A Classification-based Quantitative Approach for SILAC Data

Seongho Kim, Joohyoung Lee
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Abstract

A practical and powerful approach for stable isotope labeling is stable isotope labeling by amino acids in cell culture (SILAC). A key advantage of SILAC is the ability to detecting simultaneously the isotopically labeled peptides in a single instrument run and so guarantees relative quantitation for a large number of peptides without introducing any variation caused by separate experiments. In this work, we introduce a new quantitative approach to dealing with SILAC protein-level summary using classification-based methodologies. Unlike existing methods, our approach depends mainly on the protein ratio summary and is not restricted only to the proteins with two or more peptide hits. In particular, our approach uses Gaussian mixture model and a stochastic, metaheuristic global optimization algorithm, particle swarm optimization (PSO), to avoid either a premature of convergence or being stuck in a local optimum. Our simulation studies show that the proposed method performs the best in terms of F1 score.
一种基于分类的SILAC数据定量方法
一种实用而有效的稳定同位素标记方法是利用细胞培养物中的氨基酸进行稳定同位素标记。SILAC的一个关键优势是能够在一次仪器运行中同时检测同位素标记的肽,从而保证对大量肽的相对定量,而不会引入由单独实验引起的任何变化。在这项工作中,我们引入了一种新的定量方法来处理基于分类的SILAC蛋白水平摘要。与现有方法不同,我们的方法主要依赖于蛋白质比例汇总,而不仅仅局限于具有两个或多个肽点的蛋白质。特别是,我们的方法使用高斯混合模型和随机,元启发式全局优化算法,粒子群优化(PSO),以避免过早收敛或陷入局部最优。我们的仿真研究表明,该方法在F1分数方面表现最好。
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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