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Post-Hybridization Quality Measures for Oligos in Genome-Wide Microarray Experiments

机译:基因组全基因芯片实验中寡核苷酸的杂交后质量检测

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High-throughput microarray experiments produce vast amounts of data. Quality control methods for every step of such experiments are essential to ensure a high biological significance of the conclusions drawn from the data. This issue has been addressed for most steps of the typical microarray pipeline, but the quality of the oligonu-cleotide probes designed for microarrays has only been evaluated based on their a priori properties, such as sequence length or melting temperature predictions. We introduce new oligo quality measures that can be calculated using expression values collected in direct as well as indirect design experiments. Based on these measures, we propose combined oligo quality scores as a tool for assessing probe quality, optimizing array designs and data normalization strategies. We use simulated as well as biological data sets to evaluate these new quality scores. We show that the presented quality scores reliably identify high-quality probes. The set of best-quality probes converges with increasing number of arrays used for the calculation and the measures are robust with respect to the chosen normalization method.
机译:高通量微阵列实验可产生大量数据。对于此类实验的每个步骤,质量控制方法对于确保从数据得出的结论具有很高的生物学意义至关重要。这个问题已经在典型的微阵列流水线的大多数步骤中得到解决,但是为微阵列设计的寡核苷酸探针的质量仅基于其先验特性(例如序列长度或熔解温度预测)进行了评估。我们介绍了新的寡核苷酸质量测量方法,可以使用在直接和间接设计实验中收集的表达值来计算。基于这些措施,我们提出了组合的寡核苷酸质量评分作为评估探针质量,优化阵列设计和数据归一化策略的工具。我们使用模拟数据集和生物学数据集来评估这些新的质量得分。我们表明,提出的质量得分可以可靠地识别出高质量的探针。最佳质量的探针集会随着用于计算的阵列数量的增加而收敛,并且相对于所选的归一化方法,这些措施是可靠的。

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