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Once detected, the OP must be analysed on both axial and coronal oblique planes.
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The effects were analysed on both arms combined to test for potential treatment interactions and in each arm separately (for listing of parameters into the different models, see Supporting Information Table S3).
Sequences were analysed on both strands for common cis-regulatory elements of length 8 – 12 bp.
In this way, the data from all patients included in this study were analysed on both systems.
To evaluate the pattern of amplification, aRNA samples of all five cell lines were analysed on both denaturing agarose gels and the Agilent Bioanalyzer.
The primary end point was ORR as assessed by external independent review, which was analysed on both an intention-to-treat (ITT, all eligible patients who were randomly assigned) and per-protocol (PP, treated patients eligible and assessable for response without major protocol violations) basis.
The Sox1 GFP population profiles gained in each condition have been analysed on multiple occasions and are both reproducible and stable.
The outcome of both groups are analysed on the basis of the 'intention to treat' principle.
Both proteins were analysed on Western blots and quantified separately by densitometry.
Non polar fractions were analysed on HPLC.
All variables were analysed on logarithmic scales.
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