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30,813 results for “typing”
Harmonised LUCAS database classified by crop sequence type
<p>Assessing the benefits of crop diversification – a pillar of the agroecological transition – on a large scale requires a description of current crop sequences as a baseline, which is lacking at the scale of the European Union (EU). This work is based on the Harmonised LUCAS in-situ land cover and use database for field surveys from 2006 to 2018 in the European Union (doi: <a href="http://doi.org/10.2905/f85907ae-d123-471f-a44a-8cca993485a2">10.2905/f85907ae-d123-471f-a44a-8cca993485a2)</a> to fill this gap, We completed this dataset with a crop sequence type information for each point under non-perennial agricultural land cover in 2012, 2015 and 2018.</p> <p>The dataset lucas_classified.csv includes 31 159 points. Variables "point_id", "nuts0", "nuts2", "th_lat", "th_long", "LC1_2012", "LC1_2015", "LC1_2018" are inherited from the Harmonised LUCAS databse. Variables "cereals", "corn", "rapeseed", "sunflower", "pulses", "rootCrops", "forageLeg", "grassland" correspond to the temporal frequencies of respectively cereals, corn, rapeseed, sunflower, pulses, root crops, forage legumes and grassland within the 2012, 2015 and 2018 crop sequence for each point. Variable "crop_sequence_type" is the crop sequence type assigned to each point, among eight options: cereals, corn and cereals, forage legumes and cereals, pulses and cereals, rapeseed and cereals, root crops and cereals, sunflower and cereals, temporary grasslands.</p> <p>This dataset could be used to map current dominant crop sequences in the European Union, as illustrated in the map attached, and to assess the benefits of future crop diversification.</p> <p> </p>
Seedling emergence and biomass data of nine dryland plant species characterizing the impact of soil residual auxin herbicide across two soil types and water pulse events on greenhouse growth; Las Cruces, New Mexico, Spring 2021.
Synthetic-auxin herbicides are often used to control woody plants and aid in grassland restoration. Seed-based restoration is common alongside herbicide applications and there may be unintended effects of these herbicides on dryland plant species at the seed and seedling stages. Additionally, abiotic conditions at the time of herbicide application may influence herbicide-soil-plant interactions. We conducted a greenhouse study to examine the effects of a common shrub-control herbicide mix and its interaction with soil type and a post-herbicide water pulse on common desert plant seeds and seedlings. In this greenhouse study, we found that a subset of species responded negatively to soil residual herbicide activity of a mixture of aminopyralid, clopyralid, and triclopyr at the seed and seedling stages. Species sensitive to soil herbicide residues were primarily shrub and forb species that are often the target species of herbicide applications for woody plant control, such as Prosopis glandulosa (honey mesquite) and Larrea tridentata (creosote bush). However, two shrub species (Atriplex canescens [four-wing saltbush] and Yucca elata [soaptree yucca]) and one perennial grass species (Digitaria californica [Arizona cottontop]), which are used in dryland restoration projects, were found to be particularly sensitive to soil residual herbicide activity. Thus, if using these herbicides to control woody plants and restore herbaceous vegetation via active seeding or relying on the in situ seed bank, considerations should be given to what species are used in the seed mix, what species are already present in the soil seed bank, and other details of the circumstances of herbicide application.
Benthic community response to different disturbance type events across six islands between two timepoints in the Central Pacific
A coral reef's response to disturbance can be driven by various factors including community composition. This dataset highlights benthic cover and its changes between two timepoints at six islands across the central Pacific. The survey islands include Ant Atoll, Pakin Atoll, and Pohnpei located within the Federated States of Micronesia (FSM) as well as Upon and Savai'i in Samoa and Rarotonga in the Cook Islands. Survey years differed between sites but all sites had an estimated two-year time-difference between resampling. To extract benthic cover, photos were annotated using randomized points and labeled to their highest taxonomic resolution, down to genus-level for hard corals. Both abiotic and biotic substrate were identified and major functional groups included: hard corals, soft corals, invertebrates, turf algae, Halimeda spp., crustose coralline algae, and other (sand/debris/etc.). Disturbance type and community composition at the initial survey period drove changes in percent cover for major functional groups. Data was collected by annotating photos from transect surveys on a coral reef. This effort was completed by the 2020 SIO 'Pop-up' SURF REU that was formed in rapid response due to COVID-19 research limitations.
