Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • qPCR validation of RNA-Seq data

    I am wondering if anyone has a good and easy way of comparing RNA-Seq data and qPCR result/validation statistically. I have seen papers comparing the microarray data and qPCR but not RNA-Seq data. Any help would be highly appreciate.

  • #2
    Originally posted by upendra_35 View Post
    I am wondering if anyone has a good and easy way of comparing RNA-Seq data and qPCR result/validation statistically. I have seen papers comparing the microarray data and qPCR but not RNA-Seq data. Any help would be highly appreciate.
    There are papers with comparison of RNA-seq and qPCR data. Check out for instance Griffith et al, Nature Methods 2010, or Asmann et al BMC Genomics, 2009. Probably the Mortazavi et al too, and those from the Burge lab.

    Comment


    • #3
      Thanks Steven. I will check it out....

      Comment


      • #4
        For added convenience to people landing here ... in Griffith et al. Nature Methods. 2010 Oct;7(10):843-847 [Abstract | Full Text | PDF | Supplementary Materials] the qPCR validations are presented in Figure 2. The experiment involved qPCR validation of 192 differentially expressed exons identified in the RNA-seq data. An additional qualitative assay involving RT-PCR, gel electrophoresis and Sanger sequencing was used to validate 189 exon-skipping junctions (see Supplementary Figure 10a in the Supplementary Materials). The actual data values are available from the ALEXA-seq website here. The validation rates for the quantitative and qualitative assays were 88% and 85% respectively. The selection of targets for validation was not biased towards highly expressed exons. Actually it was biased towards lowly expressed exons that were nevertheless identified as expressed above background by RNA-seq. These likely represent minor isoforms in many cases (see Supplementary Figure 10b in the Supplementary Materials). The paper also includes direct comparison to both Affymetrix exon arrays and custom NimbleGen splicing microarrays.

        Comment


        • #5
          Hi!
          In lack of more cDNA I only have 12 genes from qPCR.. I want to compare edgeR vs DESeq2 vs Cuffdiff and see which I will use based on match with qPCR:

          YES/no indicates if it is significantly changed.

          Gene qPCR edgeR DESeq2 Cuffdiff
          1 no YES no no
          2 YES YES no no
          3 no no no no
          4 YES YES no no
          5 YES no no no
          6 no no no no
          7 no no no no
          8 no no no no
          9 no no no no
          10 no no no no
          11 no no no no
          12 no no no no

          I really want to use edgeR, but is this test good enought?

          Comment


          • #6
            I'm not sure why you tested 8 of those since they weren't DE according to any of the programs (I assume #5 was either borderline or had a huge foldchange). Given your effective n=3 of informative genes, edgeR would seem to be in the lead. However, you haven't tested any that DESeq2 or cuffdiff uniquely called DE. BTW, making more cDNA doesn't even take an hour...

            Comment


            • #7
              Yeah, actually this genes where already measured, thats why I used them, I got the message about not having cDNA, but Ill ask again tomorrow!

              How many should I aim to test from each?

              Thanks!

              Comment

              Latest Articles

              Collapse

              • seqadmin
                Advancing Precision Medicine for Rare Diseases in Children
                by seqadmin




                Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
                12-16-2024, 07:57 AM
              • seqadmin
                Recent Advances in Sequencing Technologies
                by seqadmin



                Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

                Long-Read Sequencing
                Long-read sequencing has seen remarkable advancements,...
                12-02-2024, 01:49 PM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by seqadmin, 12-17-2024, 10:28 AM
              0 responses
              33 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 12-13-2024, 08:24 AM
              0 responses
              49 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 12-12-2024, 07:41 AM
              0 responses
              34 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 12-11-2024, 07:45 AM
              0 responses
              46 views
              0 likes
              Last Post seqadmin  
              Working...
              X