skip to main content

Title: Hilbert-Type Dimension Polynomials of Intermediate Difference-Differential Field Extensions
Let K be an inversive difference-differential field and L a (not necessarily inversive) finitely generated difference-differential field extension of K. We consider the natural filtration of the extension L/K associated with a finite system \eta of its difference-differential generators and prove that for any intermediate difference-differential field F, the transcendence degrees of the components of the induced filtration of F are expressed by a certain numerical polynomial \chi_{K, F,\eta}(t). This polynomial is closely connected with the dimension Hilbert-type polynomial of a submodule of the module of K\"ahler differentials $\Omega_{L^{\ast}|K} where L^{\ast} is the inversive closure of L. We prove some properties of polynomials \chi_{K, F,\eta}(t) and use them for the study of the Krull-type dimension of the extension L/K. In the last part of the paper, we present a generalization of the obtained results to multidimensional filtrations of L/K associated with partitions of the sets of basic derivations and translations.
Award ID(s):
Publication Date:
Journal Name:
Lecture notes in computer science
Page Range or eLocation-ID:
64 - 79
Sponsoring Org:
National Science Foundation
More Like this
  1. We use the method of characteristic sets with respect to two term orderings to prove the existence and obtain a method of computation of a bivariate dimension polynomial associated with a non-reflexive difference-differential ideal in the algebra of difference-differential polynomials with several basic derivations and one translation. As a consequence, we obtain a new proof and a method of computation of the dimension polynomial of a non-reflexive prime difference ideal in the algebra of difference polynomials over an ordinary difference field. We also discuss applications of our results to systems of algebraic difference-differential equations.
  2. Abstract We prove an inequality that unifies previous works of the authors on the properties of the Radon transform on convex bodies including an extension of the Busemann–Petty problem and a slicing inequality for arbitrary functions. Let $K$ and $L$ be star bodies in ${\mathbb R}^n,$ let $0<k<n$ be an integer, and let $f,g$ be non-negative continuous functions on $K$ and $L$, respectively, so that $\|g\|_\infty =g(0)=1.$ Then $$\begin{align*} & \frac{\int_Kf}{\left(\int_L g\right)^{\frac{n-k}n}|K|^{\frac kn}} \le \frac n{n-k} \left(d_{\textrm{ovr}}(K,\mathcal{B}\mathcal{P}_k^n)\right)^k \max_{H} \frac{\int_{K\cap H} f}{\int_{L\cap H} g}, \end{align*}$$where $|K|$ stands for volume of proper dimension, $C$ is an absolute constant, the maximum is takenmore »over all $(n-k)$-dimensional subspaces of ${\mathbb R}^n,$ and $d_{\textrm{ovr}}(K,\mathcal{B}\mathcal{P}_k^n)$ is the outer volume ratio distance from $K$ to the class of generalized $k$-intersection bodies in ${\mathbb R}^n.$ Another consequence of this result is a mean value inequality for the Radon transform. We also obtain a generalization of the isomorphic version of the Shephard problem.« less
