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Dimension reduction is essential for analyzing high-dimensional data, with various techniques developed to address diverse data characteristics. However, individual methods often struggle to capture all intricate patterns and complex structures simultaneously. To overcome this limitation, we introduce ADM (Adaptive graph Diffusion for Meta-dimension reduction), a novel meta-dimension reduction method grounded in graph diffusion theory. ADM integrates results from multiple dimension reduction techniques, leveraging their individual strengths while mitigating their specific weaknesses.ADM utilizes dynamic Markov processes to transform Euclidean space results into an information space, revealing intrinsic nonlinear manifold structures that are hard to capture by conventional methods. A critical advancement in ADM is its adaptive diffusion mechanism, which dynamically selects optimal diffusion time scales for each sample, enabling effective representation of multi-scale structures. This approach generates robust, high-quality low-dimensional representations that capture both local and global data structures while reducing noise and technique-specific distortions. We demonstrate ADM’s efficacy on simulated and real-world datasets, including various omics data types. Results show that ADM provides clearer separation between biological groups and reveals more meaningful patterns compared to existing methods, advancing the analysis and visualization of complex biological data.
Dimension reduction is essential for analyzing high-dimensional data, with various techniques developed to address diverse data characteristics. However, individual methods often struggle to capture all intricate patterns and complex structures simultaneously. To overcome this limitation, we introduce ADM (Adaptive graph Diffusion for Meta-dimension reduction), a novel meta-dimension reduction method grounded in graph diffusion theory. ADM integrates results from multiple dimension reduction techniques, leveraging their individual strengths while mitigating their specific weaknesses.ADM utilizes dynamic Markov processes to transform Euclidean space results into an information space, revealing intrinsic nonlinear manifold structures that are hard to capture by conventional methods. A critical advancement in ADM is its adaptive diffusion mechanism, which dynamically selects optimal diffusion time scales for each sample, enabling effective representation of multi-scale structures. This approach generates robust, high-quality low-dimensional representations that capture both local and global data structures while reducing noise and technique-specific distortions. We demonstrate ADM’s efficacy on simulated and real-world datasets, including various omics data types. Results show that ADM provides clearer separation between biological groups and reveals more meaningful patterns compared to existing methods, advancing the analysis and visualization of complex biological data.
We study the behavior of two kernel based sensor fusion algorithms, nonparametric canonical correlation analysis (NCCA) and alternating diffusion (AD), under the nonnull setting that the clean datasets collected from two sensors are modeled by a common low-dimensional manifold embedded in a high-dimensional Euclidean space and the datasets are corrupted by high-dimensional noise. We establish the asymptotic limits and convergence rates for the eigenvalues of the associated kernel matrices assuming that the sample dimension and sample size are comparably large, where NCCA and AD are conducted using the Gaussian kernel. It turns out that both the asymptotic limits and convergence rates depend on the signal-to-noise ratio (SNR) of each sensor and selected bandwidths. On one hand, we show that if NCCA and AD are directly applied to the noisy point clouds without any sanity check, it may generate artificial information that misleads scientists’ interpretation. On the other hand, we prove that if the bandwidths are selected adequately, both NCCA and AD can be made robust to high-dimensional noise when the SNRs are relatively large.
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