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Non-parametric Quality Assessment of High-Content Screening Assays

机译:高含量筛选测定的非参数评估

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Quality control is a key component of high-content screening for novel drug discovery endeavors and phenotype-genotype mapping. Current methods such Z-factor and strictly standardized mean difference (SSMD) rely on a normal distribution assumption with control data. Unfortunately, this assumption often times is not accurate, leading to low quality scores on viable biological assessments (bioassays). This can result in lost resources, increased cost and wasted time in attempting to optimize a bioassay. We propose a novel non-parametric approach that is robust to noise and is capable of assessing the quality of bioassays where the control data may not follow a Gaussian distribution. We demonstrate that our method produces accurate results when assessing the quality of real-world siRNA and small-molecule screens. We test the proposed quality score on synthetic data using different distributions and demonstrate that our method provides a more accurate assessment of data separation on non-Gaussian datasets as well.
机译:质量控制是新型药物发现的高含量筛选的关键组成部分和表型基因型测绘。目前方法如这种Z因子和严格标准化的平均差异(SSMD)依赖于对照数据的正态分布假设。不幸的是,这种假设通常是不准确的,导致可行的生物评估(生物测定)上的低质量评分。这可能导致资源丢失,增加成本和浪费时间,以便优化生物测定。我们提出了一种新颖的非参数方法,其具有稳健的噪声,并且能够评估控制数据可能不遵循高斯分布的生物测量的质量。我们证明我们的方法在评估现实世界siRNA和小分子屏幕的质量时产生准确的结果。我们使用不同的分布测试合成数据的提出质量分数,并证明我们的方法也在提供了对非高斯数据集上的数据分离进行了更准确的评估。

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