Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • pari_89
    Member
    • Apr 2013
    • 55

    #1

    SOAPdenovo2

    Hello everyone, I am new to this forum and new to using assembly tools as well. I am trying to use SOAPdenovo2 and tried to write the configuration file which is as follows :

    #maximal read length
    max_rd_len=36
    [LIB]
    #average insert size
    avg_ins=100
    #if sequence needs to be reversed
    reverse_seq=0
    #in which part(s) the reads are used
    asm_flags=3
    f=sample.fq

    I am using soapdenovo2 in steps. I tried to use the pregraph_sparse63mer version using this command :

    /pregraph_sparse63mer -s configfile -K 63 -z 1000000 -o output_graph -p 4


    The programs starts to build the graph but no nodes are allocated and it seems to parse the file but O kmer detected etc...

    I have tried with combinations of -k 23 and smaller values because my reads are very short (36 nt) in length and it is a bacterial file 88 MB

    I do not know if my parameters are correct in the config file but I am using only ONE FASTQ file.

    Thank you.
  • mastal
    Senior Member
    • Mar 2009
    • 666

    #2
    SOAPdenovo2

    If the file with your reads is in fastq format you should have
    q=sample.fq

    in the configuration file.

    Did you get any better results with -K 23 or smaller?
    Kmer size needs to be shorter than your reads.

    Comment

    • pari_89
      Member
      • Apr 2013
      • 55

      #3
      Hi, Thank you. Yes, it started to construct the graph and when I used the command soapdenovo2 63-mer contig -g output_graph , it produced a file named output_graph.contig

      However, the contigs are very small and in this format:

      >1 length 16 cvg_0.0_tip_0
      AAAAAAAAAAAAAAAA

      is that alright?

      I used the same pregraph_sparse command but used -K 15

      Comment

      • Scaon
        Junior Member
        • Apr 2012
        • 3

        #4
        SOAPdenovo2

        Hi,

        A month ago, i was struggling with pregraph_sparse too.
        My problem was, as you stated "The programs starts to build the graph but no nodes are allocated and it seems to parse the file but O kmer detected etc..."

        I compiled from source in the first place. Then, i decided to give binaries a try, and it was finally working. Maybe this could solve your issue.

        Best,
        Erwan

        Comment

        • pari_89
          Member
          • Apr 2013
          • 55

          #5
          Hi thank you, I compiled from the source and the program is working but the length of the contigs are in the format that I stated above and does not seem right. Have you used Soapdenovo2 and are your contigs in the same format?

          Thank you.

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
            by SEQadmin2



            CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

            Despite this, “CRISPR helped turn genome editing from a specialized technique into
            ...
            07-31-2026, 11:01 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Yesterday, 10:35 AM
          0 responses
          9 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-06-2026, 07:41 AM
          0 responses
          27 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-03-2026, 10:13 AM
          0 responses
          45 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-31-2026, 02:55 AM
          0 responses
          48 views
          0 reactions
          Last Post SEQadmin2  
          Working...