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94 results for “methods: data analysis”
Supplementary Data for MOCCASIN: A method for correcting known and unknown confounders in RNA-Seq-based splicing analysis
<p>Contents</p> <ol> <li><strong>moccasin_paper_env.yaml</strong>: conda environment file with R and Python packages and modules needed to reproduce analyses.</li> <li><strong>FigureReproduction.zip</strong>: data and code to reproduce main and supplemental figures.</li> <li><strong>MOCCASIN_ExampleDataset.zip</strong>: A small subset of the simulated data with example code to run MOCCASIN.</li> <li><strong>encode_corrected.zip</strong>: Folder with batch-corrected ENCODE differential splicing quantifications (dPSI).</li> </ol> <p> </p> <p> </p> <p>(1) <strong>moccasin_paper_env.yaml</strong></p> <p>Use the moccasin_paper_env.yaml file to create a conda environment from which all analyses for the paper can be reproduced.</p> <pre><code class="language-bash"># need to first install conda. See here: # https://docs.conda.io/en/latest/miniconda.html # Next, create a conda environment: conda env create --name moccasin_paper_env --file moccasin_paper_env.yaml --force # Activate the environment: conda activate moccasin_paper_env</code></pre> <p><br> The only Python packages not included in this environment are MAJIQ & VOILA. Please see majiq.biocipers.org for installation instructions.</p> <p> </p> <p> </p> <p>(2) <strong>FigureReproduction.zip</strong></p> <p>Within FigureReproduction are folders with code and data to reproduce the main and supplemental figures of the publication. Each folder contains data, script(s) and a README.txt with instructions on how to reproduce figures.</p> <p> </p> <p> </p> <p>(3) <strong>MOCCASIN_ExampleDataset.zip</strong></p> <p>Within this folder is an example dataset to test MOCCASIN. The README.txt file contains detailed line-by-line instructions for how to run MOCCASIN and do post-MOCCASIN analyses. In this example, we show how to run MOCCASIN on a group of .majiq samples with one known confounding effect. Also demonstrated is how to run an "explore unknown residuals" analysis as described in the detailed methods in the supplemental of the paper. </p> <p> </p> <p> </p> <p>(4) <strong>encode_corrected.zip</strong></p> <p>Includes a file called ENCODE_BeforeAndAfterMOCCASIN.voila.tsv.zip which includes LSV quantifications before and after MOCCASIN. Each row in the file represents a junction from an LSV. Each column header starts with the prefix "BeforeMOCCASIN" or "AfterMOCCASIN" and headers ending in dPSI corresponds to the dPSI of an ENCODE knockdown vs control experiment. </p>
Data used in ECLIPSER methods paper and GTEx snRNA-seq cross-tissue reference map analysis
<p>The tables were used in the papers: Rouhana*, Wang* <em>et al.,</em> ECLIPSER: identifying causal cell types and genes for complex traits through single cell enrichment of e/sQTL-mapped genes in GWAS loci, bioRxiv 2021, doi: https://doi.org/10.1101/2021.11.24.469720; and Eraslan <em>et al.,</em> Single-nucleus cross-tissue molecular reference maps to decipher disease gene function, bioRxiv 2021, doi: https://doi.org/10.1101/2021.07.19.452954. '<a href="https://zenodo.org/api/files/1f8d48d0-6bf7-4bec-b6ef-5c7a9ead8079/GTEx_v8_HG38_all_variants.tsv.gz">GTEx_v8_HG38_all_variants.tsv.gz</a>' is an input file for running GWASvar2gene on GTEx v8 eQTLs and sQTLs, and all other files are input files for ECLIPSER.</p>
Datasets, reproducible codes, and results for evaluating differential expression analysis methods on population-level RNA-seq data
<p>This upload contains the necessary R codes and data to reproduce the FDR and Power results described in our correspondence "Neglecting normalization impact in semi-synthetic RNA-seq data simulation generates artificial false positives" to Li Y, Ge X, Peng F, Li W, Li JJ, Exaggerated false positives by popular differential expression methods when analyzing human population samples, <em>Genome Biology</em> 23, 79, 2022, DOI: 10.1186/s13059-022-02648-4.</p>
Data for "Tuning parameters of dimensionality reduction methods for single-cell RNA-seq analysis"
<p>The files named <code>df_scran.csv</code>, <code>df_seurat.csv</code>, <code>df_zinbwave.csv</code>, <code>df_dca.csv</code>, and <code>df_scvi.csv</code> contain one row per configuration that we ran successfully.</p> <p>The files named <code>DATASET.METHOD.h5ad</code> are encoded with anndata <code>v0.7.0</code> (be careful as they are not readable with previous versions) and contain 100 embeddings each. The embeddings are in the <code>obsm</code> attribute of the object. All the embeddings can be listed with the <code>obsm_keys()</code> method. The name of the embedding contains the parameters used to generate that embedding and are written like that <code>method=zinbwave.dims=10.epsilon=1000.features=300.gene_covariate=0</code>.</p> <p> </p> <p>For questions on this dataset please contact fraimundo@google.com</p>
