3 research outputs found
Incremental dimension reduction of tensors with random index
We present an incremental, scalable and efficient dimension reduction
technique for tensors that is based on sparse random linear coding. Data is
stored in a compactified representation with fixed size, which makes memory
requirements low and predictable. Component encoding and decoding are performed
on-line without computationally expensive re-analysis of the data set. The
range of tensor indices can be extended dynamically without modifying the
component representation. This idea originates from a mathematical model of
semantic memory and a method known as random indexing in natural language
processing. We generalize the random-indexing algorithm to tensors and present
signal-to-noise-ratio simulations for representations of vectors and matrices.
We present also a mathematical analysis of the approximate orthogonality of
high-dimensional ternary vectors, which is a property that underpins this and
other similar random-coding approaches to dimension reduction. To further
demonstrate the properties of random indexing we present results of a synonym
identification task. The method presented here has some similarities with
random projection and Tucker decomposition, but it performs well at high
dimensionality only (n>10^3). Random indexing is useful for a range of complex
practical problems, e.g., in natural language processing, data mining, pattern
recognition, event detection, graph searching and search engines. Prototype
software is provided. It supports encoding and decoding of tensors of order >=
1 in a unified framework, i.e., vectors, matrices and higher order tensors.Comment: 36 pages, 9 figure
A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection
Abstract Background The application of high-throughput sequencing in a broad range of quantitative genomic assays (e.g., DNA-seq, ChIP-seq) has created a high demand for the analysis of large-scale read-count data. Typically, the genome is divided into tiling windows and windowed read-count data is generated for the entire genome from which genomic signals are detected (e.g. copy number changes in DNA-seq, enrichment peaks in ChIP-seq). For accurate analysis of read-count data, many state-of-the-art statistical methods use generalized linear models (GLM) coupled with the negative-binomial (NB) distribution by leveraging its ability for simultaneous bias correction and signal detection. However, although statistically powerful, the GLM+NB method has a quadratic computational complexity and therefore suffers from slow running time when applied to large-scale windowed read-count data. In this study, we aimed to speed up substantially the GLM+NB method by using a randomized algorithm and we demonstrate here the utility of our approach in the application of detecting copy number variants (CNVs) using a real example. Results We propose an efficient estimator, the randomized GLM+NB coefficients estimator (RGE), for speeding up the GLM+NB method. RGE samples the read-count data and solves the estimation problem on a smaller scale. We first theoretically validated the consistency and the variance properties of RGE. We then applied RGE to GENSENG, a GLM+NB based method for detecting CNVs. We named the resulting method as “R-GENSENG". Based on extensive evaluation using both simulated and empirical data, we concluded that R-GENSENG is ten times faster than the original GENSENG while maintaining GENSENG’s accuracy in CNV detection. Conclusions Our results suggest that RGE strategy developed here could be applied to other GLM+NB based read-count analyses, i.e. ChIP-seq data analysis, to substantially improve their computational efficiency while preserving the analytic power