Nursing Home Compare has detailed information about every Medicare and Medicaid nursing home in the country. A nursing home is a place for people who can’t be cared for at home and need 24-hour nursing care. These are the official datasets used on the Medicare.gov Nursing Home Compare Website provided by the Centers for Medicare & Medicaid Services. These data allow you to compare the quality of care at every Medicare and Medicaid-certified nursing home in the country, including over 15,000 nationwide.

Comparison of OR tables between the interaction of rs7522462 and rs11945978 in the WTCCC data with the shared controls (left) and the interaction of the proxy SNPs, rs296533 and rs2089509 in the IBDGC data (right). The legend to this table is the same as that of Table 3.

Different Stages

## Overview

Different Stages is a dataset for object detection tasks - it contains Dancer annotations for 3,843 images.

## Getting Started

You can download this dataset for use within your own projects, or fork it into a workspace on Roboflow to create your own model.

  ## License

  This dataset is available under the [CC BY 4.0 license](https://creativecommons.org/licenses/CC BY 4.0).

GENERAL INFORMATION

Title of Dataset: A dataset from a survey investigating disciplinary differences in data citation

Date of data collection: January to March 2022

Collection instrument: SurveyMonkey

Funding: Alfred P. Sloan Foundation

SHARING/ACCESS INFORMATION

Licenses/restrictions placed on the data: These data are available under a CC BY 4.0 license

Links to publications that cite or use the data:

Gregory, K., Ninkov, A., Ripp, C., Peters, I., & Haustein, S. (2022). Surveying practices of data citation and reuse across disciplines. Proceedings of the 26th International Conference on Science and Technology Indicators. International Conference on Science and Technology Indicators, Granada, Spain. https://doi.org/10.5281/ZENODO.6951437

Gregory, K., Ninkov, A., Ripp, C., Roblin, E., Peters, I., & Haustein, S. (2023). Tracing data:
A survey investigating disciplinary differences in data citation. Zenodo. https://doi.org/10.5281/zenodo.7555266

DATA & FILE OVERVIEW

File List

• Filename: MDCDatacitationReuse2021Codebookv2.pdf
  Codebook
• Filename: MDCDataCitationReuse2021surveydatav2.csv
  Dataset format in csv
• Filename: MDCDataCitationReuse2021surveydatav2.sav
  Dataset format in SPSS
• Filename: MDCDataCitationReuseSurvey2021QNR.pdf
  Questionnaire

Additional related data collected that was not included in the current data package: Open ended questions asked to respondents

METHODOLOGICAL INFORMATION

Description of methods used for collection/generation of data:

The development of the questionnaire (Gregory et al., 2022) was centered around the creation of two main branches of questions for the primary groups of interest in our study: researchers that reuse data (33 questions in total) and researchers that do not reuse data (16 questions in total). The population of interest for this survey consists of researchers from all disciplines and countries, sampled from the corresponding authors of papers indexed in the Web of Science (WoS) between 2016 and 2020.

Received 3,632 responses, 2,509 of which were completed, representing a completion rate of 68.6%. Incomplete responses were excluded from the dataset. The final total contains 2,492 complete responses and an uncorrected response rate of 1.57%. Controlling for invalid emails, bounced emails and opt-outs (n=5,201) produced a response rate of 1.62%, similar to surveys using comparable recruitment methods (Gregory et al., 2020).

Methods for processing the data:

Results were downloaded from SurveyMonkey in CSV format and were prepared for analysis using Excel and SPSS by recoding ordinal and multiple choice questions and by removing missing values.

Instrument- or software-specific information needed to interpret the data:

The dataset is provided in SPSS format, which requires IBM SPSS Statistics. The dataset is also available in a coded format in CSV. The Codebook is required to interpret to values.

DATA-SPECIFIC INFORMATION FOR: MDCDataCitationReuse2021surveydata

Number of variables: 95

Number of cases/rows: 2,492

Missing data codes: 999 Not asked

Refer to MDCDatacitationReuse2021Codebook.pdf for detailed variable information.

