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通过高斯过程模型从破坏性时间序列实验中解码潜在行为

Decoding underlying behaviour from destructive time series experiments through Gaussian process models
课程网址: http://videolectures.net/licsb2010_honkela_dub/  
主讲教师: Antti Honkela
开课单位: 阿尔托大学
开课时间: 2010-05-03
课程语种: 英语
中文简介:
生物学时间序列的主要问题是通常实验(例如使用微阵列或RNA seq的基因表达测量)需要破坏生物体或细胞。这意味着特定的时间序列通常是在不同时间对不同生物(或细胞批次)的一系列测量。生物学重复通常由同时测量的单独生物样品组成。随着单细胞表达实验的出现,目前无法在不破坏细胞的情况下进行基因组范围的基因表达测量,我们期望这样的设置得以持续。许多现有的转录数据建模方法假设连续的微分方程模型时间表达谱,重复观察出现。对重复实验进行建模的两种方法是将重复观察视为来自共享配置文件,或者来自完全独立的配置文件。前一种方法假设每个实验的基因表达谱不变,而后一种方法假设基因表达谱之间没有关系。对于许多实验装置,我们可能期望在这两个极端之间存在某些东西,其中每个单独的测量来自不同的细胞集合或不同的生物体,实验设置大致相同。因此,我们期望对实验产生一些共同的影响和一些独立的影响。在这项工作中,我们提出了一个集成的高斯过程框架来分析这些实验。在我们的方法中,实验的独立方面被建模为独立的高斯过程绘制,而实验中的共同轮廓通过单独的高斯过程建模。该方法通过共享共同轮廓的重复来增加功率,同时对来自各个流氓实验的异常值具有鲁棒性。
课程简介: A major problem for biological time series is that often experiments (such as gene expression measurements using microarrays or RNA-seq) require the organism or cells to be destroyed. This means that a particular time series is often a series of measurements of different organisms (or batches of cells) at different times. Biological replicates normally consist of a separate biological sample measured at the same time. With the advent of single cell expression experiments, where it is not currently conceivable to make genome-wide gene expression measurements without destroying the cell, we expect such set ups to be sustained. Many existing approaches to modelling transcriptional data postulate a differential equation model for continuous-time expression profiles from which the repeated observations arise. Two ways of modelling repeat experiments would be either to handle repeated observations as being from a shared profile, or from completely independent profiles. The former approach assumes that gene expression profile for each experiment does not vary, whilst the latter approach assumes no relationship between the gene expression profiles. For many experimental set ups we might expect something in between these two extremes where, whilst each individual measurement comes from a different collection of cells or a different organism, the experimental set up is broadly the same. We therefore expect some shared affects and some independent affects for the experiments. In this work we propose an integrated Gaussian process framework for analysis of such experiments. In our approach, independent aspects of the experiments are modelled as independent Gaussian process draws, while the common profile across the experiments is modelled by a separate Gaussian process. The method adds power through sharing of replicates for the common profile while being robust to outliers from individual rogue experiments.
关 键 词: 时间序列; 单细胞; 转录数据建模
课程来源: 视频讲座网
最后编审: 2019-05-14:lxf
阅读次数: 54