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All divergence analyses were calibrated by placing calibration priors on nine nodes in the phylogeny (see Additional file 3).

Both the ionization chamber and the electrometer were calibrated by Accredited Dosimetry Calibration Laboratory (ADCL) at the University of Wisconsin.

All assays were calibrated by use of Dade Dimension human calibrator (Dade Behring Inc, Newark, USA).

The growth rates were calibrated by RHEED specular spot oscillations.

Doping levels were calibrated by Hall measurements with separate samples.

The predictive equations were calibrated by using the literature database.

Binding energies were calibrated by using the containment carbon (C1s = 284.6 eV).

The spring constants of the cantilevers were calibrated by the thermal tune method [21].

Simple models with several descriptors for different subsets were calibrated by multilinear regression (MLR).

The mass flow controllers for SiH4 and CO2 were calibrated by N2.

The charge effects were calibrated by setting the C 1-s photoemission at 284.6 eV.