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This book is written for statisticians, data analysts, programmers, researchers, teachers, students, professionals, and general consumers on how to perform different types of statistical data analysis for research purposes using the R programming language. R is an open-source software and object-oriented programming language with a development environment (IDE) called RStudio for computing statistics and graphical displays through data manipulation, modelling, and calculation. R packages and supported libraries provides a wide range of functions for programming and analyzing of data. Unlike many of the existing statistical softwares, R has the added benefit of allowing the users to write more efficient codes by using command-line scripting and vectors. It has several built-in functions and libraries that are extensible and allows the users to define their own (customized) functions on how they expect the program to behave while handling the data, which can also be stored in the simple object system.For all intents and purposes, this book serves as both textbook and manual for R statistics particularly in academic research, data analytics, and computer programming targeted to help inform and guide the work of the R users or statisticians. It provides information about different types of statistical data analysis and methods, and the best scenarios for use of each case in R. It gives a hands-on step-by-step practical guide on how to identify and conduct the different parametric and non-parametric procedures. This includes a description of the different conditions or assumptions that are necessary for performing the various statistical methods or tests, and how to understand the results of the methods. The book also covers the different data formats and sources, and how to test for reliability and validity of the available datasets. Different research experiments, case scenarios and examples are explained in this book. It is the first book to provide a comprehensive description and step-by-step practical hands-on guide to carrying out the different types of statistical analysis in R particularly for research purposes with examples. Ranging from how to import and store datasets in R as Objects, how to code and call the methods or functions for manipulating the datasets or objects, factorization, and vectorization, to better reasoning, interpretation, and storage of the results for future use, and graphical visualizations and representations. Thus, congruence of Statistics and Computer programming for Research.
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Each R script replicates all of the example code from one chapter from the book. All required data for each script are also uploaded, as are all data used in the practice problems at the end of each chapter. The data are drawn from a wide array of sources, so please cite the original work if you ever use any of these data sets for research purposes.
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TwitterEmory University (analyzed the urine samples for pyrethroid metabolites). This dataset is not publicly accessible because: EPA cannot release personally identifiable information regarding living individuals, according to the Privacy Act and the Freedom of Information Act (FOIA). This dataset contains information about human research subjects. Because there is potential to identify individual participants and disclose personal information, either alone or in combination with other datasets, individual level data are not appropriate to post for public access. Restricted access may be granted to authorized persons by contacting the party listed. It can be accessed through the following means: Contact Researcher. Format: Pyrethroid metabolite concentration data for 50 adults over six-weeks. This dataset is associated with the following publication: Morgan , M., J. Sobus , D.B. Barr, C. Croghan , F. Chen , R. Walker, L. Alston, E. Andersen, and M. Clifton. Temporal variability of pyrethroid metabolite levels in bedtime, morning, and 24-hr urine samples for 50 adults in North Carolina. ENVIRONMENT INTERNATIONAL. Elsevier Science Ltd, New York, NY, USA, 144: 81-91, (2015).
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TwitterThe dataset is a relational dataset of 8,000 households households, representing a sample of the population of an imaginary middle-income country. The dataset contains two data files: one with variables at the household level, the other one with variables at the individual level. It includes variables that are typically collected in population censuses (demography, education, occupation, dwelling characteristics, fertility, mortality, and migration) and in household surveys (household expenditure, anthropometric data for children, assets ownership). The data only includes ordinary households (no community households). The dataset was created using REaLTabFormer, a model that leverages deep learning methods. The dataset was created for the purpose of training and simulation and is not intended to be representative of any specific country.
The full-population dataset (with about 10 million individuals) is also distributed as open data.
The dataset is a synthetic dataset for an imaginary country. It was created to represent the population of this country by province (equivalent to admin1) and by urban/rural areas of residence.
Household, Individual
The dataset is a fully-synthetic dataset representative of the resident population of ordinary households for an imaginary middle-income country.
ssd
The sample size was set to 8,000 households. The fixed number of households to be selected from each enumeration area was set to 25. In a first stage, the number of enumeration areas to be selected in each stratum was calculated, proportional to the size of each stratum (stratification by geo_1 and urban/rural). Then 25 households were randomly selected within each enumeration area. The R script used to draw the sample is provided as an external resource.
other
The dataset is a synthetic dataset. Although the variables it contains are variables typically collected from sample surveys or population censuses, no questionnaire is available for this dataset. A "fake" questionnaire was however created for the sample dataset extracted from this dataset, to be used as training material.
