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The highest sensitivities for all the primers tested were determined using DNA extracted from whole blood samples, while the lowest sensitivities were obtained when DNA was extracted from filter paper preparations.
Significant differences between EC50 values between compounds tested were determined using Student's t tests.
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Linkage disequilibrium among SNPs tested was determined using the Haploview program [ 26].
Error bars represent standard error as indicated and significance in differences between arrays of data tested was determined using two-tailed Student T test (Microsoft Excel).
Subsequently, assuming that a given amount of TD recording resources was available, the number of possible sires that could be tested was determined using equation (13).
Error bars represent S.D. as indicated and significance in differences between arrays of data tested was determined using two-tailed Student t-test (MicroStudent t-test
Analysis of variance by Duncan's test and Pearson's product-moment correlation coefficient test were determined using SPSS version 10.0 software (SPSS Institute, Inc., Chicago, IL, USA).
Significance levels (P values of t-tests) were determined using InStat Software GraphPad Softwaree).
Independent factors associated with recent HIV testing were determined using logistic regression.
Optimal conditions for clinical chemosensitivity testing were determined using established SCLC lines.
All spectrophotometric tests were determined using an UV-visible spectrophotometer (Shimadzu, Columbia, MD, USA).
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