This paper applies probabilistic amplitude shaping (PAS) to cyclic redundancy check (CRC)-aided tail-biting trellis-coded modulation (TCM). CRC-TCM-PAS produces practical codes for short block lengths on the additive white Gaussian noise (AWGN) channel. In the transmitter, equally likely message bits are encoded by a distribution matcher (DM) generating amplitude symbols with a desired distribution. A CRC is appended to the sequence of amplitude symbols, and this sequence is then encoded and modulated by TCM to produce real-valued channel input signals. This paper proves that the sign values produced by the TCM are asymptotically equally likely to be positive or negative. The CRC-TCM-PAS scheme can thus generate channel input symbols with a symmetric capacity-approaching probability mass function. The paper provides an analytical upper bound on the frame error rate of the CRC-TCM-PAS system over the AWGN channel. This FER upper bound is the objective function used for jointly optimizing the CRC and convolutional code. Additionally, this paper proposes a multi-composition DM, which is a collection of multiple constant-composition DMs. The optimized CRC-TCM-PAS systems achieve frame error rates below the random coding union (RCU) bound in AWGN and outperform the short-blocklength PAS systems with various other forward error correction codes studied in [2].
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This paper derives a union bound on the frame error rate (FER) of a probabilistic amplitude shaping (PAS) system which uses a CRC-aided, rate −k/k+1 , systematic, recursive trellis-coded modulation (TCM). A tail-biting convolutional code (TBCC) provides the feed-forward error correction (FEC) code for the TCM. The system is referred as CRC-TCM-PAS [1]. In order to derive the union bound, we first prove that the concatenation of a CRC and a rate −k/k+1 convolutional code is equivalent to a new convolutional code. Then, we give the generating function of the new convolutional code using Biglieri's product-state-diagram approach. A union bound can be calculated using the generating function. Simulation results show that the derived union bound is tight in the high signal-to-noise ratio (SNR) regime and can be used to design the convolutional and CRC codes. Simulation results also show that the optimized CRC-TCM-PAS system exceeds the random coding union (RCU) bound and outperforms the PAS systems with various FEC codes studied in [2] for the same number of input bits and the same transmission rate.more » « less
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This paper presents a method for computing a finite-blocklength converse for the rate of fixed-length codes with feedback used on discrete memoryless channels (DMCs). The new converse is expressed in terms of a stochastic control problem whose solution can be efficiently computed using dynamic programming and Fourier methods. For channels such as the binary symmetric channel (BSC) and binary erasure channel (BEC), the accuracy of the proposed converse is similar to that of existing special-purpose converse bounds, but the new converse technique can be applied to arbitrary DMCs. We provide example applications of the new converse technique to the binary asymmetric channel (BAC) and the quantized amplitude-constrained AWGN channel.more » « less
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Previously, dynamic-assignment Blahut-Arimoto (DAB) was used to find capacity-achieving probability mass functions (PMFs) for binomial channels and molecular channels. As it turns out, DAB can efficiently identify capacity-achieving PMFs for a wide variety of channels. This paper applies DAB to power-constrained (PC) additive white Gaussian Noise (AWGN) Channels and amplitude-constrained (AC) AWGN Channels.This paper modifies DAB to include a power constraint and finds low-cardinality PMFs that approach capacity on PC-AWGN Channels. While a continuous Gaussian PDF is well-known to be capacity-achieving on the PC-AWGN channel, DAB identifies low-cardinality PMFs within 0.01 bits of the mutual information provided by a Gaussian PDF. Recall the results of Ozarow and Wyner requiring a constellation cardinality of ⌈2 ^ (C+1) ⌉ to approach capacity C to within the asymptotic shaping loss of 1.53 dB at high SNR. PMF's found by DAB approach capacity with essentially no shaping loss with cardinality less than 2 ^ (C+1.2) . As expected, DAB's numerical approach identifies PMFs with better mutual information vs. SNR performance than the analytical approaches to finite-support constellations examined by Wu and Verdu. This paper also uses DAB to find capacity-achieving PMFs with small cardinality support sets for AC-AWGN Channels. The resulting evolution of capacity-achieving PMFs as a function of SNR is consistent with the approximate cardinality transition points of Sharma and Shamai.more » « less
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Abstract Introduction Benign epilepsy with centrotemporal spikes (BECTS) is a common form of childhood epilepsy with the majority of those afflicted remitting during their early teenage years. Seizures arise from the lower half of the sensorimotor cortex of the brain (e.g. seizure onset zone) and the abnormal epileptiform discharges observed increase during NREM sleep. To date no clinical factors reliably predict disease course, making determination of ongoing seizure risk a significant challenge. Prior work in BECTS have shown abnormalities in beta band (14.9–30 Hz) oscillations during movement and rest. Oscillations in this frequency band are modulated by state of consciousness and thought to reflect intrinsic inhibitory mechanisms.
Methods We used high density EEG and source localization techniques to examine beta band activity in the seizure onset zone (sensorimotor cortex) in a prospective cohort of children with BECTS and healthy controls during sleep. We hypothesized that beta power in the sensorimotor cortex would be different between patients and healthy controls, and that beta abnormalities would improve with resolution of disease in this self‐limited epilepsy syndrome. We further explored the specificity of our findings and correlation with clinical features. Statistical testing was performed using logistic and standard linear regression models.
Results We found that beta band power in the seizure onset zone is different between healthy controls and BECTS patients. We also found that a longer duration of time spent seizure‐free (corresponding to disease remission) correlates with lower beta power in the seizure onset zone. Exploratory spatial analysis suggests this effect is not restricted to the sensorimotor cortex. Exploratory frequency analysis suggests that this phenomenon is also observed in alpha and gamma range activity. We found no relationship between beta power and the presence or rate of epileptiform discharges in the sensorimotor cortex or a test of sensorimotor performance.
Conclusion These results provide evidence that cortical beta power in the seizure onset zone may provide a dynamic physiological biomarker of disease in BECTS.
