Ameliorative missing value imputation for robust biological knowledge inference

Sehgal, Shoaib M.; Gondal, Iqbal; Dooley, Laurence D. and Coppel, Ross (2008). Ameliorative missing value imputation for robust biological knowledge inference. Journal of Biomedical Informatics, 41(4) pp. 499–514.



Gene expression data is widely used in various post genomic analyses. The data is often probed using microarrays due to their ability to simultaneously measure the expressions of thousands of genes. The expression data, however, contains significant numbers of missing values, which can impact on subsequent biological analysis. To minimize the impact of these missing values, several imputation algorithms including Collateral Missing Value Estimation (CMVE), Bayesian Principal Component Analysis (BPCA), Least Square Impute (LSImpute), Local Least Square Impute (LLSImpute), and K-Nearest Neighbour (KNN) have been proposed. These algorithms, however, exploit either only the global or local correlation structure of the data, which normally can lead to higher estimation errors. This paper presents an Ameliorative Missing Value Imputation (AMVI) technique which has ability to exploit global/local and positive/negative correlations in a given dataset by automatic selection of the optimal number of predictor genes k using a wrapper non-parametric method based on Monte Carlo simulations. The AMVI technique has CMVE strategy at its core because CMVE has demonstrated improved performance compared to both low variance methods like BPCA, LLSImpute, and high variance methods such as KNN and ZeroImpute, as CMVE exploits positive/negative correlations. The performance of AMVI is compared with CMVE, BPCA, LLSImpute, and KNN by randomly removing between 1% and 15% missing values in eight different ovarian, breast cancer and yeast datasets. Together with the standard NRMS error metric, the True Positive (TP) rate of the significant genes selection, biological significance of the selected genes and the statistical significance test results are presented to investigate the impact of missing values on subsequent biological analysis. The enhanced performance of AMVI was demonstrated by its lower NRMS error, improved TP rate, bio significance of the selected genes and statistical significance test results, when compared with the aforementioned imputation methods across all the datasets. The results show that AMVI adapted to the latent correlation structure of the data and proved to be an effective and robust approach compared with the trial and error methodology for selecting k. The results confirmed that AMVI can be successfully applied to accurately impute missing values prior to any microarray data analysis.

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