Creates a realistic synthetic cell-culture microscopy data set for
demonstration and testing. The simulated experiment has six
treatment groups, four replicates per group and 96 wells in total.
Four fluorescence channels are generated: a nuclear stain (DAPI),
a damage marker (marker_1), a viability marker (marker_2) and a
secondary readout (marker_3).
Examples
exp <- cr_example_experiment(seed = 1, n_cells_per_well = 20)
print(exp)
#> ── cr_experiment ───────────────────────────────────────────────────────────────
#> • Cells: 1961 across 96 wells
#> • Channels: "DAPI", "marker_1", "marker_2", and "marker_3"
#> • Design: 6 treatment groups
#> • QC steps applied: 0
#> ℹ Metadata fields: project and sop