Instead, the bounds of uncertain microphone mismatches [16, 17] or the limited knowledge of mean and variance of microphone mismatches [18] may be practically available to a designer.
When limited knowledge of mean and variance of microphone mismatches is available to a designer, the robust FSBB design approach based on the worst-case mean performance (WCMP) optimization with the passband response variance (PRV) constraint is developed.
When limited knowledge of mean and variance of microphone mismatches is available, a robust FSBB design approach based on the worst-case mean performance optimization with the passband response variance (PRV) constraint is devised.
In Section 4, we develop the robust FSBB design using the WCMP optimization with the PRV constraint, when the limited knowledge of mean and variance of microphone mismatches is available.
When the limited knowledge of mean and variance of microphone mismatches is available, the robust FSBB design approach based on the WCMP optimization with the PRV constraint has been presented.
To enhance the robustness of the FSBB, i.e., to improve its stability of passband response and hence to reduce target signal distortion, we hereby consider to incorporate the PRV constraint into the design procedures by using the bounded variances of microphone mismatches.
EEG: Electroencephalogram; EPN: Early posterior negativity; ERP: Event-related potentials; MANOVA: Multivariate analyses of variance; MMN: Mismatch negativity; vMMN: Visual mismatch negativity.
This estimate of the contribution of mismatches to the variance of log2 signal ratios is likely to be an underestimate due to the large numbers of unknown mismatches; less than 50% of SNP are included in the Perlegen dataset and indels are very poorly represented and were not incorporated in our study [ 14].
It should be emphasized that the small contributions of mismatch position and mismatch type to the variance in signal ratio does not mean that these effects are insignificant.
ARLEQUIN version 3.5.1.3 [ 60] was used for the calculation of mismatch distributions, molecular diversity indices, and analyses of molecular variance (AMOVA) with entire control region sequences (16024 576) excluding C-insertions on positions 16193, 309, 315 and 573.
