Closed shntnu closed 4 years ago
In https://github.com/broadinstitute/cmQTL/issues/47#issuecomment-687181206 @jatinarora-upmc asked:
@gwaygenomics @bethac07 @shntnu just following up on cell health readouts, was it feasible to align the features?
We did not embark down this path yet. Legacy CellProfiler datasets lose value if we are unable to align features between CellProfiler versions. We need to do this in a systematic way so that past and future datasets can be interoperable. The Cell Health dataset and LINCS dataset are two major examples.
The cmQTL dataset is another great example demonstrating the need for interoperable CellProfiler features. Because we are analyzing the CellProfiler features like we would individual genes, we need to make sure that the feature measurements retain biological signal across CellProfiler versions.
Another critical point (the other side of the same coin) is that to increase value of CellProfiler features, we need to make sure that we optimize their internal sensitivity within
Let's reopen if we decide to pursue this again
Being addressed here https://github.com/broadinstitute/cmQTL/pull/51
Discussion context: https://github.com/broadinstitute/cmQTL/issues/47#issuecomment-661617001