稀释系列实验中粒子数的估计

Yajie Duan, C. Lin, D. Sargsyan, Javier Cabrera, Christine M Livingston, R. Vogel, J. Sendecki, W. Talloen, H. Geys, Surya Mohanty
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引用次数: 0

摘要

一个多世纪以来,样品(细菌细胞或病毒颗粒)中微生物浓度的估计一直是生物医学实验的焦点。在免疫学、病毒学和制药工业中,样品的连续稀释常用于估计靶浓度。一种新的方法,称为联合似然估计(JLE),提出了估计粒子,如微生物的数量,从计数获得的连续稀释样品。该模型计算来自整个单一稀释系列的数据,而不是仅使用特定稀释度。理论框架以二项分布和泊松分布为基础,与实际实验过程相吻合。目标浓度的估计是通过MLE与观测计数的联合似然函数(包括右截距值)得到的。仿真结果表明,与现有方法相比,该方法显著提高了估算的精密度和准确度。它可以应用于具有类似实验设计的各种研究,特别是当整齐样品中的颗粒数量非常大时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Particle count estimation in dilution series experiments
Estimation of microorganism concentration in samples (bacterial cells or viral particles) has been a focal point in biomedical experiments for more than a century. Serial dilution of the samples is often used to estimate the target concentrations in immunology, virology, and pharmaceutical industry. A new methodology, called joint likelihood estimation (JLE), is proposed to estimate particles such as the number of microorganisms in a sample from counts obtained by serially diluting the sample. It models count data from the entire single dilution series rather than using only specific dilutions. The theoretical framework is based on the binomial and the Poisson distributions and is consistent with the actual experimental process. The estimator of the target concentration is obtained by MLE with derived joint likelihood functions of the observed counts including right‐censored values. Simulations demonstrated that the new JLE method significantly increases precision and accuracy of the estimate compared to the existing methods. It can be applied to a variety of studies with similar experimental designs, especially when the number of particles in the neat sample is very large.
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