Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Could not locate a bowtie index corresponding to basename -- tried posted solutions

    Hi,

    I am running on Ubuntu 16 and am trying to analyze my data with Bowtie2. I have managed to get this exact script to work on a windows machine running cygwin, but can't figure out this problem that arose on Linux.

    I am getting the classic "Could not located Bowtie index corresponding to basename "directory", yet I have listed a path directing to the base file name 'mm10', not the folder as many people here have posted about before.

    Things that I have tried:

    Changing to directory the index is located and running bowtie2.

    Adding the directory the index is located in to PATH.

    Placed the index in a folder in the bowtie2 directory, in my downloads directory, and the desktop. All with the same result.

    I have tried building an index from scratch or downloading a prebuilt one from bowtie2.

    I am running the code within a script to align multiple reads, but I have also tried manually calling bowtie to individual fastq files.
    Code:
    bowtie2 index:
    /user/home/Downloads/mm10/mm10
    call to bowtie2: 
    bowtie2 --local --very-sensitive-local --no-unal -q --phred33 --threads 12 -x /user/home/Downloads/mm10/mm10 -U BS_P384R_S_S30_L002_R1_001.fastq > BS_P384R_S
    Could not locate a Bowtie index corresponding to basename "/user/home/Downloads/mm10/mm10"
    Error: Encountered internal Bowtie 2 exception (#1)
    Command: /home/user/anaconda3/bin/bowtie2-align-s --wrapper basic-0 --local --very-sensitive-local -q --phred33 --threads 12 -x /user/home/Downloads/mm10/mm10 --passthrough -U BS_P384R_S_S30_L002_R1_001.fastq 
    (ERR): bowtie2-align exited with value 1
    Traceback (most recent call last):
      File "/home/user/phd/fastq_to_sams.py", line 92, in <module>
        py_bowtie_single_end('/home/user/phd/NGYHF03', list_output_sam = outputs, bowtie2_index = mm10)
      File "/home/user/phd/fastq_to_sams.py", line 87, in py_bowtie_single_end
        check_output(temp_str, shell=True)
      File "/home/user/anaconda3/lib/python3.6/subprocess.py", line 336, in check_output
        **kwargs).stdout
      File "/home/user/anaconda3/lib/python3.6/subprocess.py", line 418, in run
        output=stdout, stderr=stderr)
    subprocess.CalledProcessError: Command 'bowtie2 --local --very-sensitive-local --no-unal -q --phred33 --threads 12 -x /user/home/Downloads/mm10/mm10 -U BS_P384R_S_S30_L002_R1_001.fastq > BS_P384R_S' returned non-zero exit status 1
    .



    Any suggestions on something to try?

Latest Articles

Collapse

  • seqadmin
    Essential Discoveries and Tools in Epitranscriptomics
    by seqadmin


    The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
    Today, 07:01 AM
  • 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

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by seqadmin, 04-11-2024, 12:08 PM
0 responses
37 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-10-2024, 10:19 PM
0 responses
41 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-10-2024, 09:21 AM
0 responses
35 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-04-2024, 09:00 AM
0 responses
54 views
0 likes
Last Post seqadmin  
Working...
X