Populations Can Be Essential in Tracking Dynamic Optima.
Ontology highlight
ABSTRACT:
SUBMITTER: Dang DC
PROVIDER: S-EPMC5479466 | biostudies-other | 2017
REPOSITORIES: biostudies-other
Similar Datasets
Project description:Optical tracking is often combined with conventional flat panel solar cells to maximize electrical power generation over the course of a day. However, conventional trackers are complex and often require costly and cumbersome structural components to support system weight. Here we use kirigami (the art of paper cutting) to realize novel solar cells where tracking is integral to the structure at the substrate level. Specifically, an elegant cut pattern is made in thin-film gallium arsenide solar cells, which are then stretched to produce an array of tilted surface elements which can be controlled to within ±1°. We analyze the combined optical and mechanical properties of the tracking system, and demonstrate a mechanically robust system with optical tracking efficiencies matching conventional trackers. This design suggests a pathway towards enabling new applications for solar tracking, as well as inspiring a broader range of optoelectronic and mechanical devices.
| S-EPMC4569711 | biostudies-literature
Project description:We describe a chemical method to label and purify 4-thiouridine (s4U) -containing RNA. We demonstrate that methanethiolsulfonate (MTS) reagents form disulfide bonds with s4U more efficiently than the commonly used HPDP-biotin, leading to higher yields and less biased enrichment. This increase in efficiency allowed us to use s4U-labeling to study global microRNA (miRNA) turnover in proliferating cultured human cells without perturbing global miRNA levels or the miRNA processing machinery. This improved chemistry will enhance methods that depend on tracking different populations of RNA such as 4-thiouridine-tagging to study tissue-specific transcription and dynamic transcriptome analysis (DTA) to study RNA turnover. s4U metabolic labeling of RNA in 293T cells, followed by biochemical enrichment of labeled RNA with two biotinylation reagents, RNAs >200nt and miRNAs in separate experiments
2015-09-03 | E-GEOD-60988 | biostudies-arrayexpress
Project description:We describe a chemical method to label and purify 4-thiouridine (s4U) -containing RNA. We demonstrate that methanethiolsulfonate (MTS) reagents form disulfide bonds with s4U more efficiently than the commonly used HPDP-biotin, leading to higher yields and less biased enrichment. This increase in efficiency allowed us to use s4U-labeling to study global microRNA (miRNA) turnover in proliferating cultured human cells without perturbing global miRNA levels or the miRNA processing machinery. This improved chemistry will enhance methods that depend on tracking different populations of RNA such as 4-thiouridine-tagging to study tissue-specific transcription and dynamic transcriptome analysis (DTA) to study RNA turnover.
2015-09-03 | GSE60988 | GEO
Project description:3D dynamic surface tracking is an important research problem and plays a vital role in many computer vision and medical imaging applications. However, it is still challenging to efficiently register surface sequences which has large deformations and strong noise. In this paper, we propose a novel automatic method for non-rigid 3D dynamic surface tracking with surface Ricci flow and Teichmüller map methods. According to quasi-conformal Teichmüller theory, the Techmüller map minimizes the maximal dilation so that our method is able to automatically register surfaces with large deformations. Besides, the adoption of Delaunay triangulation and quadrilateral meshes makes our method applicable to low quality meshes. In our work, the 3D dynamic surfaces are acquired by a high speed 3D scanner. We first identified sparse surface features using machine learning methods in the texture space. Then we assign landmark features with different curvature settings and the Riemannian metric of the surface is computed by the dynamic Ricci flow method, such that all the curvatures are concentrated on the feature points and the surface is flat everywhere else. The registration among frames is computed by the Teichmüller mappings, which aligns the feature points with least angle distortions. We apply our new method to multiple sequences of 3D facial surfaces with large expression deformations and compare them with two other state-of-the-art tracking methods. The effectiveness of our method is demonstrated by the clearly improved accuracy and efficiency.
| S-EPMC5844492 | biostudies-literature
Project description:ES cells grown in culture are heterogeneous with respect to their transcriptional profiles, their methylation landscape and, functionally, their potency. This study is investigating overall changes in transcriptional landscape of ES cells upon overexpression of epigenetic regulators which can indicate a shift in the distribution of subpopulations.Epigenetic regulators are expressed in human embryonic stem cells, and their effect on the transcriptional landscape is analysed.This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/
2015-02-17 | E-ERAD-329 | biostudies-arrayexpress
Project description:Background:Hashtags are widely used for communication in online media. As a condensed version of information, they characterize topics and discussions. For their analysis, we apply methods from network science and propose novel tools for tracing their dynamics in time-dependent data. The observations are characterized by bursty behaviors in the increases and decreases of hashtag usage. These features can be reproduced with a novel model of dynamic rankings. Hashtag communities in time:We build temporal and weighted co-occurrence networks from hashtags. On static snapshots, we infer the community structure using customized methods. On temporal networks, we solve the bipartite matching problem of detected communities at subsequent timesteps by taking into account higher-order memory. This results in a matching protocol that is robust toward temporal fluctuations and instabilities of the static community detection. The proposed methodology is broadly applicable and its outcomes reveal the temporal behavior of online topics. Modeling topic-dynamics:We consider the size of the communities in time as a proxy for online popularity dynamics. We find that the distributions of gains and losses, as well as the interevent times are fat-tailed indicating occasional, but large and sudden changes in the usage of hashtags. Inspired by typical website designs, we propose a stochastic model that incorporates a ranking with respect to a time-dependent prestige score. This causes occasional cascades of rank shift events and reproduces the observations with good agreement. This offers an explanation for the observed dynamics, based on characteristic elements of online media.
