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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Group Sequential Methods and Sample Size Savings in Biomarker-Disease Association Studies
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Group Sequential Methods and Sample Size Savings in Biomarker-Disease Association Studies

机译:生物标志物-疾病关联研究中的组序贯方法和样本量节省

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摘要

Molecular epidemiological association studies use valuable biosamples and incur costs. Statistical methods for early genotyping termination may conserve biosamples and costs. Group sequential methods (GSM) allow early termination of studies on the basis of interim comparisons. Simulation studies evaluated the application of GSM using data from a case-control study of GST genotypes and prostate cancer. Group sequential boundaries (GSB) were defined in the EAST-2000 software and were evaluated for study termination when early evidence suggested that the null hypothesis of no association between genotype and disease was unlikely to be rejected. Early termination of GSTM1 genotyping, which demonstrated no association with prostate cancer, occurred in 90% of the simulated studies. On average, 36.4% of biosamples were saved from unnecessary genotyping. In contrast, for GSTT1 , which demonstrated a positive association, inappropriate termination occurred in only 6.6%. GSM may provide significant cost and sample savings in molecular epidemiology studies.
机译:分子流行病学关联研究使用有价值的生物样本并产生费用。早期基因分型终止的统计方法可以节省生物样本和成本。团体顺序法(GSM)允许在中期比较的基础上尽早终止研究。模拟研究使用GST基因型和前列腺癌病例对照研究的数据评估了GSM的应用。当早期证据表明基因型与疾病之间没有关联的无效假设不太可能被拒绝时,在EAST-2000软件中定义了组序边界(GSB),并评估了该序列是否终止研究。超过90%的模拟研究中发生了GSTM1基因型的早期终止,这表明与前列腺癌无关。平均而言,从不必要的基因分型中节省了36.4%的生物样品。相反,对于表现出正关联的GSTT1,仅6.6%发生了不适当的终止。 GSM在分子流行病学研究中可能会节省大量成本并节省样本。

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