Browsing by Author "Shen, Minjie"

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    Comparative assessment and novel strategy on methods for imputing proteomics data
    Shen, Minjie; Chang, Yi-Tan; Wu, Chiung-Ting; Parker, Sarah J.; Saylor, Georgia; Wang, Yizhi; Yu, Guoqiang; Van Eyk, Jennifer E.; Clarke, Robert; Herrington, David M.; Wang, Yue (2022-01-20)
    Missing values are a major issue in quantitative proteomics analysis. While many methods have been developed for imputing missing values in high-throughput proteomics data, a comparative assessment of imputation accuracy remains inconclusive, mainly because mechanisms contributing to true missing values are complex and existing evaluation methodologies are imperfect. Moreover, few studies have provided an outlook of future methodological development. We first re-evaluate the performance of eight representative methods targeting three typical missing mechanisms. These methods are compared on both simulated and masked missing values embedded within real proteomics datasets, and performance is evaluated using three quantitative measures. We then introduce fused regularization matrix factorization, a low-rank global matrix factorization framework, capable of integrating local similarity derived from additional data types. We also explore a biologically-inspired latent variable modeling strategy—convex analysis of mixtures—for missing value imputation and present preliminary experimental results. While some winners emerged from our comparative assessment, the evaluation is intrinsically imperfect because performance is evaluated indirectly on artificial missing or masked values not authentic missing values. Nevertheless, we show that our fused regularization matrix factorization provides a novel incorporation of external and local information, and the exploratory implementation of convex analysis of mixtures presents a biologically plausible new approach.
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    Cosbin: cosine score-based iterative normalization of biologically diverse samples
    Wu, Chiung-Ting; Shen, Minjie; Du, Dongping; Cheng, Zuolin; Parker, Sarah J.; Lu, Yingzhou; Van Eyk, Jennifer E.; Yu, Guoqiang; Clarke, Robert; Herrington, David M.; Wang, Yue (Oxford University Press, 2022)
    Motivation: Data normalization is essential to ensure accurate inference and comparability of gene expression measures across samples or conditions. Ideally, gene expression data should be rescaled based on consistently expressed reference genes. However, to normalize biologically diverse samples, the most commonly used reference genes exhibit striking expression variability and size-factor or distribution-based normalization methods can be problematic when the amount of asymmetry in differential expression is significant. Results: We report an efficient and accurate data-driven method-Cosine score-based iterative normalization (Cosbin)-to normalize biologically diverse samples. Based on the Cosine scores of cross-condition expression patterns, the Cosbin pipeline iteratively eliminates asymmetric differentially expressed genes, identifies consistently expressed genes, and calculates sample-wise normalization factors. We demonstrate the superior performance and enhanced utility of Cosbin compared with six representative peer methods using both simulation and real multi-omics expression datasets. Implemented in open-source R scripts and specifically designed to address normalization bias due to significant asymmetry in differential expression across multiple conditions, the Cosbin tool complements rather than replaces the existing methods and will allow biologists to more accurately detect true molecular signals among diverse phenotypic groups. Availability and implementation: The R scripts of Cosbin pipeline are freely available at https://github.com/MinjieSh/Cosbin. Supplementary information: Supplementary data are available at Bioinformatics Advances online.
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    A Study of Machine Learning Approaches for Biomedical Signal Processing
    Shen, Minjie (Virginia Tech, 2021-06-10)
    The introduction of high-throughput molecular profiling technologies provides the capability of studying diverse biological systems at molecular level. However, due to various limitations of measurement instruments, data preprocessing is often required in biomedical research. Improper preprocessing will have negative impact on the downstream analytics tasks. This thesis studies two important preprocessing topics: missing value imputation and between-sample normalization. Missing data is a major issue in quantitative proteomics data analysis. While many methods have been developed for imputing missing values in high-throughput proteomics data, comparative assessment on the accuracy of existing methods remains inconclusive, mainly because the true missing mechanisms are complex and the existing evaluation methodologies are imperfect. Moreover, few studies have provided an outlook of current and future development. We first report an assessment of eight representative methods collectively targeting three typical missing mechanisms. The selected methods are compared on both realistic simulation and real proteomics datasets, and the performance is evaluated using three quantitative measures. We then discuss fused regularization matrix factorization, a popular low-rank matrix factorization framework with similarity and/or biological regularization, which is extendable to integrating multi-omics data such as gene expressions or clinical variables. We further explore the potential application of convex analysis of mixtures, a biologically inspired latent variable modeling strategy, to missing value imputation. The preliminary results on proteomics data are provided together with an outlook into future development directions. While a few winners emerged from our comparative assessment, data-driven evaluation of imputation methods is imperfect because performance is evaluated indirectly on artificial missing or masked values not authentic missing values. Imputation accuracy may vary with signal intensity. Fused regularization matrix factorization provides a possibility of incorporating external information. Convex analysis of mixtures presents a biologically plausible new approach. Data normalization is essential to ensure accurate inference and comparability of gene expressions across samples or conditions. Ideally, gene expressions should be rescaled based on consistently expressed reference genes. However, for normalizing biologically diverse samples, the most commonly used reference genes have exhibited striking expression variability, and distribution-based approaches can be problematic when differentially expressed genes are significantly asymmetric. We introduce a Cosine score based iterative normalization (Cosbin) strategy to normalize biologically diverse samples. The between-sample normalization is based on iteratively identified consistently expressed genes, where differentially expressed genes are sequentially eliminated according to scale-invariant Cosine scores. We evaluate the performance of Cosbin and four other representative normalization methods (Total count, TMM/edgeR, DESeq2, DEGES/TCC) on both idealistic and realistic simulation data sets. Cosbin consistently outperforms the other methods across various performance criteria. Implemented in open-source R scripts and applicable to grouped or individual samples, the Cosbin tool will allow biologists to detect subtle yet important molecular signals across known or novel phenotypic groups.