منابع مشابه
Voiceprint Biometric Authentication System
Speech recognition systems employ a number of standard system architectures and methodologies. While some of these can be optimized to work well with text independent identification and verification systems, the Pace University voiceprint system is optimized for textdependent identification. The second version of the system described here include analysis of the voice fundamental and formant fr...
متن کاملHandling the “Voiceprint” Issue
What was and is “Voiceprint”/Aural-Spectrographic Identification? Throughout the years, going all the way back to the Second World War, speaker identification by spectrograms has had an influence on Forensic Speaker Identification. The method has been criticized and embraced by different people at different points in time. This paper describes the issues diachronically, using the most important...
متن کاملKey Genaration Forimage Scrambling Using Voiceprint
ABSTRACT:-This paper presents a new algorithm to scramble color image using voiceprint and linear predicative coding (LPC). The speech signal pass through pre-processing stage which includes sampling and segmentation into many frames. All frames are windowed using rectangular window and fed to linear predicative predicator, the linear predicator is used to obtain the coefficient of the p th ord...
متن کاملA report of two cases of pyknodysostosis in two children
pyknodysostosis is a rare bone disease characterzed with short stature,wide fontaneles,small chin,hyperdensity of bones,erosion of tufts of the disatl phalanges,and narrowing of the mandibular angle. pyknodysostosis is inheritted as an autosomal recessive disease and may be seen in both sexes at any age.the patients have normal life span.short stature and bone fractures are their major problems...
متن کاملT Sachs disease in two children: report two cases
Background and aim: Tachyx is a rare autosomal recessive and neurological disorder caused by glycosfenolipid accumulation (GM2 ganglioside) in cell lysosomes. The accumulation of GM2 ganglioside is due to the mutation in the beta-hexose aminase gene (HEXA), which reduces the activity and deficiency of the HEXA enzyme. The aim of this study was to report 2 cases of T.Sax disease. Case report:...
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ژورنال
عنوان ژورنال: The Journal of the Acoustical Society of America
سال: 1974
ISSN: 0001-4966
DOI: 10.1121/1.3437934