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Post-test calculations were performed using a version of SCDAP/RELAP5/MOD3.2.

First, single-marker analyses were performed using a version of principal component analysis, which is designed for allelic frequencies (%PCA).

Detection of microsatellite and SNP outlier loci was performed using a version of DFDIST modified by r.

In addition, a test for endogeneity of the insurance variable is performed using a version of the Durbin-Wu-Hausman class of tests for endogeneity [ 21].

Quantifications were performed by comparisons with known amounts of standard Starch extraction was performed using a version of the method of Klein and Betz [ 17].

All blending evaluations were performed using a version of the BLUPF90 program [ 24] modified to implement the equations (1), (3) and (4).

Statistical analysis was performed using a trial version of GraphPad InStat version 3.1.

The cells were sorted in a FACScalibur flow cytometer (BD, USA) using CellQuest Pro software (Becton Dickinson, USA) and a quantitative analysis of the cell cycle distribution was performed using a trial version of the ModFit LT software, version 4.0.

This analysis was performed using a modified version of the SSPACE Premium scaffolder version 2.3 [ 80].

All ligand-based VS experiments were performed using a modified version of the Directory of Useful Decoys (DUD) Release 2 [53] 53].

Searches for and the identification of peptides were performed using a licensed version of MASCOT software (Matrix Science) with a peptide tolerance of 50 ppm.