Meta-learning with Latent Space Clustering in Generative Adversarial Network for Speaker Diarization. Academic Article uri icon

Overview

abstract

  • The performance of most speaker diarization systems with x-vector embeddings is both vulnerable to noisy environments and lacks domain robustness. Earlier work on speaker diarization using generative adversarial network (GAN) with an encoder network (ClusterGAN) to project input x-vectors into a latent space has shown promising performance on meeting data. In this paper, we extend the ClusterGAN network to improve diarization robustness and enable rapid generalization across various challenging domains. To this end, we fetch the pre-trained encoder from the ClusterGAN and fine tune it by using prototypical loss (meta-ClusterGAN or MCGAN) under the meta-learning paradigm. Experiments are conducted on CALLHOME telephonic conversations, AMI meeting data, DIHARD-II (dev set) which includes challenging multi-domain corpus, and two child-clinician interaction corpora (ADOS, BOSCC) related to the autism spectrum disorder domain. Extensive analyses of the experimental data are done to investigate the effectiveness of the proposed ClusterGAN and MCGAN embeddings over x-vectors. The results show that the proposed embeddings with normalized maximum eigengap spectral clustering (NME-SC) back-end consistently outperform the Kaldi state-of-the-art x-vector diarization system. Finally, we employ embedding fusion with x-vectors to provide further improvement in diarization performance. We achieve a relative diarization error rate (DER) improvement of 6.67% to 53.93% on the aforementioned datasets using the proposed fused embeddings over x-vectors. Besides, the MCGAN embeddings provide better performance in the number of speakers estimation and short speech segment diarization compared to x-vectors and ClusterGAN on telephonic conversations.

publication date

  • February 26, 2021

Identity

PubMed Central ID

  • PMC8118028

Scopus Document Identifier

  • 85101834777

Digital Object Identifier (DOI)

  • 10.1109/taslp.2021.3061885

PubMed ID

  • 33997106

Additional Document Info

volume

  • 29