“…Key methods include micropipette aspiration [10, 11], atomic force microscopy [12, 13], optical tweezers [14-16], diffraction phase microscopy [17-19], and magnetic twisting cytometry [20]. Although these techniques have varying levels of force and displacement resolutions for probing cellular and subcellular components in living cells, they often suffer from low throughput, cumbersome experimental set-up and data interpretation, limited portability, and/or applicability only to specific testing and geometry conditions [3-5, 21]. Microfluidic platforms for assessing cell biorheology, on the other hand, offer the means to probe large cell populations in high throughput [22-25], but are often limited in their flexibility to quantitatively determine specific cell mechanical properties using label-free methods(i.e., methods without using any biochemical or immunological tagging techniques).…”