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In our measurements, we maintained the magnetic field constant at 19 T.
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To perform such measurements, we first maintain (P_text{{u}}) is at a constant pressure of 0.2 MPa using a gas bottle for at least 1 h; this allows for complete pore fluid saturation of the sample.
Reliability was good during hospital measurements and was maintained when we conducted follow-up assessments in the home.
In order to establish an assay which would allow the effective measurement of fluorescence of epithelial and mesenchymal markers, we first determined the confocal settings in the range of which linearity of fluorescent measurements is maintained.
Measurements are maintained in the switches and are asynchronously sent to a SDN controller.
The water saturated state of the sample is controlled using permeability measurements and maintained throughout the experiment.
The temperature during the measurements was maintained at approximately 302 K (84°F), leading to the -176.8 dBm/Hz expected value for the two-sided PSD of the thermal noise.
The flow rate of HBS-EP buffer during all measurements was maintained at 10 μl/min.
The sample temperature for all CD measurements was maintained at 293 K. Sedimentation velocity analyses were conducted using a Beckman Optima XL-I analytical ultracentrifuge in the University of Massachusetts Medical School Ultracentrifuge Facility.
Repeated measurements showed maintained mean Hb levels of 11.3 g/dL (95% CI: 11.3 11.4) for the restrictive transfusion group and 12.2 g/dL (95% CI: 12.2 12.3) for the liberal group.
In addition, the complete separation between trisomy 18 and euploid measurements achievable with the original measurements was not maintained after repeat masking (see Supplementary Figure S3 online).
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