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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/35550?offset=110</link>
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	<description><![CDATA[]]></description>
	
	<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>
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	<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>
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<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>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/41586/primer-blast</guid>
	<pubDate>Tue, 28 Apr 2020 00:28:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/41586/primer-blast</link>
	<title><![CDATA[Primer BLAST !]]></title>
	<description><![CDATA[<p>BLAST team added a new feature (Max 3' match), shown in Figure 1, to Primer-BLAST that limits the length of 3' exon matches when designing exon-exon spanning primers. This makes it less likely that primers specifically designed to amplify transcripts will also amplify genomic DNA contamination in expression assays. See the NCBI Insights post (<a href="https://go.usa.gov/xvUT4" target="_blank"><span>https://go.usa.gov/xvUT4</span></a>) for more details.</p><p>&nbsp;</p><p><span>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<sup><span><img src="https://mail.google.com/mail/u/0?ui=2&amp;ik=024a8aa0b9&amp;attid=0.1&amp;permmsgid=msg-f:1665129030912557674&amp;th=171bba0808bbc26a&amp;view=fimg&amp;sz=s0-l75-ft&amp;attbid=ANGjdJ-yC7WlxAuBOITc1ND1AN0YIdrtaQ3utEJuH_vnvOTM3uh8Wwn652wjlqDQ6HJOKApVPRJNpBRVd3H_AisXJXRWtzl0Y9alARMC05_yINEwa2lkBGoA7Q93-GU&amp;disp=emb" width="13" height="12" alt="image" style="border: 0px;"></span></sup></a></span></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/44515/cleaner-blast-databases-for-more-accurate-results</guid>
	<pubDate>Tue, 23 Apr 2024 01:23:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/44515/cleaner-blast-databases-for-more-accurate-results</link>
	<title><![CDATA[Cleaner BLAST Databases for More Accurate Results]]></title>
	<description><![CDATA[<p>Do you use&nbsp;<a href="https://blast.ncbi.nlm.nih.gov/Blast.cgi?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=blast-cleaner-20240422">BLAST</a><span style="font-size: 12.8px; font-weight: normal;">&nbsp;to identify a sequence or the evolutionary scope of a gene? That can be challenging if contaminated and misclassified sequences are in the BLAST databases and show up in your search results. To address</span><span style="font-size: 12.8px; font-weight: normal;">&nbsp;this problem</span><span style="font-size: 12.8px; font-weight: normal;">, we now use the NCBI quality assurance tools listed below to systematically remove these misleading sequences from the default nucleotide (nt) and protein (nr) BLAST databases.</span><span style="font-size: 12.8px; font-weight: normal;">&nbsp;</span></p><div><ul>
<li><a href="https://github.com/ncbi/fcs">Foreign Contamination Screen tool for genome cross-species screening (FCS-GX)</a>&nbsp;detects contamination from foreign organisms in genomes and other sequences using the genome cross-species aligner (GX)&nbsp;</li>
<li><a href="https://ncbiinsights.ncbi.nlm.nih.gov/2022/05/27/ani-for-assembly-validation?utm_source=ncbi_insights&amp;utm_medium=referral&amp;utm_campaign=blast-cleaner-20240422">Average Nucleotide Identity (ANI)</a>&nbsp;evaluates the taxonomic classification of prokaryotic genome assemblies. Sequences from genomes marked up as &lsquo;unverified source organism&rsquo; are considered suspect and removed.&nbsp;</li>
</ul><p>Ref&nbsp;https://ncbiinsights.ncbi.nlm.nih.gov/2024/04/22/cleaner-blast-databases-more-accurate-results/</p></div>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<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>
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	<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>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/1182/installing-perl-gd-module</guid>
	<pubDate>Mon, 22 Jul 2013 14:02:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/1182/installing-perl-gd-module</link>
	<title><![CDATA[Installing Perl GD Module]]></title>
	<description><![CDATA[<div><p>In comparative genome analysis work, we usually compare more than two genomes and looks for syntenic regions amongst them. In my research I used Evolution Highway (RH) <a href="http://eh-demo.ncsa.uiuc.edu/">http://eh-demo.ncsa.uiuc.edu/</a>, which is a collaborative project designed to provide a visual means for simultaneously comparing genomes of multiple amniote species. The tool removes the burden of manually aligning these maps and allows cognitive skills to be used toward something more valuable than preparation and transformation of data. In addition to EH, attractive Circos (<a href="http://circos.ca/">http://circos.ca/</a>) is also very popular for this kind of analysis.</p><p>The EH is available online, and can be easily access and use, whereas Circos installation is not entirely straightforward. One of the most difficult parts of the installation involves installing the GD library. Since there weren't good instructions for installing this library on the internet I decided to post instructions here in case they are useful to anyone else.</p><p><strong>Following are the steps to install GD modules in Mac OS</strong><br /><br />1. Setup<br /><br />Create a folder for the files:<br /><br />$ mkdir -p /SourceCache<br />$ cd /SourceCache<br /><br />Get and unpack the required Jpeg-6b and GD libraries:<br />Download Jpeg-6b (<a href="http://code.google.com/p/google-desktop-for-linux-mirror/downloads/detail?name=jpeg-6b.tar.gz&amp;can=2&amp;q">http://code.google.com/p/google-desktop-for-linux-mirror/downloads/detail?name=jpeg-6b.tar.gz&amp;can=2&amp;q</a>)<br />Download GD (<a href="http://search.cpan.org/%7Elds/GD-2.46/">http://search.cpan.org/~lds/GD-2.46/</a>)<br /><br />Place the "tar.gz" files in "/SourceCache" and double click to unpack.