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Sequence traces were analysed using SEQUENCHER software.
Sequence traces were analysed using NovoSNP (Weckx et al, 2005).
All sequence traces were analysed using Sequencher® 4.10 (Gene Codes Corporation).
Resuspended products were analysed using a DNA analyzer 3730xl (Applied Biosystems) and the resulting sequence traces were analysed using Sequence Analysis 5.2.2 (Applied Biosystems).
Sequencing traces were analysed using Sequencher software (GeneCodes Corporation, Ann Arbor, MI, USA), and multiple sequences aligned to aid mutation detection.
All electronically stored traces were analysed using Spike II software (Cambridge Electronic Design) according to previously documented criteria of a stable baseline and triangular MAP morphology, rapid upstroke phase and a consistent amplitude (Knollmann et al. 2001).
Similar(50)
DNA structures were analysed using 3DNA26.
Group differences were analysed using repeated measures ANOVAs.
Results from the four SST variants were analysed using response times (RTs) and accuracy measures.
The quantification results were analysed using 7300 SDS v1.3.1 Software (Applied Biosystems).
Images were analysed using Volocity®V5.3.2, ZEN software (Zeiss) and Leica LCS Confocal software.
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