scholarly journals Scalable Spatio-Temporal Video Indexing Using Sparse Multiscale Patches

2009 ◽  
Author(s):  
Paolo Piro ◽  
Sandrine Anthoine ◽  
Eric Debreuve ◽  
Michel Barlaud
Keyword(s):  
Video Indexing ◽  
Spatio Temporal

scholarly journals IDENTIFYING OVERLAPPED OBJECTS FOR VIDEO INDEXING AND MODELING IN MULTIMEDIA DATABASE SYSTEMS

2001 ◽  
Vol 10 (04) ◽  
pp. 715-734 ◽  
Author(s):  
SHU-CHING CHEN ◽  
MEI-LING SHYU ◽  
CHENGCUI ZHANG ◽  
R. L. KASHYAP
Keyword(s):  
Spatial Information ◽  
Video Segmentation ◽  
Database Systems ◽  
Video Indexing ◽  
Video Data ◽  
Multimedia Database ◽  
Current Frame ◽  
Data Indexing ◽  
Spatio Temporal ◽  
Input Strings

The identification of the overlapped objects is a great challenge in object tracking and video data indexing. For this purpose, a backtrack-chain-updation split algorithm is proposed to assist an unsupervised video segmentation method called the "simultaneous partition and class parameter estimation" (SPCPE) algorithm to identify the overlapped objects in the video sequence. The backtrack-chain-updation split algorithm can identify the split segment (object) and use the information in the current frame to update the previous frames in a backtrack-chain manner. The split algorithm provides more accurate temporal and spatial information of the semantic objects so that the semantic objects can be indexed and modeled by multimedia input strings and the multimedia augmented transition network (MATN) model. The MATN model is based on the ATN model that has been used in artificial intelligence (AI) areas for natural language understanding systems, and its inputs are modeled by the multimedia input strings. In this paper, we will show that the SPCPE algorithm together with the backtrack-chain-updation split algorithm can significantly enhance the efficiency of spatio-temporal video indexing by improving the accuracy of multimedia database queries related to semantic objects.

Video Caption Extraction Using Spatio-Temporal Slices

2018 ◽  
Vol 18 (02) ◽  
pp. 1850009 ◽  
Author(s):  
Liang-Hua Chen ◽  
Chih-Wen Su
Keyword(s):  
Video Indexing ◽  
Experimental Results ◽  
Bar Code ◽  
Structure Information ◽  
Indexing And Retrieval ◽  
Scan Line ◽  
Video Indexing And Retrieval ◽  
Spatio Temporal ◽  
Novel Algorithm

Captions in videos play an important role for video indexing and retrieval. In this paper, we propose a novel algorithm to extract multilingual captions from video. Our approach is based on the analysis of spatio-temporal slices of video. If the horizontal (or vertical) scan line contains some pixels of caption region then the corresponding spatio-temporal slice will have bar-code like patterns. By integrating the structure information of bar-code like patterns in horizontal and vertical slices, the spatial and temporal positions of video captions can be located accurately. Experimental results show that the proposed algorithm is effective and outperforms some existing techniques.

E3 ubiquitin ligases

2005 ◽  
Vol 41 ◽  
pp. 15-30 ◽  
Author(s):  
Helen C. Ardley ◽  
Philip A. Robinson
Keyword(s):  
Protein Complexes ◽  
Loss Of Function ◽  
Direct Role ◽  
Cellular Processes ◽  
Substrate Protein ◽  
Protein Ubiquitination ◽  
C Terminus ◽  
Full Complement ◽  
Spatio Temporal ◽  
Eukaryotic Organisms

The selectivity of the ubiquitin–26 S proteasome system (UPS) for a particular substrate protein relies on the interaction between a ubiquitin-conjugating enzyme (E2, of which a cell contains relatively few) and a ubiquitin–protein ligase (E3, of which there are possibly hundreds). Post-translational modifications of the protein substrate, such as phosphorylation or hydroxylation, are often required prior to its selection. In this way, the precise spatio-temporal targeting and degradation of a given substrate can be achieved. The E3s are a large, diverse group of proteins, characterized by one of several defining motifs. These include a HECT (homologous to E6-associated protein C-terminus), RING (really interesting new gene) or U-box (a modified RING motif without the full complement of Zn2+-binding ligands) domain. Whereas HECT E3s have a direct role in catalysis during ubiquitination, RING and U-box E3s facilitate protein ubiquitination. These latter two E3 types act as adaptor-like molecules. They bring an E2 and a substrate into sufficiently close proximity to promote the substrate's ubiquitination. Although many RING-type E3s, such as MDM2 (murine double minute clone 2 oncoprotein) and c-Cbl, can apparently act alone, others are found as components of much larger multi-protein complexes, such as the anaphase-promoting complex. Taken together, these multifaceted properties and interactions enable E3s to provide a powerful, and specific, mechanism for protein clearance within all cells of eukaryotic organisms. The importance of E3s is highlighted by the number of normal cellular processes they regulate, and the number of diseases associated with their loss of function or inappropriate targeting.

Elucidating cyclic AMP signaling in subcellular domains with optogenetic tools and fluorescent biosensors

2019 ◽  
Vol 47 (6) ◽  
pp. 1733-1747 ◽  
Author(s):  
Christina Klausen ◽  
Fabian Kaiser ◽  
Birthe Stüven ◽  
Jan N. Hansen ◽  
Dagmar Wachten
Keyword(s):  
Cyclic Amp ◽  
Adenosine Monophosphate ◽  
Adenylyl Cyclases ◽  
Temporal Precision ◽  
Fluorescent Biosensors ◽  
Subcellular Domains ◽  
Spatio Temporal ◽  
Hydrolysis Of ◽  
Shed Light ◽  
Cyclic Amp Signaling

The second messenger 3′,5′-cyclic nucleoside adenosine monophosphate (cAMP) plays a key role in signal transduction across prokaryotes and eukaryotes. Cyclic AMP signaling is compartmentalized into microdomains to fulfil specific functions. To define the function of cAMP within these microdomains, signaling needs to be analyzed with spatio-temporal precision. To this end, optogenetic approaches and genetically encoded fluorescent biosensors are particularly well suited. Synthesis and hydrolysis of cAMP can be directly manipulated by photoactivated adenylyl cyclases (PACs) and light-regulated phosphodiesterases (PDEs), respectively. In addition, many biosensors have been designed to spatially and temporarily resolve cAMP dynamics in the cell. This review provides an overview about optogenetic tools and biosensors to shed light on the subcellular organization of cAMP signaling.

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