Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • hong_sunwoo
    Member
    • Jan 2010
    • 11

    #1

    Gene information in Cuffdiff output files

    Hello.
    I am now trying RNA-seq data analysis using Tophat-Cufflinks process.
    I have two human RNA-seq data from Solexa sequencing (single-end) and my goal is comparing gene expression level and alternative splicing patterns of each data.

    Without any option, I ran tophat with UCSC hg19 and obtained two accepted_hits.sam files.
    Then, through cufflinks and cuffcompare, single gtf file, stdout.combined.gtf file is made and used for cuffdiff along with two sam files.

    After cuffdiff run, I could see several files such as gene_exp.diff.

    My question is below.
    When I open the cuffdiff results files, I can not find gene information as below.
    Code:
    test_id    gene    locus    sample_1    sample_2    status    value_1    value_2    ln(fold_change)    test_stat    p_value    significant
    XLOC_000001    -    chr1:763004-764484    q1    q2    NOTEST    0    9.91482    2.13631e-314    1.79769e+308    0    no
    XLOC_000002    -    chr1:895380-897112    q1    q2    NOTEST    6.56765    2.24444    -1.0737    1.38868    0.16493    no
    XLOC_000003    -    chr1:897214-901465    q1    q2    NOTEST    11.9247    2.23374    -1.67493    4.67081    3.00007e-06    no
    XLOC_000004    -    chr1:908878-909553    q1    q2    NOTEST    0    4.13402    2.14785e-314    1.79769e+308    0    no
    How can I get gene information?
  • Cole Trapnell
    Senior Member
    • Nov 2008
    • 213

    #2
    Originally posted by micrornas View Post
    Hello.
    I am now trying RNA-seq data analysis using Tophat-Cufflinks process.
    I have two human RNA-seq data from Solexa sequencing (single-end) and my goal is comparing gene expression level and alternative splicing patterns of each data.

    Without any option, I ran tophat with UCSC hg19 and obtained two accepted_hits.sam files.
    Then, through cufflinks and cuffcompare, single gtf file, stdout.combined.gtf file is made and used for cuffdiff along with two sam files.

    After cuffdiff run, I could see several files such as gene_exp.diff.

    My question is below.
    When I open the cuffdiff results files, I can not find gene information as below.
    Code:
    test_id    gene    locus    sample_1    sample_2    status    value_1    value_2    ln(fold_change)    test_stat    p_value    significant
    XLOC_000001    -    chr1:763004-764484    q1    q2    NOTEST    0    9.91482    2.13631e-314    1.79769e+308    0    no
    XLOC_000002    -    chr1:895380-897112    q1    q2    NOTEST    6.56765    2.24444    -1.0737    1.38868    0.16493    no
    XLOC_000003    -    chr1:897214-901465    q1    q2    NOTEST    11.9247    2.23374    -1.67493    4.67081    3.00007e-06    no
    XLOC_000004    -    chr1:908878-909553    q1    q2    NOTEST    0    4.13402    2.14785e-314    1.79769e+308    0    no
    How can I get gene information?
    That field is for the "gene_name" attribute for each transcript. Your GTF file needs to have the "gene_name" attribute attached to it in order to anything to show up there. Ensembl and other annotation sources attach these to their GTF records, and Cuffcompare tries to preserve them in its *.combined.gtf files.

    Comment

    • hong_sunwoo
      Member
      • Jan 2010
      • 11

      #3
      Thanks Cole.
      I will try cuffcompare using annotation file from Ensemble!

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        How Immunogenomics Decodes Immunity’s Genetic Blueprint
        by SEQadmin2




        The immune system’s power comes from its genetic diversity, allowing myriad threats to be neutralized through first recognizing foreign antigens. That diversity is also what makes the immune system so difficult to study. Recent advances in sequencing technology and computational biology, however, are giving researchers new tools to understand immune responses and immune-related diseases in greater detail.

        This convergence of genetics, immunology, and computation...
        Yesterday, 05:41 AM
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 08-24-2026, 10:32 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-20-2026, 11:17 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-18-2026, 10:05 AM
      0 responses
      55 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-13-2026, 12:22 PM
      0 responses
      50 views
      0 reactions
      Last Post SEQadmin2  
      Working...