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Gene expression profiling by estimating parameters of gene regulatory network using simulated annealing: A comparative study

机译:通过模拟退火估算基因调控网络参数进行基因表达谱分析:一项比较研究

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Gene regulation is either an intra-cellular, inter-cellular, intra-tissue or inter-tissue biochemical phenomenon in an organism where a few genes may regulate the expression(s) of any other gene(s), even the expression of itself. The regulation is performed through proteins, metabolites and other genetic spin-offs resulting from the change in environment that genes experience in the cellular context. The gene regulatory network which originates from the regulation process is a potential source from which different physiological, behavioral, medicinal and disease-related issues of an organism can be uncovered. Computational inference of the network is a well-known bioinformatics task. Easy availability of time series gene expression data has made the work easier. But this data suffers from the curse of dimensionality as columns (time points) are few in number in comparison with rows (genes). Methods which are proposed here take the microarray time series gene expression data as input and simulate a time series of larger number of rows with regular small intervals. The parameters of the gene regulatory network are estimated using three variants of Simulated Annealing, viz. Basic Simulated Annealing (BSA), Tabu Simulated Annealing (TSA) and Greedy Simulated Annealing (GSA). During the estimation of parameters, the main focus is on minimizing the cost between actual and simulated time series in successive iterations. The final parameter set is used to produce the simulated time series, each row of which is the expression profile of a gene. With an available synthetic data set, original expression profiles are compared to the expression profiles produced by three different methods. The simulated profiles show close correspondence to the original ones. GSA shows the closest correspondence and TSA proves to be the most efficient in terms of time and number of iterations. The simulated time series may be used for GRN reconstruction or other problems.
机译:基因调节是生物体中的细胞内,细胞间,组织内或组织间生化现象,其中一些基因可以调节任何其他基因的表达,甚至是其自身的表达。调节是通过蛋白质,代谢物和其他遗传衍生产物进行的,这些衍生产物是基因在细胞环境中经历的环境变化产生的。源自调节过程的基因调节网络是潜在的来源,可以从中发现生物体的不同生理,行为,医学和疾病相关问题。网络的计算推理是众所周知的生物信息学任务。时间序列基因表达数据的容易获得使工作变得更加容易。但是,由于列(时间点)的数量少于行(基因)的数量,因此该数据遭受了维数的诅咒。这里提出的方法将微阵列时间序列基因表达数据作为输入,并以规则的小间隔模拟更多行的时间序列。基因调节网络的参数是使用模拟退火的三种变体来估算的,即。基本模拟退火(BSA),禁忌模拟退火(TSA)和贪婪模拟退火(GSA)。在参数估计期间,主要重点是使连续迭代中的实际时间序列和模拟时间序列之间的成本最小化。最终参数集用于产生模拟的时间序列,其中的每一行都是基因的表达谱。利用可用的合成数据集,将原始表达谱与通过三种不同方法产生的表达谱进行比较。模拟的轮廓显示与原始轮廓非常接近。 GSA显示了最接近的对应关系,并且在时间和迭代次数方面,TSA被证明是最有效的。模拟的时间序列可用于GRN重建或其他问题。

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