The synthetic data generation process included a set of "validators" (consistency checks, based on which synthetic observation were assessed and rejected/replaced when needed). Also, some post-processing was applied to the data to result in the distributed data files.
This is a synthetic dataset; the "response rate" is 100%.
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{# General information# The script runs with R (Version 3.1.1; 2014-07-10) and packages plyr (Version 1.8.1), XLConnect (Version 0.2-9), utilsMPIO (Version 0.0.25), sp (Version 1.0-15), rgdal (Version 0.8-16), tools (Version 3.1.1) and lattice (Version 0.20-29)# --------------------------------------------------------------------------------------------------------# Questions can be directed to: Martin Bulla (bulla.mar@gmail.com)# -------------------------------------------------------------------------------------------------------- # Data collection and how the individual variables were derived is described in: #Steiger, S.S., et al., When the sun never sets: diverse activity rhythms under continuous daylight in free-living arctic-breeding birds. Proceedings of the Royal Society B: Biological Sciences, 2013. 280(1764): p. 20131016-20131016. # Dale, J., et al., The effects of life history and sexual selection on male and female plumage colouration. Nature, 2015. # Data are available as Rdata file # Missing values are NA. # --------------------------------------------------------------------------------------------------------# For better readability the subsections of the script can be collapsed # --------------------------------------------------------------------------------------------------------}{# Description of the method # 1 - data are visualized in an interactive actogram with time of day on x-axis and one panel for each day of data # 2 - red rectangle indicates the active field, clicking with the mouse in that field on the depicted light signal generates a data point that is automatically (via custom made function) saved in the csv file. For this data extraction I recommend, to click always on the bottom line of the red rectangle, as there is always data available due to a dummy variable ("lin") that creates continuous data at the bottom of the active panel. The data are captured only if greenish vertical bar appears and if new line of data appears in R console). # 3 - to extract incubation bouts, first click in the new plot has to be start of incubation, then next click depict end of incubation and the click on the same stop start of the incubation for the other sex. If the end and start of incubation are at different times, the data will be still extracted, but the sex, logger and bird_ID will be wrong. These need to be changed manually in the csv file. Similarly, the first bout for a given plot will be always assigned to male (if no data are present in the csv file) or based on previous data. Hence, whenever a data from a new plot are extracted, at a first mouse click it is worth checking whether the sex, logger and bird_ID information is correct and if not adjust it manually. # 4 - if all information from one day (panel) is extracted, right-click on the plot and choose "stop". This will activate the following day (panel) for extraction. # 5 - If you wish to end extraction before going through all the rectangles, just press "escape". }{# Annotations of data-files from turnstone_2009_Barrow_nest-t401_transmitter.RData dfr-- contains raw data on signal strength from radio tag attached to the rump of female and male, and information about when the birds where captured and incubation stage of the nest1. who: identifies whether the recording refers to female, male, capture or start of hatching2. datetime_: date and time of each recording3. logger: unique identity of the radio tag 4. signal_: signal strength of the radio tag5. sex: sex of the bird (f = female, m = male)6. nest: unique identity of the nest7. day: datetime_ variable truncated to year-month-day format8. time: time of day in hours9. datetime_utc: date and time of each recording, but in UTC time10. cols: colors assigned to "who"--------------------------------------------------------------------------------------------------------m-- contains metadata for a given nest1. sp: identifies species (RUTU = Ruddy turnstone)2. nest: unique identity of the nest3. year_: year of observation4. IDfemale: unique identity of the female5. IDmale: unique identity of the male6. lat: latitude coordinate of the nest7. lon: longitude coordinate of the nest8. hatch_start: date and time when the hatching of the eggs started 9. scinam: scientific name of the species10. breeding_site: unique identity of the breeding site (barr = Barrow, Alaska)11. logger: type of device used to record incubation (IT - radio tag)12. sampling: mean incubation sampling interval in seconds--------------------------------------------------------------------------------------------------------s-- contains metadata for the incubating parents1. year_: year of capture2. species: identifies species (RUTU = Ruddy turnstone)3. author: identifies the author who measured the bird4. nest: unique identity of the nest5. caught_date_time: date and time when the bird was captured6. recapture: was the bird capture before? (0 - no, 1 - yes)7. sex: sex of the bird (f = female, m = male)8. bird_ID: unique identity of the bird9. logger: unique identity of the radio tag --------------------------------------------------------------------------------------------------------}