  3. Byrka, Jaroslaw ; Meka, Raghu (Ed.)
    In this work, we prove new relations between the bias of multilinear forms, the correlation between multilinear forms and lower degree polynomials, and the rank of tensors over F₂. We show the following results for multilinear forms and tensors. Correlation bounds. We show that a random d-linear form has exponentially low correlation with low-degree polynomials. More precisely, for d = 2^{o(k)}, we show that a random d-linear form f(X₁,X₂, … , X_d) : (F₂^{k}) ^d → F₂ has correlation 2^{-k(1-o(1))} with any polynomial of degree at most d/2 with high probability. This result is proved by giving near-optimal bounds onmore »the bias of a random d-linear form, which is in turn proved by giving near-optimal bounds on the probability that a sum of t random d-dimensional rank-1 tensors is identically zero. Tensor rank vs Bias. We show that if a 3-dimensional tensor has small rank then its bias, when viewed as a 3-linear form, is large. More precisely, given any 3-dimensional tensor T: [k]³ → F₂ of rank at most t, the bias of the 3-linear form f_T(X₁, X₂, X₃) : = ∑_{(i₁, i₂, i₃) ∈ [k]³} T(i₁, i₂, i₃)⋅ X_{1,i₁}⋅ X_{2,i₂}⋅ X_{3,i₃} is at least (3/4)^t. This bias vs tensor-rank connection suggests a natural approach to proving nontrivial tensor-rank lower bounds. In particular, we use this approach to give a new proof that the finite field multiplication tensor has tensor rank at least 3.52 k, which is the best known rank lower bound for any explicit tensor in three dimensions over F₂. Moreover, this relation between bias and tensor rank holds for d-dimensional tensors for any fixed d.« less
  4. Obeid, Iyad Selesnick (Ed.)
    Electroencephalography (EEG) is a popular clinical monitoring tool used for diagnosing brain-related disorders such as epilepsy [1]. As monitoring EEGs in a critical-care setting is an expensive and tedious task, there is a great interest in developing real-time EEG monitoring tools to improve patient care quality and efficiency [2]. However, clinicians require automatic seizure detection tools that provide decisions with at least 75% sensitivity and less than 1 false alarm (FA) per 24 hours [3]. Some commercial tools recently claim to reach such performance levels, including the Olympic Brainz Monitor [4] and Persyst 14 [5]. In this abstract, we describemore »our efforts to transform a high-performance offline seizure detection system [3] into a low latency real-time or online seizure detection system. An overview of the system is shown in Figure 1. The main difference between an online versus offline system is that an online system should always be causal and has minimum latency which is often defined by domain experts. The offline system, shown in Figure 2, uses two phases of deep learning models with postprocessing [3]. The channel-based long short term memory (LSTM) model (Phase 1 or P1) processes linear frequency cepstral coefficients (LFCC) [6] features from each EEG channel separately. We use the hypotheses generated by the P1 model and create additional features that carry information about the detected events and their confidence. The P2 model uses these additional features and the LFCC features to learn the temporal and spatial aspects of the EEG signals using a hybrid convolutional neural network (CNN) and LSTM model. Finally, Phase 3 aggregates the results from both P1 and P2 before applying a final postprocessing step. The online system implements Phase 1 by taking advantage of the Linux piping mechanism, multithreading techniques, and multi-core processors. To convert Phase 1 into an online system, we divide the system into five major modules: signal preprocessor, feature extractor, event decoder, postprocessor, and visualizer. The system reads 0.1-second frames from each EEG channel and sends them to the feature extractor and the visualizer. The feature extractor generates LFCC features in real time from the streaming EEG signal. Next, the system computes seizure and background probabilities using a channel-based LSTM model and applies a postprocessor to aggregate the detected events across channels. The system then displays the EEG signal and the decisions simultaneously using a visualization module. The online system uses C++, Python, TensorFlow, and PyQtGraph in its implementation. The online system accepts streamed EEG data sampled at 250 Hz as input. The system begins processing the EEG signal by applying a TCP montage [8]. Depending on the type of the montage, the EEG signal can have either 22 or 20 channels. To enable the online operation, we send 0.1-second (25 samples) length frames from each channel of the streamed EEG signal to the feature extractor and the visualizer. Feature extraction is performed