微阵列数据分析与PCA在一个DBMS

W. Rinsurongkawong, C. Ordonez
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引用次数: 4

摘要

微阵列数据集包含数千个基因的表达水平。这些数据集的统计分析通常在DBMS之外使用统计包或数学库执行。在这项工作中,我们将重点放在在DBMS中分析它们。这是一个困难的问题,因为微阵列数据集具有高维,但尺寸小。首先,由于DBMS对每个表的最大列数的限制,在分析之前必须对数据集进行pivot和转换。更重要的是,数万个基因的相关矩阵有数百万个值。虽然大多数高维数据集可以用经典的主成分分析方法进行分析,但小而高维的数据集只能用奇异值分解(SVD)进行分析。采用Householder三对角化和QR分解数值方法求解数据库内部的奇异值分解问题。由于这些数学方法需要大量的矩阵运算,而这些运算很难用SQL来表达,因此需要开发查询优化和高效的udf来获得良好的性能。我们提出的技术实现了与R包(一个著名的统计工具)相当的处理时间。实验表明,我们的方法在高维情况下具有良好的可扩展性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microarray data analysis with PCA in a DBMS
Microarray data sets contain expression levels of thousands of genes. The statistical analysis of such data sets is typically performed outside a DBMS with statistical packages or mathematical libraries. In this work, we focus on analyzing them inside the DBMS. This is a difficult problem because microarray data sets have high dimensionality, but small size. First, due to DBMS limitations on a maximum number of columns per table, the data set has to be pivoted and transformed before analysis. More importantly, the correlation matrix on tens of thousands of genes has millions of values. While most high dimensional data sets can be analyzed with the classical PCA method, small, but high dimensional, data sets can only be analyzed with Singular Value Decomposition (SVD). We adapt the Householder tridiagonalization and QR factorization numerical methods to solve SVD inside the DBMS. Since these mathematical methods require many matrix operations, which are hard to express in SQL, query optimizations and efficient UDFs are developed to get good performance. Our proposed techniques achieve processing times comparable with those from the R package, a well-known statistical tool. We experimentally show our methods scale well with high dimensionality.
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