Sample 3D image data from RIMS method for image analysis code demo
<p>Sample 3D image data from RIMS method applied to mechanical test on hydrogel sphere packings, to be used in image analysis code demo as demonstrated in the ALERT Geomechanics doctoral school 2022. The data is a small subset from a larger set of data as found on Dryad via 10.5061/dryad.6djh9w0x8 and is separated here on Zenodo to make the subset more machine-readable.</p>
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019) in Variability of the gene cyt b in the Korean field mouse Apodemus peninsulae Thomas, 1906 - a reservoir host of AMRV in the Khasansky District of Primorsky Krai
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019)
Data for: "A high-throughput microscopy method for single-cell analysis of event-time correlations in nanoparticle-induced cell death"
<p>Data related to the publication Murschhauser <em>et al.</em>: <a href="https://doi.org/10.1038/s42003-019-0282-0">A high-throughput microscopy method for single-cell analysis of event-time correlations in nanoparticle-induced cell death</a>. It contains fluorescence time traces of single cells marked with cell-event markers and observed by time-lapse microscopy. The cells were treated with nanoparticles at different doses (NP25 and NP100), with staurosporine (sts) or were left untreated for control (ctrl). See the above-mentioned publication for more details.</p> <p>The format of the data is described below.</p> <p>The file <code>Data_A549.zip</code> contains data measured with A549 cells, and the file <code>Data_Huh7.zip</code> contains data measured with Huh7 cells. Both files have the same structure. Each file contains the directories <code>Raw</code> and <code>Fitted</code> as well as a checksum file. The <code>Raw</code> directory contains single-cell fluorescence time courses as obtained by time-lapse microscopy. The <code>Fitted</code> directory contains the results of fitting model functions as well as properties of identified events, such as event times. The checksum file contains SHA256 checksums of all files within these directories and can be used to check file integrity.</p> <p>Both directories contain measurement directories. Each measurement directory contains the data corresponding to one experiment. The name of the measurement directory is the measurement identifier. Each measurement directory contains condition directories. Each condition directory contains data corresponding to one condition measured in the measurement and is named after the condition. Each condition directory contains marker directories. They are named after the fluorescence markers measured and contain files with single-cell data corresponding to the respective markers.</p> <p>The names of those files consist of multiple parts separated by underscores. The first two parts identify a position of the microscope. Since pairs of markers were measured, each position is present in two marker directories. The third part is the measurement identifier. The other parts will be described below.</p> <p>The <code>Raw</code> directory contains only CSV files with the raw fluorescence time courses. The filenames contain no other parts and have the suffix “.txt”. The first row of each CSV file is the time (in units of 10 minutes), and the other rows are the fluorescence time courses of the cells observed at the corresponding position (in arbitrary units). Each file in the <code>Raw</code> directory corresponds to a group of files in the <code>Fitted</code> directory.</p> <p>The <code>Fitted</code> directory contains three types of CSV files. Their names have “ALL” as fourth part, a session identifier as sixth part and the suffix “.csv”. The fifth part indicates the type of file and is one of the following:</p> <ul> <li>“PARAMS” indicates the estimated values for the model parameters. Each row stands for one cell and each column for a parameter of the model function fitted to the data. The model functions are published with the <a href="https://doi.org/10.5281/zenodo.1418465">fitting software</a>.</li> <li>“SIMULATED” indicates the fitted traces. The traces are calculated using the model functions and the estimated parameters. The format is the same as for the raw traces, but the time is in units of hours and has a higher resolution.