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  • #46
    The latest V2.05 is available to download for not-for-profit and research use. There are no restrictions if you would like to use it in your research work.

    Added features e.g. BS-alignemnt, multithreading, etc are available in the 'Pro'/commercial version.

    Originally posted by seq_GA View Post
    Hi Colin,

    I am wondering whether novocraft 2.04 version is free to download for reaserch purpose?

    Thanks

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    • #47
      Novoalign is still available free for use in non-profit organizations but some of the new features are disabled. The free version will do DNA, miRNA, RNA alignment of single end and paired end reads.
      The commercial versions adds multi-threading, bi-seq alignment, base quality calibration and buying a license also helps fund further development.

      Colin

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      • #48
        sequence identifiers like >chrY_random

        retracting comment. I have to check some more on my side first.
        Sorry,
        Bernd
        Last edited by BAJ; 08-26-2009, 04:41 AM. Reason: see comment

        Comment


        • #49
          It's OK. Some copies of Human Genome have some additional sequence files like:

          chr7_random.fa
          >chr7_random
          gatcatgctattgcactccagcctgggcgacagagtgaaactccatctca
          gaaaaaataaataaaTGAGAGGATCAGCCAACGCATCAGCAAATGTCAGC
          CGGACGGTTTAATTTCCACTCATCCCACGACACGAGGCAACCCTCAAACA
          CACAGGTCCTGGCCATGAAGCCTTCAGGGAATCACAGGACTGGGTGCTGA
          CCCAGAAAACTCTACAAAGCTTTGTGACCAAAGAGGTTCGAGTCCCAAGT
          CCCCTTCAGGAAGAGCTGCAGTCTGCTCATGtgtctaagtttgcctctgt
          tgcttataacaacataccggaaactgggtaaattataaaggaaaggcatt
          tatttctcacagttatgaggctggataaatccagggtcgagtggccacaa
          tggctttcttgctggaggggacttttcagggttcccaggtggcacaggcc

          Some of these must have been included in your index build.
          Colin

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