Hello, all:
I've performed an initial analysis, which contains all of the data except for Rice replicate #1 (which appears to have only partially uploaded).
For all of the significant fluorescence samples, the geo.std. of group means for the three matched groups is only:
(MG, SG, MR, SR) = 1.3088 2.6344 1.1969 1.1459
when Rice's unmatched flow cytometer is added, these go up to:
1.4765 2.3276 1.4137 1.3791
Meanwhile, the standard deviation between replicates within each group is:
Stanford: 1.1771 1.3559 1.0497 1.0893
Gaitherburg: 1.1854 3.0373 1.1159 1.1247
MIT: 1.0984 2.3766 1.1726 1.1092
Rice: 1.0656 2.0192 1.1000 1.0621
Key takeaways:
1. SG should be discarded as a failed sample: it is all over the place because it contains a mixed population with many non-fluorescing cells. See attached "SG-debug" comparing 3 Gaithersburg samples.
2. The precision that we are seeing is significantly better than our target: we aimed for 1.5x - 2.0x, and got 1.15x - 1.31x
3. For the most part, inter-group precision is only barely worse than the worst intra-group precision.
Bottom line: as hypothesized, beads appear to be work excellently for comparison, even if we don't exactly know what their units mean!
I look forward to detailed discussion this afternoon, including of the path forward from here.
Thanks,
-Jake