Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ohofmann
    Member
    • Jan 2009
    • 37

    #1

    Helicos SRF to FASTQ

    Dear all,



    been trying to explore a number of Helicos runs. I have access to the read data both in Helicos' SMS format as well as their implementation of SRF (which does not bode well). Using the Staden iolib package it is straightforward to convert reads to FASTA using the srf2fasta command:

    >HE-0243693211002-14-2-2-4250
    CAGAGTATAGACCTA
    Trying the same with srf2fastq results in:

    Zero or greater than one CNF chunks found.
    My guess is that the quality information is encoded differently in the Helicos' implementation which would explain why Helisphere also only ships with a '2fasta' option.

    Is there *any* way to get FASTQ (or a equivalent expressive format) out of Helicos? I'd love to throw the data at a few standard pipelines that usually start with FASTQ data, and seem to be out of options.

    Thanks!
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Originally posted by ohofmann View Post
    Dear all,



    been trying to explore a number of Helicos runs. I have access to the read data both in Helicos' SMS format as well as their implementation of SRF (which does not bode well). Using the Staden iolib package it is straightforward to convert reads to FASTA using the srf2fasta command:



    Trying the same with srf2fastq results in:



    My guess is that the quality information is encoded differently in the Helicos' implementation which would explain why Helisphere also only ships with a '2fasta' option.

    Is there *any* way to get FASTQ (or a equivalent expressive format) out of Helicos? I'd love to throw the data at a few standard pipelines that usually start with FASTQ data, and seem to be out of options.

    Thanks!
    Convert to FASTA and then insert dummy quality values (not the best but it will work).

    Comment

    • ohofmann
      Member
      • Jan 2009
      • 37

      #3
      Sorry, should have clarified that -- Helisphere even provides scripts that insert dummy quality values, but since we are trying to get a better handle on error profiles that is of course less than ideal. Can't even do basic filtering by quality, or re-evaluate the quality distribution after trimming with FASTX.

      Ah well. Guess there's always room for yet-another-format.

      Comment

      • kmcarr
        Senior Member
        • May 2008
        • 1181

        #4
        Originally posted by ohofmann View Post
        Trying the same with srf2fastq results in:
        Zero or greater than one CNF chunks found.
        You need to use srf2fastq with the '-c' option, which tells the program to use the Calibrated Quality scores in chunk CNF1. Without it you get that oh so unhelpful error message. This also happens with SRF files of Illumina data created using illumina2srf in the SequenceRead 2.0 package.

        Code:
        % srf2fastq -c myFile.srf > myFile.fastq

        Comment

        • ohofmann
          Member
          • Jan 2009
          • 37

          #5
          Getting the same error using the `-c` flag; maybe indicative of something being wrong with my SRF files rather than the conversion process. I'll see if I can get this to work on public Helicos data first.

          Thanks again!

          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, Yesterday, 11:13 AM
          0 responses
          16 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, Yesterday, 10:48 AM
          0 responses
          15 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-15-2026, 10:52 AM
          0 responses
          35 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          42 views
          0 reactions
          Last Post SEQadmin2  
          Working...