Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • nicedad
    Member
    • May 2011
    • 49

    #1

    how to get rid of singletones

    Hi everyone,
    After mining the file 454NewblerMetrics.txt I found 134002 singletones my question is whether this number sounds normal?? and how to get rid of these? with which tool?

    thanks in advance,
    Last edited by nicedad; 08-19-2011, 12:47 AM.
  • westerman
    Rick Westerman
    • Jun 2008
    • 1104

    #2
    That number doesn't sound too bad. Looking at a recent run we had 720K reads of which 240K were singletons and the most of the rest collapsed into assemblies.

    As for how to get rid of them, look at the 454ReadStatus.txt file. From that you can separate the reads into Assembled, Partially Assembled, Singletons, etc.

    Comment

    • nicedad
      Member
      • May 2011
      • 49

      #3
      Thanks westerman. my problem is I could not figure out the principle of how to get rid of these from the 454Allcontigs file? I mean, what is the correlation between singletons in 454ReadStatus and 454Allcontigs since the later one will be used for further analysis.
      Ok, I separated them (with grap) but what I got are only the name of all singletons and not sequences!!
      sorry unconveniece as am getting my feet wet in this domain.

      However, how is the wether in Indiana right now, I was a grad student in Indy!!

      Comment

      • flxlex
        Moderator
        • Nov 2008
        • 412

        #4
        You are in luck: singletons (sequences, that is) are not included in any if the output files, so no need to remove them...

        Comment

        • nicedad
          Member
          • May 2011
          • 49

          #5
          really? this are good news. thanks flxlex.

          Comment

          • westerman
            Rick Westerman
            • Jun 2008
            • 1104

            #6
            I meant to reply but the weekend got in the way. flxlex is correct in that the Singletons are not included in the 454AllContigs file. In fact for our customers we make up a new file that includes both the contigs and the singletons so that they have a "one stop" method of seeing all of their relevant data. After all just because a read is classified as a Singleton because it can not align with any other read does not make the Singleton read irrelevant.

            Comment

            • samanta
              Senior Member
              • Feb 2010
              • 108

              #7
              Agree with other experts. Singletons are single people (reads), who did not find some other read to marry. That does not make them bad people (reads) by any measure.

              Do you want to eliminate them all? What kind of world will that be like?
              http://homolog.us

              Comment

              • nicedad
                Member
                • May 2011
                • 49

                #8
                Originally posted by samanta View Post
                Agree with other experts. Singletons are single people (reads), who did not find some other read to marry. That does not make them bad people (reads) by any measure.

                Do you want to eliminate them all? What kind of world will that be like?
                If singletones are useful, they would not be removed from 454Allcontigs file!
                Furthermore, I wana remove them because this is done in the almost manuscrits of this area of research, if you want I can post some.

                However, does anyone know how to get their weight (Mb)?

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                  by SEQadmin2



                  Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                  Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                  ...
                  10-14-2026, 09:55 AM
                • SEQadmin2
                  New Genomics Technologies Take Aim at Long-Standing Limits
                  by SEQadmin2


                  Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                  We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                  ...
                  09-28-2026, 10:25 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, 10-22-2026, 11:13 AM
                0 responses
                28 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-22-2026, 10:48 AM
                0 responses
                20 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-15-2026, 10:52 AM
                0 responses
                38 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-14-2026, 05:39 AM
                0 responses
                44 views
                0 reactions
                Last Post SEQadmin2  
                Working...