124 research outputs found
Heisenberg Uniqueness Pairs and the wave equation
Given a curve and a set in the plane, the concept of the
Heisenberg uniqueness pair was first introduced by
Hedenmalm and Motes-Rodr\'{\i}gez (Ann. of Math. 173(2),1507-1527, 2011,
\cite{HM}) as a variant of the uncertainty principle for the Fourier transform.
The main results of Hedenmalm and Motes-Rodr\'{\i}gez concern the hyperbola
() and lattice-crosses
(), where it's proved that
is a Heisenberg uniqueness pair if
and only if .
In this paper, we aim to study the endpoint case (i.e., in
) and investigate the following problem: what's the minimal
amount of information required on (the zero set) to form a Heisenberg
uniqueness pair? When is contained in the union of two curves in the
plane, we give characterizations in terms of some dynamical system conditions.
The situation is quite different in higher dimensions and we obtain
characterizations in the case that is the union of two hyperplanes.Comment: 24 page
Constructing Cooking Ontology for Live Streams
We build a cooking domain knowledge by using an ontology schema that reflects natural language processing and enhances ontology instances with semantic query. Our research helps audiences to better understand live streaming, especially when they just switch to a show. The practical contribution of our research is to use cooking ontology, so we may map clips of cooking live stream video and instructions of recipes. The architecture of our study presents three sections: ontology construction, ontology enhancement, and mapping cooking video to cooking ontology. Also, our preliminary evaluations consist of three hierarchies—nodes, ordered-pairs, and 3-tuples—that we use to referee (1) ontology enhancement performance for our first experiment evaluation and (2) the accuracy ratio of mapping between video clips and cooking ontology for our second experiment evaluation. Our results indicate that ontology enhancement is effective and heightens accuracy ratios on matching pairs with cooking ontology and video clips
Spiking Inception Module for Multi-layer Unsupervised Spiking Neural Networks
Spiking Neural Network (SNN), as a brain-inspired approach, is attracting
attention due to its potential to produce ultra-high-energy-efficient hardware.
Competitive learning based on Spike-Timing-Dependent Plasticity (STDP) is a
popular method to train an unsupervised SNN. However, previous unsupervised
SNNs trained through this method are limited to a shallow network with only one
learnable layer and cannot achieve satisfactory results when compared with
multi-layer SNNs. In this paper, we eased this limitation by: 1)We proposed a
Spiking Inception (Sp-Inception) module, inspired by the Inception module in
the Artificial Neural Network (ANN) literature. This module is trained through
STDP-based competitive learning and outperforms the baseline modules on
learning capability, learning efficiency, and robustness. 2)We proposed a
Pooling-Reshape-Activate (PRA) layer to make the Sp-Inception module stackable.
3)We stacked multiple Sp-Inception modules to construct multi-layer SNNs. Our
algorithm outperforms the baseline algorithms on the hand-written digit
classification task, and reaches state-of-the-art results on the MNIST dataset
among the existing unsupervised SNNs.Comment: Published at the 2020 International Joint Conference on Neural
Networks (IJCNN); Extended from arXiv:2001.0168
SparseSpikformer: A Co-Design Framework for Token and Weight Pruning in Spiking Transformer
As the third-generation neural network, the Spiking Neural Network (SNN) has
the advantages of low power consumption and high energy efficiency, making it
suitable for implementation on edge devices. More recently, the most advanced
SNN, Spikformer, combines the self-attention module from Transformer with SNN
to achieve remarkable performance. However, it adopts larger channel dimensions
in MLP layers, leading to an increased number of redundant model parameters. To
effectively decrease the computational complexity and weight parameters of the
model, we explore the Lottery Ticket Hypothesis (LTH) and discover a very
sparse (90%) subnetwork that achieves comparable performance to the
original network. Furthermore, we also design a lightweight token selector
module, which can remove unimportant background information from images based
on the average spike firing rate of neurons, selecting only essential
foreground image tokens to participate in attention calculation. Based on that,
we present SparseSpikformer, a co-design framework aimed at achieving sparsity
in Spikformer through token and weight pruning techniques. Experimental results
demonstrate that our framework can significantly reduce 90% model parameters
and cut down Giga Floating-Point Operations (GFLOPs) by 20% while maintaining
the accuracy of the original model
THE IDENTIFICATION OF NOTEWORTHY HOTEL REVIEWS FOR HOTEL MANAGEMENT
The rapid emergence of user-generated content (UGC) inspires knowledge sharing among Internet users. A good example is the well-known travel site TripAdvisor.com, which enables users to share their experiences and express their opinions on attractions, accommodations, restaurants, etc. The UGC about travel provide precious information to the users as well as staff in travel industry. In particular, how to identify reviews that are noteworthy for hotel management is critical to the success of hotels in the competitive travel industry. We have employed two hotel managers to conduct an examination on Taiwan’s hotel reviews in Tripadvisor.com and found that noteworthy reviews can be characterized by their content features, sentiments, and review qualities. Through the experiments using tripadvisor.com data, we find that all three types of features are important in identifying noteworthy hotel reviews. Specifically, content features are shown to have the most impact, followed by sentiments and review qualities. With respect to the various methods for representing content features, LDA method achieves comparable performance to TF-IDF method with higher recall and much fewer features
The Research on the Detection of Noteworthy Symptom Descriptions
