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A staining intensity index was used, defined as the product of staining intensity (0-3) and proportion of immunoreactive cells (less than 10% = 1, 10-50% = 2, more than 50% = 3).
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The Cufflinks program [41] was used define transcribed regions using the SAM mapping file as the input.
As common utility metric the mean opinion score is used, defined by the vector (11).
In original paper, modal superposition method was used as defined.
As detailed above, the classification of "unhealthy" that was used was defined conservatively.
Consensus was used to define the final set of triggers.
Dollo parsimony was used to define intron gains, whereas standard parsimony was used to define intron losses.
The cutpoint of ≥3200 cpm 16 was used to define MVPA and <1100 cpm 17 was used to define SB.
AES was used to define concentration profiles.
A mathematical model was used to define synchronizability criteria.
Molecular modeling was used to define chiral recognition by FPR2.
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