https://www.selleckchem.com/pr....oducts/brigimadlin.h
As missing values are frequently present in genomic data, practical methods to handle missing data are necessary for downstream analyses that require complete data sets. State-of-the-art imputation techniques, including methods based on singular value decomposition and K-nearest neighbors, can be computationally expensive for large data sets and it is difficult to modify these algorithms to handle certain cases not missing at random. In this work, we use a deep-learning framework based on the variational auto-encoder (VAE) for genom
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