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  • Error running Shrimp aligner

    Hi all

    I'm trying to map some reads that were found unmapped using bwa with Shrimp agaist chr18.

    The command I'm running is as follows:

    gmapper-cs -N 8 -E -Q Unmapped-reads.fq chrm-18/chr18-
    homo.fasta

    However I'm getting the following output/error.

    Output:

    --------------------------------------------------------------------------------
    gmapper: COLOUR SPACE (AB SOLiD).
    SHRiMP 2.1.1b
    [ICC Intel(R) C++ g++ 4.1 mode]
    --------------------------------------------------------------------------------
    Settings:
    Spaced Seeds (weight/span) 111110001111111 (12/15)
    111100111001001111 (12/18)
    111001001000111001111 (12/21)
    1111001000010001001001111 (12/25)
    Number of Outputs per Read: 10
    Window Generation Mode: 2
    Window Length: 140.00%
    Window Overlap Length: 20.00%

    SW Match Score: 10
    SW Mismatch Score: -15
    SW Gap Open Score (Ref): -40
    SW Gap Open Score (Qry): -40
    SW Gap Extend Score (Ref): -7
    SW Gap Extend Score (Qry): -7
    SW Crossover Score: -14

    Window Generation Threshold: 55.00%
    SW Vector Hit Threshold: 50.00%
    SW Full Hit Threshold: 55.00%

    Paired mode: none

    Gapless mode: no
    Number of threads: 8
    Thread chunk size: 1000
    Hash Filter Calls: yes
    Anchor Width: 8
    - Processing genome file [/chrm-18/chr18-homo.fasta]
    - Processing contig gi|224589809|ref|NC_000018.9|
    Loaded Genome
    Automatically trimming genome index lists longer than: 1000
    - Processing read file [Unmapped-reads.fq]
    gmapper-cs: common/fasta.c:380: bool fasta_get_next_read_with_range(_fasta_t *, read_entry *): Assertion `quality_length <= sequence_length' failed.

    Any suggestions is highly appreciated.

    Thanks
    Mahtab

  • #2
    It would appear that you have some sequences that have longer qualities than there are bases in the sequence - i.e. the length of the quality is not less than or equal to the sequence length, which is what that error is suggesting.

    Comment


    • #3
      Thanks for you response.

      The problem is I'm getting the same error across different sets of input fastq data both synthetic and real data which I had previously mapped using bwa.

      Comment

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