Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • pederworning
    Junior Member
    • Feb 2011
    • 5

    #1

    VelvetOptimiser sam format

    Dear Bioinformatic forum,

    I am using VelvetOptimiser to see which parameters to use for Velvet denovo assembly, but I cannot get it to read sam files. It can read fasta and fastq but not sam.
    I am using Ubuntu 10.04 LTS installation and I have Velvet version 1.0.18 and VelvetOptimiser.pl version 2.2.0 My velveth can read the sam files!

    When I do the following command I get the error message below:
    > VelvetOptimiser.pl -s 15 -e 31 -f '-shortPaired -sam s_7_001.sam' -t 4 -g 3.0
    MSG: The sequence does not appear to be FASTA format (lacks a descriptor line '>')

    I have tried to shuffle the -shotPaired and -sam and if I type -fastq instead of -sam I get a different error message:
    MSG: Missing sequence and/or quality data; line: 23774387
    So it can read fastq but not sam.

    Have anyone tried to read sam files with VelvetOptimiser and do you have any suggestions of what to do.

    Thanks
    Peder Worning
  • mht
    Member
    • May 2012
    • 23

    #2
    Hi, I'm now trying to use velvetoptimiser on sam files too. Did u get any feedback on this issue?

    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
    23 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
    36 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...