Hello,
I am working with the Biomark HD Fluidigm high throughput qPCR transcriptomics datasets (consists of 240 target genes and 8 housekeeping genes). The dataset consists of 250 samples processed in 5 different batches (50 samples/batch). Dataset of each batch was normalized to calculate Delta Ct
(Difference between the Target gene and Geometric mean of 8 housekeeping gene (i.e GM_HKgs)). Then, transformed to - Delta Ct
(negative delta Ct) because we want to apply downstream analyses like ANOVA to log-scale normalized relative expression values, as just using -1 * Delta Ct
as readout is quite valid too. I understand from various posts removebatcheffects
(limma
package) would be best to use. My question is what data type should be used as input, Delta Ct or Negative Delta Ct (-1*Delta Ct).
Hi Gordon Smyth Thank you for the inputs and suggestions. I will also try to run the limma DE for the qPCR Ct values and benchmark the data.
Meanwhile, if I would like to use
removeBatchEffect
for continuity of the qPCR data analysis. Can I still use the same? Additionally, the resultant matrix (y2) generated from this function could be used for further downstream analysis like t-test/ANOVA/plots or just utilized only for the visualization purposes like PCA and Heatmap?I'm not sure what you mean by "continuity". I recommend that
removeBatchEffect
only be used for visualization, as is said on the help page for that function.Hi Gordon Smyth Noted. I will use
removeBatchEffect
on my Negative Delta Ct values for the visualization only. Thank you very much.