SIGRN: Inferring Gene Regulatory Network with Soft Introspective Variational Autoencoders.

Gene regulatory networks (GRNs) exhibit the complex regulatory relationships among genes, which are essential for understanding developmental biology and uncovering the fundamental aspects of various biological phenomena. It is an effective and economical way to infer GRNs from single-cell RNA sequencing (scRNA-seq) with computational methods. Recent researches have been done on the problem by using variational autoencoder (VAE) and structural equation model (SEM).

Identification of Cancer Driver Genes based on Dynamic Incentive Model.

Cancer is a complex genomic mutation disease, and identifying cancer driver genes promotes the development of targeted drugs and personalized therapies. The current computational method takes less consideration of the relationship among features and the effect of noise in protein-protein interaction(PPI) data, resulting in a low recognition rate. In this paper, we propose a cancer driver genes identification method based on dynamic incentive model, DIM.

Identification of cancer driver genes based on hierarchical weak consensus model.

Unlabelled: Cancer is a complex gene mutation disease that derives from the accumulation of mutations during somatic cell evolution. With the advent of high-throughput technology, a large amount of omics data has been generated, and how to find cancer-related driver genes from a large number of omics data is a challenge. In the early stage, the researchers developed many frequency-based driver genes identification methods, but they could not identify driver genes with low mutation rates well.

AGImpute: imputation of scRNA-seq data based on a hybrid GAN with dropouts identification.

Motivation: Dropout events bring challenges in analyzing single-cell RNA sequencing data as they introduce noise and distort the true distributions of gene expression profiles. Recent studies focus on estimating dropout probability and imputing dropout events by leveraging information from similar cells or genes. However, the number of dropout events differs in different cells, due to the complex factors, such as different sequencing protocols, cell types, and batch effects.

Essential proteins discovery based on dominance relationship and neighborhood similarity centrality.

Essential proteins play a vital role in development and reproduction of cells. The identification of essential proteins helps to understand the basic survival of cells. Due to time-consuming, costly and inefficient with biological experimental methods for discovering essential proteins, computational methods have gained increasing attention.

Mdwgan-gp: data augmentation for gene expression data based on multiple discriminator WGAN-GP.

Background: Although gene expression data play significant roles in biological and medical studies, their applications are hampered due to the difficulty and high expenses of gathering them through biological experiments. It is an urgent problem to generate high quality gene expression data with computational methods. WGAN-GP, a generative adversarial network-based method, has been successfully applied in augmenting gene expression data.

Identifying driver pathways based on a parameter-free model and a partheno-genetic algorithm.

Background: Tremendous amounts of omics data accumulated have made it possible to identify cancer driver pathways through computational methods, which is believed to be able to offer critical information in such downstream research as ascertaining cancer pathogenesis, developing anti-cancer drugs, and so on. It is a challenging problem to identify cancer driver pathways by integrating multiple omics data.

Results: In this study, a parameter-free identification model SMCMN, incorporating both pathway features and gene associations in Protein-Protein Interaction (PPI) network, is proposed.

Identification of cancer-related module in protein-protein interaction network based on gene prioritization.

With the rapid development of deep sequencing technologies, a large amount of high-throughput data has been available for studying the carcinogenic mechanism at the molecular level. It has been widely accepted that the development and progression of cancer are regulated by modules/pathways rather than individual genes. The investigation of identifying cancer-related active modules has received an extensive attention.

A novel extended Pareto Optimality Consensus model for predicting essential proteins.

Essential proteins have vital functions, when they are destroyed in cells, the cells will die or stop reproducing. Therefore, it is very important to identify essential proteins from a large number of other proteins. Due to the time-consuming, expensive, and inefficient process in biological experimental methods, computational methods become more and more popular to recognize them.

United Neighborhood Closeness Centrality and Orthology for Predicting Essential Proteins.

Identifying essential proteins plays an important role in disease study, drug design, and understanding the minimal requirement for cellular life. Computational methods for essential proteins discovery overcome the disadvantages of biological experimental methods that are often time-consuming, expensive, and inefficient. The topological features of protein-protein interaction (PPI) networks are often used to design computational prediction methods, such as Degree Centrality (DC), Betweenness Centrality (BC), Closeness Centrality (CC), Subgraph Centrality (SC), Eigenvector Centrality (EC), Information Centrality (IC), and Neighborhood Centrality (NC).

Predicting essential proteins based on subcellular localization, orthology and PPI networks.

Background: Essential proteins play an indispensable role in the cellular survival and development. There have been a series of biological experimental methods for finding essential proteins; however they are time-consuming, expensive and inefficient. In order to overcome the shortcomings of biological experimental methods, many computational methods have been proposed to predict essential proteins.