</li> <li>“STATE” indicates additional information extracted from the fitted traces. Each row stands for a cell and each column for a property. The first column is the number of the cell. The second column is the event time found (in hours); non-finite values indicate that no event time was found. The third and fourth columns contain the absolute and relative amplitude of the trace, respectively. The fifth column is the logarithmic likelihood of the best fit. The sixth column indicates an algorithm used for postprocessing, and the seventh column indicates the trace slope at the event. See the fitting software for details.</li> </ul> <p> </p>
Data from: A new digital method of data collection for spatial point pattern analysis in grassland communities
<p>A major objective of plant ecology research is to determine the underlying processes responsible for the observed spatial distribution patterns of plant species. Plants can be approximated as points in space for this purpose, and thus, spatial point pattern analysis has become increasingly popular in ecological research. The basic piece of data for point pattern analysis is a point location of an ecological object in some study region. Therefore, point pattern analysis can only be performed if data can be collected. However, due to the lack of a convenient sampling method, a few previous studies have used point pattern analysis to examine the spatial patterns of grassland species. This is unfortunate because being able to explore point patterns in grassland systems has widespread implications for population dynamics, community-level patterns and ecological processes. In this study, we develop a new method to measure individual coordinates of species in grassland communities. This method records plant growing positions via digital picture samples that have been sub-blocked within a geographical information system (GIS). Here, we tested out the new method by measuring the individual coordinates of <i>Stipa</i><i> grandis</i> in grazed and ungrazed <i>S. grandis</i> communities in a temperate steppe ecosystem in China. Furthermore, we analyzed the pattern of <i>S. grandis</i> by using the pair correlation function <i>g</i>(<i>r</i>) with both a homogeneous Poisson process and a heterogeneous Poisson process. Our results showed that individuals of <i>S. grandis</i> were overdispersed according to the homogeneous Poisson process at 0-0.16 m in the ungrazed community, while they were clustered at 0.19 m according to the homogeneous and heterogeneous Poisson processes in the grazed community. These results suggest that competitive interactions dominated the ungrazed community, while facilitative interactions dominated the grazed community. In sum, we successfully executed a new sampling method, using digital photography and a Geographical Information System, to collect experimental data on the spatial point patterns for the populations in this grassland community.</p>
Comparative Analysis of Methods to Estimate Geodetic Strain Rates from GNSS Data in Italy
<p>This dataset comprises GNSS velocity field and strain rate maps for Italy.</p> <p><strong>List of Files:</strong></p> <ol> <li> <p><strong>velocity_dataset.dat</strong></p> <ul> <li>GNSS velocity field of stations with time series longer than 4.5 years.</li> <li>Columns: Longitude (degrees), Latitude (degrees), East component of velocity (mm/yr), North component of velocity (mm/yr), Uncertainty on the East component (mm/yr), Uncertainty on the North component (mm/yr), Station Name.</li> </ul> </li> <li> <p><strong>velocity_dataset_filtr.dat</strong></p> <ul> <li>Filtered velocity field.</li> <li>Columns: Longitude (degrees), Latitude (degrees), East component of velocity (mm/yr), North component of velocity (mm/yr), Uncertainty on the East component (mm/yr), Uncertainty on the North component (mm/yr), Station Name.</li> <li>Stations ending with 'GPM' represent velocity values obtained by merging neighboring stations.</li> </ul> </li> <li> <p><strong>strain_rate_nn.dat (strain_rate_visr.dat, strain_rate_wav.dat)</strong></p> <ul> <li>Strain rate computed on cells spaced by 0.025°.</li> <li>Suffixes in the file names: 'nn' refers to the Nearest Neighbor method, 'visr' refers to the VISR method, and 'wav' refers to the Wavelet-based method</li> <li>Columns: Longitude (degrees), Latitude (degrees), exx (east) component of the strain rate tensor (nstr/yr), exy (east, north) component of the strain rate tensor (nstr/yr), eyy (north) component of the strain rate tensor, second invariant of the strain rate (nstr/yr), most extensive eigenvalue (nstr/yr), most compressive eigenvalue (nstr/yr), angle between north and the direction of the eigenvector corresponding to the most compressive eigenvalue (degrees, positive clockwise).</li> </ul> </li> </ol> <p><strong>Reference:</strong></p> <p>For further details, please refer to the article "Comparative Analysis of Methods to Estimate Geodetic Strain Rates from GNSS Data in Italy", published in <em>Annals of Geophysics</em>.</p>
