Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Blaize
    Member
    • Jul 2008
    • 17

    #1

    Velvet - hybrid assembly failure

    Dear Velvet users,

    I try to do some hybrid assembly with Abi Solid and Roche 454 reads, when encountered memory / swap out error.
    We have a 48Gb RAMed / 24Gb swapped 2*8 Xeon workstation, runs on the latest Ubuntu Linux 64bit.

    Reads stat:

    Solid: mate pair, ~37 000 000 reads, 2*50nt length
    454: frag ~160000 reads, ~400nt length

    Predicted genome size: 7Mb

    Steps:

    1.a ./saet_mp solidreads_F3.csfasta solidreads _F3_QV.qual 7000000 -numcores 16 -globalrounds 2 -qvupdate -qvhigh -nosampling OK!!!

    1.a ./saet_mp solidreads _R3.csfastas olidreads _R3_QV.qual 7000000 -numcores 16 -globalrounds 2 -qvupdate -qvhigh -nosampling OK!!!

    1c. ./encodeFasta.py -l -n -a 454reads.fna > samplebacteria.de (colorizer from Corona Lite package) OK!!!


    2. ./solid_denovo_preprocessor_v1.2.pl --run_type mates --output preproced_dir_name --f3 solidreads _F3.csfasta --r3 solidreads_R3.csfasta OK!!!


    3. ./velveth_de hashed/ 21 -shortPaired doubleEncoded_input.de -long samplebacteria.de OK!!!


    4. ./velvetg_de hashed/ -exp_cov 20 -ins_length 2600 -min_contig_lgth 200 -cov_cutoff 2

    At this step I ran out of memory/swap and the process automatically killed by the OS.

    .
    .
    [3502.183999] 25532000 nodes visited
    [3502.252314] Concatenation...
    [3504.923849] Renumbering nodes
    [3504.923874] Initial node count 13837915
    [3505.706345] Removed 384358 null nodes
    [3505.706369] Concatenation over!
    [3505.706372] Clipping short tips off graph, drastic
    [3515.809932] Concatenation...
    [3560.510149] Renumbering nodes
    [3560.510170] Initial node count 13453557
    [3560.980761] Removed 3542018 null nodes
    [3560.980778] Concatenation over!
    [3560.980781] 9911539 nodes left
    [3561.090558] Writing into graph file hashed//Graph2...
    [6433.379904] Removing contigs with coverage < -2.000000...
    [6521.066093] Concatenation...
    [6573.221114] Renumbering nodes
    [6573.221139] Initial node count 9911539
    [6573.252071] Removed 0 null nodes
    [6573.252101] Concatenation over!
    [6573.691763] Concatenation...
    [6575.770354] Renumbering nodes
    [6575.770376] Initial node count 9911539
    [6575.789992] Removed 0 null nodes
    [6575.790011] Concatenation over!
    [6575.790476] Clipping short tips off graph, drastic
    [6576.074753] Concatenation...
    [6578.174284] Renumbering nodes
    [6578.174312] Initial node count 9911539
    [6578.193785] Removed 0 null nodes
    [6578.193809] Concatenation over!
    [6578.193811] 9911539 nodes left
    [6578.193971] Read coherency...
    [6578.891643] Identifying unique nodes
    [6579.250084] Done, 8196 unique nodes counted
    [6579.250108] Trimming read tips
    [6598.101153] Renumbering nodes
    [6598.101177] Initial node count 9911539
    [6605.287075] Removed 1511 null nodes
    [6605.500090] Renumbering nodes
    [6605.500105] Initial node count 9910028
    [6605.520381] Removed 0 null nodes
    [6605.520400] Confronted to 5 multiple hits and 15329 null over 16845
    [6605.520403] Read coherency over!
    [6610.547042] Starting pebble resolution...
    [6610.910790] Preparing to correct graph with cutoff 0.200000
    [6635.017686] Computing read to node mapping array sizes
    Killed

    Intermediate file sizes:

    55Gb Graph2
    2,7Gb sequences
    2,8Gb roadmaps
    533Mb pregraph

    What can be wrong? I've made successful hybrid assembly with the CLC Geno Workbench on the same dataset, generated ~200 long contigs with ~7Mb summarized lenght.

    Thank you for any idea:

    Blaize
  • lcollado
    Member
    • Jun 2009
    • 65

    #2
    Hello Blaize,

    You should probably ask this question on the Velvet mailing list where Daniel Zerbino will most likely answer it:


    Greetings,
    Leonardo
    L. Collado Torres, Ph.D. student in Biostatistics.

    Comment

    • Blaize
      Member
      • Jul 2008
      • 17

      #3
      Hi Leonardo,

      I've already did it (without any reply

      Originally posted by lcollado View Post
      Hello Blaize,

      You should probably ask this question on the Velvet mailing list where Daniel Zerbino will most likely answer it:


      Greetings,
      Leonardo

      Comment

      • lcollado
        Member
        • Jun 2009
        • 65

        #4
        Hello Blaize,

        I just checked (a few times) the recent mails from the list and I cannot find yours. So it most likely didn't get sent to the mailing list and I recommend you to re-send it.

        Greetings,
        Leonardo
        L. Collado Torres, Ph.D. student in Biostatistics.

        Comment

        • Blaize
          Member
          • Jul 2008
          • 17

          #5
          Yeah, I've resent it.

          Comment

          • Blaize
            Member
            • Jul 2008
            • 17

            #6
            Hi, Leonardo,

            Daniel recommends to raise the cutoff value, I hope it'll help us!

            B

            Comment

            • Temima
              Member
              • Sep 2010
              • 12

              #7
              Did This work?

              Would love to hear if you actually pulled off this hybrid assembly

              Comment

              • Blaize
                Member
                • Jul 2008
                • 17

                #8
                Hi Temima,

                we did the job, evaluating the results going now

                B

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
                  by SEQadmin2




                  NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
                  Today, 06:46 AM
                • 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

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, 10-28-2026, 09:57 AM
                0 responses
                22 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-28-2026, 09:51 AM
                0 responses
                14 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-22-2026, 11:13 AM
                0 responses
                67 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 10-22-2026, 10:48 AM
                0 responses
                47 views
                0 reactions
                Last Post SEQadmin2  
                Working...