sequentially on each channel. The signal preprocessor writes the sample frames into two streams to facilitate these modules. In the first stream, the feature extractor receives the signals using stdin. In parallel, as a second stream, the visualizer shares a user-defined file with the signal preprocessor. This user-defined file holds raw signal information as a buffer for the visualizer. The signal preprocessor writes into the file while the visualizer reads from it. Reading and writing into the same file poses a challenge. The visualizer can start reading while the signal preprocessor is writing into it. To resolve this issue, we utilize a file locking mechanism in the signal preprocessor and visualizer. Each of the processes temporarily locks the file, performs its operation, releases the lock, and tries to obtain the lock after a waiting period. The file locking mechanism ensures that only one process can access the file by prohibiting other processes from reading or writing while one process is modifying the file [9]. The feature extractor uses circular buffers to save 0.3 seconds or 75 samples from each channel for extracting 0.2-second or 50-sample long center-aligned windows. The module generates 8 absolute LFCC features where the zeroth cepstral coefficient is replaced by a temporal domain energy term. For extracting the rest of the features, three pipelines are used. The differential energy feature is calculated in a 0.9-second absolute feature window with a frame size of 0.1 seconds. The difference between the maximum and minimum temporal energy terms is calculated in this range. Then, the first derivative or the delta features are calculated using another 0.9-second window. Finally, the second derivative or delta-delta features are calculated using a 0.3-second window [6]. The differential energy for the delta-delta features is not included. In total, we extract 26 features from the raw sample windows which add 1.1 seconds of delay to the system. We used the Temple University Hospital Seizure Database (TUSZ) v1.2.1 for developing the online system [10]. The statistics for this dataset are shown in Table 1. A channel-based LSTM model was trained using the features derived from the train set using the online feature extractor module. A window-based normalization technique was applied to those features. In the offline model, we scale features by normalizing using the maximum absolute value of a channel [11] before applying a sliding window approach. Since the online system has access to a limited amount of data, we normalize based on the observed window. The model uses the feature vectors with a frame size of 1 second and a window size of 7 seconds. We evaluated the model using the offline P1 postprocessor to determine the efficacy of the delayed features and the window-based normalization technique. As shown by the results of experiments 1 and 4 in Table 2, these changes give us a comparable performance to the offline model. The online event decoder module utilizes this trained model for computing probabilities for the seizure and background classes. These posteriors are then postprocessed to remove spurious detections. The online postprocessor receives and saves 8 seconds of class posteriors in a buffer for further processing. It applies multiple heuristic filters (e.g., probability threshold) to make an overall decision by combining events across the channels. These filters evaluate the average confidence, the duration of a seizure, and the channels where the seizures were observed. The postprocessor delivers the label and confidence to the visualizer. The visualizer starts to display the signal as soon as it gets access to the signal file, as shown in Figure 1 using the “Signal File” and “Visualizer” blocks. Once the visualizer receives the label and confidence for the latest epoch from the postprocessor, it overlays the decision and color codes that epoch. The visualizer uses red for seizure with the label SEIZ and green for the background class with the label BCKG. Once the streaming finishes, the system saves three files: a signal file in which the sample frames are saved in the order they were streamed, a time segmented event (TSE) file with the overall decisions and confidences, and a hypotheses (HYP) file that saves the label and confidence for each epoch. The user can plot the signal and decisions using the signal and HYP files with only the visualizer by enabling appropriate options. For comparing the performance of different stages of development, we used the test set of TUSZ v1.2.1 database. It contains 1015 EEG records of varying duration. The any-overlap performance [12] of the overall system shown in Figure 2 is 40.29% sensitivity with 5.77 FAs per 24 hours. For