Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Independent filtering by using fold change in DESeq2

    Hi everyone,
    Thanks for reading my post.

    I know DESeq2 uses normalized mean count as independent filtering to improve the performance of multiple testing error correction. I would like to know is it possible I can add the criteria, |log2FC| > 1, together with normalized mean count as the independent filtering? If so, how could I add this criteria? by using "filter=" or "filterFun=" argument? How to write the command?

    What I know now is to change the "lfcThreshold=" to 1, but this only change the null hypothesis from 0 to 1, not actually filter any genes.

    Many Thanks in advance!

  • #2
    No you can't use fold-change in independent filtering, it wouldn't then be independent. You can filter genes after the fact for the fold-change threshold you want.

    Comment


    • #3
      Originally posted by dpryan View Post
      No you can't use fold-change in independent filtering, it wouldn't then be independent. You can filter genes after the fact for the fold-change threshold you want.
      Hi dpryan,
      Thanks for your reply. You mean I should run DESeq for DE analysis first and then filter out the genes with small fold change? If so, could I only perform multiple testing error correction for those genes remained instead of all the genes tested? Since this would give me more significant DE genes with big fold change.

      Thanks.

      Comment


      • #4
        But that is a violation of independent filtering principle, you cannot filter for something you are testing for. Obviously it is great for your p-values, but also completely invalid and should be considered p-value-hacking.

        Comment


        • #5
          Originally posted by wdecoster View Post
          But that is a violation of independent filtering principle, you cannot filter for something you are testing for. Obviously it is great for your p-values, but also completely invalid and should be considered p-value-hacking.
          Hi wdecoster,
          Thanks for you reply.
          So nothing we can do by using fold change to filter the genes? any suggestion? Thanks

          Comment


          • #6
            You can filter genes by fold-change after calculating p-values and adjusting for multiple testing. If you do anything like that beforehand odds are good that you'll end up with me as a reviewer and I will guarantee that your paper is rejected.

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Latest Developments in Precision Medicine
              by seqadmin



              Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

              Somatic Genomics
              “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
              05-24-2024, 01:16 PM
            • seqadmin
              Recent Advances in Sequencing Analysis Tools
              by seqadmin


              The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
              05-06-2024, 07:48 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, Yesterday, 06:55 AM
            0 responses
            12 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 05-30-2024, 03:16 PM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 05-29-2024, 01:32 PM
            0 responses
            28 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 05-24-2024, 07:15 AM
            0 responses
            215 views
            0 likes
            Last Post seqadmin  
            Working...
            X