CycleGAN with Dual Adversarial Loss for Bone-Conducted Speech Enhancement

Compared with air-conducted speech, bone-conducted speech has the unique advantage of shielding background noise. Enhancement of bone-conducted speech helps to improve its quality and intelligibility. In this paper, a novel CycleGAN with dual adversarial loss (CycleGAN-DAL) is proposed for bone-conducted speech enhancement. The proposed method uses an adversarial loss and a cycle-consistent loss simultaneously to learn forward and cyclic mapping, in which the adversarial loss is replaced with the classification adversarial loss and the defect adversarial loss to consolidate the forward mapping. Compared with conventional baseline methods, it can learn feature mapping between bone-conducted speech and target speech without additional air-conducted speech assistance. Moreover, the proposed method also avoids the oversmooth problem which is occurred commonly in conventional statistical based models. Experimental results show that the proposed method outperforms baseline methods such as CycleGAN, GMM, and BLSTM. Keywords: Bone-conducted speech enhancement, dual adversarial loss, Parallel CycleGAN, high frequency speech reconstruction

Logistic Regression Augmented Community Detection for Network Data with Application in Identifying Autism-Related Gene Pathways

When searching for gene pathways leading to specific disease outcomes, additional information on gene characteristics is often available that may facilitate to differentiate genes related to the disease from irrelevant background when connections involving both types of genes are observed and their relationships to the disease are unknown. We propose method to single out irrelevant background genes with the help of auxiliary information through a logistic regression, and cluster relevant genes into cohesive groups using the adjacency matrix. Expectation-maximization algorithm is modified to maximize a joint pseudo-likelihood assuming latent indicators for relevance to the disease and latent group memberships as well as Poisson or multinomial distributed link numbers within and between groups. A robust version allowing arbitrary linkage patterns within the background is further derived. Asymptotic consistency of label assignments under the stochastic blockmodel is proven. Superior performance and robustness in finite samples are observed in simulation studies. The proposed robust method identifies previously missed gene sets underlying autism related neurological diseases using diverse data sources including de novo mutations, gene expressions and protein-protein interactions.