Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • chariko
    Member
    • Jun 2010
    • 56

    #1

    RnaSeq vs Microarray correlation

    Hi all,

    I have an experiment with 80 samples both of them run with microarray and RnaSeq. I want to correlate the results between the two technologies.

    I received the results from the RnaSeq experiment in two ways:

    a) Raw data (fastq files)
    b)Table of ensembl id´s counts (no idea how this analysis was done).

    I did the analysis in two ways:

    1)
    For the RnaSeq experiment I took the ensembl id´s counts, translated them into Gene Symbol identifiers (various ensembl Id`s derived in the same Gene Symbol so I just used one of them randomly selected and the other ensembl id´s were discarded), and normalized them with voom (log2 with some modifications).

    For the Microarray experiment I normalized them (RMA) using a curated database (hgu133plus2hsentrezgcdf). I translated the entrez id´s probes into Gene Symbol identifiers.

    I did the correlation between microarray and RnaSeq (cor.test, two sides, spearman method)) and I obtained good results for all the samples (07-0.9). Attached figure 1 with the scatterplot of sample 1.

    2)
    I took the fastq files and analyzed them taking into account the HG19 GRC 37 RefSeq as reference. I translated the refseq id´s into gene symbol. I randomly selected one gene symbol per refseq id.

    Same microarray data was used for the correlation.

    I did the same correlatin as before but the results were worse (0.3-48). Figure 2 shows scatterplot of sample 1.

    My question is, does anybody have a clue about why starting with refseq id´s is not giving the same good results? Any clues?

    Thanks in advance.
    Attached Files

Latest Articles

Collapse

  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    by SEQadmin2



    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
    ...
    10-14-2026, 09:55 AM
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    by SEQadmin2


    Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

    We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
23 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
20 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Working...