The Meta-Dataset benchmark is a large few-shot learning benchmark and consists of multiple datasets of different data distributions. It does not restrict few-shot tasks to have fixed ways and shots, thus representing a more realistic scenario. It consists of 10 datasets from diverse domains:

ILSVRC-2012 (the ImageNet dataset, consisting of natural images with 1000 categories) Omniglot (hand-written characters, 1623 classes) Aircraft (dataset of aircraft images, 100 classes) CUB-200-2011 (dataset of Birds, 200 classes) Describable Textures (different kinds of texture images with 43 categories) Quick Draw (black and white sketches of 345 different categories) Fungi (a large dataset of mushrooms with 1500 categories) VGG Flower (dataset of flower images with 102 categories), Traffic Signs (German traffic sign images with 43 classes) MSCOCO (images collected from Flickr, 80 classes).

All datasets except Traffic signs and MSCOCO have a training, validation and test split (proportioned roughly into 70%, 15%, 15%). The datasets Traffic Signs and MSCOCO are reserved for testing only.

This online application gives manufacturers the ability to compare Iowa to other states on a number of different topics including: business climate, education, operating costs, quality of life and workforce.

This dataset is about books. It has 1 row and is filtered where the book is Ordinary difference-differential equations. It features 7 columns including author, publication date, language, and book publisher.

This dataset provides values for WORLD reported in several countries. The data includes current values, previous releases, historical highs and record lows, release frequency, reported unit and currency.

Regions of common inter-individual DNA methylation differences in human monocytes – potential function and genetic basis WGBS Data of Samples: 43_Hm03_BlMo_Ct, 43_Hm02_BlMo_Ct, 43_Hm05_BlMo_Ct, 43_Hm01_BlMo_Ct For details about sequencing or sample metadata check http://deep.dkfz.de/

Published at 12th AIAA Aviation Technology, Integration, and Operations (ATIO) Conference and 14th AIAA/ISSM 17 - 19 September 2012, Indianapolis, Indiana

The NADAC Weekly Comparison identifies the drug products with current NADAC rates that are replaced with new NADAC rates. Other changes (e.g. NDC additions and terminations) to the NADAC file are not reflected in this comparison. Note: Effective Date was not recorded in the dataset until 6/7/2017

This Location Data & Foot traffic dataset available for all countries include enriched raw mobility data and visitation at POIs to answer questions such as:

-How often do people visit a location? (daily, monthly, absolute, and averages). -What type of places do they visit ? (parks, schools, hospitals, etc) -Which social characteristics do people have in a certain POI? - Breakdown by type: residents, workers, visitors. -What's their mobility like enduring night hours & day hours?
-What's the frequency of the visits partition by day of the week and hour of the day?

Extra insights -Visitors´ relative income Level. -Visitors´ preferences as derived by their visits to shopping, parks, sports facilities, churches, among others.

Overview & Key Concepts Each record corresponds to a ping from a mobile device, at a particular moment in time and at a particular latitude and longitude. We procure this data from reliable technology partners, which obtain it through partnerships with location-aware apps. All the process is compliant with applicable privacy laws.

We clean and process these massive datasets with a number of complex, computer-intensive calculations to make them easier to use in different data science and machine learning applications, especially those related to understanding customer behavior.

Featured attributes of the data Device speed: based on the distance between each observation and the previous one, we estimate the speed at which the device is moving. This is particularly useful to differentiate between vehicles, pedestrians, and stationery observations.

Night base of the device: we calculate the approximated location of where the device spends the night, which is usually their home neighborhood.

Day base of the device: we calculate the most common daylight location during weekdays, which is usually their work location.

Income level: we use the night neighborhood of the device, and intersect it with available socioeconomic data, to infer the device’s income level. Depending on the country, and the availability of good census data, this figure ranges from a relative wealth index to a currency-calculated income.

POI visited: we intersect each observation with a number of POI databases, to estimate check-ins to different locations. POI databases can vary significantly, in scope and depth, between countries.

Category of visited POI: for each observation that can be attributable to a POI, we also include a standardized location category (park, hospital, among others). Coverage: Worldwide.

