Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • komalsrathi
    Member
    • Aug 2013
    • 14

    #1

    tophat-fusion-post: ValueError: invalid literal for int() with base 10: 'exonCount'

    Hi everyone,

    I am running tophat-fusion-post like this:

    Code:
    tophat-fusion-post -o ./fusion_results -p 8 --num-fusion-reads 1 --num-fusion-pairs 2 --num-fusion-both 5 /mnt/isilon/cbmi/variome/reference/bowtie_indexes/hg38_no_alt/Homo_sapiens/NCBI/GRCh38/Sequence/BowtieIndex/genome
    My root folder is tophat-fusion. I have 4 tophat output folders under it: CHP212, SHSY5Y, SKNAS and SKNSH, each of which contain a fusions.out file. I have created symbolic links to refGene.txt, ensGene.txt and blast database (blast) in the same folder.

    This is my directory structure where I have run tophat:

    Code:
    $ tree -L 2 ./tophat-fusion
    
    ./
    |-- CHP212
    |   |-- accepted_hits.bam
    |   |-- align_summary.txt
    |   |-- deletions.bed
    |   |-- fusions.out
    |   |-- insertions.bed
    |   |-- junctions.bed
    |   |-- logs
    |   |-- prep_reads.info
    |   `-- unmapped.bam
    |-- CHP212.sh
    |-- CHP212_R1.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/CHP212_R1.fastq.gz
    |-- CHP212_R2.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/CHP212_R2.fastq.gz
    |-- IMR32.sh
    |-- IMR32_R1.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/IMR32_R1.fastq.gz
    |-- IMR32_R2.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/IMR32_R2.fastq.gz
    |-- SHSY5Y
    |   |-- accepted_hits.bam
    |   |-- align_summary.txt
    |   |-- deletions.bed
    |   |-- fusions.out
    |   |-- insertions.bed
    |   |-- junctions.bed
    |   |-- logs
    |   |-- prep_reads.info
    |   `-- unmapped.bam
    |-- SHSY5Y.sh
    |-- SHSY5Y_R1.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SHSY5Y_R1.fastq.gz
    |-- SHSY5Y_R2.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SHSY5Y_R2.fastq.gz
    |-- SKNAS
    |   |-- accepted_hits.bam
    |   |-- align_summary.txt
    |   |-- deletions.bed
    |   |-- fusions.out
    |   |-- insertions.bed
    |   |-- junctions.bed
    |   |-- logs
    |   |-- prep_reads.info
    |   `-- unmapped.bam
    |-- SKNAS.sh
    |-- SKNAS_R1.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SKNAS_R1.fastq.gz
    |-- SKNAS_R2.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SKNAS_R2.fastq.gz
    |-- SKNSH
    |   |-- accepted_hits.bam
    |   |-- align_summary.txt
    |   |-- deletions.bed
    |   |-- fusions.out
    |   |-- insertions.bed
    |   |-- junctions.bed
    |   |-- logs
    |   |-- prep_reads.info
    |   `-- unmapped.bam
    |-- SKNSH.sh
    |-- SKNSH_R1.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SKNSH_R1.fastq.gz
    |-- SKNSH_R2.fastq.gz -> /mnt/isilon/maris_lab/target_nbl_ngs/CellLineRNASeq/rawfiles/cat_fastq/SKNSH_R2.fastq.gz
    |-- blast -> /mnt/isilon/cbmi/variome/reference/blast_db/hg38
    |-- ensGene.txt -> /mnt/isilon/cbmi/variome/reference/blast_db/hg38/ensGene.txt
    |-- fusion_results
    |   |-- fusion_seq.bwtout
    |   |-- fusion_seq.fa
    |   |-- fusion_seq.map
    |   |-- logs
    |   `-- tmp
    |-- refGene.txt -> /mnt/isilon/cbmi/variome/reference/blast_db/hg38/refGene.txt
    `-- tophat-fusion.sh
    When I run tophat-fusion-post under this directory, I am getting the following errors:

    Code:
    [Fri Mar 17 15:09:18 2017] Beginning TopHat-Fusion post-processing run (v2.1.0)
    -----------------------------------------------
    [Fri Mar 17 15:09:18 2017] Extracting 23-mer around fusions and mapping them using Bowtie
    [Fri Mar 17 15:09:30 2017] Filtering fusions
    Traceback (most recent call last):
      File "/home/rathik/tools/miniconda3/envs/fusion-env/bin/tophat-fusion-post", line 2924, in <module>
        sys.exit(main())
      File "/home/rathik/tools/miniconda3/envs/fusion-env/bin/tophat-fusion-post", line 2895, in main
        filter_fusion(bwt_idx_prefix, params)
      File "/home/rathik/tools/miniconda3/envs/fusion-env/bin/tophat-fusion-post", line 965, in filter_fusion
        ensGene_list = read_genes("ensGene.txt")
      File "/home/rathik/tools/miniconda3/envs/fusion-env/bin/tophat-fusion-post", line 917, in read_genes
        num_exons = int(line[7])
    ValueError: invalid literal for int() with base 10: 'exonCount'
    Komal Rathi
    Bioinformatics Application Developer
    University of Pennsylvania
  • Enraico
    Junior Member
    • Feb 2012
    • 5

    #2
    remove header line from the ensGene.txt file
    Code:
    mv ensGene.txt ensGene.txt.bk
    grep -v "^#" ensGene.txt.bk > ensGene.txt

    Comment

    • warrenfelsh
      Junior Member
      • Apr 2020
      • 1

      #3
      The error message invalid literal for int() with base 10 would seem to indicate that you are passing a string that's not an integer to the int() function . In other words it's either empty, or has a character in it other than a digit.

      You can solve this error by using Python isdigit() method to check whether the value is number or not. The returns True if all the characters are digits, otherwise False .

      if val.isdigit():

      The other way to overcome this issue is to wrap your code inside a Python try...except block to handle this error.

      Python2.x and Python3.x

      Sometimes the difference between Python2.x and Python3.x that leads to this ValueError: invalid literal for int() with base 10 .

      With Python2.x , int(str(3/2)) gives you "1". With Python3.x , the same gives you ("1.5"): ValueError: invalid literal for int() with base 10: "1.5".

      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...