Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • mgbfx9
    Member
    • Sep 2015
    • 25

    #1

    Assembler:SOAPdenovo

    Hello everyone,

    I am newbie. I am working on de novo assembly of human genome.
    I am new in the field, but not getting any help. So I would appreciate any sort of help to proceed.

    I made the DNA library, and I got my sequencing data from the sequencing facility. They ran my samples on Illumina MiSeq 2x250. This is a 250 bp PE MiSeq multiplex run. I have 4 samples, paired end reads, each has R1 and R2.

    I checked the quality by running on FastQC. I chose to run SOAP de novo now, and from the literature I found out that I don't need to trim the edges, or all the preliminary things before assembly, as SOAP de novo has all the tools. I downloaded SOAP de novo assembler, but please help me to start to use it.

    Thanks,
  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    A MiSeq run will not produce enough data to allow you to do a de novo assembly. You should probably run Bowtie2 or some other mapping engine instead to map your reads to a human reference genome.

    --
    Phillip

    Comment

    • mgbfx9
      Member
      • Sep 2015
      • 25

      #3
      Assembler:SOAPdenovo

      Thank you, Phillip.for your suggestion.

      I have haploid genome for sequencing. You said that I won't have enough data to do de novo assembly. May I ask you how much data do I need to do de novo assembly? I have more than 5 GB data. Could you please let me know?

      Thanks,
      mgbfx9

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        I would think 20-30X, at a minimum, for a de novo assembly. So for a human, 60 billion bases. Below that, you would almost certainly get more usable results by mapping your reads to the reference human genome sequence.

        --
        Phillip

        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
        28 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        21 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        44 views
        0 reactions
        Last Post SEQadmin2  
        Working...