Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • knightfeng
    Junior Member
    • Oct 2009
    • 4

    SeqGenomeBrowser : A mini genome browser for NGS data

    Hi, all
    If you need to visualize your next-generation seqeuencing data, you can try a new mini local genome browser, SeqGenomeBrowser, which is :

    1. very easy to use
    2. ligtht and fast
    3. no preliminary installation or configuration needed
    4. handle large data and use little memory (less than 50M)
    5. support standard USCS file format such as bed, wig and refFlat
    6. cross platform

    SeqGenomeBrowser is available at http://sourceforge.net/projects/seqgenomebrowse/
  • sklages
    Senior Member
    • May 2008
    • 628

    #2
    Hi,

    after downloading & extracting on a 64bit linux platform,

    $ ./bin/SeqGenomeBrowser
    QMetaObject::connectSlotsByName: No matching signal for on_GotoChrRange_clicked()
    ./bin/SeqGenomeBrowser: symbol lookup error: ./bin/SeqGenomeBrowser: undefined symbol: FT_Library_SetLcdFilter

    cheers,
    Sven

    Comment

    • steven
      Senior Member
      • Aug 2009
      • 269

      #3
      Originally posted by knightfeng View Post
      Hi, all
      If you need to visualize your next-generation seqeuencing data, you can try a new mini local genome browser, SeqGenomeBrowser, which is :

      1. very easy to use
      2. ligtht and fast
      3. no preliminary installation or configuration needed
      4. handle large data and use little memory (less than 50M)
      5. support standard USCS file format such as bed, wig and refFlat
      6. cross platform

      SeqGenomeBrowser is available at http://sourceforge.net/projects/seqgenomebrowse/
      Nice app! Light and fast indeed, convenient for a quick overview. A bit restrictive on the input format though (only 4 or 6 columns bed files are accepted).

      Comment

      • knightfeng
        Junior Member
        • Oct 2009
        • 4

        #4
        Originally posted by sklages View Post
        Hi,

        after downloading & extracting on a 64bit linux platform,

        $ ./bin/SeqGenomeBrowser
        QMetaObject::connectSlotsByName: No matching signal for on_GotoChrRange_clicked()
        ./bin/SeqGenomeBrowser: symbol lookup error: ./bin/SeqGenomeBrowser: undefined symbol: FT_Library_SetLcdFilter

        cheers,
        Sven
        Could the GUI be launched correctly after the warning message? If not, it may be a bug on linux 64 system. SeqGenomeBrowser was expected to has the same behavior on Windows, linux and Mac. Could you tell what linux systerm you used?

        Thanks.

        Zhixing

        Comment

        • knightfeng
          Junior Member
          • Oct 2009
          • 4

          #5
          Originally posted by steven View Post
          Nice app! Light and fast indeed, convenient for a quick overview. A bit restrictive on the input format though (only 4 or 6 columns bed files are accepted).
          Thank you for using SeqGenomeBrowser and your nice suggestion. More file formats including the full version bed format will be supported in the next version.

          Best.

          Zhixing

          Comment

          • lh3
            Senior Member
            • Feb 2008
            • 686

            #6
            Before you go further, it may be worth thinking what features make your viewer unique to other existing viewers which are largely covered in this thread:

            Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

            Comment

            • krobison
              Senior Member
              • Nov 2007
              • 734

              #7
              Also, please create an entry for your tool in the wiki

              Comment

              • Xi Wang
                Senior Member
                • Oct 2009
                • 317

                #8
                Nice, you come here to market your software.

                Before you go further, it may be worth thinking what features make your viewer unique to other existing viewers which are largely covered in this thread:

                http://seqanswers.com/forums/showthread.php?t=3904
                Thanks, Heng, a pretty sharp suggestion.
                Xi Wang

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  Cancer Drug Resistance: The Lingering Barrier to Rising Survival
                  by SEQadmin2



                  Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

                  There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
                  Today, 05:17 AM
                • GATTACAT
                  Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                  by GATTACAT
                  Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                  07-01-2026, 11:43 AM
                • SEQadmin2
                  Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                  by SEQadmin2


                  I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

                  Here are nine questions we think about, in roughly the order they matter, before...
                  06-18-2026, 07:11 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, Today, 10:08 AM
                0 responses
                6 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, Yesterday, 11:05 AM
                0 responses
                8 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-02-2026, 11:08 AM
                0 responses
                31 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 06-30-2026, 05:37 AM
                0 responses
                29 views
                0 reactions
                Last Post SEQadmin2  
                Working...