Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Yilong Li
    Member
    • Dec 2010
    • 41

    #1

    SOAPdenovo map question

    Dear fellow sequencers,

    I am trying to assemble some reads using SOAPdenovo and map the reads to the assembled contigs. In SOAPdenovo, there is a utility SOAPdenovo map, that is supposed to do this. But when I do this, the resulting *readOnContig is empty (leave header line). The output I get from SOAPdenovo-63mer map is:


    Version 1.05: released on July 29th, 2010

    K = 31
    contig len cutoff: 33

    there're 1125597 contigs in file: test_fasta_020611, max seq len 5161, min seq len 32, max name len 10
    time spent on parse contigs file 11s
    8 thread created
    time spent on hash reads: 5s
    16173369 nodes allocated, 17130136 kmer in reads, 17130136 kmer processed
    time spent on De bruijn graph construction: 16s

    time spent on mapping long reads: 1s

    In file: config.txt, max seq len 85, max name len 256

    8 thread created
    2250827 edges in graph
    0 out of 0 (nan)% reads mapped to contigs
    no paired reads found
    [LIB] 0, avg_ins 0, reverse 0
    time spent on mapping reads: 1s

    overall time for alignment: 0m


    I am using the same config file and read file for both the assembly and the mapping. So what could be the reason for the failed mapping?


    Yilong
  • xysheep
    Junior Member
    • Jul 2011
    • 2

    #2
    I have faced the same problem with you.
    Let's pray for a master-hand to give a solution.

    Comment

    • Yilong Li
      Member
      • Dec 2010
      • 41

      #3
      Hi xysheep,

      I asked this from SOAPdenovo support back some time ago, and they told me that the map function only works with paired end reads. Hope this helps you!

      Yilong

      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
        ...
        Today, 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
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Today, 02:55 AM
      0 responses
      7 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-23-2026, 11:41 AM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-20-2026, 11:10 AM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Working...