Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • indugun
    Junior Member
    • Apr 2013
    • 4

    #1

    Transcript quatification tools

    Which is best tool for transcript quantification (RSEM,cufflinks or any other) ?
  • AdrianP
    Senior Member
    • Apr 2011
    • 130

    #2
    I am actually interested in finding out an answer to that question as well.

    I am looking through this paper http://www.nature.com/nmeth/journal/...meth.1226.html talk about the ERANGE software. However, this software seems to consist of scripts that need to be modified with specific data being analysed before any work can be done. Not sure I am up to the task.

    I got a genome sequenced and assembled, and a transcription sequenced, assembled and annotated. Now I need to know gene expression relative to alpha tubulin.

    Comment

    • chadn737
      Senior Member
      • Jan 2009
      • 392

      #3
      Nobody uses ERANGE anymore. That is so 2008. It really depends on what you want to do with the data. Differential expression between conditions, isoform discovery or alternative splicing, or comparing gene expression within a sample. Know the specific goal of the research and then that will define the tool or lack thereof.

      Comment

      • Jeremy
        Senior Member
        • Nov 2009
        • 190

        #4
        I don't think this really has an answer yet. Different tools give different sets of DE genes, but which one is more correct is not easy to find out.

        Comment

        • AdrianP
          Senior Member
          • Apr 2011
          • 130

          #5
          Can I at least have some examples of some tools?

          Really, all I got is RNA-seq from 1 sample, and within that sample I need relative expression to alpha tubulin.

          Comment

          • shi
            Wei Shi
            • Feb 2010
            • 236

            #6
            Hi AdrianP,

            I don't quite understand how you can get relative expression from only 1 sample. But for the quantification, you may try featureCounts. See this post for more info about featureCounts - http://seqanswers.com/forums/showpos...21&postcount=1

            Cheers,
            Wei

            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, Today, 07:41 AM
            0 responses
            9 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...