Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • guoweiguowei@gmail.com
    Junior Member
    • Apr 2010
    • 4

    see segmentation fault in soapsnp

    When I run the following command in linux
    2bwt-builder ref.fasta
    soap -a reads.fastq -D ref.fasta.index -o reads.soap
    msort -k n9 reads.soap > sort.reads.soap
    soapsnp -i sort.reads.soap -d ref.fasta -o reads.soapsnp

    soap and msort (or use linux sort command) works well. But when I run soapsnp to call SNPs, I found
    'segmentation fault'.

    No idea about this.
  • jgibbons1
    Senior Member
    • Oct 2009
    • 135

    #2
    sounds like a memory issue...

    how much ram do you have?

    Comment

    • guoweiguowei@gmail.com
      Junior Member
      • Apr 2010
      • 4

      #3
      I run this in a unix server which have 20GB memory. If soap does not have its own memory limit, I do not think this is caused by it.

      Comment

      • JohnK
        Senior Member
        • Feb 2010
        • 106

        #4
        I get segment faults every now and then. I'd try increasing memory or changing permissions first.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Cancer Drug Resistance: The Lingering Barrier to Rising Survival
          by SEQadmin2



          Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

          There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
          Today, 05:17 AM
        • GATTACAT
          Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by GATTACAT
          Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
          07-01-2026, 11:43 AM
        • 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

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Today, 10:08 AM
        0 responses
        6 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 11:05 AM
        0 responses
        8 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-02-2026, 11:08 AM
        0 responses
        31 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-30-2026, 05:37 AM
        0 responses
        28 views
        0 reactions
        Last Post SEQadmin2  
        Working...