
for example, here is an experiment i've made on three different days of the week. even though isolated analysis show no crossing bars between groups (therefore showing some significance), the effect size observed on each experiment is different, and when I analyze the whole data I end up losing the effect. How can I get the best approach to this situation?
Some extra information for context:
- The experiment in question uses "technical replicates" and each bar on the graph shows all data from that day's triplicate.
- Flow cytometry uses High-troughput analysis and measures mean population fluorescence. Each observation is merely the median from the distribution of all cells in that cell plate.
- Given the criteria from homogeneity and normality met, the experiment in question would use an ANOVA.
- I am well aware that non-paramatric analysis can be a solution. However, I would like to check for every possibility that doesn't rank or normalize the data.
Thanks in advance!