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All p values reported were obtained using two-sided tests of statistical significance.

The segregation data of two RAPD markers ('OPB' markers) and one STS marker ('SICAS'), which were not previously reported, were obtained using the HR × R130 mapping population.

All results reported were obtained using a commercially available plastic tip (part no 1004763, Advion Inc., Itacha, NY), with a syringe needle acting as an inner electrode, E1.

The one exception was F1023, where the intensity of the cascade blue labelling did not allow accurate cell counts to be made under brightfield illumination and so the values reported were obtained using fluorescence microscopy.

The results reported were obtained using a plane wave cutoff energy of 780 eV and a Monkhorst Pack Brillouin zone sampling grid of spacing 2π × 0.07 Å–1; the required force tolerance for a successful geometry optimization in each run was 0.05 eV Å 1 (section 2.2 of the Supporting Information).

Second, figures in previous report were obtained using non-confluent ME180 cells, whereas adhesion ratios reported here were obtained with cells at higher densities (sub-confluent).

Raw probe intensities (x, y and signal reports) were obtained using NimbleScan software (v2.4, Roche NimbleGen, Inc).

The results presented throughout this report were obtained using a ROI seed radius of 5 mm for each seed-based correlation map (i.e., each instance of neighbor identification).

En-face images with a size of 1.5 : 1 in width over height in this report are obtained using suitable amplitudes for the voltages applied to the X and Y-galvoscanners.

The peptide fiber widths reported herein were obtained using the deconvolution method reported by Fung et al [30].

Since most of the reported results were obtained using synchrotron radiation, a brief description of the European Synchrotron Radiation Facility ESRFF) is presented, followed by a description of the two techniques.