Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • limericksean
    Junior Member
    • Jan 2011
    • 4

    bowtie terminate called error

    Hi,
    I'm using bowtie 0.12.7 to align 100bp PE reads. I'm crashing with the error:

    Too few quality values for read: -
    are you sure this is a FASTQ-int file?
    terminate called after throwing an instance of 'int'

    Aside from finding out why this happened, I'd be particularly happy for bowtie to report this error as a warning and then continue with the run.
    Is it possible to set a flag to get bowtie to throw the read instead of crashing?

    Here's my call with arguments:
    bowtie -X 20000 -q -p 12 -k 2 -m 2 --un no_align.fq --max mult_align.fq hg18.index -1 fastq_1 -2 fastq_2 align.aln

    The last reported read before terminate is called can be found in no_align.fq (bowtie reports 2 files - 1 for each mate) :

    tail -4 no_align_1.fq
    @HWI-ST1096:2181WHPACXX:5:2316:16714:101026 1:N:0:TAAGGCG
    NGATGAGATGATCGACGTCATCGGGGTGACCAAGGGCAAAGGCTACAAAGGGGTCACCAGTCGTTGGCACACCAAGAAGCTGCCCCGCAAGACCCACCGA
    +
    #1=?DDDDFFFFFDFII@@GFBCFEE@FDFFFEFFEFFFIIIIIIIIIEFFFDBDCCCCCBBB?BBBBBBBBBBBBBBBBABBBBBBBBBBBBBBBBB@9

    &

    tail -4 no_align_2.fq
    @HWI-ST1096:2181WHPACXX:5:2316:16714:101026 2:N:0:TAAGGCG
    CCAGAGCCCGCCGCTTCGTCTGCACCAGCAAGGACTTGCGGAGGGTGAGCGCCCGCTTCTTGGTTCCCACCGCACAGCCTTTCGGCATGACGGAGTCATT
    +
    1:?A1ADDF1@D1<CG<EHHEGHGJ@GD?)?DD2DG>=CHIIHFD;?=@@',33;@BBBA>>:@+>A@:A9&)09<(28CCDD(&&)08>A(&)0<9CCC


    I've noticed other threads mentioning stretches of multiple B's at the end of sequences being a trigger for low quality reads. Not sure if this is the case here. Either way, can I force bowtie to not terminate on this instance if indeed this is the case.
    One other thing, I have checked all reported align files (max-align, un-align & align) to see whether the next read in the original fastq file (i.e. after the one above) is actually reported just to make sure termination is in fact called & it is not there in any file. Therefore my run is incomplete.

    Any ideas or fixes would be greatfully appreciated.

    Thanks,
    Sean.
  • mastal
    Senior Member
    • Mar 2009
    • 666

    #2
    bowtie terminate called error

    Hi,

    I don't think the problem is the read quality values, but rather the number of base qualities compared to the number of bases for that read.

    I found a link to the part of the bowtie code that throws this error:



    Hope this helps,
    Maria

    Comment

    • limericksean
      Junior Member
      • Jan 2011
      • 4

      #3
      Thanks for the reply & tip.

      However, this fills me with dread! I have to pre-check the qual & seq character lengths from the sequencing prior to alignments now. Man!
      This has occurred in literally hundreds of different samples - it just can't be that they're all buggy.

      S.

      Comment

      Latest Articles

      Collapse

      • mylaser
        Reply to Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by mylaser
        The world of online gaming has grown tremendously over the past few years, giving players access to exciting sports, casino games, and interactive entertainment from the comfort of their homes. Among the platforms gaining attention, Kheloyaar has become a trusted destination for users seeking a fast, secure, and engaging gaming experience.
        Whether you're a first-time visitor or an existing user, understanding the features of Kheloyar and the Kheloyaar login process can help you enjoy everything...
        Today, 12:33 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        Yesterday, 11:48 AM
      • SEQadmin2
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 11:10 AM
      0 responses
      8 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-13-2026, 10:26 AM
      0 responses
      30 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-09-2026, 10:04 AM
      0 responses
      39 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-08-2026, 10:08 AM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Working...