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Residual signals

If we apply the iaverse-filtering technique to each frame in the entire speech waveform, we create a sequence of residual signals, one for each frame. A single residual waveform for the whole utterance can be made from these residual frames but, since the details of this are somewhat subtle, a description of this is left until Section 12.6.5. [Pg.373]

How do we now find the glottal-source signal from the residual x[n] Recall that in the z-domain the main filter expression is [Pg.373]


Instrumentation. H and NMR spectra were recorded on a Bruker AV 400 spectrometer (400.2 MHz for proton and 100.6 MHz for carbon) at 310 K. Chemical shifts (< are expressed in ppm coupling constants (J) in Hz. Deuterated DMSO and/or water were used as solvent chemical shift values are reported relative to residual signals (DMSO 5 = 2.50 for H and 5 = 39.5 for C). ESl-MS data were obtained on a VG Trio-2000 Fisons Instruments Mass Spectrometer with VG MassLynx software. Vers. 2.00 in CH3CN/H2O at 60°C. Isothermal titration calorimetry (ITC) experiments were conducted on a VP isothermal titration calorimeter from Microcal at 30°C. [Pg.456]

Fig. 27. ESR Spectra of nitroxyl methylcobinamide. (a) Before photolysis and (b) after anaerobic photolysis. In (b) the spectrometer signal level is set much higher than in (a) so that the residual signal intensity is only a few percent of initial intensity... Fig. 27. ESR Spectra of nitroxyl methylcobinamide. (a) Before photolysis and (b) after anaerobic photolysis. In (b) the spectrometer signal level is set much higher than in (a) so that the residual signal intensity is only a few percent of initial intensity...
This is a very polar solvent, suitable for salts and extremely polar compounds. Like DMSO it has a very high affinity for water and is almost impossible to keep dry. Its water peak is sharper and occurs more predictably at around 4.8 ppm. The residual CD2HOD signal is of similar appearance to the D6-DMSO residual signal and is observed at 3.3 ppm. [Pg.17]

Consequently, the signal fractions of 51 f(r)/51 f(0) can be calculated and compared with simulations. For samples prepared by bacterial expression, correction of the background signals can be carried out in a similar fashion [48, 53, 54], It is noteworthy that spin geometries deviated from linearity, which may occur in the side-chain 13C nuclei such as C , would produce more rapid signal decays and smaller residual signal fraction [55],... [Pg.54]

Table 2 13C chemical shifts (with respect to the residual signal of CDCI3 at 77.0 ppm) as well as the Jc-p coupling constants of the imidazo[1,2-c][1,3,2]oxazaphosphinine derivative 49... [Pg.963]

Since the natural abundance levels of 13C and 15N are on the order of 1%, interference from residual signals of the unlabeled moiety can be neglected as long as it is not present in large excess. Furthermore, nonoptimized editing (from imperfections in the pulse sequence etc.) will just lower the overall sensitivity, but not affect the selectivity. [Pg.378]

All standard pulse sequences for these experiments include some mechanism for selecting xH-X pairs and suppressing the other XH signals (phase cycling and/or pulsed field gradients, see below). As a further advantage, residual signal intensity of protons not bound to X (because of imperfect suppression) will not lead to a cross peak in the xH,X plane after Fourier transformation, but merely contribute to axial peaks at the spec-... [Pg.379]

In analytical redundancy schemes, the resulting difference generated from the consistency checking of different variables is called a residual signal. The residual should be by convention zero-valued when the system is normal and should diverge from zero when a fault occurs. This zero and non-zero property of the residual is used to determine whether or not a fault has occurred. Analytical redundancy makes use of a quantitative model of the monitored process and is therefore often referred to as the model-based approach to fault diagnosis. [Pg.205]

These spectra demonstrate that with the multiselective method a clean separation of the subspectra of the three independent spin systems may be achieved. They furthermore prove that - compared to the basic ID TOCSY experiment - spectra of the same quality with respect to the suppression of residual signals originating from the other spin systems and with respect to the signal-to-noise ratios can be measured. [Pg.31]

