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Early termination in step (2/10)

pmhgrt
2023-12-07
2024-09-26
  • pmhgrt

    pmhgrt - 2023-12-07

    Dear @barryghall & @shea0,

    We just tried to use some Candida auris assemblies using kSNP4.1. We have multiple contigs in each files. We tried to run the program but we got a early termination in step 2.

    (base) pmh@pmh-Alienware-Aurora-R13:~/program/kSNP4.1/Test/CAUR$ /home/pmh/program/kSNP4.1/kSNP4.1_Linux_package/kSNP4.1_Linux_package/kSNP4.1pkg/kSNP4 -in Test01.in -outdir Run1 -k 11 | tee Run3Log
    fasta_list: /home/pmh/program/kSNP4.1/Test/CAUR/Test01.in
    Output directory: /home/pmh/program/kSNP4.1/Test/CAUR/Run1
    Starting kSNP4.1
    Thursday, December 07, 2023 PM06:28:05 HKT
    Configuration for this run:
    input fasta_list: /home/pmh/program/kSNP4.1/Test/CAUR/Test01.in
    output / working directory: /home/pmh/program/kSNP4.1/Test/CAUR/Run1
    k=11
    annotate_list file:
    Maximum number of open files: 10240
    Automatically determining number of CPUs to use:
    The operating system is Linux
    Discovered 24
    Number CPUs: 24
    Python version to be used:
    Python 3.9.17
    SNPS_ALL_INPUT=
    GENBANKFILEINPUT=
    CORE=0
    ML=0
    NJ=0
    VCF=0
    DEBUG=0
    [00:00:00] (1/10) Preprocessing
    [00:00:00] (2/10) Running jellyfish to get kmer counts

    We also tried to delete the multiple contigs into only one contig and it run completely.

    May we know if kSNP4.1 could only handle one contig per fasta file?

    Thanks a lot.

    Best regards,
    GRT

     
  • Rita

    Rita - 2024-02-12

    This is happening to me as well. I don't think it's due to only handling one contig per file as I was previously able to successfully run over 150 samples each with 16 contigs in the individual files. However, now I have about 172 samples (each with 16 contigs) and now it hangs and crashes on that step. Is there something I can add to the command I am using to account for more memory or CPU?

     
  • Rita

    Rita - 2024-03-11

    It was the RAM on those samples and I was able to fix it and have it run. However, those were on assembled genomes and now I am trying to run with raw (quality checked and trimmed) paired-end combined Illumina fasta files and it hangs on the second step. I have attached the log file describing the error.

     
  • Rita

    Rita - 2024-03-11
     

    Last edit: Rita 2024-03-11
  • hansen wang

    hansen wang - 2024-09-26

    the error you encounter is the same as me. Do you get some response for this, how do you resolve this?

     

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