Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • biofreak
    Member
    • Jun 2011
    • 44

    #1

    GFT file for rat

    I want to run tophat for rat samples. Where do I download the gtf file from?
    thanks
  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    You can find it here:

    http://www.ensembl.org/info/data/ftp/index.html

    --
    Phillip

    Comment

    • HSV-1
      Member
      • Jul 2012
      • 38

      #3
      the same is much bigger than the one from ucsc, why?

      Comment

      • mbblack
        Senior Member
        • Aug 2009
        • 245

        #4
        Originally posted by HSV-1 View Post
        the same is much bigger than the one from ucsc, why?
        How did you get your one from UCSC? If you make a RefGene based GTF from TableBrowser, it only includes coding features. The pre-built GTF from Ensembl includes all coding and non-coding features. Plus the actual annotations are longer text strings (all the Ensembl accessions for gene ID, exon ID, transcript ID, name, biotype,...) so in raw text the Ensembl file will be larger.

        Also note that the UCSC file uses the notation "chr1", etc while the fist column in the Ensembl will just be "1" etc (some software will expect the prefix "chr").
        Michael Black, Ph.D.
        ScitoVation LLC. RTP, N.C.

        Comment

        • HSV-1
          Member
          • Jul 2012
          • 38

          #5
          This is probably the reason.
          How to fix?
          From the same sequence data with ensemble gft I should get more accepted hits by tophat .



          Originally posted by mbblack View Post
          How did you get your one from UCSC? If you make a RefGene based GTF from TableBrowser, it only includes coding features. The pre-built GTF from Ensembl includes all coding and non-coding features. Plus the actual annotations are longer text strings (all the Ensembl accessions for gene ID, exon ID, transcript ID, name, biotype,...) so in raw text the Ensembl file will be larger.

          Also note that the UCSC file uses the notation "chr1", etc while the fist column in the Ensembl will just be "1" etc (some software will expect the prefix "chr").

          Comment

          • mbblack
            Senior Member
            • Aug 2009
            • 245

            #6
            Originally posted by HSV-1 View Post
            From the same sequence data with ensemble gft I should get more accepted hits by tophat .
            No, not for a reasonably mature genome such as the Rat. Ensembl's build may include a handful of novel and/or predicted coding genes, but not many. Ensembl Rat rel. 66.34 had 22,938 coding genes, 22,921 of which were known and have Refseq annotation (I only know this as I'm writing up data that used 66.34 as the reference - you would have to look on Ensembl's web site for the stats for the current release).

            The annotation really should not have any significant affect on your summarized mapping results for a mature feature set like the Rat - it would only matter if there were a large number of novel, unknown or predicted genes in one annotation versus another, or if the splice boundaries of the annotation features were still largely undetermined. But once summarized by gene, your mapped count data should be unaffected given the genome build is fairly well characterized and stable at this point.
            Michael Black, Ph.D.
            ScitoVation LLC. RTP, N.C.

            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
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            26 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            39 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...