Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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

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

    Comment


    • #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

      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM
      • seqadmin
        Strategies for Sequencing Challenging Samples
        by seqadmin


        Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
        03-22-2024, 06:39 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      25 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      24 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      52 views
      0 likes
      Last Post seqadmin  
      Working...
      X