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Our initial analyses were performed to assess the selectivity and sensitivity of our protocol and focused on an early time point (5 minutes), which would presumably reveal strong responses and be less influenced by pathway cross-talk.
Initial analyses were performed using descriptive statistics.
Initial analyses were performed without discounting.
Initial analyses were performed using SDS software (Applied Biosystems).
Initial analyses were performed on the cell line DNAs from the two individuals.
Labeling, hybridization and initial analyses were performed at MOGENE LC, St . Louis MO, USA.
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Initial sequence analyses were performed by Fasteris SA, Switzerland.
Initial data analyses were performed using the pedstats and QTDT software including gender as a covariate.
Initial image analyses were performed using Zeiss LSM Image Browser software, and later Adobe Photoshop was used to adjust image brightness and generate overlays.
Initial STRUCTURE analyses were performed under assumptions of different numbers of population groups (K) ranging from two to twelve (K = 2 to K = 12) without any pre-assignment of population affiliation.
Initial data analyses were performed and statistical tests were conducted to assess the susceptibility of each SNP marker [ 25].
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