Digisonde Data files used for JGR-Space Physics paper "A simplified method of true height analysis to estimate the real height of sporadic E layers"
<p>paper submitted for publication in JGR-Space Physics.</p> <p>Digisonde Data files used for analysis</p> <p> </p> <p>A simplified method of true height analysis to estimate the real height of sporadic E layers</p> <p> </p> <p>Christos Haldoupis</p> <p>Department of Physics, University of Crete, Heraklion, Greece</p> <p>Haris Haralambous</p> <p>Frederick University and Frederick Research Center, Nicosia, Cyprus</p> <p>Chris Meek</p> <p>Institute of Space and Atmospheric Studies, University of Saskatchewan, Saskatoon, SK, Canada</p>
Data and code for the publication "Multi-method analysis of microplastic distribution by flood frequency and local topography in Rhine floodplains"
<p><strong>Background</strong></p> <p>The dataset contains data on soil properties and microplastic abundance in soil samples taken in the floodplains Langel-Merkenich, Poller Wiesen and Westhovener Aue (Cologne, Germany). They were analysed in the paper by M. Rolf, H. Laermanns, J. Horn, L. Kienzler, C. Pohl, G. Dierkes, S. Kernchen, C. Laforsch, M.G.J. Löder and C. Bogner, “Multi-method analysis of microplastic distribution by flood frequency and local topography in Rhine floodplains” <a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.scitotenv.2024.171927" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.scitotenv.2024.171927</a>) published in Science of the Total Environment.</p>
Cross-spectra used in "Detailed S-wave velocity structure of sediment and crust off Sanriku, Japan by a new analysis method for distributed acoustic sensing data using a seafloor cable and seismic interferometry"
<p>Cross-spectra used in "Detailed S-wave velocity structure of sediment and crust off Sanriku, Japan, derived from distributed acoustic sensing data collected using a seafloor cable with seismic interferometry", by Shun Fukushima, Masanao Shinohara, Kiwamu Nishida, Akiko Takeo, Tomoaki Yamada, and Kiyoshi Yomogida </p> <p>For more information, please contact Shun Fukushima (s-fuku@eri.u-tokyo.ac.jp)</p>
Raw Data for the article: A Radioactive-Free Method for the Thorough Analysis of the Kinetics of Cell Cytotoxicity
<p>The cytotoxic activity of T cells and Natural Killer cells is usually measured with the chromium release assay (CRA), which involves the use of 51Chromium (<sup>51</sup>Cr), a radioactive substance dangerous to the operator and expensive to handle and dismiss. The accuracy of the measurements depends on how well the target cells incorporate <sup>51</sup>Cr during labelling which, in turn, depends on cellular division. Due to bystander metabolism, the target cells spontaneously release <sup>51</sup>Cr, producing a high background noise. Alternative radioactive-free methods have been developed. Here, we compare a bioluminescence (BLI)-based and a carboxyfluorescein succinimidyl ester (CFSE)-based cytotoxicity assay to the standard radioactive CRA. In the first assay, the target cells stably express the enzyme luciferase, and vitality is measured by photon emission upon the addition of the substrate d-luciferin. In the second one, the target cells are labelled with CFSE, and the signal is detected by Flow Cytometry. We used these two protocols to measure cytotoxicity induced by treatment with NK cells. The cytotoxicity of NK cells was determined by adding increasing doses of human NK cells. The results obtained with the BLI method were consistent with those obtained with the CRA- or CFSE-based assays 4 hours after adding the NK cells. Most importantly, with the BLI assay, the kinetic of NK cells' killing was thoroughly traced with multiple time point measurements, in contrast with the single time point measurement the other two methods allow, which unveiled additional information on NK cell killing pathways.</p>