A second electrolysis at —0.3 V restores the initial red solution. The voltammogram (curve (e)) performed immediately after the reductive electrolysis of the redox couple of 7"+ is invariant with time. As all the pentacoordinate copper(I) species formed electrochemically are quantitatively transformed into tetracoordinate copper(I) species during the electrolysis, we can give a lower limit of 10 4 s 1 for the rate constant of the chemical reaction. The residual signal at —0.03 V simply reflects an incomplete electrolysis. [Pg.439]

The Adjust Point option available from the Process pull-down menu allows you to move single points in y - dimension to correct faulty data points, e.g. spikes. The same function has alreday been used to correct "wrong values in the FID. Adjust Point should not be used to purify your sample, by removing the residual signals of impurities or of a solvent. [Pg.205]

Fig. 2. Time resolved fluorescence spectra of all-trans PRSB in methanol (black) and octanol (grey) for a) t<50 fs and b) t>50 fs. The intensity of the octanol spectra is adjusted the methanol spectra. The spectra are not corrected for self-absorption (for >19.500 cm 1), or for the detector response function. A residual signal appearing at energies <14.000 cm"1 is due to incomplete background subtraction (see above). Fig. 2. Time resolved fluorescence spectra of all-trans PRSB in methanol (black) and octanol (grey) for a) t<50 fs and b) t>50 fs. The intensity of the octanol spectra is adjusted the methanol spectra. The spectra are not corrected for self-absorption (for >19.500 cm 1), or for the detector response function. A residual signal appearing at energies <14.000 cm"1 is due to incomplete background subtraction (see above).
The gene for arginine vasopressin is that of a 166-residue precursor protein carrying a 19-residue signal sequence at the N terminus.84 This sequence is followed by that of vasopressin, then after a GKR linker by the 95-residue neurophysin II. Finally, after one additional arginine there is a 39-residue glycopeptide. Oxytocin originates in a parallel way from its own precursor.85... [Pg.1748]

Both Met-enkephalin and Leu-enkephalin have their own pro- and prepro forms.29 Bovine preproenkephalin A is a 268-residue protein containing a 20-residue signal sequence and four sequences of Met-enkephalin and one of Leu-enkephalin, each flanked by pairs of basic residues. There are also Met-enkephalin-Arg-Gly-Leu (YGGFMRGL) and Met-enkephalin-Arg-Phe sequences. Not all of these are cut out cleanly, and other peptides such as Met-enkephalin-Arg-Arg-Val-NH2 are also found in brain. Proenkephalin B contains three copies of Leu-enkephalin contained within longer peptides. One of these, P-dynorphin (Table 30-4), is also a potent opioid compound. The enkephalins are thought to act as neurotransmitters, which are rapidly degraded after their release by two or three membrane-bound... [Pg.1752]

Processing of insulin. Insulin is synthesized by membrane-bound polysomes in the /3 cells of the pancreas. The primary translation product is preproinsulin, which contains a 24-residue signal peptide preceding the 81-residue proinsulin molecule. The signal peptide is removed by signal peptidase, cutting between Ala (—1) and Phe (+1), as the nascent chain is transported into the lumen of the endoplasmic reticulum. Proinsulin folds and two disulfide bonds crosslink the ends of the molecule as shown. Before secretion, a trypsinlike enzyme cleaves after a pair of basic residues 31, 32 and 59, 60 then a carboxypeptidase B-like enzyme removes these basic residues to generate the mature form of insulin. [Pg.758]

Photoresponse properties. Photoresponse properties are very important properties for imaging devices, especially in broadcasting use. The amount of decay lag can be defined as the ratio of the residual signal current... [Pg.77]


See other pages where Residual signals is mentioned: [Pg.403]    [Pg.97]    [Pg.64]    [Pg.133]    [Pg.185]    [Pg.60]    [Pg.140]    [Pg.17]    [Pg.114]    [Pg.378]    [Pg.236]    [Pg.312]    [Pg.14]    [Pg.41]    [Pg.895]    [Pg.305]    [Pg.257]    [Pg.236]    [Pg.757]    [Pg.725]    [Pg.157]    [Pg.240]    [Pg.52]    [Pg.263]    [Pg.26]    [Pg.209]    [Pg.460]    [Pg.176]    [Pg.187]    [Pg.439]    [Pg.442]    [Pg.59]    [Pg.305]    [Pg.96]   


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