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EIT scans were generated using the weighted backprojection reconstruction procedure along equipotential lines [ 7].
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The block diagram of the simulated signal generator is represented in Figure 5. Several signals (A-scans) were generated using this model.
All arrays were scanned and the corresponding CEL files were generated using the Affymetrix® GeneChip® Genotyping Analysis Software Version 4.0 [ 18].
The models were generated using skull CT scan data.
Spatial patterns of risk, disease clusters and cold and hot spots were generated using a spatial scan statistic and a Getis-Ord Gi* statistic.
The data shown in Figure 1 were generated using the mismatch scanning array.
A GenePix 4000B scanner (Axon Instruments, Union City, CA, USA) was used to scan individual chips and median spot intensities were generated using GenePix 4.0 (Axon Instruments).
Whole mount images of fly wings were generated using the Zeiss Mirax Scan digital imaging platform.
Following scanning, non-scaled RNA signal intensity files (.cel) were generated using the Command Console software (Affymetrix).
Microarrays were scanned using a ScanArray 5000 (Perkin Elmer) and signal intensity files were generated using NimbleScan software.
Transgenic mice were generated using standard procedures.
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