Improved downstream functional analysis of single-cell RNA-sequence data using DGAN.

The dramatic increase in the number of single-cell RNA-sequence (scRNA-seq) investigations is indeed an endorsement of the new-fangled proficiencies of next generation sequencing technologies that facilitate the accurate measurement of tens of thousands of RNA expression levels at the cellular resolution. Nevertheless, missing values of RNA amplification persist and remain as a significant computational challenge, as these data omission induce further noise in their respective cellular data and ultimately impede downstream functional analysis of scRNA-seq data. Consequently, it turns imperative to develop robust and efficient scRNA-seq data imputation methods for improved downstream functional analysis outcomes. To overcome this adversity, we have designed an imputation framework namely deep generative autoencoder network [DGAN]. In essence, DGAN is an evolved variational autoencoder designed to robustly impute data dropouts in scRNA-seq data manifested as a sparse gene expression matrix. DGAN principally reckons count distribution, besides data sparsity utilizing a gaussian model whereby, cell dependencies are capitalized to detect and exclude outlier cells via imputation. When tested on five publicly available scRNA-seq data, DGAN outperformed every single baseline method paralleled, with respect to downstream functional analysis including cell data visualization, clustering, classification and differential expression analysis. DGAN is executed in Python and is accessible at https://github.com/dikshap11/DGAN .