对活力数据和相关细胞功能曲线进行归一化。

ALTEX Pub Date : 2018-01-01 DOI:10.14573/1803231
Alice Krebs, Johanna Nyffeler, Jörg Rahnenführer, Marcel Leist
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引用次数: 20

摘要

细胞生物学、药理学和毒理学中许多类型的测定产生的数据是在参考系统(阴性对照)中测量参数,然后在压力增加或药物暴露的条件下测量参数。为了使这些数据易于比较,它们被归一化,即,系统的初始值(例如,生存能力或传输函数)被设置为100%,并且所有数据都相对于该值表示。然后,通过数据点拟合曲线,确定系统行为的汇总数据。为此,给出基准响应(BMR)(例如,曲线下降15%或50%),并确定相应的基准浓度(BMC15或BMC50)。特别是对于低bmr,该过程不是很健壮,并且经常导致不正确的汇总数据。为了使数据适合于曲线拟合,第二次归一化(再归一化)是必要的,这一点经常被忽视。这也经常被忽视,这需要了解系统在非常低的应力条件下的行为。在这里,为再归一化过程提供了良好的体外实践指导,以便生成和呈现更高保真度的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Normalization of data for viability and relative cell function curves.

Many types of assays in cell biology, pharmacology and toxicology generate data in which a parameter is measured in a reference system (negative control) and then also under conditions of increasing stress or drug exposure. To make such data easily comparable, they are normalized, i.e., the initial value of the system (e.g., viability or transport function) is set to 100%, and all data are indicated relative to this value. Then, curves are fitted through the data points and summary data of the system behavior are determined. For this, a benchmark response (BMR) is given (e.g., a curve drop by 15 or 50%), and the corresponding benchmark concentration (BMC15 or BMC50) is determined. Especially for low BMRs, this procedure is not very robust and often results in incorrect summary data. It is often neglected that a second normalization (re-normalization) is necessary to make the data suitable for curve fitting. It is also frequently overlooked that this requires knowledge of the system behavior at very low stress conditions. Here, good in vitro practice guidance for the re-normalization procedure is provided so that data of higher fidelity can be generated and presented.

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