Input data of the multi-patch geometries used in: A. Farahat, H. M. Verhelst, J. Kiendl, M. Kapl, Isogeometric analysis for multi-patch structured Kirchhoff–Love shells, Computer Methods in Applied Mechanics and Engineering 411 (2023) 116060 DOI: 10.1016/j.cma.2023.116060
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Data from: Individual Movement - Sequence Analysis Method (IM-SAM): characterising spatio-temporal patterns of animal trajectories across scales and landscapes
<p>Dataset included in Zenodo supports the analyses performed in "<em>Individual Movement - Sequence Analysis Methods (IM-SAM) characterising spatio-temporal patterns of animal trajectories across scales and landscapes.</em>"</p> <p>The dataset includes one RDS file, that can be easily loaded into R using the readRDS function. The RDS file consists out of a list including two objects per animal:</p> <ul> <li>Object 1 contains a data frame with the real and simulated sequences for an animal. e.g., ls[[1]][[1]] </li> <li>Object 2 contains the home range in raster format of an animal. e.g., ls[[1]][[2]]</li> </ul> <p>The data frames in object 1 contain real habitat use sequences and corresponding simulated habitat use sequences generated in the home range of the specific individual (900 simulated sequences: 6 habitat selection rules x 3 selection coefficients x 50 repetitions). Open and closed habitats are respectively encoded by 0 and 1. The first 96 columns of each row in a data frame represent a 16-day habitat use sequence, with a fixed 4-hour relocation interval (0, 4, 8, 12, 16 and 20h). Column names are named as follows: Day_1_0h, Day_1_4h,..., Day_16_20h. In the next columns we provide the selection coefficients (columns 97-99), the habitat selection rules (or pattern, columns 100-102) and the number of missing values (mvs, columns, 103-104) for each of the real and simulated sequences. Note that simulated sequences have no missing values (i.e. values are always 0.00) and for real sequences there is no selection coefficient or habitat selection rule (i.e. values are always xxx).</p> <p>Rownames of simulated sequences are composed out of the habitat selection rule (c, o, a24, a33, a42 and u), the selection coefficient (5, 10, 50) and the replicate (1 to 50), separated by dashes. For example, the first simulated sequence in the first data frame (ls[[1]][[1]][1,]) is described as a24_10_1. The rownames of real sequences instead are composed out of the individuals' identifier, the biweekly period (1 to 23) and the year. For example, the first real sequence in the first data frame (ls[[1]][[1]][901,]) is described as 1_5_2006.</p> <p><br> </p>
Data for 'Comparative Analysis of Single-Cell RNA Sequencing Methods'
<p>Raw sequencing data to "Comparative Analysis of Single-Cell RNA Sequencing Methods". </p> <p>https://www.ncbi.nlm.nih.gov/pubmed/28212749</p> <p> </p> <p>In addition to the GEO submission https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE75790, you can find here raw bam files for UMI-methods tagged with cell barcode and UMI sequences.</p> <p>MD5 checksum: f10825509952fffd9c4dc0c1dcb9eb8e</p>
Code + simulated + publically accessable data for "Evaluating health facility access using Bayesian spatial models and location analysis methods"
<p># README</p> <p>These files contain r data objects and R files that represent the key details of the paper, "Evaluating health facility access using Bayesian spatial models and location analysis methods".</p> <p>The following datasources are available for simulation of some of the ideas in the paper.</p> <p>- dat_grid_sim: simulated data of the grid and grid cells<br> - dat_ohca_cv_sim: simulated data containing the cross validated test/training sets of OHCA data<br> - dat_ohca_sim: simulated OHCA event data<br> - dat_aed_sim: simulated AED location data<br> - dat_bldg_sim: simulated building location data<br> - dat_municipality_sim: simulated municipality information<br> - table_1: Table 1 information containing key demographic data</p> <p>These data were produced using the code in 01-create-sim-data.R, and one of the statistical models is demonstrated in 02-demo-inla-model.R</p> <p>In terms of the paper itself, the functions and code used in the manuscript are located in:</p> <p>* 01_tidy.Rmd - analysis code used to tidy up the data</p> <p>* 02_fit_fixed_all_cv.Rmd - analysis code used to place AEDs</p> <p>* 02_model.Rmd - analysis code used to fit the model in INLA</p> <p>* 03_manuscript.Rmd - Full code and text used to create the paper</p> <p>* 04_supp_materials.Rmd - full code and text used to create the supplementary materials</p> <p>The following files are a part of an R package "swatial" that was developed along with the paper. These files are:</p> <p>* DESCRIPTION</p> <p>* NAMESPACE</p> <p>* LICENSE</p> <p>* LICENSE.md</p> <p>* decay.R</p> <p>* spherical-distance.R</p> <p>* test-figure-data-matches.R</p> <p>* test-table-data-matches.R</p> <p>* testthat.R</p> <p>* tidy-inla.R</p> <p>* tidy-posterior-coefs.R</p> <p>* tidy-predictions.R</p> <p>* utils-pipe.R</p> <p>* All files that end in .Rd are documentation files for the functions.