Hi all,
I am analysing relative RT-PCR data. The mean normalized relative quantities of the various genes for each sample analysed, as well as the corresponding standard errors, are best calculated using a simple spreadsheet due to the complexity of the calculations (see for ex. The Plant Cell 2009;21:1031-3 for details).
As such, I end up with a table of relative quantities and standard errors for each gene/sample.
As suggested in the literature, it is appropriate to perform an ANOVA for differences between samples / groups of samples.
The question is: how to perform an ANOVA (or any other statistical test) in STATA by feeding only means and SE's, instead of the whole dataset of observations, as is needed to do when, like in this case, the calculations for means and SE are done outside of STATA?
Thanks in advance,
I am analysing relative RT-PCR data. The mean normalized relative quantities of the various genes for each sample analysed, as well as the corresponding standard errors, are best calculated using a simple spreadsheet due to the complexity of the calculations (see for ex. The Plant Cell 2009;21:1031-3 for details).
As such, I end up with a table of relative quantities and standard errors for each gene/sample.
As suggested in the literature, it is appropriate to perform an ANOVA for differences between samples / groups of samples.
The question is: how to perform an ANOVA (or any other statistical test) in STATA by feeding only means and SE's, instead of the whole dataset of observations, as is needed to do when, like in this case, the calculations for means and SE are done outside of STATA?
Thanks in advance,
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