Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • john_gamble
    Junior Member
    • Feb 2017
    • 2

    #1

    Advice RNA-Seq experimental design

    Hello,

    I've recently started working in a group that would like to start doing RNA-Seq experiments in order to compare the transcriptomes of pancreatic islets undergoing different treatments.

    As I'm new to this kind of work, I was wondering if anyone could offer advice on experimental design - specifically, how do you choose the correct number of samples (technical and biological replicates) and the depth of sequencing to give statistically meaningful results? Is it necessary to carry out a 'power' analysis to answer these questions? If so, how do you do that?

    I've spent some time going through the literature on this, but frankly, it's quite confusing and seems inaccessible to anyone without a background in advanced maths or statistics. (I have neither.)

    However, on the basis of what I've read, I've decided to run a pilot sequencing experiment with a limited number of samples and then enter the data into the 'Scotty' web-tool as described here:



    This then returns information on number of samples and read-depth required to achieve a specific statistical 'power'.

    Does that sound like a reasonable course of action?

    Any advice on this matter would be much appreciated. In fact, any advice, or pointers to worthwhile reading material/resources in the area of RNA-Seq difference analysis would be a huge help.

    Thanks for any advice offered.

    Regards,

    John

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

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 10:35 AM
0 responses
9 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-06-2026, 07:41 AM
0 responses
27 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
45 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-31-2026, 02:55 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Working...