Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • ksherwood
    Junior Member
    • Apr 2011
    • 4

    Identifying nde genes as controls

    Hi all,

    Most of us are interested in identifying differentially expressed genes within datasets, however I was wondering if anyone had tried to identify NON DIFFERENTIALLY EXPRESSED genes- perhaps as a way of picking control genes?

    I haven't even got any idea how one would go about doing this? All and any suggestions would be greatly appreciated!

    thanks,
    k
  • Bukowski
    Senior Member
    • Jan 2010
    • 388

    #2
    This paper: http://www.biomedcentral.com/1471-2164/12/156

    and this R package:



    Which is aimed at identifying the best 'housekeeping' genes for normalisation in qPCR

    Comment

    • ksherwood
      Junior Member
      • Apr 2011
      • 4

      #3
      Identifying NDE genes as controls

      Thank you very much for that help!

      I was wondering if the R package would work for miRNA data? I have a miRNA seq dataset (nanostring) of ~700miRNA and need to identify the least variable (i.e. Non differentially expressed) miRNA's between a disease vs control comparison.

      much appreciated!
      karen

      Comment

      • steven
        Senior Member
        • Aug 2009
        • 269

        #4
        Originally posted by ksherwood View Post
        Thank you very much for that help!

        I was wondering if the R package would work for miRNA data? I have a miRNA seq dataset (nanostring) of ~700miRNA and need to identify the least variable (i.e. Non differentially expressed) miRNA's between a disease vs control comparison.

        much appreciated!
        karen
        mhm.. if you consider the qPCR world (again) the endogenous control classical approaches (like GeNorm and NormFinder) may not be optimal for miRNAs.
        Have a look at this paper:
        A novel and universal method for microRNA RT-qPCR data normalization.
        The idea is more or less to build a virtual control gene using the median expression. In your case the upper quartile may be more appropriate (like proposed for RNA-seq by Bullard et al I think).

        Comment

        • ksherwood
          Junior Member
          • Apr 2011
          • 4

          #5
          Thank you for all the useful pointers!

          From a slightly different angle;

          Rather than trying to identify a few stably expressed miRNA to use for normalization, are there any suggestions for an approach to identify a NDE profile, thereby giving a unchanged 'background' for your condition of interest? Especially when dealing with NG methods, which can differ from qRT-PCR analytical methods (although eventually findings generally have to be validated in PCR).

          It comes from this idea that there should be a 'healthy' profile or baseline, as opposed to a 'disease' profile, which might be more popular as personalized medicine becomes more of a reality.

          Thanks again!

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
            by SEQadmin2


            Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


            The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
            ...
            06-02-2026, 10:05 AM
          • SEQadmin2
            Single-Cell Sequencing at an Inflection Point: Early Impacts of New Platforms and Emerging Trends
            by SEQadmin2


            With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.


            Introduction

            Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...
            05-22-2026, 06:42 AM
          • SEQadmin2
            Environmental Genomics in the Age of NGS: From Microbes to Conservation Strategies
            by SEQadmin2

            Studying ecosystems means dealing with complex, multi-species communities that are hard to observe at scale. This complexity, however, hides many important questions to be answered, from how biogeochemical cycles work and how climate change can affect species distribution to how conservation strategies can work best.


            Genomics, particularly since the expansion of NGS, has transformed ecosystem ecology. By sequencing environmental DNA, we can now assess biodiversity without direct...
            05-06-2026, 09:04 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Yesterday, 08:59 AM
          0 responses
          13 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-02-2026, 12:03 PM
          0 responses
          22 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-02-2026, 11:40 AM
          0 responses
          19 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 05-28-2026, 11:40 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Working...