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13,064 results for “predictions”
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 4. Drawing of autocorrelation function and partial correlation for males primary stage students
<p>We get to notice the stability of the time series, and to be more accurate we draw each (Autocorrelation Function) ACF, and (Partial Autocorrelation Function) PACF in a row to ensure the stability according to the figure (4).</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 5. Drawing the time series for primary stage female students
<p>We use the Unit Radix Dickey-Fuller Test to assure the series’ stability. The results are: Dickey-Fuller Test Estimated Value = 0.233403, Statistic Test = 0.125769, P-Value = 0.6405 The values above P-Value = 0.6405 is noted on the abstract level of 0.05 which leads to refusing the Null Hypothesis and accepting the Alternative Hypothesis (The Nonexistence of a Radix Unit) implies that the time series is stable. Figure 5 represents the Time series of Female Primary Stage Students.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 8. Drawing of autocorrelation function and partial correlation for Females primary stage students
<p>The stability of the time series is observed and to be more accurate we draw each (Autocorrelation Function) ACF, and (Partial Autocorrelation Function) PACF in a row to assure the stability according to the figure (8).</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 3. Drawing the time series for Males primary stage students after getting the first difference
<p>The Unit Radix Dickey-Fuller Test is used to assure the series’ stability. The results are: Dickey-Fuller Test Estimated Value = 0.276151, Statistic Test = 0.87796, P-Value = 0.8984 We get to notice from the values above P-Value = 0.8984 on the abstract level of 0.05 which leads to accepting the Null Hypothesis and refusing the Alternative Hypothesis (Existence of a Radix Unit) implies that the time series is instable. By taking the first difference, it is observed that the stability of the Time Series has been accomplished . See figure 3.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 2. Drawing of autocorrelation function and partial correlation for males primary stage
<p>We get to notice the instability of the time series, and to be more precise we draw each (Autocorrelation Function) ACF, and (Partial Autocorrelation Function) PACF in a row to ensure the stability according to the figure 2.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 1. Drawing the time series for males primary stage
<p>After collecting all the students’ dropout proportion for both males and females in the<br> primary stage, the first step of the Box-Jenkins is to draw the time chain data to understand the<br> chain's attitude.</p>
Data to accompany the paper "Improved fragment-based protein structure prediction by redesign of search heuristics"
<p>This repository contains the older and newer input fragment sets and other data used for the analyses in our paper. The filenames for each tarball contain the PDB identifier of each protein along with a chain ID if applicable, followed by 'old' or 'new' for old and new fragments, respectively. Each tarball contains: a .fasta file of the input sequence, a matching PDB structure file, the relevant PSIPRED secondary structure prediction file, and the 9mer and 3mer fragment files. <br> <br> An additional tarball, ScoreRMSDplots_3protocols.tgz, contains extended versions of Figure 3 which show score and RMSD distributions clearly. Additionally, the same data is shown for equivalent experiments using the older fragment set.</p>
Data for "Sounding out Ecoacoustic Metrics: Avian species richness is predicted by acoustic indices in temperate but not tropical habitats"
<p>This deposit contains the data for the paper <strong>A Multi-habitat, Comparative Evaluation of Ecoacoustic Indices for Biodiversity Monitoring: Acoustic Indices Predict Avian Species Richness in Temperate but not Tropical Habitats. (Ecological Indicators) </strong>The dataset contains a series of 1 min wav files recorded across UK and Ecuadorian habitats. Each one has 26 acoustic indices calculated on it, and a full list of avian species and abundances and GPS data for each sample site.</p> <p>Abstract</p> <p>Affordable, autonomous recording devices facilitate large scale acoustic monitoring and Rapid Acoustic Survey is emerging as a cost-effective approach to ecological monitoring; the success of the approach rests on the development of computational methods by which biodiversity metrics can be automatically derived from remotely collected audio data. Dozens of indices have been proposed to date, but systematic validation against classical, in situ diversity measures. This study conducted the most comprehensive comparative evaluation to date of the relationship between avian species diversity and a suite of acoustic indices across a wide range of ecological conditions. Acoustic surveys were carried out across habitat gradients in temperate and tropical biomes. Baseline avian species richness and subjective multi-taxa biophonic density estimates were established through aural counting by expert ornithologists. 