Delivery schemas We can deliver the data in three different formats:

Full dataset: one record per mobile ping. These datasets are very large, and should only be consumed by experienced teams with large computing budgets.

Visitation stream: one record per attributable visit. This dataset is considerably smaller than the full one but retains most of the more valuable elements in the dataset. This helps understand who visited a specific POI, characterize and understand the consumer's behavior.

Audience profiles: one record per mobile device in a given period of time (usually monthly). All the visitation stream is aggregated by category. This is the most condensed version of the dataset and is very useful to quickly understand the types of consumers in a particular area and to create cohorts of users.

Data for a Brief Report/Short Communication published in Body Image (2021). Details of the study are included below via the abstract from the manuscript. The dataset includes online experimental data from 167 women who were recruited via social media and institutional participant pools. The experiment was completed in Qualtrics.Women viewed either neutral travel images (control), body positivity posts with an average-sized model (e.g., ~ UK size 14), or body positivity posts with a larger model (e.g., UK size 18+); which images women viewed is show in the ‘condition’ variable in the data.The data includes the age range, height, weight, calculated BMI, and Instagram use of participants. After viewing the images, women responded to the Positive and Negative Affect Schedule (PANAS), a state version of the Body Satisfaction Scale (BSS), and reported their immediate social comparison with the images (SAC items). Women then selected a lunch for themselves from a hypothetical menu; these selections are detailed in the data, as are the total calories calculated from this and the proportion of their picks which were (provided as a percentage, and as a categorical variable [as used in the paper analyses]). Women also reported whether they were on a special diet (e.g., vegan or vegetarian), had food intolerances, when they last ate, and how hungry they were.

Women also completed trait measures of Body Appreciation (BAS-2) and social comparison (PACS-R). Women also were asked to comment on what they thought the experiment was about. Items and computed scales are included within the dataset.This item includes the dataset collected for the manuscript (in SPSS and CSV formats), the variable list for the CSV file (for users working with the CSV datafile; the variable list and details are contained within the .sav file for the SPSS version), and the SPSS syntax for our analyses (.sps). Also included are the information and consent form (collected via Qualtrics) and the questions as completed by participants (both in pdf format).Please note that the survey order in the PDF is not the same as in the datafiles; users should utilise the variable list (either in CSV or SPSS formats) to identify the items in the data.The SPSS syntax can be used to replicate the analyses reported in the Results section of the paper. Annotations within the syntax file guide the user through these.

A copy of SPSS Statistics is needed to open the .sav and .sps files.

Manuscript abstract:

Body Positivity (or ‘BoPo’) social media content may be beneficial for women’s mood and body image, but concerns have been raised that it may reduce motivation for healthy behaviours. This study examines differences in women’s mood, body satisfaction, and hypothetical food choices after viewing BoPo posts (featuring average or larger women) or a neutral travel control. Women (N = 167, 81.8% aged 18-29) were randomly assigned in an online experiment to one of three conditions (BoPo-average, BoPo-larger, or Travel/Control) and viewed three Instagram posts for two minutes, before reporting their mood and body satisfaction, and selecting a meal from a hypothetical menu. Women who viewed the BoPo posts featuring average-size women reported more positive mood than the control group; women who viewed posts featuring larger women did not. There were no effects of condition on negative mood or body satisfaction. Women did not make less healthy food choices than the control in either BoPo condition; women who viewed the BoPo images of larger women showed a stronger association between hunger and calories selected. These findings suggest that concerns over BoPo promoting unhealthy behaviours may be misplaced, but further research is needed regarding women’s responses to different body sizes.

The dataset is designed to simulate password-related events, creating a synthetic representation of actions related to password management. It includes fields like timestamp, action, event type, location, IP address, password, hour, and time difference.

• The dataset comprises 50,000 records representing a variety of password-related events.
• A list of commonly used passwords is incorporated to mimic real-world scenarios.
• Timestamps are spread throughout the current year.
• Features like 'hour' and 'time_difference' are derived to provide additional insights into the temporal aspects of the events.

