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  • IMPORTANT SERVICE ANNOUNCEMENT Entrez and BLAST services will stop working in November for MacVector 15.0.3 and earlier.

    UPDATE – November 8, 2016 – Although the official switch off date is not until Wednesday the 9th, Entrez and BLAST are NOT currently working from MacVector 15.0.3 and earlier. We suspect this change is now permanent. UPDATE – November 7, 2016 – We have just been notified by the NCBI that they will be…

    Read more: IMPORTANT SERVICE ANNOUNCEMENT Entrez and BLAST services will stop working in November for MacVector 15.0.3 and earlier.
    Oct 19, 2016

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    by

    Chris
    in Releases

  • Highlighting sequence using color and lower case in the Editor tab

    You can very quickly annotate a region of interest in your sequence in the Editor tab. For example, showing introns in lower case or highlighting CDS features with a colored background. Using the TRANSFORMATIONS menu To enter sequences as mixed case. Enable Edit | Transformations | Enable Mixed Case Entry Type your sequence using SHIFT…

    Read more: Highlighting sequence using color and lower case in the Editor tab
    Oct 17, 2016

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    by

    Chris
    in Tips

  • Estimating insert length quickly for a read pair

    [Edit December 20, 2017 – As of MacVector 15.5 you can simply right click a READ and select “SEE MATCHING READS” to view the pair of reads. The total sequence length is selected. ] Insert length is the length of the sequence in between a pair of reads. Sequencers are supplied DNA samples in fragments of…

    Read more: Estimating insert length quickly for a read pair
    Oct 7, 2016

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    by

    Chris
    in Tips

  • Restriction enzyme analysis in MacVector and REBASE

    Although there are two different ways to perform restriction enzyme analysis with MacVector, there are also additional places where restriction enzyme sites are shown. All these tools use the same set of restriction enzyme files to recognise enzymes. These files are updated regularly from the REBASE database. The restriction enzymes are divided into multiple files.…

    Read more: Restriction enzyme analysis in MacVector and REBASE
    Oct 7, 2016

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    by

    Chris
    in Techniques

  • Drag and drop to quickly annotate ORFs

    You can use the Analyze | Open Reading Frames function to very quickly find ORFs on a sequence. Did you know that you can very quickly turn those results into permanent CDS features on your sequence? After running the Open Reading Frames analysis, simply drag and drop the ORF objects you are interested in from…

    Read more: Drag and drop to quickly annotate ORFs
    Oct 3, 2016

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    by

    Chris
    in Tips

  • 101 things you (maybe) didn’t know about MacVector: #50 – Using Align To Folder to “clone” genes from NGS data

    The Database | Align To Folder… function in MacVector is remarkably powerful. Its like having your own personal BLAST search except that it can also scan through millions of Reads in fasta or fastq formatted files to identify those matching an input sequence, which can be DNA OR protein. In addition, it understands about paired-end…

    Read more: 101 things you (maybe) didn’t know about MacVector: #50 – Using Align To Folder to “clone” genes from NGS data
    Sep 22, 2016

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    by

    Kevin
    in 101 Tips

  • Download the latest published version of your favorite sequence with its accession number

    It’s very quick to download the latest version of a sequence if you know its accession number. When you start working with a new sequence, it’s the best place to start. Go to DATABASE > ENTREZ Enter the accession number of your favorite sequence Click SEARCH Double click on the result to open up your…

    Read more: Download the latest published version of your favorite sequence with its accession number
    Sep 20, 2016

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    by

    Chris
    in Tips

  • How to change the default appearance of RE sites

    MacVector is extremely customizable. If you don’t like the defaults we supply, its very easy to change them. Lets look at restriction enzyme sites. By default we show unique sites in small red letters and sites that cut more than once in small blue letters. But suppose you want something bigger, bolder and, well, more…

    Read more: How to change the default appearance of RE sites
    Sep 14, 2016

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    by

    Chris
    in Tips

  • NIH Research Festival September 14-16, 2016

    We’re at the NIH Research Festival this week. Please drop by our booth on Thursday or Friday, when the big, white exhibitors tent is open. We’re on booth #562. We’ll be able to show you our latest release, MacVector 15 and we’ll have some goodies too!

    Read more: NIH Research Festival September 14-16, 2016
    Sep 13, 2016

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    by

    Chris
    in Meetings

  • Working with digested fragments in the Cloning Clipboard

    The Cloning Clipboard is an easy, and flexible, way to design and document your cloning strategies. Here’s two tips on manipulating a single fragment. – If you drag a fragment from the Cloning Clipboard to a vector, then you’ll get the ligation dialog. However, if you have already selected a pair of enzyme sites, then…

    Read more: Working with digested fragments in the Cloning Clipboard
    Aug 30, 2016

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    by

    Chris
    in Tips
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