Logical Experimental Design and Execution in the Biomedical Sciences

Q2 Pharmacology, Toxicology and Pharmaceutics
Daniel J. Holder, Michael J. Marino
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引用次数: 6

Abstract

Lack of reproducibility has been highlighted as a significant problem in biomedical research. The present unit is devoted to describing ways to help ensure that research findings can be replicated by others, with a focus on the design and execution of laboratory experiments. Essential components for this include clearly defining the question being asked, using available information or information from pilot studies to aid in the design the experiment, and choosing manipulations under a logical framework based on Mill's “methods of knowing” to build confidence in putative causal links. Final experimental design requires systematic attention to detail, including the choice of controls, sample selection, blinding to avoid bias, and the use of power analysis to determine the sample size. Execution of the experiment is done with care to ensure that the independent variables are controlled and the measurements of the dependent variables are accurate. While there are always differences among laboratories with respect to technical expertise, equipment, and suppliers, execution of the steps itemized in this unit will ensure well-designed and well-executed experiments to answer any question in biomedical research. © 2017 by John Wiley & Sons, Inc.

生物医学科学中的逻辑实验设计与执行
缺乏可重复性已成为生物医学研究中的一个重要问题。本单元致力于描述有助于确保研究成果可以被其他人复制的方法,重点是实验室实验的设计和执行。这一过程的基本组成部分包括明确定义要问的问题,利用现有信息或来自试点研究的信息来帮助设计实验,并在基于密尔“认知方法”的逻辑框架下选择操作,以建立对假定因果关系的信心。最终的实验设计需要系统地关注细节,包括选择对照、样本选择、盲法避免偏倚,以及使用功率分析来确定样本量。实验的执行是谨慎的,以确保自变量得到控制,因变量的测量是准确的。虽然实验室之间在技术专长、设备和供应商方面总是存在差异,但执行本单元列出的步骤将确保设计良好、执行良好的实验,以回答生物医学研究中的任何问题。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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