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Pathogen diversity resulting in quasispecies can enable persistence and adaptation to host defenses and therapies. However, accurate quasispecies characterization can be impeded by errors introduced during sample handling and sequencing which can require extensive optimizations to overcome. We present complete laboratory and bioinformatics workflows to overcome many of these hurdles. The Pacific Biosciences single molecule real-time platform was used to sequence PCR amplicons derived from cDNA templates tagged with universal molecular identifiers (SMRT-UMI). Optimized laboratory protocols were developed through extensive testing of different sample preparation conditions to minimize between-template recombination during PCR and the use of UMI allowed accurate template quantitation as well as removal of point mutations introduced during PCR and sequencing to produce a highly accurate consensus sequence from each template. Handling of the large datasets produced from SMRT-UMI sequencing was facilitated by a novel bioinformatic pipeline, Probabilistic Offspring Resolver for Primer IDs (PORPIDpipeline), that automatically filters and parses reads by sample, identifies and discards reads with UMIs likely created from PCR and sequencing errors, generates consensus sequences, checks for contamination within the dataset, and removes any sequence with evidence of PCR recombination or early cycle PCR errors, resulting in highly accurate sequence datasets. The optimized SMRT-UMI sequencing method presented here represents a highly adaptable and established starting point for accurate sequencing of diverse pathogens. These methods are illustrated through characterization of human immunodeficiency virus (HIV) quasispecies.
Methods
This serves as an overview of the analysis performed on PacBio sequence data that is summarized in Analysis Flowchart.pdf and was used as primary data for the paper by Westfall et al. "Optimized SMRT-UMI protocol produces highly accurate sequence datasets from diverse populations – application to HIV-1 quasispecies"
Five different PacBio sequencing datasets were used for this analysis: M027, M2199, M1567, M004, and M005
For the datasets which were indexed (M027, M2199), CCS reads from PacBio sequencing files and the chunked_demux_config files were used as input for the chunked_demux pipeline. Each config file lists the different Index primers added during PCR to each sample. The pipeline produces one fastq file for each Index primer combination in the config. For example, in dataset M027 there were 3–4 samples using each Index combination. The fastq files from each demultiplexed read set were moved to the sUMI_dUMI_comparison pipeline fastq folder for further demultiplexing by sample and consensus generation with that pipeline. More information about the chunked_demux pipeline can be found in the README.md file on GitHub.
The demultiplexed read collections from the chunked_demux pipeline or CCS read files from datasets which were not indexed (M1567, M004, M005) were each used as input for the sUMI_dUMI_comparison pipeline along with each dataset's config file. Each config file contains the primer sequences for each sample (including the sample ID block in the cDNA primer) and further demultiplexes the reads to prepare data tables summarizing all of the UMI sequences and counts for each family (tagged.tar.gz) as well as consensus sequences from each sUMI and rank 1 dUMI family (consensus.tar.gz). More information about the sUMI_dUMI_comparison pipeline can be found in the paper and the README.md file on GitHub.
The consensus.tar.gz and tagged.tar.gz files were moved from sUMI_dUMI_comparison pipeline directory on the server to the Pipeline_Outputs folder in this analysis directory for each dataset and appended with the dataset name (e.g. consensus_M027.tar.gz). Also in this analysis directory is a Sample_Info_Table.csv containing information about how each of the samples was prepared, such as purification methods and number of PCRs. There are also three other folders: Sequence_Analysis, Indentifying_Recombinant_Reads, and Figures. Each has an .Rmd file with the same name inside which is used to collect, summarize, and analyze the data. All of these collections of code were written and executed in RStudio to track notes and summarize results.
Sequence_Analysis.Rmd has instructions to decompress all of the consensus.tar.gz files, combine them, and create two fasta files, one with all sUMI and one with all dUMI sequences. Using these as input, two data tables were created, that summarize all sequences and read counts for each sample that pass various criteria. These are used to help create Table 2 and as input for Indentifying_Recombinant_Reads.Rmd and Figures.Rmd. Next, 2 fasta files containing all of the rank 1 dUMI sequences and the matching sUMI sequences were created. These were used as input for the python script compare_seqs.py which identifies any matched sequences that are different between sUMI and dUMI read collections. This information was also used to help create Table 2. Finally, to populate the table with the number of sequences and bases in each sequence subset of interest, different sequence collections were saved and viewed in the Geneious program.
