp;</span></span></span></p><p><span> Learn more:&nbsp;https://ncbiinsights.ncbi.nlm.nih.gov/2024/07/18/new-blast-core-nucleotide-database/</span></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>

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