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. 2017 Sep 7;19(4):81. doi: 10.1007/s10544-017-0222-z

Fig. 2.

Fig. 2

Image analysis workflow including: segmentation (identification of objects, measurements and tracking) in multiple frames from different microfluidic chambers at different time points; assembly of data in tables including measurements for cells at different time points and gradient intensity profiles; and final merge of the data into graphs representing cell morphology measurements as a function of Cytochalasin D concentration