<br /><br />2. Install libjpeg<br /><br />Copy the "config.sub" and "config.guess" files to "/SourceCache". Note that your "config.sub" and ""config.guess" files may be in a slightly different location. The commands below show where they were on my machine:<br /><br />$ cd /SourceCache/jpeg-6b/src<br />$ cp /usr/share/libtool/config/config.sub .<br />$ cp /usr/share/libtool/config/config.guess .<br /><br />Configure libjpeg as follows. Note that this was installed on a 64 bit machine. However, this method may configure it in a 32 bit format. This may not be the best way to configure the installation but it works.<br /><br />$ .configure --enable-shared<br />$ make<br /><br />Check to see if the following directories exist on your machine. Create the missing directories in the following manner:<br /><br />$ mkdir -p /usr/local/include<br />$ mkdir -p /usr/local/bin<br />$ mkdir -p /usr/local/lib<br />$ mkdir -p /usr/local/man/man1<br /><br />Finish making and installing libjpeg:<br /><br />$ make install<br /><br />3. Install GD<br /><br />$ cd /SourceCache/GD-2.46/GD/<br />$ perl Makefile.PL<br />$ make<br />$ make test (optional)<br />$ make html (optional)<br />$ make install</p><p><strong>Other way for Mac OS</strong><br />The easiest way to get a lot of these is with a program called Fink, which is similar in nature to the CPAN installer, but installs common GNU utilities. Fink is available from &lt;<a href="http://sourceforge.net/projects/fink/%3E">http://sourceforge.net/projects/fink/&gt;</a>.<br /><br />Follow the instructions for setting up Fink. Once it's installed, you'll want to run the following as root: fink install gd<br /><br />It will prompt you for a number of dependencies, type 'y' and hit enter to install all of the dependencies. Then watch it work.<br /><br />To prevent creating conflicts with the software that Apple installs by default, Fink creates its own directory tree at /sw where it installs most of the software that it installs. This means your libraries and headers for libgd will be at /sw/lib and /sw/include instead of /usr/lib and /usr/local/include. Because of these changed locations for the libraries, the Perl GD module will not install directly via CPAN, because it looks for the specific paths instead of getting them from your environment. But there's a way around that :-)<br /><br />Instead of typing "install GD" at the cpan&gt; prompt, type look GD. This should go through the motions of downloading the latest version of the GD module, then it will open a shell and drop you into the build directory. Apply below patch to the Makefile.PL file (save the patch into a file and use the command patch &lt; patchfile.)<br /><br />Then, run these commands to finish the installation of the GD module:<br /><br />perl Makefile.PL<br />make<br />make test<br />make install<br />And don't forget to run exit to get back to CPAN.</p><p>&nbsp;</p><p><strong>Install on MS Window, using PPM</strong></p><p>C:\Documents and Settings\Owner&gt;ppm<br />PPM interactive shell (2.2.0) - type 'help' for available commands.<br />PPM&gt; install GD<br />Install package 'GD?' (y/N): y<br />Installing package 'GD'...<br />Downloading <a href="http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW">http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW</a>. ...<br />Installing C:\Perl\site\lib\auto\GD\GD.bs<br />Installing C:\Perl\site\lib\auto\GD\GD.dll<br />Installing C:\Perl\site\lib\auto\GD\GD.exp<br />Installing C:\Perl\site\lib\auto\GD\GD.lib<br />Installing C:\Perl\html\site\lib\GD.html<br />Installing C:\Perl\site\lib\GD.pm<br />Installing C:\Perl\site\lib\qd.pl<br />Installing C:\Perl\site\lib\auto\GD\autosplit.ix<br />PPM&gt;<br /><br /><br />If you can't install it from ppm. You can download it:<br /><a href="http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW">http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW</a>.<br /><br /><br />BTW,All Perl 5.6.1 Modules are located at:<br /><br /><a href="http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW">http://ppm.ActiveState.com/PPMPackages/5.6plus/MSW</a>.</p><p>&nbsp;</p><p><strong>Install the Perl GD Module on Linux</strong><br /><br />$ sudo perl -MCPAN -e shell<br /><br />Since it was the first time I had run this command on this particular machine I had to answer a lot of questions but simply selected the defaults for everything as this usually works for me. Once in the CPAN shell I entered<br /><br />$ install Bundle::CPAN<br /><br />and selected all of the defaults again. Once the CPAN bundle had finished installing I tried to install GD::Graph by typing<br /><br />$ install GD::Graph<br /><br />but it failed with hundreds of errors &ndash; the first of which was<br /><br />GD.xs:7:16: error: gd.h: No such file or directory<br /><br />This was fixed with the following apt-get command (in the bash shell)<br /><br />$ sudo apt-get install libgd2-xpm-dev<br /><br />back in the CPAN shell I still couldn&rsquo;t get GD::Graph to build and I guessed this was because of some left over files from the failed build. I don&rsquo;t know the command to clean things up inside the CPAN shell and am too lazy to read the docs so I simply went into the .cpan/build directory in my home directory and deleted anything that started with GD &ndash; eg<br /><br />$ rm -rf GD-2.35-HC_vkB<br /><br />$ rm -rf GDGraph-1.44-Evfibe<br /><br />and so on. Those strings at the end (VkB and so on) look random so they might be different on your machine. Then I went back into the CPAN shell and ran<br /><br />$ install GD::Graph<br /><br />There were a few dependencies which the script fetched and installed for me but everything worked smoothly.</p><p>Manual and other Perl Module instalation are mentioned in my previous blog @ <a href="http://bioinformaticsonline.com/blog/view/710/how-to-install-perl-modules-manually-using-cpan-command-and-other-quick-ways">http://bioinformaticsonline.com/blog/view/710/how-to-install-perl-modules-manually-using-cpan-command-and-other-quick-ways</a></p></div>]]></description>
	<dc:creator>Jit</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>
	
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