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Predictive models in neuroscience and bioinformatics.

机译:神经科学和生物信息学中的预测模型。

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摘要

This dissertation discusses how predictive models are being used for scientific inquiry. Statistical and computational advances have given rise to high-dimensional models that can be fit on relatively small samples but still predict well the behavior of complex systems. Scientists try to use such models to learn about complex biological systems; but it is not always clear how prediction accuracy translates to understanding the underlying system. In the chapters below, I present different approaches to learn from predictive models in bioinformatics and neuroscience. In each of these collaborative works, we tailor models that would both fit well and be interpretable in the context of the scientific questions.;In the first chapter, we fit and compare predictive models for the GC-content bias, an important confounder in DNA-sequencing. We develop a high-resolution model that treats each base-pair in the genome as a separate example; this allows us to compare many representations of GC-content, identifying which representation best predicts the variation in the coverage. To deal with the huge volumes of data, we develop a new conditional dependence measure that efficiently compares different models. Selection of the model that maximizes this dependence reveals a recurring association with an experimental parameter: the selected model in each sample corresponds to a window size almost identical to the average size of DNA fragments in the sample. This recurring result can be used both for correcting the bias and for learning about the causes for the bias.;In the next chapter, we propose a new estimator for interpreting prediction-accuracy results of models for neural activity in the visual cortex. Our shuffle estimator targets the explainable variance - the proportion of signal in the measured response - while accounting for auto-correlation in the noise. Re-analyzing models of functional MRI voxels within visual area V1, we observe a strong linear correlation between the signal-to-noise and prediction accuracy.;In the final chapter we analyze neurophysiology data recorded from visual area V4, and present a full cycle of scientific investigation using prediction models in neuroscience. Whereas the previous chapters developed metrics for evaluating feature sets and prediction models, this chapter takes an extra leap: we use optimization algorithms together with prior scientific knowledge to propose a new feature-set. We then fit regularized linear models based on this representation that generalize well to a validation data set. Finally, novel visualization and model-summary techniques help interpret the resulting prediction models, revealing rich patterns of activity in the different neurons and unexpected categories of neurons.
机译:本文讨论了如何将预测模型用于科学探究。统计和计算方面的进步已经产生了高维模型,该模型可以适合相对较小的样本,但仍可以很好地预测复杂系统的行为。科学家试图使用这种模型来了解复杂的生物系统。但并非总是很清楚预测精度如何转化为对底层系统的理解。在下面的章节中,我介绍了从生物信息学和神经科学的预测模型中学习的不同方法。在所有这些协作工作中,我们都对模型进行了调整,这些模型既适合科学问题,又可以在科学问题的背景下解释。在第一章中,我们拟合并比较了GC含量偏差的预测模型,GC含量偏差是DNA的重要混杂因素。 -测序。我们开发了一个高分辨率模型,该模型将基因组中的每个碱基对作为一个单独的示例进行处理;这使我们可以比较GC含量的许多表示形式,确定哪种表示形式最能预测覆盖率的变化。为了处理大量数据,我们开发了一种新的条件依赖度量,可以有效地比较不同模型。最大化这种依赖性的模型的选择揭示了与实验参数的反复关联:每个样品中的选定模型对应的窗口大小几乎与样品中DNA片段的平均大小相同。该重复结果可用于纠正偏差和了解偏差的原因。在下一章中,我们提出了一种新的估计器,用于解释视觉皮层神经活动模型的预测准确性结果。我们的混洗估计器以可解释的方差为目标-信号在测得的响应中所占的比例-同时考虑了噪声中的自相关。重新分析视觉区域V1中功能性MRI体素的模型,我们观察到信噪比与预测准确性之间存在很强的线性相关性。在最后一章中,我们分析了视觉区域V4中记录的神经生理学数据,并提出了一个完整的周期使用神经科学中的预测模型进行科学调查的方法。前面的章节开发了用于评估特征集和预测模型的指标,而本章则进行了一次额外的飞跃:我们将优化算法与现有的科学知识一起使用,以提出新的特征集。然后,我们基于此表示拟合正则化线性模型,该模型可以很好地推广到验证数据集。最后,新颖的可视化和模型摘要技术有助于解释所得的预测模型,揭示出不同神经元和神经元意外类别中丰富的活动模式。

著录项

  • 作者

    Benjamini, Yuval.;

  • 作者单位

    University of California, Berkeley.;

  • 授予单位 University of California, Berkeley.;
  • 学科 Statistics.;Bioinformatics.;Neurosciences.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 111 p.
  • 总页数 111
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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