The advance of mobile devices and communication technologies enable patients to communicate with their doctors in a more convenient way. We have developed an App that allows patients to record their symptoms and submit them to their doctors. Physicians can keep track of patients’ conditions by looking at the self-report messages. Nevertheless, physicians are usually busy and may be overwhelmed by the large amount of incoming messages. As a result, critical messages may not receive immediate attentions, and patient care is compromised. It is imperative to identify the messages that require physicians’ attention, called noteworthy messages. In this research, we propose an approach that applies text-mining technologies to identify medical symptoms conveyed in the messages and their associated sentiment orientation, as well as other factors. Noteworthy messages are subsequently characterized by symptom sentiment and symptom change features. We then construct a prediction model to identify messages that are noteworthy to the physicians. We show from our experiments using data collected from a teaching hospital in Taiwan that the different features have different degrees of impact on the performance of the prediction model, and our proposed approach can effectively identify noteworthy messages
Identification and Characterization of microRNAs from Peanut (Arachis hypogaea L.) by High-Throughput Sequencing
BACKGROUND: MicroRNAs (miRNAs) are noncoding RNAs of approximately 21 nt that regulate gene expression in plants post-transcriptionally by endonucleolytic cleavage or translational inhibition. miRNAs play essential roles in numerous developmental and physiological processes and many of them are conserved across species. Extensive studies of miRNAs have been done in a few model plants; however, less is known about the diversity of these regulatory RNAs in peanut (Arachis hypogaea L.), one of the most important oilseed crops cultivated worldwide. RESULTS: A library of small RNA from peanut was constructed for deep sequencing. In addition to 126 known miRNAs from 33 families, 25 novel peanut miRNAs were identified. The miRNA* sequences of four novel miRNAs were discovered, providing additional evidence for the existence of miRNAs. Twenty of the novel miRNAs were considered to be species-specific because no homolog has been found for other plant species. qRT-PCR was used to analyze the expression of seven miRNAs in different tissues and in seed at different developmental stages and some showed tissue- and/or growth stage-specific expression. Furthermore, potential targets of these putative miRNAs were predicted on the basis of the sequence homology search. CONCLUSIONS: We have identified large numbers of miRNAs and their related target genes through deep sequencing of a small RNA library. This study of the identification and characterization of miRNAs in peanut can initiate further study on peanut miRNA regulation mechanisms, and help toward a greater understanding of the important roles of miRNAs in peanut
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High-throughput monitoring of wild bee diversity and abundance via mitogenomics
1. Bee populations and other pollinators face multiple, synergistically acting threats, which have led to population declines, loss of local species richness and pollination services, and extinctions. However, our understanding of the degree, distribution and causes of declines is patchy, in part due to inadequate monitoring systems, with the challenge of taxonomic identification posing a major logistical barrier. Pollinator conservation would benefit from a high-throughput identification pipeline.
2. We show that the metagenomic mining and resequencing of mitochondrial genomes (mitogenomics) can be applied successfully to bulk samples of wild bees. We assembled the mitogenomes of 48 UK bee species and then shotgun-sequenced total DNA extracted from 204 whole bees that had been collected in 10 pan-trap samples from farms in England and been identified morphologically to 33 species. Each sample data set was mapped
against the 48 reference mitogenomes.
3. The morphological and mitogenomic data sets were highly congruent. Out of 63 total species detections in the morphological data set, the mitogenomic data set made 59 correct detections (93�7% detection rate) and detected
six more species (putative false positives). Direct inspection and an analysis with species-specific primers suggested that these putative false positives were most likely due to incorrect morphological IDs. Read frequency
significantly predicted species biomass frequency (R2 = 24�9%). Species lists, biomass frequencies, extrapolated
species richness and community structure were recovered with less error than in a metabarcoding pipeline.
4. Mitogenomics automates the onerous task of taxonomic identification, even for cryptic species, allowing the
tracking of changes in species richness and istributions. A mitogenomic pipeline should thus be able to contain
costs, maintain consistently high-quality data over long time series, incorporate retrospective taxonomic revisions and provide an auditable evidence trail. Mitogenomic data sets also provide estimates of species counts within samples and thus have potential for tracking population trajectories
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
Funder: NCI U24CA211006Abstract: The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) curated consensus somatic mutation calls using whole exome sequencing (WES) and whole genome sequencing (WGS), respectively. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we compare WES and WGS side-by-side from 746 TCGA samples, finding that ~80% of mutations overlap in covered exonic regions. We estimate that low variant allele fraction (VAF < 15%) and clonal heterogeneity contribute up to 68% of private WGS mutations and 71% of private WES mutations. We observe that ~30% of private WGS mutations trace to mutations identified by a single variant caller in WES consensus efforts. WGS captures both ~50% more variation in exonic regions and un-observed mutations in loci with variable GC-content. Together, our analysis highlights technological divergences between two reproducible somatic variant detection efforts
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