Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • NGS_New_User
    Member
    • Sep 2012
    • 41

    help using velvet for de novo assembly

    Hi everyone, i'm trying to run de novo assembly using velvet on short (100bp long) paired end reads.
    I first ran velveth and it created only two files named: Log and Sequences.
    It also gave me this error:
    velveth: Can't malloc 121 chars: Cannot allocate memory

    I tried to run velvetg but then I got an error:
    [0.000000] No Roadmap file to build upon! Please run velveth (see manual)

    This is what I ran using velveth:
    $ velveth output_assem 35 -shortPaired -fasta file_PE-1.fa file_PE-2.fa

    The two fasta files are already in paired
    What does this mean? This is my first time using velvet, and I will appreciate anyone's help. Thanks a lot in advance
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    I think velvet wants the fastqs to be interleaved. It least older versions did, and they used to include a little perl script that would do that,

    Comment

    • kmcarr
      Senior Member
      • May 2008
      • 1181

      #3
      Originally posted by swbarnes2 View Post
      I think velvet wants the fastqs to be interleaved. It least older versions did, and they used to include a little perl script that would do that,
      Currrent versions of velvet accept interleaved or separate input files for paired end reads. The default is interleaved; if you are using separate files you have to add the '-separate' option. For your example this would be:
      Code:
      $ velveth output_assem 35 -shortPaired -fasta -separate file_PE-1.fa file_PE-2.fa

      Comment

      • NGS_New_User
        Member
        • Sep 2012
        • 41

        #4
        Thanks for the suggestions! I do appreciate them! I am going to try them, hopefully no errors will pop up

        Comment

        • madhavi
          Member
          • Jan 2015
          • 14

          #5
          Hii can anyone help me to run velvet with higher hash value rather than 31 and also how to run velvet optimiser? (illumina short paied end reads)
          thanks in advance

          Comment

          • mastal
            Senior Member
            • Mar 2009
            • 666

            #6
            to use kmer sizes greater than 31, you need to recompile velvet with

            'make ’MAXKMERLENGTH= ’, and put in the max value that you want to be able to use.

            See the velvet manual

            Comment

            • madhavi
              Member
              • Jan 2015
              • 14

              #7
              Hello mastal
              first of all thanks for ur reply.
              i have tried this too but it is showing an error as 'compilation terminated.make: *** [obj/readSet.o] Error 1'

              Comment

              Latest Articles

              Collapse

              • 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
              • SEQadmin2
                From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
                by SEQadmin2


                Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


                The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
                ...
                06-02-2026, 10:05 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 06-26-2026, 11:10 AM
              0 responses
              14 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-17-2026, 06:09 AM
              0 responses
              48 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-09-2026, 11:58 AM
              0 responses
              107 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-05-2026, 10:09 AM
              0 responses
              125 views
              0 reactions
              Last Post SEQadmin2  
              Working...