</p> <p>## Regarding data sources</p> <p>Census information for Ticino was transcribed from the Annual Statistical Report of Canton Ticino from years 2010 to 2015. This data was taken from their publicly accessible annual reports - for example: (https://www3.ti.ch/DFE/DR/USTAT/allegati/volume/ast_2015.pdf). The raw data was extracted from these annual reports, and placed into the file: "swiss_census_popn_2010_2015.xlsx". These data are put into analysis ready format in the file “01_tidy.Rmd”</p> <p>Housing and other relevant geospatial data can be accessed via http://map.housing-stat.ch/ and https://data.geo.admin.ch/. The maps of buildings from the REA (Register of Buildings and Dwellings) can be found here: https://map.geo.admin.ch/?zoom=11&bgLayer=ch.swisstopo.pixelkarte-grau&lang=en&topic=ech&layers=ch.bfs.gebaeude_wohnungs_register,ch.swisstopo.swissboundaries3d-gemeinde-flaeche.fill,ch.bfs.volkszaehlung-gebaeudestatistik_gebaeude,ch.bfs.volkszaehlung-gebaeudestatistik_wohnungen,ch.swisstopo.swissbuildings3d_1.metadata,ch.swisstopo.swissbuildings3d_2.metadata&E=2717616.28&N=1096597.25&catalogNodes=687,696&layers_timestamp=,,2016,2016,,&layers_visibility=true,false,false,false,false,false&layers_opacity=1,1,1,1,1,0.75</p> <p>For further enquiries on this data, contact the Swiss federal Office of Statistics at the details listed here: https://www.bfs.admin.ch/bfs/en/home/services/contact.html</p> <p>The shapefiles of the Comuni can be accessed here: https://www4.ti.ch/dfe/de/ucr/documentazione/download-file/?noMobile=1</p> <p>Data from the people living in the Municipalities in Ticino can be downloaded here: https://www3.ti.ch/DFE/DR/USTAT/index.php?fuseaction=dati.home&tema=33&id2=61&id3=65&c1=01&c2=02&c3=02</p> <p>## Future work</p> <p>In the future, these functions from the paper may be generalised and put into their own package. If that happens, this repository will be updated with a link to updated functions.</p>
Data Appendix for Lack, P., "Using Word Analysis to Track the Evolution of Emotional Well-being in Nineteenth-Century Industrializing Britain", Historical Methods (forthcoming)
<p>This file contains the data associated with the publication Lack, P., "Using Word Analysis to Track the Evolution of Emotional Well-being in Nineteenth-Century Industrializing Britain", <em>Historical Methods</em> (forthcoming). It quantifies the trend in emotional well-being expressed in a corpus of British pamphlets published between 1800 and 1900. The first page of the excel document presents this key data on the trend in emotional well-being. Sheet 1A presents summary statistics on the trend in emotional well-being and its correlation with GDP per capita and real wages. </p>
Data for "Advanced Structural Health Monitoring Method by Integrated Isogeometric Analysis and Distributed Fiber Optic Sensing"
<p>This dataset includes the experiment and simulation data of a new structural health monitoring system using distributed fiber optic sensing (DFOS) and Isogeometric Analysis (IGA).</p> <p>The experiment setup was a 5mm thick PVC pipe with a fiber optic cable wrapped around the outer surface of the pipe. The PVC pipe was subjected to an applied deformation and the distributed strains along the optical fiber was measured with a Neubrescope (NBX7031) instrument using Rayleigh backscattering technology.</p> <p>The simulation was performed using the in-house code JWRIAN-IGA developed in Joining and Welding Research Institute, Osaka University. The simulated data includes deformation, stress and strain distributions of the pipe, and projected one-dimensional fiber strains. The visualization files are post-processed with ParaView software.</p>
Ice-Flow Perturbation Analysis: A method to estimate ice-sheet bed topography and conditions from surface datasets (data)
<p>This dataset accompanies the paper 'Ice-Flow Perturbation Analysis: A method to estimate ice-sheet bed topography and conditions from surface datasets' in Journal of Glaciology, and can be used alongside the provided code to reproduce the figures,</p>
ScienceDex guides
Understand access before you commit
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.