To investigate the cause of sequences where the sUMI and dUMI sequences do not match, tagged.tar.gz was decompressed and for each family with discordant sUMI and dUMI sequences the reads from the UMI1_keeping directory were aligned using geneious. Reads from dUMI families failing the 0.7 filter were also aligned in Genious. The uncompressed tagged folder was then removed to save space. These read collections contain all of the reads in a UMI1 family and still include the UMI2 sequence. By examining the alignment and specifically the UMI2 sequences, the site of the discordance and its case were identified for each family as described in the paper. These alignments were saved as "Sequence Alignments.geneious". The counts of how many families were the result of PCR recombination were used in the body of the paper.
Using Identifying_Recombinant_Reads.Rmd, the dUMI_ranked.csv file from each sample was extracted from all of the tagged.tar.gz files, combined and used as input to create a single dataset containing all UMI information from all samples. This file dUMI_df.csv was used as input for Figures.Rmd.
Figures.Rmd used dUMI_df.csv, sequence_counts.csv, and read_counts.csv as input to create draft figures and then individual datasets for eachFigure. These were copied into Prism software to create the final figures for the paper.
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This dataset contains fish and jellyfish sample information from R/V Centennial trawl surveys in the Hood Canal, WA from 2012-2013. The sample number, length, weight, and species are included.
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Download this sample dataset and proceed with the assignment as described.
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By SocialGrep [source]
A subreddit dataset is a collection of posts and comments made on Reddit's /r/datasets board. This dataset contains all the posts and comments made on the /r/datasets subreddit from its inception to March 1, 2022. The dataset was procured using SocialGrep. The data does not include usernames to preserve users' anonymity and to prevent targeted harassment
For more datasets, click here.
- 🚨 Your notebook can be here! 🚨!
In order to use this dataset, you will need to have a text editor such as Microsoft Word or LibreOffice installed on your computer. You will also need a web browser such as Google Chrome or Mozilla Firefox.
Once you have the necessary software installed, open the The Reddit Dataset folder and double-click on the the-reddit-dataset-dataset-posts.csv file to open it in your preferred text editor.
In the document, you will see a list of posts with the following information for each one: title, sentiment, score, URL, created UTC, permalink, subreddit NSFW status, and subreddit name.
You can use this information to analyze trends in data sets posted on /r/datasets over time. For example, you could calculate the average score for all posts and compare it to the average score for posts in specific subReddits. Additionally, sentiment analysis could be performed on the titles of posts to see if there is a correlation between positive/negative sentiment and upvotes/downvotes
- Finding correlations between different types of datasets
- Determining which datasets are most popular on Reddit
- Analyzing the sentiments of post and comments on Reddit's /r/datasets board
If you use this dataset in your research, please credit the original authors.
License
License: CC0 1.0 Universal (CC0 1.0) - Public Domain Dedication No Copyright - You can copy, modify, distribute and perform the work, even for commercial purposes, all without asking permission. See Other Information.
File: the-reddit-dataset-dataset-comments.csv | Column name | Description | |:-------------------|:---------------------------------------------------| | type | The type of post. (String) | | subreddit.name | The name of the subreddit. (String) | | subreddit.nsfw | Whether or not the subreddit is NSFW. (Boolean) | | created_utc | The time the post was created, in UTC. (Timestamp) | | permalink | The permalink for the post. (String) | | body | The body of the post. (String) | | sentiment | The sentiment of the post. (String) | | score | The score of the post. (Integer) |
File: the-reddit-dataset-dataset-posts.csv | Column name | Description | |:-------------------|:---------------------------------------------------| | type | The type of post. (String) | | subreddit.name | The name of the subreddit. (String) | | subreddit.nsfw | Whether or not the subreddit is NSFW. (Boolean) | | created_utc | The time the post was created, in UTC. (Timestamp) | | permalink | The permalink for the post. (String) | | score | The score of the post. (Integer) | | domain | The domain of the post. (String) | | url | The URL of the post. (String) | | selftext | The self-text of the post. (String) | | title | The title of the post. (String) |
If you use this dataset in your research, please credit the original authors. If you use this dataset in your research, please credit SocialGrep.