comparison, the previous state-of-the-art model developed on this database performed at 30.71% sensitivity with 6.77 FAs per 24 hours [3]. The individual performances of the deep learning phases are as follows: Phase 1’s (P1) performance is 39.46% sensitivity and 11.62 FAs per 24 hours, and Phase 2 detects seizures with 41.16% sensitivity and 11.69 FAs per 24 hours. We trained an LSTM model with the delayed features and the window-based normalization technique for developing the online system. Using the offline decoder and postprocessor, the model performed at 36.23% sensitivity with 9.52 FAs per 24 hours. The trained model was then evaluated with the online modules. The current performance of the overall online system is 45.80% sensitivity with 28.14 FAs per 24 hours. Table 2 summarizes the performances of these systems. The performance of the online system deviates from the offline P1 model because the online postprocessor fails to combine the events as the seizure probability fluctuates during an event. The modules in the online system add a total of 11.1 seconds of delay for processing each second of the data, as shown in Figure 3. In practice, we also count the time for loading the model and starting the visualizer block. When we consider these facts, the system consumes 15 seconds to display the first hypothesis. The system detects seizure onsets with an average latency of 15 seconds. Implementing an automatic seizure detection model in real time is not trivial. We used a variety of techniques such as the file locking mechanism, multithreading, circular buffers, real-time event decoding, and signal-decision plotting to realize the system. A video demonstrating the system is available at: The final conference submission will include a more detailed analysis of the online performance of each module. ACKNOWLEDGMENTS Research reported in this publication was most recently supported by the National Science Foundation Partnership for Innovation award number IIP-1827565 and the Pennsylvania Commonwealth Universal Research Enhancement Program (PA CURE). Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the official views of any of these organizations. REFERENCES [1] A. Craik, Y. He, and J. L. Contreras-Vidal, “Deep learning for electroencephalogram (EEG) classification tasks: a review,” J. Neural Eng., vol. 16, no. 3, p. 031001, 2019. [2] A. C. Bridi, T. Q. Louro, and R. C. L. Da Silva, “Clinical Alarms in intensive care: implications of alarm fatigue for the safety of patients,” Rev. Lat. Am. Enfermagem, vol. 22, no. 6, p. 1034, 2014. [3] M. Golmohammadi, V. Shah, I. Obeid, and J. Picone, “Deep Learning Approaches for Automatic Seizure Detection from Scalp Electroencephalograms,” in Signal Processing in Medicine and Biology: Emerging Trends in Research and Applications, 1st ed., I. Obeid, I. Selesnick, and J. Picone, Eds. New York, New York, USA: Springer, 2020, pp. 233–274. [4] “CFM Olympic Brainz Monitor.” [Online]. Available: [Accessed: 17-Jul-2020]. [5] M. L. Scheuer, S. B. Wilson, A. Antony, G. Ghearing, A. Urban, and A. I. Bagic, “Seizure Detection: Interreader Agreement and Detection Algorithm Assessments Using a Large Dataset,” J. Clin. Neurophysiol., 2020. [6] A. Harati, M. Golmohammadi, S. Lopez, I. Obeid, and J. Picone, “Improved EEG Event Classification Using Differential Energy,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium, 2015, pp. 1–4. [7] V. Shah, C. Campbell, I. Obeid, and J. Picone, “Improved Spatio-Temporal Modeling in Automated Seizure Detection using Channel-Dependent Posteriors,” Neurocomputing, 2021. [8] W. Tatum, A. Husain, S. Benbadis, and P. Kaplan, Handbook of EEG Interpretation. New York City, New York, USA: Demos Medical Publishing, 2007. [9] D. P. Bovet and C. Marco, Understanding the Linux Kernel, 3rd ed. O’Reilly Media, Inc., 2005. [10] V. Shah et al., “The Temple University Hospital Seizure Detection Corpus,” Front. Neuroinform., vol. 12, pp. 1–6, 2018. [11] F. Pedregosa et al., “Scikit-learn: Machine Learning in Python,” J. Mach. Learn. Res., vol. 12, pp. 2825–2830, 2011. [12] J. Gotman, D. Flanagan, J. Zhang, and B. Rosenblatt, “Automatic seizure detection in the newborn: Methods and initial evaluation,” Electroencephalogr. Clin. Neurophysiol., vol. 103, no. 3, pp. 356–362, 1997.« less
  5. We present a method of Gröbner bases with respect to several term orderings and use it to obtain new results on multivariate dimension polynomials of inversive difference modules. Then we use the difference structure of the module of Kahler differentials associated with a finitely generated inversive difference field extension of a given difference transcendence degree to describe the form of a multivariate difference dimension polynomial of the extension.