Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • tophat-fusion-post result sam_header empty

    Hi all,

    I’m having a problem with tophat-fusion-post. I run it, but the output is empty.
    I think a sam_header file may cause that problem.

    I use the version of
    tophat : 2.1.0
    bowtie : 1.2.2
    on Windows Subsystem for Linux.

    My command like this:

    tophat-fusion-post -o /home/onsh/src/tophat-2.1.0/tophat_SRR064286/post_out/ \
    --num-threads 16 --num-fusion-reads 1 --num-fusion-pairs 2 --num-fusion-both 5 \
    /home/onsh/src/tophat-2.1.0/Homo_sapiens.GRCh38.small

    Bowtie indexes are downloaded from Ensembl. In the original file,
    I added a word “chr” to each chromosome numbers because the chromosome number is just a number.

    My directory structure like this:

    onsh@PC3:~/src/tophat-2.1.0$ ll
    drwxrwxrwx 0 onsh onsh 512 May 14 16:22 blast/
    -rwxrwxrwx 1 onsh onsh 22661379 May 14 16:02 ensGene.txt
    -rwxrwxrwx 1 onsh onsh 982498668 May 14 15:12 Homo_sapiens.GRCh38.small.1.bt2
    -rwxrwxrwx 1 onsh onsh 842742636 May 14 15:12 Homo_sapiens.GRCh38.small.1.ebwt
    -rwxrwxrwx 1 onsh onsh 733719256 May 14 15:12 Homo_sapiens.GRCh38.small.2.bt2
    -rwxrwxrwx 1 onsh onsh 366859632 May 14 15:12 Homo_sapiens.GRCh38.small.2.ebwt
    -rwxrwxrwx 1 onsh onsh 8945 May 14 15:12 Homo_sapiens.GRCh38.small.3.bt2
    -rwxrwxrwx 1 onsh onsh 8945 May 14 15:12 Homo_sapiens.GRCh38.small.3.ebwt
    -rwxrwxrwx 1 onsh onsh 733719249 May 14 15:12 Homo_sapiens.GRCh38.small.4.bt2
    -rwxrwxrwx 1 onsh onsh 733719249 May 14 15:12 Homo_sapiens.GRCh38.small.4.ebwt
    -rwxrwxrwx 1 onsh onsh 3150052344 May 14 15:12 Homo_sapiens.GRCh38.small.fa
    -rwxrwxrwx 1 onsh onsh 982498668 May 14 17:15 Homo_sapiens.GRCh38.small.rev.1.bt2
    -rwxrwxrwx 1 onsh onsh 842742636 May 14 17:15 Homo_sapiens.GRCh38.small.rev.1.ebwt
    -rwxrwxrwx 1 onsh onsh 733719256 May 14 17:15 Homo_sapiens.GRCh38.small.rev.2.bt2
    -rwxrwxrwx 1 onsh onsh 366859632 May 14 17:15 Homo_sapiens.GRCh38.small.rev.2.ebwt
    -rwxrwxrwx 1 onsh onsh 20767330 May 14 16:02 refGene.txt
    -rwxr-xr-x 1 onsh onsh 171175 Jul 23 2015 tophat
    -rwxr-xr-x 1 onsh onsh 233 Jul 23 2015 tophat2
    -rwxr-xr-x 1 onsh onsh 118420 May 15 13:39 tophat-fusion-post
    drwxrwxrwx 0 onsh onsh 512 May 15 15:06 tophat_SRR064286/

    In the tophat_SRR064286/ directory, I have some files:

    onsh@PC3:~/src/tophat-2.1.0/tophat_SRR064286$ ll
    -rw-rw-rw- 1 onsh onsh 2754640914 May 14 15:04 accepted_hits.bam
    -rw-rw-rw- 1 onsh onsh 569 May 14 15:04 align_summary.txt
    -rw-rw-rw- 1 onsh onsh 1646739 May 14 15:04 deletions.bed
    -rw-rw-rw- 1 onsh onsh 16228495 May 14 15:04 fusions.out
    -rw-rw-rw- 1 onsh onsh 1380426 May 14 15:04 insertions.bed
    -rw-rw-rw- 1 onsh onsh 6025364 May 14 15:04 junctions.bed
    drwxrwxrwx 0 onsh onsh 512 May 15 13:58 post_out/ # <— output directory
    -rw-rw-rw- 1 onsh onsh 180 May 14 15:04 prep_reads.info
    -rw-rw-rw- 1 onsh onsh 75130369 May 14 15:04 unmapped.bam

    I dig the tophat-fusion-post code, it seems that “get_chromosome_order()” function doesn’t work.
    A sam_header file is empty.

    bowtie_header_filename = tmp_dir + "sam_header"
    subprocess.call(bowtie_header_cmd,
    stdout=open(bowtie_header_filename, "w"),
    stderr=open("/dev/null"))

    The chrs variable which the function returns is also empty in spite of using chrs variable in the subsequent processes.

    Could you anybody solve this?

    Thank you all,

    onsh
    Last edited by onsh; 05-15-2018, 09:28 PM.

  • #2
    Originally posted by onsh View Post
    Bowtie indexes are downloaded from Ensembl. In the original file,
    I added a word “chr” to each chromosome numbers because the chromosome number is just a number.
    onsh
    I'm sorry that the sentence above is not correct.

    <CORRECTION>
    FASTA of genome sequences are downloaded from Ensembl. In the original file, I added a word “chr” to each chromosome numbers because the chromosome number is just number.
    Bowtie indexes were built by bowtie 1.2.2.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM
    • seqadmin
      Strategies for Sequencing Challenging Samples
      by seqadmin


      Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
      03-22-2024, 06:39 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    18 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    22 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    47 views
    0 likes
    Last Post seqadmin  
    Working...
    X