This synthetic dataset can be used for training and testing machine learning models related to cyber security, anomaly detection, or password management. It allows researchers and practitioners to experiment with data resembling real-world scenarios without compromising actual user information.

This is the updated version of the dataset from 10.5281/zenodo.6320761 Information The diverse publicly available compound/bioactivity databases constitute a key resource for data-driven applications in chemogenomics and drug design. Analysis of their coverage of compound entries and biological targets revealed considerable differences, however, suggesting benefit of a consensus dataset. Therefore, we have combined and curated information from five esteemed databases (ChEMBL, PubChem, BindingDB, IUPHAR/BPS and Probes&Drugs) to assemble a consensus compound/bioactivity dataset comprising 1144648 compounds with 10915362 bioactivities on 5613 targets (including defined macromolecular targets as well as cell-lines and phenotypic readouts). It also provides simplified information on assay types underlying the bioactivity data and on bioactivity confidence by comparing data from different sources. We have unified the source databases, brought them into a common format and combined them, enabling an ease for generic uses in multiple applications such as chemogenomics and data-driven drug design. The consensus dataset provides increased target coverage and contains a higher number of molecules compared to the source databases which is also evident from a larger number of scaffolds. These features render the consensus dataset a valuable tool for machine learning and other data-driven applications in (de novo) drug design and bioactivity prediction. The increased chemical and bioactivity coverage of the consensus dataset may improve robustness of such models compared to the single source databases. In addition, semi-automated structure and bioactivity annotation checks with flags for divergent data from different sources may help data selection and further accurate curation. This dataset belongs to the publication: https://doi.org/10.3390/molecules27082513 Structure and content of the dataset Dataset structure ChEMBL ID PubChem ID IUPHAR ID Target Activity type Assay type Unit Mean C (0) ... Mean PC (0) ... Mean B (0) ... Mean I (0) ... Mean PD (0) ... Activity check annotation Ligand names Canonical SMILES C ... Structure check (Tanimoto) Source The dataset was created using the Konstanz Information Miner (KNIME) (https://www.knime.com/) and was exported as a CSV-file and a compressed CSV-file. Except for the canonical SMILES columns, all columns are filled with the datatype ‘string’. The datatype for the canonical SMILES columns is the smiles-format. We recommend the File Reader node for using the dataset in KNIME. With the help of this node the data types of the columns can be adjusted exactly. In addition, only this node can read the compressed format. Column content: ChEMBL ID, PubChem ID, IUPHAR ID: chemical identifier of the databases Target: biological target of the molecule expressed as the HGNC gene symbol Activity type: for example, pIC50 Assay type: Simplification/Classification of the assay into cell-free, cellular, functional and unspecified Unit: unit of bioactivity measurement Mean columns of the databases: mean of bioactivity values or activity comments denoted with the frequency of their occurrence in the database, e.g. Mean C = 7.5 *(15) -> the value for this compound-target pair occurs 15 times in ChEMBL database Activity check annotation: a bioactivity check was performed by comparing values from the different sources and adding an activity check annotation to provide automated activity validation for additional confidence no comment: bioactivity values are within one log unit; check activity data: bioactivity values are not within one log unit; only one data point: only one value was available, no comparison and no range calculated; no activity value: no precise numeric activity value was available; no log-value could be calculated: no negative decadic logarithm could be calculated, e.g., because the reported unit was not a compound concentration Ligand names: all unique names contained in the five source databases are listed Canonical SMILES columns: Molecular structure of the compound from each database Structure check (Tanimoto): To denote matching or differing compound structures in different source databases match: molecule structures are the same between different sources; no match: the structures differ. We calculated the Jaccard-Tanimoto similarity coefficient from Morgan Fingerprints to reveal true differences between sources and reported the minimum value; 1 structure: no structure comparison is possible, because there was only one structure available; no structure: no structure comparison is possible, because there was no structure available. Source: From which databases the data come from

This file compiles the different datasets used and analysis made in the paper "Visual Continuous Time Preferences". Both RStudio and Stata were used for the analysis. The first was used for descriptive statistics and graphs, the second for regressions. We join the datasets for both analysis.