26 acoustic indices were calculated and compared to observed variations in species diversity. Five acoustic diversity indices (Bioacoustic Index, Acoustic Diversity Index, Acoustic Evenness Index, Acoustic Entropy, and the Normalised Difference Sound Index) were assessed as well as three simple acoustic descriptors (root-mean-square, spectral centroid and zero-crossing rate). Highly significant correlations, of up to 65%, between acoustic indices and avian species richness were observed across temperate habitats, supporting the use of automated acoustic indices in biodiversity monitoring where a single vocal taxon dominates. Significant, weaker correlations were observed in neotropical habitats which host multiple non-avian vocalizing species. Multivariate classification analyses suggest that AIs also track observed differences in habitat-dependent community composition and that each habitat has a distinct soundscape. Multivariate analyses of the relative predictive power of AIs show that compound indices are more powerful predictors of avian species richness than any single index and simple descriptors contribute to predicting avian diversity in multi-taxa tropical environments. Our results support the use of community level acoustic indices as a proxy for species richness and point to the potential for tracking of habitat-dependent changes in community composition. Recommendations for the design of compound indices for multi-taxa community composition appraisal are put forward, with consideration for the requirements of next generation, low power remote monitoring networks.</p> <p> </p> <p><strong>Sampling Methods (extract from paper)</strong></p> <p>Acoustic surveys were carried out along a gradient of habitat degradation (1 forested, 2 regenerating forest and 3 agricultural land) in South East (SE) England and North Western (NW) Ecuador. The six sites (UK1, UK2, UK3, EC1, EC2, EC3) were sampled consecutively from May 6th - Aug 25th 2015.</p> <p>All UK sites were in the county of Sussex, in SE England, an area of weald clays (Fig. 2, left) and included ancient woodland (UK1), regenerating farmland with patches of woodland (UK2) and a downland barley farm (UK3).1 min mono audio recordings made every 15 minutes at three different habitats in the UK</p> <p>Ten day acoustic surveys were carried out consecutively at each study site using 15 Wildlife Acoustics Song Meter audio field recorders. Sampling points were arranged in a grid at a minimum distance of 200 m to minimise pseudo replication (the sound of most species being attenuated over this distance in all biomes). Altitudinal range of sample points across sites was minimised in order to prevent introduction of extraneous, confounding gradients (UK varied between 10 m – 50 m and Ecuador 130 m – 390 m). Recording schedules captured 1 min every 15 min around the clock for 10 days at each site, resulting in 960 recordings at each of 15 sample points for 3 habitat types in 2 different climates (86,400 1 minute recordings in total). Data across the 15 sample points was pooled; inter-site variation was not explored in the current analyses. In the UK 3½ hours of each dawn chorus was sampled starting at 1 hour before sunrise. This range was determined to capture the onset, progression and peak of the dawn chorus, creating a temporal gradient. The equatorial dawn chorus is more compact and was sampled for 2¼ hours starting 15 mins before sunrise, capturing a comparable chorus onset and peak.</p> <p> </p> <p> </p>
Data archive for Allen and Nettle, 'Hunger and socioeconomic background additively predict impulsivity in humans'
<p>This archive contains the raw data from Allen and Nettle, 'Hunger and socioeconomic background additively predict impulsivity in humans', plus R code for the data analyses. The impulsivity measure (HMDT) used in studies 2 and 3 is also included here. </p> <p>The R script 'IndividualAnalysis.R' performs the analysis of each study individually. 'MetaAnalysis.R' performs the meta-analysis. The three .csv files are the raw data from the three studies respectively. </p>
Atmospheric_river_precipitation_predictability_data
<p>Data for the manuscript entitled "Predictability of Extreme Precipitation Associated With Atmospheric Rivers in Western U.S. Watersheds".</p> <p> </p> <p>It includes daily precipitation data from WRF and PRISM. Also includes atmospheric river information derived from ARTMIP Tier 1 archive.</p> <p> </p> <p>The tools used to generate the figures in the paper is at: <a href="https://github.com/lucas-uw/Chen-2018-GRL">https://github.com/lucas-uw/Chen-2018-GRL</a></p> <p> </p> <p>If you use this dataset, please cite the following paper:</p> <p> </p> <p>Chen, X., Leung, L. R., Gao, Y., Liu, Y., Wigmosta, M., & Richmond, M. (2018). Predictability of extreme precipitation in western U.S. watersheds based on atmospheric river occurrence, intensity, and duration. Geophysical Research Letters, 45, 11,693–11,701. <a href="http://doi.org/10.1029/2018GL079831">https://doi.org/10.1029/2018GL079831</a></p> <p> </p> <p>Chen, X., Leung, L. R., Wigmosta, M., & Richmond, M. (2019). Impact of Atmospheric Rivers on Surface Hydrological Processes in Western U.S. Watersheds. Journal of Geophysical Research: Atmospheres, <a href="http://doi.org/10.1029/2019JD03468">https://doi.org/10.1029/2019JD03468</a></p>
Partially automatically annotated corpus to predict gestural cues in Embodied Conversational Agents
