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. 2011 May 25;2(6):1717–1726. doi: 10.1364/BOE.2.001717

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©2011 Optical Society of America

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

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Fig. 2 — Typical pairs of measured diffraction images (1) and intensified GLCM images (2) of single flowing cells acquired at λ = 532nm: (a1/a2) Jurkat; (b1/b2) NALM-6; (c1/c2) U937; (d1/d2) MCF-7; (e1/e2) B16F10; (f1/f2) TRAMP-C1. The GLCM images are placed to the right of the diffraction images respectively. The scale bar on the left indicates the pixel values of the normalized diffraction images after conversion to 8-bit pixel values and the one on the right indicates the values of GLCM elements with p_max = (a2) 0.0172; (b2) 0.0204; (c2) 0.0160; (d2) 0.00302; (e2) 0.00175; (f2) 0.00297.