Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • How DESeq2 Handles counts

    Hypothetically

    If I have 24 samples and I submit them to a facility to run my RNA-seq then can this happen?

    The technician puts in varying amount of prepped library into the lanes so how does DESeq2 account for this variability in it's normalization?

    If I put in 20 ng if DNA in lane one and 50 ng in lane 2 how is this accounted for by the software or is this something I should be aware of and account for by myself.

  • #2
    The normal packages (DESeq2, edgeR, etc.) will deal with this just fine and it's not something you normally need to concern yourself with. The method used in DESeq2 was described in the original DESeq paper (the end of page 2 and the beginning of page 3).

    Having said that, it's often good to have a look at the size factors. It's sometimes the case that if that of one sample differs by 10x or more from the others that you get spurious results.

    Comment


    • #3
      Originally posted by dpryan View Post
      The normal packages (DESeq2, edgeR, etc.) will deal with this just fine and it's not something you normally need to concern yourself with. The method used in DESeq2 was described in the original DESeq paper (the end of page 2 and the beginning of page 3).

      Having said that, it's often good to have a look at the size factors. It's sometimes the case that if that of one sample differs by 10x or more from the others that you get spurious results.
      thanks you have been a great PI in my research so far


      quick code in R for size factors?

      Comment


      • #4
        Code:
        sizeFactors(dds)
        where "dds" is a "DESeqDataSet" object.

        Comment


        • #5
          excellent thank you

          size factors are around 0.9 - 1.1 bla bla bla

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Essential Discoveries and Tools in Epitranscriptomics
            by seqadmin


            The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
            Today, 07:01 AM
          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          37 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          41 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          35 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          54 views
          0 likes
          Last Post seqadmin  
          Working...
          X