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TwitterIn September 2013, an experiment using Distributed Acoustic Sensing (DAS) was conducted at Garner Valley, a test site of the University of California Santa Barbara (Lancelle et al., 2014). This submission includes one 45 kN shear shaker (called "large shaker" on the basemap) test for three different measurement systems. The shaker swept from a rest, up to 10 Hz, and back down to a rest over 60 seconds. Lancelle, C., N. Lord, H. Wang, D. Fratta, R. Nigbor, A. Chalari, R. Karaulanov, J. Baldwin, and E. Castongia (2014), Directivity and Sensitivity of Fiber-Optic Cable Measuring Ground Motion using a Distributed Acoustic Sensing Array (abstract # NS31C-3935), AGU Fall Meeting.
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Complete dataset of “Film Circulation on the International Film Festival Network and the Impact on Global Film Culture”
A peer-reviewed data paper for this dataset is in review to be published in NECSUS_European Journal of Media Studies - an open access journal aiming at enhancing data transparency and reusability, and will be available from https://necsus-ejms.org/ and https://mediarep.org
Please cite this when using the dataset.
Detailed description of the dataset:
1 Film Dataset: Festival Programs
The Film Dataset consists a data scheme image file, a codebook and two dataset tables in csv format.
The codebook (csv file “1_codebook_film-dataset_festival-program”) offers a detailed description of all variables within the Film Dataset. Along with the definition of variables it lists explanations for the units of measurement, data sources, coding and information on missing data.
The csv file “1_film-dataset_festival-program_long” comprises a dataset of all films and the festivals, festival sections, and the year of the festival edition that they were sampled from. The dataset is structured in the long format, i.e. the same film can appear in several rows when it appeared in more than one sample festival. However, films are identifiable via their unique ID.
The csv file “1_film-dataset_festival-program_wide” consists of the dataset listing only unique films (n=9,348). The dataset is in the wide format, i.e. each row corresponds to a unique film, identifiable via its unique ID. For easy analysis, and since the overlap is only six percent, in this dataset the variable sample festival (fest) corresponds to the first sample festival where the film appeared. For instance, if a film was first shown at Berlinale (in February) and then at Frameline (in June of the same year), the sample festival will list “Berlinale”. This file includes information on unique and IMDb IDs, the film title, production year, length, categorization in length, production countries, regional attribution, director names, genre attribution, the festival, festival section and festival edition the film was sampled from, and information whether there is festival run information available through the IMDb data.
2 Survey Dataset
The Survey Dataset consists of a data scheme image file, a codebook and two dataset tables in csv format.
The codebook “2_codebook_survey-dataset” includes coding information for both survey datasets. It lists the definition of the variables or survey questions (corresponding to Samoilova/Loist 2019), units of measurement, data source, variable type, range and coding, and information on missing data.
The csv file “2_survey-dataset_long-festivals_shared-consent” consists of a subset (n=161) of the original survey dataset (n=454), where respondents provided festival run data for films (n=206) and gave consent to share their data for research purposes. This dataset consists of the festival data in a long format, so that each row corresponds to the festival appearance of a film.
The csv file “2_survey-dataset_wide-no-festivals_shared-consent” consists of a subset (n=372) of the original dataset (n=454) of survey responses corresponding to sample films. It includes data only for those films for which respondents provided consent to share their data for research purposes. This dataset is shown in wide format of the survey data, i.e. information for each response corresponding to a film is listed in one row. This includes data on film IDs, film title, survey questions regarding completeness and availability of provided information, information on number of festival screenings, screening fees, budgets, marketing costs, market screenings, and distribution. As the file name suggests, no data on festival screenings is included in the wide format dataset.
3 IMDb & Scripts
The IMDb dataset consists of a data scheme image file, one codebook and eight datasets, all in csv format. It also includes the R scripts that we used for scraping and matching.
The codebook “3_codebook_imdb-dataset” includes information for all IMDb datasets. This includes ID information and their data source, coding and value ranges, and information on missing data.
The csv file “3_imdb-dataset_aka-titles_long” contains film title data in different languages scraped from IMDb in a long format, i.e. each row corresponds to a title in a given language.
