Combining vocal tract length normalization with hierarchial linear transformations

Recent research has demonstrated the effectiveness of vocal tract length normalization (VTLN) as a rapid adaptation technique for statistical parametric speech synthesis. VTLN produces speech with naturalness preferable to that of MLLR-based adaptation techniques, being much closer in quality to that generated by the original av-erage voice model. However with only a single parameter, VTLN captures very few speaker specific characteristics when compared to linear transform based adaptation techniques. This paper pro-poses that the merits of VTLN can be combined with those of linear transform based adaptation in a hierarchial Bayesian frame-work, where VTLN is used as the prior information. A novel tech-nique for propagating the gender information from the VTLN prior through constrained structural maximum a posteriori linear regres-sion (CSMAPLR) adaptation is presented. Experiments show that the resulting transformation has improved speech quality with better naturalness, intelligibility and improved speaker similarity. Index Terms — Statistical parametric speech synthesis, hidden Markov models, speaker adaptation, vocal tract length normaliza-tion, constrained structural maximum a posteriori linear regression 1

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

A major use of the 1000 Genomes Project (1000GP) data is genotype imputation in genome-wide association studies (GWAS). Here we develop a method to estimate haplotypes from low-coverage sequencing data that can take advantage of single-nucleotide polymorphism (SNP) microarray genotypes on the same samples. First the SNP array data are phased to build a backbone (or 'scaffold') of haplotypes across each chromosome. We then phase the sequence data 'onto' this haplotype scaffold. This approach can take advantage of relatedness between sequenced and non-sequenced samples to improve accuracy. We use this method to create a new 1000GP haplotype reference set for use by the human genetic community. Using a set of validation genotypes at SNP and bi-allelic indels we show that these haplotypes have lower genotype discordance and improved imputation performance into downstream GWAS samples, especially at low-frequency variants. © 2014 Macmillan Publishers Limited. All rights reserved

Transcribing meetings with the AMIDA systems

In this paper, we give an overview of the AMIDA systems for transcription of conference and lecture room meetings. The systems were developed for participation in the Rich Transcription evaluations conducted by the National Institute for Standards and Technology in the years 2007 and 2009 and can process close talking and far field microphone recordings. The paper first discusses fundamental properties of meeting data with special focus on the AMI/AMIDA corpora. This is followed by a description and analysis of improved processing and modeling, with focus on techniques specifically addressing meeting transcription issues such as multi-room recordings or domain variability. In 2007 and 2009, two different strategies of systems building were followed. While in 2007 we used our traditional style system design based on cross adaptation, the 2009 systems were constructed semi-automatically, supported by improved decoders and a new method for system representation. Overall these changes gave a 6%-13% relative reduction in word error rate compared to our 2007 results while at the same time requiring less training material and reducing the real-time factor by five times. The meeting transcription systems are available at www.webasr.org

Culturally centering social change communication: subaltern critiques of, resistance to, and re-imagination of development

10.1080/17447143.2018.1446440Journal of Multicultural Discourses13287-10