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高通量筛选中标准差的分布。

The Distribution of Standard Deviations Applied to High Throughput Screening.

机构信息

School of Science and Technology, Nottingham Trent University Clifton Lane, Nottingham, NG11 8NS, United Kingdom.

出版信息

Sci Rep. 2019 Feb 4;9(1):1268. doi: 10.1038/s41598-018-36722-4.

Abstract

High throughput screening (HTS) assesses compound libraries for "activity" using target assays. A subset of HTS data contains a large number of sample measurements replicated a small number of times providing an opportunity to introduce the distribution of standard deviations (DSD). Applying the DSD to some HTS data sets revealed signs of bias in some of the data and discovered a sub-population of compounds exhibiting high variability which may be difficult to screen. In the data examined, 21% of 1189 such compounds were pan-assay interference compounds. This proportion reached 57% for the most closely related compounds within the sub-population. Using the DSD, large HTS data sets can be modelled in many cases as two distributions: a large group of nearly normally distributed "inactive" compounds and a residual distribution of "active" compounds. The latter were not normally distributed, overlapped inactive distributions - on both sides -, and were larger than typically assumed. As such, a large number of compounds are being misclassified as "inactive" or are invisible to current methods which could become the next generation of drugs. Although applied here to HTS, it is applicable to data sets with a large number of samples measured a small number of times.

摘要

高通量筛选 (HTS) 使用靶标测定法评估化合物文库的“活性”。HTS 数据的一部分包含大量样本测量值,这些测量值的复制次数很少,这为标准偏差分布 (DSD) 的引入提供了机会。将 DSD 应用于一些 HTS 数据集揭示了一些数据中存在偏差的迹象,并发现了具有高变异性的化合物亚群,这些化合物可能难以筛选。在所检查的数据中,1189 种此类化合物中有 21%是泛分析干扰化合物。在亚群中最相关的化合物中,这一比例达到了 57%。在许多情况下,使用 DSD 可以将大型 HTS 数据集建模为两个分布:一大组几乎呈正态分布的“非活性”化合物和一个“活性”化合物的剩余分布。后者不是正态分布的,与活性分布重叠 - 在两侧 - 并且比通常假设的要大。因此,大量化合物被错误地归类为“非活性”或当前方法无法检测到,这些化合物可能成为下一代药物。虽然这里应用于 HTS,但它也适用于样本数量很少但复制次数很多的数据集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d3/6361996/cd88f2b6db87/41598_2018_36722_Fig1_HTML.jpg

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