The csv file “3_imdb-dataset_awards_long” contains film award data in a long format, i.e. each row corresponds to an award of a given film.
The csv file “3_imdb-dataset_companies_long” contains data on production and distribution companies of films. The dataset is in a long format, so that each row corresponds to a particular company of a particular film.
The csv file “3_imdb-dataset_crew_long” contains data on names and roles of crew members in a long format, i.e. each row corresponds to each crew member. The file also contains binary gender assigned to directors based on their first names using the GenderizeR application.
The csv file “3_imdb-dataset_festival-runs_long” contains festival run data scraped from IMDb in a long format, i.e. each row corresponds to the festival appearance of a given film. The dataset does not include each film screening, but the first screening of a film at a festival within a given year. The data includes festival runs up to 2019.
The csv file “3_imdb-dataset_general-info_wide” contains general information about films such as genre as defined by IMDb, languages in which a film was shown, ratings, and budget. The dataset is in wide format, so that each row corresponds to a unique film.
The csv file “3_imdb-dataset_release-info_long” contains data about non-festival release (e.g., theatrical, digital, tv, dvd/blueray). The dataset is in a long format, so that each row corresponds to a particular release of a particular film.
The csv file “3_imdb-dataset_websites_long” contains data on available websites (official websites, miscellaneous, photos, video clips). The dataset is in a long format, so that each row corresponds to a website of a particular film.
The dataset includes 8 text files containing the script for webscraping. They were written using the R-3.6.3 version for Windows.
The R script “r_1_unite_data” demonstrates the structure of the dataset, that we use in the following steps to identify, scrape, and match the film data.
The R script “r_2_scrape_matches” reads in the dataset with the film characteristics described in the “r_1_unite_data” and uses various R packages to create a search URL for each film from the core dataset on the IMDb website. The script attempts to match each film from the core dataset to IMDb records by first conducting an advanced search based on the movie title and year, and then potentially using an alternative title and a basic search if no matches are found in the advanced search. The script scrapes the title, release year, directors, running time, genre, and IMDb film URL from the first page of the suggested records from the IMDb website. The script then defines a loop that matches (including matching scores) each film in the core dataset with suggested films on the IMDb search page. Matching was done using data on directors, production year (+/- one year), and title, a fuzzy matching approach with two methods: “cosine” and “osa.” where the cosine similarity is used to match titles with a high degree of similarity, and the OSA algorithm is used to match titles that may have typos or minor variations.
The script “r_3_matching” creates a dataset with the matches for a manual check. Each pair of films (original film from the core dataset and the suggested match from the IMDb website was categorized in the following five categories: a) 100% match: perfect match on title, year, and director; b) likely good match; c) maybe match; d) unlikely match; and e) no match). The script also checks for possible doubles in the dataset and identifies them for a manual check.
The script “r_4_scraping_functions” creates a function for scraping the data from the identified matches (based on the scripts described above and manually checked). These functions are used for scraping the data in the next script.
The script “r_5a_extracting_info_sample” uses the function defined in the “r_4_scraping_functions”, in order to scrape the IMDb data for the identified matches. This script does that for the first 100 films, to check, if everything works. Scraping for the entire dataset took a few hours. Therefore, a test with a subsample of 100 films is advisable.
The script “r_5b_extracting_info_all” extracts the data for the entire dataset of the identified matches.
The script “r_5c_extracting_info_skipped” checks the films with missing data (where data was not scraped) and tried to extract data one more time to make sure that the errors were not caused by disruptions in the internet connection or other technical issues.
The script “r_check_logs” is used for troubleshooting and tracking the progress of all of the R scripts used. It gives information on the amount of missing values and errors.
4 Festival Library Dataset
The Festival Library Dataset consists of a data scheme image file, one codebook and one dataset, all in csv format.
The codebook (csv file “4_codebook_festival-library_dataset”) offers a detailed description of all variables within the Library Dataset. It lists the definition of variables, such as location and festival name, and festival categories, units of measurement, data sources and coding and missing data.
