Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • abh
    Member
    • Aug 2012
    • 13

    #1

    Tophat with bowtie2

    Hi,

    I want to align the Rna-seq data using bowtie2.so here are the steps i did(i installed tophat,bowtie2 and samtools and kept in bashprofile)

    i got the reference genome from bowtie2(hg19) and i ran the makescript for indexing them.i got
    6 index files(hg19.1.bt2 hg19.2.bt2 hg19.3.bt2 hg19.4.bt2 hg19.rev.1.bt2 hg19.rev.2.bt2)and i kept in genome folder hg19

    now i want to run the tophat by takine these index files and the fastq file like this but i am getting error
    [ab RNASEQ]$ tophat /net/gs/vol3/shared/lab/RNASEQ/hg19/hg19 C_RNAseq_1.fq

    [Thu Nov 29 23:45:21 2012] Beginning TopHat run (v1.4.1)
    -----------------------------------------------
    [Thu Nov 29 23:45:21 2012] Preparing output location ./tophat_out/
    [Thu Nov 29 23:45:21 2012] Checking for Bowtie index files
    Error: Could not find Bowtie index files /net/gs/vol3/shared/lab/RNASEQ/hg19.*

    can anyone help me with this?i am new in using the tophat

    Thank you
  • mknut
    Member
    • Jul 2012
    • 23

    #2
    It looks like tophat thinks that your index is in
    Code:
    /net/gs/vol3/shared/lab/RNASEQ/
    not
    Code:
    /net/gs/vol3/shared/lab/RNASEQ/hg19/
    . Try moving your index to a folder that does not include "hg19" in its name - it seems to be confusing tophat. Say
    Code:
    /net/gs/vol3/shared/lab/RNASEQ/my_index/
    should do the trick.

    EDIT: It looks like I did not notice the elephant in the room - you are using TopHat v1.4.1 which does not support Bowtie 2. Use Tophat version >2.0. From TopHat website:
    Version 2.0.0 is a major release adding Bowtie 2 support
    Last edited by mknut; 11-30-2012, 01:53 AM. Reason: misread the question

    Comment

    • masterpiece
      Member
      • Mar 2009
      • 40

      #3
      [Thu Nov 29 23:45:21 2012] Beginning TopHat run (v1.4.1)
      You cannot run tophat 1.4 with Bowtie2. You have to install Tophat version 2.0.* if you want to use Bowtie2.

      kamal

      Comment

      • abh
        Member
        • Aug 2012
        • 13

        #4
        thank you

        Its working now

        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, Yesterday, 07:41 AM
        0 responses
        11 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Working...