Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • virg4l
    Junior Member
    • May 2015
    • 7

    #1

    HTseq-count errors

    I put 10 .bam files (from Tophat) through the same samtools & htseq-count commands, and 3/10 didn't work (each with their own error) in htseq.

    $ samtools view -h -o sample.sam sample.bam

    $ htseq-count --stranded no -i gene_id sample.sam genes.gtf > sample.gene.counts

    The errors are:

    1) ...596437 GFF lines processed.
    Error occured when reading beginning of SAM/BAM file.
    [Exception type: StopIteration, raised in count.py:84]

    This one particularly confuses me since the program didn't choke on any of the other sam files that were prepared the same way.

    2) ...20000000 SAM alignment records processed.
    Error occured when processing SAM input (line 20080682 of file TH2/DEprep/BR2_N2In.sam):
    ('SAM line does not contain at least 11 tab-delimited fields.', 'line 20080682 of file TH2/DEprep/BR2_N2In.sam')
    [Exception type: ValueError, raised in _HTSeq.pyx:1276]

    3) ...35089676 SAM alignments processed.
    [Errno 5] Input/output error
    [Exception type: IOError, raised in count.py:212]


    Any suggestions for how I should fix these problems?
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    I wonder if you're having hard drive corruption issues.

    In any case, make sure you're using the most recent version of htseq-count. Also, check line 20080682 of the sam file mentioned and ensure it's not malformed.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 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
      ...
      07-20-2026, 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, 08-06-2026, 07:41 AM
    0 responses
    13 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    30 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    40 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    26 views
    0 reactions
    Last Post SEQadmin2  
    Working...