The csv file “4_festival-library_dataset_imdb-and-survey” contains data on all unique festivals collected from both IMDb and survey sources. This dataset appears in wide format, all information for each festival is listed in one row. This
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The R Manual for QCA entails a PDF file that describes all the steps and code needed to prepare and conduct a Qualitative Comparative Analysis (QCA) study in R. This is complemented by an R Script that can be customized as needed. The dataset further includes two files with sample data, for the set-theoretic analysis and the visualization of QCA results. The R Manual for QCA is the online appendix to "Qualitative Comparative Analysis: An Introduction to Research Design and Application", Georgetown University Press, 2021.
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The retailer wants to target customers with suggestions on itemset that a customer is most likely to purchase .I was given dataset contains data of a retailer; the transaction data provides data around all the transactions that have happened over a period of time. Retailer will use result to grove in his industry and provide for customer suggestions on itemset, we be able increase customer engagement and improve customer experience and identify customer behavior. I will solve this problem with use Association Rules type of unsupervised learning technique that checks for the dependency of one data item on another data item.
Association Rule is most used when you are planning to build association in different objects in a set. It works when you are planning to find frequent patterns in a transaction database. It can tell you what items do customers frequently buy together and it allows retailer to identify relationships between the items.
Assume there are 100 customers, 10 of them bought Computer Mouth, 9 bought Mat for Mouse and 8 bought both of them. - bought Computer Mouth => bought Mat for Mouse - support = P(Mouth & Mat) = 8/100 = 0.08 - confidence = support/P(Mat for Mouse) = 0.08/0.09 = 0.89 - lift = confidence/P(Computer Mouth) = 0.89/0.10 = 8.9 This just simple example. In practice, a rule needs the support of several hundred transactions, before it can be considered statistically significant, and datasets often contain thousands or millions of transactions.
Number of Attributes: 7
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First, we need to load required libraries. Shortly I describe all libraries.
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Next, we need to upload Assignment-1_Data. xlsx to R to read the dataset.Now we can see our data in R.
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After we will clear our data frame, will remove missing values.
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To apply Association Rule mining, we need to convert dataframe into transaction data to make all items that are bought together in one invoice will be in ...
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minimum_sample_sizes_code.R includes the complete set of instructions used to carry out the analyses in the related manuscript, plus save the computed data files and generate the text figures. data_files.tar.gz includes all of the files generated by the R code.
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This dataset contains measurements from Niskin bottle samples from R/V New Horizon cruise NH1417 from August 18th to September 16th of 2014 in the Eastern Pacific between San Diego and Hawaii. The R/V New Horizon cruise NH1417 was a Nutrient Effects on Marine microOrganisms (NEMO) cruise.
Measurements from Fast Repetition Rate Fluorometry (FRRF): initial fluorescence, maximum photochemical efficiency of photostream II, and functional absorption of cross-section.
CTD measurements: temperature, salinity, pressure, PAR, in-situ chlorophyll a, dissolved oxygen, fluorescence.
Derived values: Extracted chlorophyll a, 15N2 enrichment, 14C primary production.
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TwitterThis archive contains code and data for reproducing the analysis for “Replication Data for Revisiting ‘The Rise and Decline’ in a Population of Peer Production Projects”. Depending on what you hope to do with the data you probabbly do not want to download all of the files. Depending on your computation resources you may not be able to run all stages of the analysis. The code for all stages of the analysis, including typesetting the manuscript and running the analysis, is in code.tar. If you only want to run the final analysis or to play with datasets used in the analysis of the paper, you want intermediate_data.7z or the uncompressed tab and csv files. The data files are created in a four-stage process. The first stage uses the program “wikiq” to parse mediawiki xml dumps and create tsv files that have edit data for each wiki. The second stage generates all.edits.RDS file which combines these tsvs into a dataset of edits from all the wikis. This file is expensive to generate and at 1.5GB is pretty big. The third stage builds smaller intermediate files that contain the analytical variables from these tsv files. The fourth stage uses the intermediate files to generate smaller RDS files that contain the results. Finally, knitr and latex typeset the manuscript. A