<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Plasmid Maps on Michael’s Domain</title><link>https://jeltsch.org/en/tags/plasmid-maps/</link><description>Recent content in Plasmid Maps on Michael’s Domain</description><generator>Hugo</generator><language>en-us</language><copyright>Copyright © 2002 - 2026 Michael Jeltsch.</copyright><lastBuildDate>Fri, 24 Jul 2026 00:18:18 +0300</lastBuildDate><atom:link href="https://jeltsch.org/en/tags/plasmid-maps/index.xml" rel="self" type="application/rss+xml"/><item><title>Opening old plasmid map files</title><link>https://jeltsch.org/en/gck/</link><pubDate>Sat, 01 Jan 2022 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/gck/</guid><description>&lt;p&gt;For a new cloning project, we needed to access the plasmid maps of an old construct of mine (pSecTagN2, which was a precursor of 
 &lt;a href="https://doi.org/10.1074/jbc.M511593200" target="_blank" rel="noopener noreferrer nofollow"&gt;pMosaic&amp;nbsp;






 
 
 
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, aka pSecTagI) which I had composed from many different sources in 1999. In 1999, I was working in 
 &lt;a href="https://www2.helsinki.fi/en/researchgroups/translational-cancer-biology" target="_blank" rel="noopener noreferrer nofollow"&gt;Kari Alitalo’s laboratory&amp;nbsp;






 
 
 
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 as a Ph.D. student. We were at the &amp;ldquo;cutting edge&amp;rdquo; of technology because we used a software program called 
 &lt;a href="http://www.textco.com/gene-construction-kit.php" target="_blank" rel="noopener noreferrer nofollow"&gt;Gene Construction Kit&amp;nbsp;






 
 
 
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 (GCK) to keep track of our clonings. Last Wednesday, I spent 4 hours of my working time opening one file created with GCK version 2.5 in 1999.&lt;/p&gt;</description></item><item><title>SnapGene - Simply the best DNA manipulation software</title><link>https://jeltsch.org/en/snapgene_simply_the_best_dna_manipulation_software/</link><pubDate>Fri, 01 Jan 2016 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/snapgene_simply_the_best_dna_manipulation_software/</guid><description>&lt;p&gt;Our lab has been using different software packages to plan, document and visualize DNA constructs. Among those that we liked a lot for a long time were Textco&amp;rsquo;s 
 &lt;a href="http://www.textco.com/gene-construction-kit.php" target="_blank" rel="noopener noreferrer nofollow"&gt;GeneConstructionKit&amp;nbsp;






 
 
 
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 (GCK) and 
 &lt;a href="http://www.scied.com/pr_cmpro.htm" target="_blank" rel="noopener noreferrer nofollow"&gt;Clone Manager (Professional)&amp;nbsp;






 
 
 
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. The latter runs unfortunately only under Windows. However, since several of our computers run 
 &lt;a href="http://www.ubuntu.com/desktop" target="_blank" rel="noopener noreferrer nofollow"&gt;Ubuntu Linux&amp;nbsp;






 
 
 
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, we did run GCK versions 2.5 and 3 using 
 &lt;a href="https://www.winehq.org/" target="_blank" rel="noopener noreferrer nofollow"&gt;WINE&amp;nbsp;






 
 
 
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 (a compatibility layer that allows us to run native Windows programs under Linux). However, with the upgrade to version 4, GCK became unusably slow under WINE and we were looking for a replacement. We contacted the developers of GCK, but they apparently were either not willing or able to help us. I suppose that the codebase of GCK is probably more than 20 years old and for that reason nobody dares to touch it. Just around that time, 
 &lt;a href="http://www.snapgene.com" target="_blank" rel="noopener noreferrer nofollow"&gt;SnapGene&amp;nbsp;






 
 
 
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 was released and it fulfilled almost all of our requirements:&lt;/p&gt;</description></item><item><title>EMBOSS and GCK for the assembly and documentation of construct sequences</title><link>https://jeltsch.org/en/emboss_and_gck_for_the_assembly_and_documentation_of_construct_sequences/</link><pubDate>Thu, 05 Apr 2007 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/emboss_and_gck_for_the_assembly_and_documentation_of_construct_sequences/</guid><description>&lt;p&gt;I am trying to use EMBOSS for the assembly of vector sequences. Long time ago, I used the CGC seqed program for this purpose and at the moment I use the 
 &lt;a href="http://www.textco.com" target="_blank" rel="noopener noreferrer nofollow"&gt;Gene Construction Kit&amp;nbsp;






 
 
 
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. EMBOSS doesn&amp;rsquo;t have a straight equivalent for seqed and one has to use a bunch of other tools to replace its functionality. Look at this 
 &lt;a href="http://helix.nih.gov/apps/bioinfo/emboss-gcg.html" target="_blank" rel="noopener noreferrer nofollow"&gt;comparison between CGC and EMBOSS&amp;nbsp;






 
 
 
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.&lt;/p&gt;</description></item></channel></rss>