Setting
A cell biology lab at a major Scandinavian research university, running longitudinal imaging studies on 3 different ZEISS and Leica confocal systems across two facilities.
The lab's multi-site study was generating inconsistent fluorescence intensity measurements across instruments — making it impossible to pool data from different imaging sessions without manual rescaling.
Cross-instrument CV reduced from ~37% to <7% after Cytely standardization. Data pooled from 3 systems without manual correction.