stage will only run if the outputs from the previous stages do not exist. So if the intermediate files exist they will not be regenerated. Only the final analysis will run. The exception is that stage 4, fitting models and generating plots, always runs. If you only want to replicate from the second stage onward, you want wikiq_tsvs.7z. If you want to replicate everything, you want wikia_mediawiki_xml_dumps.7z.001 wikia_mediawiki_xml_dumps.7z.002, and wikia_mediawiki_xml_dumps.7z.003. These instructions work backwards from building the manuscript using knitr, loading the datasets, running the analysis, to building the intermediate datasets. Building the manuscript using knitr This requires working latex, latexmk, and knitr installations. Depending on your operating system you might install these packages in different ways. On Debian Linux you can run apt install r-cran-knitr latexmk texlive-latex-extra. Alternatively, you can upload the necessary files to a project on Overleaf.com. Download code.tar. This has everything you need to typeset the manuscript. Unpack the tar archive. On a unix system this can be done by running tar xf code.tar. Navigate to code/paper_source. Install R dependencies. In R. run install.packages(c("data.table","scales","ggplot2","lubridate","texreg")) On a unix system you should be able to run make to build the manuscript generalizable_wiki.pdf. Otherwise you should try uploading all of the files (including the tables, figure, and knitr folders) to a new project on Overleaf.com. Loading intermediate datasets The intermediate datasets are found in the intermediate_data.7z archive. They can be extracted on a unix system using the command 7z x intermediate_data.7z. The files are 95MB uncompressed. These are RDS (R data set) files and can be loaded in R using the readRDS. For example newcomer.ds <- readRDS("newcomers.RDS"). If you wish to work with these datasets using a tool other than R, you might prefer to work with the .tab files. Running the analysis Fitting the models may not work on machines with less than 32GB of RAM. If you have trouble, you may find the functions in lib-01-sample-datasets.R useful to create stratified samples of data for fitting models. See line 89 of 02_model_newcomer_survival.R for an example. Download code.tar and intermediate_data.7z to your working folder and extract both archives. On a unix system this can be done with the command tar xf code.tar && 7z x intermediate_data.7z. Install R dependencies. install.packages(c("data.table","ggplot2","urltools","texreg","optimx","lme4","bootstrap","scales","effects","lubridate","devtools","roxygen2")). On a unix system you can simply run regen.all.sh to fit the models, build the plots and create the RDS files. Generating datasets Building the intermediate files The intermediate files are generated from all.edits.RDS. This process requires about 20GB of memory. Download all.edits.RDS, userroles_data.7z,selected.wikis.csv, and code.tar. Unpack code.tar and userroles_data.7z. On a unix system this can be done using tar xf code.tar && 7z x userroles_data.7z. Install R dependencies. In R run install.packages(c("data.table","ggplot2","urltools","texreg","optimx","lme4","bootstrap","scales","effects","lubridate","devtools","roxygen2")). Run 01_build_datasets.R. Building all.edits.RDS The intermediate RDS files used in the analysis are created from all.edits.RDS. To replicate building all.edits.RDS, you only need to run 01_build_datasets.R when the int... Visit https://dataone.org/datasets/sha256%3Acfa4980c107154267d8eb6dc0753ed0fde655a73a062c0c2f5af33f237da3437 for complete metadata about this dataset.
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Subsets of these data were published in the papers listed in the "Related Resources" section.
Related dataset:
* ScanFish Optical Plankton Counter (OPC) data: https://www.bco-dmo.org/dataset/746081
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Location of sample Points configured in the Commonwealth Environmental Water Holder (CEWH) Monitoring Data Management System (MDMS) that stores monitoring data from the Long Term Intervention Monitoring (LTIM) project and CEWO Monitoring, Evaluation and Research (Flow-MER) program. Includes Selected Area monitoring locations and Basin stream-flow gauging sites used in hydrology models (model nodes).\r \r Flow-MER Program (2019-2023)\r \r Long Term Intervention Monitoring (LTIM) project (2014-2019)\r \r
\r The Commonwealth Environmental Water Holder and Flow-MER program participants acknowledge the First Nations peoples as the Traditional Owners and Custodians of the lands, waterways and skies of the Murray-Darling Basin. We respect their continuing connection to culture and Country, and we thank them for their knowledge and science and the values reflected in these data.\r \r
\r CEWH Flow-MER (2023) MDMS sample points (Flow-MER monitoring locations). Flow-MER Program. Commonwealth Environmental Water Holder, Australian Government Department of Climate Change, Energy, the Environment and Water. Sourced from https://data.gov.au/data/dataset/mdms-monitoring-locations on [date sourced].
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Samples of FY-3E/GNOS-II GNSS-R L1 data on 20240530.A data format document is included.
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