<p>#Structure of the corpus</p> <p>This corpus has been built using speeches of Spanish politicians freely available <a href="http://www.congreso.es/portal/page/portal/Congreso/Congreso/Intervenciones">here</a> along with their transcriptions.</p> <p>Each transcription has been analyzed in terms of:</p> <ul> <li>Surface Syntactic Structure*</li> <li>Deep Syntactic Structure*</li> <li>Morphology (Part of Speech)*</li> <li>Communicative Structure</li> </ul> <p>Gestures (beat vs. no gesture tags) have been annotated using the videos.</p> <p>*All those features have been automatically retrieved using the parser freely available in https://github.com/TalnUPF/miis. The other features have been annotated manually.</p> <p>#Concerns about the corpus</p> <p>This corpus has been mostly annotated manually. Annotation agreement has not been computed.</p> <p>Moreover, it is small. In order to extract reliable correlations from it, it should be extended.</p>
DBv5 features and codified complexes used in BIPSPI: a method for the prediction of partner-specific protein–protein interfaces
<p>Features and protein complexes codified for DBv5 BIPSPI paper</p> <p>(BIPSPI: a method for the prediction of partner-specific protein–protein interfaces</p> <p><a>Ruben Sanchez-Garcia</a> <a>C O S Sorzano</a> <a>J M Carazo</a> <a>Joan Segura</a></p> <p><em>Bioinformatics</em>, bty647, <a href="https://doi.org/10.1093/bioinformatics/bty647">https://doi.org/10.1093/bioinformatics/bty647</a>)</p>
The Results of Applying Potential Predictability (PP)
<p>Author: Mao-Lin Shen (E-mail: maolin.shen@uib.no)</p> <p>Figures of the potential predictability based on signal-to-noise ratio.</p>
Distinguishing between pan assay interference compounds (PAINS) that are promiscuous or represent dark chemical matter - data set and prediction models
<p>Data sets of promiscuous PAINS (PROM_PAINS) and dark chemical matter PAINS (DCM_PAINS) are provided and support vector machine models built on the basis of original and balanced training data (see readme.txt).<br> </p>
Italian Tweet Embeddings Used For Emoji Prediction
<p>This dataset contains 100d word embeddings trained on 48M Italian tweets using fastText and employed by our team to predict emojis during ITAmoji competition of EVALITA 2018 Evaluation Campaign.</p>
Predictive simulations of ionization energies of solvated halide ions with relativistic embedded Equation of Motion Coupled-Cluster Theory: Dataset
<p>This dataset collects the unprocessed (= outputs from calculations) and processed (= plots, average values for ionization energies) results discussed in the paper titled "Predictive simulations of ionization energies of solvated halide ions with relativistic embedded Equation of Motion Coupled-Cluster Theory", by Yassine Bouchafra, Avijit Shee, Florent Réal, Valérie Vallet and André Severo Pereira Gomes.</p> <p>In each archive file there is a README explaining how to use the bundled scripts to process the data.</p>
Enzymes from the BRENDA database annotated with organism growth temperatures and predicted Topt
<p>Experimental as well as predicted organism growth temperatures were used to annotate enzymes from the BRENDA database (doi: 10.1093/nar/gky1048, https://www.brenda-enzymes.org) version 2018.2 (July 2018). The growth temperature annotation can be used as an estimate of the enzymes catalytic optima. In addition to this, the sequence of each enzyme was taken into account to predict catalytic optima, which are more accurate than simply using OGT as an estimate.</p> <p>The "enzyme_ogt_topt.tsv" file is a tab-separated file with the data headers: ec, uniprot_id, domain, organism, ogt, ogt_source, topt and topt_source. The ec column lists enzyme classes. The uniprot_id lists UniProt identifiers. The domain column lists the domain of life (superkingdom), either Archaea, Bacteria, or Eukarya. The organism column lists organism names, with strain designations removed and formatted to lowercase characters with an underscore _ separating the name parts. The ogt column lists, in degrees centigrade, the organism growth temperature. The ogt_source column lists whether experimental growth temperatures or predicted ones were used for the annotation. The topt column lists the enzyme catalytic optimum. Finally, the topt_source column lists whether experimental or predicted topt was used for the annotation.</p> <p>The "brenda_sequences_20180109.fasta" file follows the standard FASTA format and contains the protein sequences for all annotated enzymes. UniProt identifiers are used as a header for each of the sequences.</p> <p> </p>
Overview of available toxicity data for calystegines - results of the in silico genotoxicity predictions
<p>Results of the<em> in silico</em> genotoxicity predictions complementing the EFSA scientific report on calystegines: https://doi.org/10.2903/j.efsa.2019.5574</p>
AbDb processed and pickled for use in deep learning CDR-H3 Structure prediction
<p>This is a pickle file, ready for training by the neural network described in "Improving CDR-H3 modelling in Antibodies" found at the following URL:</p> <p><a href="https://github.com/OniDaito/MRes">https://github.com/OniDaito/MRes</a></p> <p>The data is derived from the AbDb dataset found at:</p> <p><a href="http://www.bioinf.org.uk/abs/abdb/">http://www.bioinf.org.uk/abs/abdb/</a></p>
Permeability Prediction in Rocks Experiencing Mineral Precipitation and Dissolution: A Numerical Study
<p>Data sets for the Publication 'Permeability Prediction in Rocks Experiencing Mineral Precipitation and Dissolution: A Numerical Study' in Water Resources Research.</p>
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.