"Analysis VCTP - RStudio.R" is the RStudio analysis. "Analysis VCTP - Stata.do" is the Stata analysis.

The RStudio datasets are: "data_Seville.xlsx" is the dataset of observations. "FormularioEng.xlsx" is the dataset of control variables.

The Stata datasets are: "data_Seville_Stata.dta" is the dataset of observations. "FormularioEng.dta" is the dataset of control variables

Additionally, the experimental instructions of the six experimental conditions are also available: "Hypothetical MPL-VCTP.pdf" is the instructions and task for hypothetical payment and MPL answered before VCTP. "Hypothetical VCTP-MPL.pdf" is the instructions and task for hypothetical payment and VCTP answered before MPL. "OneTenth MPL-VCTP.pdf" is the instructions and task for BRIS payment and MPL answered before VCTP. "OneTenth VCTP-MPL.pdf" is the instructions and task for BRIS payment and VCTP answered before MPL. "Real MPL-VCTP.pdf" is the instructions and task for real payment and VCTP answered before MPL. "Real VCTP-MPL.pdf" is the instructions and task for real payment and VCTP answered before MPL.

Dataset for A Comparison of In Vitro Points of Departure with Human Biomonitoring Levels for Per- and Polyfluoroalkyl Substances (PFAS), to be published by Environmental Health Perspectives (EHP). This dataset is associated with the following publication: Judson, R., D. Smith, M. Devito, J. Wambaugh, B. Wetmore, K. Friedman, G. Patlewicz, R. Thomas, R. Sayre, J. Olker, S. Degitz, S. Padilla, J. Harrill, T. Shafer, and K. Carstens. A Comparison of In Vitro Points of Departure with Human Blood Levels for Per- and Polyfluoroalkyl Substances (PFAS) (Toxics). Toxics. MDPI, Basel, SWITZERLAND, 12(4): 271, (2024).

The Dataset contains the data, that was created simulating and measuring different control strategies for the impact actuator. Each table contains the time value, the set position and the actual position for the base axes as well as the actuators when executing a reference contour. There are two tables for each of the four control strategies, both simulative and experimental: EdgeStop: Reference Profile with acceleration an jerk limits ImpRef: Previous Impact Control Strategie ImpNewWithoutReset: New Strategie, but without controller reset ImpNew: New Impact Conctrol strategie

Missing data is a prevalent problem that requires attention, as most data analysis techniques are unable to handle it. This is particularly critical in Multi-Label Classification (MLC), where only a few studies have investigated missing data in this application domain. MLC differs from Single-Label Classification (SLC) by allowing an instance to be associated with multiple classes. Movie classification is a didactic example since it can be “drama” and “bibliography” simultaneously. One of the most usual missing data treatment methods is data imputation, which seeks plausible values to fill in the missing ones. In this scenario, we propose a novel imputation method based on a multi-objective genetic algorithm for optimizing multiple data imputations called Multiple Imputation of Multi-label Classification data with a genetic algorithm, or simply EvoImp. We applied the proposed method in multi-label learning and evaluated its performance using six synthetic databases, considering various missing values distribution scenarios. The method was compared with other state-of-the-art imputation strategies, such as K-Means Imputation (KMI) and weighted K-Nearest Neighbors Imputation (WKNNI). The results proved that the proposed method outperformed the baseline in all the scenarios by achieving the best evaluation measures considering the Exact Match, Accuracy, and Hamming Loss. The superior results were constant in different dataset domains and sizes, demonstrating the EvoImp robustness. Thus, EvoImp represents a feasible solution to missing data treatment for multi-label learning.

The NIST Computational Chemistry Comparison and Benchmark Database is a collection of experimental and ab initio thermochemical properties for a selected set of gas-phase molecules. The goals are to provide a benchmark set of experimental data for the evaluation of ab initio computational methods and allow the comparison between different ab initio computational methods for the prediction of gas-phase thermochemical properties. The data files linked to this record are a subset of the experimental data present in the CCCBDB.