| S-EPMC6208799 | biostudies-other
Project description:Adaptive optics optical coherence tomography (AO-OCT) is a highly sensitive and noninvasive method for three dimensional imaging of the microscopic retina. Like all in vivo retinal imaging techniques, however, it suffers the effects of involuntary eye movements that occur even under normal fixation. In this study we investigated dynamic retinal tracking to measure and correct eye motion at KHz rates for AO-OCT imaging. A customized retina tracking module was integrated into the sample arm of the 2nd-generation Indiana AO-OCT system and images were acquired on three subjects. Analyses were developed based on temporal amplitude and spatial power spectra in conjunction with strip-wise registration to independently measure AO-OCT tracking performance. After optimization of the tracker parameters, the system was found to correct eye movements up to 100 Hz and reduce residual motion to 10 µm root mean square. Between session precision was 33 µm. Performance was limited by tracker-generated noise at high temporal frequencies.
| S-EPMC4102363 | biostudies-other
Project description:Evaluation of the magnitudes of intrinsically rewarding stimuli is essential for assigning value and guiding behavior. By combining parametric manipulation of a primary reward, medial forebrain bundle (MFB) microstimulation, with functional magnetic imaging (fMRI) in rodents, we delineated a broad network of structures activated by behaviorally characterized levels of rewarding stimulation. Correlation of psychometric behavioral measurements with fMRI response magnitudes revealed regions whose activity corresponded closely to the subjective magnitude of rewards. The largest and most reliable focus of reward magnitude tracking was observed in the shell region of the nucleus accumbens (NAc). Although the nonlinear nature of neurovascular coupling complicates interpretation of fMRI findings in precise neurophysiological terms, reward magnitude tracking was not observed in vascular compartments and could not be explained by saturation of region-specific hemodynamic responses. In addition, local pharmacological inactivation of NAc changed the profile of animals' responses to rewards of different magnitudes without altering mean reward response rates, further supporting a hypothesis that neural population activity in this region contributes to assessment of reward magnitudes.
| S-EPMC5619692 | biostudies-literature
Project description:DNA methylation is a stable epigenetic modification, extremely polymorphic and driven by stochastic and deterministic events. Most of the current techniques used to analyse methylated sequences identify methylated cytosines (mCpGs) at a single-nucleotide level and compute the average methylation of CpGs in the population of molecules. Stable epialleles, i.e. CpG strings with the same DNA sequence containing a discrete linear succession of phased methylated/non-methylated CpGs in the same DNA molecule, cannot be identified due to the heterogeneity of the 5'-3' ends of the molecules. Moreover, these are diluted by random unstable methylated CpGs and escape detection. We present here MethCoresProfiler, an R-based tool that provides a simple method to extract and identify combinations of methylated phased CpGs shared by all components of epiallele families in complex DNA populations. The methylated cores are stable over time, evolve by acquiring or losing new methyl sites and, ultimately, display high information content and low stochasticity. We have validated this method by identifying and tracing rare epialleles and their families in synthetic or in vivo complex cell populations derived from mouse brain areas and cells during postnatal differentiation. MethCoresProfiler is written in R language. The software is freely available at https://github.com/84AP/MethCoresProfiler/.
| S-EPMC7671405 | biostudies-literature
Project description:In order to realize many of the potential benefits associated with robotically assisted minimally invasive surgery, the robot must be more than a remote controlled device. Currently, using a surgical robot can be challenging, fatiguing, and time consuming. Teaching the robot to actively assist surgical tasks, such as suturing, has the potential to vastly improve both patient outlook and the surgeon's efficiency. One obstacle to completing surgical sutures autonomously is the difficulty in tracking surgical suture threads. This paper presents novel stereo image processing algorithms for the detection, initialization, and tracking of a surgical suture thread. A Non Uniform Rational B-Spline (NURBS) curve is used to model a thin, deformable, and dynamic length thread. The NURBS model is initialized and grown from a single selected point located on the thread. The NURBS curve is optimized by minimizing the image matching energy between the projected stereo NURBS image and the segmented thread image. The algorithms are evaluated using suture threads, a calibrated test pattern, and a simulated thread image. Additionally, the accuracy of the algorithms presented are validated as they track a suture thread undergoing translation, deformation, and apparent length changes. All of the tracking is in real-time. Note to Practioners: Abstract-The problem of tracking a surgical suture thread was addressed in this work. Since the suture thread is highly deformable, any tracking algorithm must be robust to intersections, occlusions, knot tying, and length changes. The detection algorithm introduced in this paper is capable of distinguishing different threads when they intersect. The tracking algorithm presented here demonstrate that it is possible, using polynomial curves, to track a suture thread as it deforms, becomes occluded, changes length, and even ties a knot in real time. The detection algorithm can enhance directional thin features while the polynomial curve modeling can track any string like structure. Further integration of the polynomial curve with a feed-forward thread model could improve the stability and robustness of the thread tracking.
| S-EPMC6034738 | biostudies-literature