Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Luka
    Member
    • Nov 2012
    • 10

    #16
    Originally posted by GenoMax View Post
    I think this may point to the problem. The VM may not have enough RAM allocated to it.

    How big are the sequence files that you are trying to work with BTW?
    I was suspecting that, but I managed to process big sequence files so far using other programs, using different files I have done QC, trimming, assembly , alignment.
    Now I just wanted to process some files, thus I created a test file containing 4 150bp sequences, that should be doable.

    However, there must be some limitation in this remote connection, which is causing this error.

    Can you run the command "free -g" (without quotes of course) while logged into your VM and send the output? That should tell us how much RAM is allocated to your VM.
    total used free shared buffers cached
    Mem: 3 2 0 0 0 1
    -/+ buffers/cache: 1 2
    Swap: 5 2 3

    This does not look good?

    Originally posted by westerman View Post
    3) Luka: Even without a sysadmin you should be able to install your own copy of fastX tools (from the web page I posted earlier). It may be frustrating but, heck, welcome to the "wonderful" world of bioinformatics.
    I guess that, but I does not seem easy, however , it has it charms. Anyway, I truly appreciate the effort you've put into this.
    My goal is actually to have a computer with Unix so we can install and use these tools directly on it, rather then like this.

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #17
      Your VM has 3 GB of RAM allocated to it which is probably ok for QC type things (which you have already done). Since you have already done alignments that amount of RAM has not been an issue (perhaps you are working with a small genome).

      Is there someone else you can ask to verify the fastx_toolkit install through their account?

      Comment

      • Luka
        Member
        • Nov 2012
        • 10

        #18
        Originally posted by GenoMax View Post
        Your VM has 3 GB of RAM allocated to it which is probably ok for QC type things (which you have already done). Since you have already done alignments that amount of RAM has not been an issue (perhaps you are working with a small genome).

        Is there someone else you can ask to verify the fastx_toolkit install through their account?
        Hi, thank you for your post.

        As suggested, I actually talked to IT people responsible for the installation of the fastax_toolkit and their reply was that this error has nothing to do with my remote access and that "buffer overflow detected" means that there's a bug in the program that causes it to crash.

        And I have some more info I guess it can be useful, it is a RHEV (KVM) virtual machine with 4 GB RAM and 60 GB disk. It is running stock Fedora 17 with FASTX 0.0.13 from the official Fedora package repository (fastx_toolkit-0.0.13-6.fc17.x86_64).
        Last edited by Luka; 11-16-2012, 02:19 AM.

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #19
          Sounds like if you want to use the fastx_toolkit you have to take the extra bit of effort and install it in your home directory as Rick had suggested. You can even get the precompiled binary for 64-bit Linux so all you would need to do is un-zip the archive.

          Code:
           
          wget http://hannonlab.cshl.edu/fastx_toolkit/fastx_toolkit_0.0.13_binaries_Linux_2.6_amd64.tar.bz2
          
          tar -xvjf fastx_toolkit_0.0.13_binaries_Linux_2.6_amd64.tar.bz2
          When that works (no obvious reason why it should not) then you can go back to your IT and suggest that they use the original package to redo the install.

          Comment

          • Luka
            Member
            • Nov 2012
            • 10

            #20
            Originally posted by GenoMax View Post
            Sounds like if you want to use the fastx_toolkit you have to take the extra bit of effort and install it in your home directory as Rick had suggested. You can even get the precompiled binary for 64-bit Linux so all you would need to do is un-zip the archive.

            Code:
             
            wget http://hannonlab.cshl.edu/fastx_toolkit/fastx_toolkit_0.0.13_binaries_Linux_2.6_amd64.tar.bz2
            
            tar -xvjf fastx_toolkit_0.0.13_binaries_Linux_2.6_amd64.tar.bz2
            When that works (no obvious reason why it should not) then you can go back to your IT and suggest that they use the original package to redo the install.
            Hi, before doing what suggested I forwarded your suggestion to my IT and their reply was simply that to reinstall the toolkit to my home directory will not solve this issue.

            Comment

            • westerman
              Rick Westerman
              • Jun 2008
              • 1104

              #21
              Originally posted by Luka View Post
              Hi, before doing what suggested I forwarded your suggestion to my IT and their reply was simply that to reinstall the toolkit to my home directory will not solve this issue.
              So what is their solution? FastX does not have an obvious bug. The rest of us use it all of the time without problems. Certainly I can take the 1-sequence file you gave us and run fastx_renamer on it without problem. If you can not do the same then the problem is clearly in your or your IT's department setup.

              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
              23 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              20 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-15-2026, 10:52 AM
              0 responses
              36 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              42 views
              0 reactions
              Last Post SEQadmin2  
              Working...