Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Harmakhis
    Junior Member
    • Dec 2012
    • 4

    How to collapse forward & reverse Sanger reads into consensus sequence?

    Hi everybody,

    I relatively new to this, so I thought I'd ask about way to solve my problem in the most easy way.

    I have *.ab1 files from an Applied Biosystem's 3730xl DNA Analyzer from different individuals for different genes each sequenced with a forward and a reverse primer.

    In the past I constructed the consensus sequences by hand in BioEdit while looking at the chromatogram in Geospiza's FinchTV but that's a lot of work and quite subjective.

    I thought there must be an easier and more objective way to do this... Is there a way/workflow to automatically combine my two reads per gene and individual in a consensus sequence using some kind of objective quality score and outputting that as a FASTA file or similar? Ideally, there should be a way to flag heterozygotes, too.

    Any help would be greatly appreciated.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Commercial software programs (Sequencher, Vector NTI Alignx, CLC Workbench, Geneious etc) can do this very easily but I assume you are looking for a free/open source alternative.

    Comment

    • Harmakhis
      Junior Member
      • Dec 2012
      • 4

      #3
      You're right, an open-source/freeware program would be best. I came across SeqTrace but I have trouble getting it to work. Somehow when I input my *.ab1 files no confidence score is displayed and that stops the program from calculating a consensus sequence.

      Comment

      • Harmakhis
        Junior Member
        • Dec 2012
        • 4

        #4
        Okay, just as information: it seems SeqTrace is doing what I want. The problem now is that it needs embedded Phred Quality Scores in the chromatogram to work.

        The files I get from my sequence provider are ab1-files withOUT the quality scores. I can download the quality scores as seperate .qual files.

        Is there anyway to combine those (preferably .abi or .scf files, as those are the file types SeqTrace reads)?

        Comment

        • maubp
          Peter (Biopython etc)
          • Jul 2009
          • 1544

          #5
          You could try a basecaller like TraceTuner to recall the bases from the chromatograms, that should give you ABI files with bases and PHRED quality scores.

          Comment

          • Harmakhis
            Junior Member
            • Dec 2012
            • 4

            #6
            This didn't work either, and I finally know why: I got a reply from my service provider and it seems there was something wrong with the files. I got new ones and now I have the PHRED quality scores and such.

            Thanks for your help!

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
              by SEQadmin2


              Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

              The systematic characterization of the human proteome has
              ...
              07-20-2026, 11:48 AM
            • SEQadmin2
              Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
              by SEQadmin2



              Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
              ...
              07-09-2026, 11:10 AM
            • 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...
              07-08-2026, 05:17 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            16 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            18 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-20-2026, 11:10 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-13-2026, 10:26 AM
            0 responses
            37 views
            0 reactions
            Last Post SEQadmin2  
            Working...