Biomass totals and root biomass (partitioned by percent of total leaf area) for species, tissue type, and functional group for the Arctic LTER experimental 1981 mesic acidic tussock tundra (MAT81) for the 2000 and 2015 harvests, Toolik Field Station, Alaska.
Whole plant biomass totals and root biomass (partitioned by percent of total leaf area) for species, tissue type, and functional group for the Arctic LTER experimental 1981 mesic acidic tussock tundra (MAT81) for the 2000 and 2015 harvests. Because most of the root biomass could not be identified to species in either 2000 or 2015, the calculation of root biomass and element content for roots not identified to species was estimated by the proportion of those species’ contributions to total leaf area. Specific Leaf Area (SLA = leaf area per gram leaf, centimeter squared per gram) values were available from several previous harvests of this experiment; in the present study, we used measurements from the 1995 harvest (Shaver et al. 2001).
Multiple Element Limitation in Northern Hardwood Ecosystems (MELNHE): Soil Profile Rock Characteristics by Bedrock Type in Bartlett and Hubbard Brook, 2004-2018
Soils in our northeastern forests were formed in parent materials deposited by glaciers. The direction and distance of glacial movement can be used to predict the source of glacial till at “downstream” points on the landscape (Bailey 1992). The goal of this project was to identify the rocks excavated from the soil pits in each of the plots and then to use that data to validate the glacial till model. The minority of rocks in the soil pits matched the bedrock, showing the importance of glacial movement. Additional detail on the MELNHE project, including a data table of site descriptions and a pdf file with the project description and diagram of plot configuration can be found in this data package: https://portal.edirepository.org/nis/mapbrowse?scope=knb-lter-hbr&identifier=344. These data were gathered as part of the Hubbard Brook Ecosystem Study (HBES). The HBES is a collaborative effort at the Hubbard Brook Experimental Forest, which is operated and maintained by the USDA Forest Service, Northern Research Station. Literature cited: Bailey, S.W., 1992. Lithologic composition and rock weathering potential of forested, glacial-till soils (Vol. 662). US Department of Agriculture, Forest Service, Northeastern Forest Experiment Station.
MiRoR11 - P2 - Annotated dataset for spin-related types of statements (statements of similarity and within-group comparisons)
<p>180 abstracts / 2401 sentences annotated for 2 types of spin-related statements: statements of similarity and within-group comparisons.</p>
Data: Algorithms for new types of fair stable matchings
<p>This data corresponds to the data and experiments described in Section 5 of<br> the following paper:</p> <p>Algorithms for new types of fair stable matchings<br> Authors: Frances Cooper and David Manlove</p> <ul> <li>The paper is located at: <a href="https://arxiv.org/abs/2001.10875">https://arxiv.org/abs/2001.10875</a></li> <li>The software is located at: <a href="https://zenodo.org/record/3630383">https://zenodo.org/record/3630383</a></li> <li>The data is located at: <a href="https://zenodo.org/record/3630349">https://zenodo.org/record/3630349</a></li> </ul> <p>See the README for more information.</p>
3D scans of two types of railway ballast including shape analysis information
<p>This data set contains 3D scanner data of two types of railway ballast “Calcite” (stems from Croatia) and “Kieselkalk”, also known as Helvetic Siliceous Limestone, (stems from Switzerland).<br> From each type of ballast 25 stones are scanned. The files are provided in .ply format.<br> For the scanned meshes several shape descriptors are provided: elongation, flatness, sphericity, convexity index.<br> Additional to the 3D scans, both simplified and rounded versions of the meshes are included.<br> For these meshes information on three different angularity indices are available.<br> The scanned ballast types are the same, as previously investigated in uniaxial compression tests and direct shear tests:<br> Suhr, Bettina, & Six, Klaus. (2018).<br> "Compression tests and direct shear test of two types of railway ballast [Data set]"<br> Zenodo. http://doi.org/10.5281/zenodo.1423742</p> <p> </p> <p>A detailed shape analysis of the results is conducted in:<br> Bettina Suhr, William A. Skipper, Roger Lewis, and Klaus Six<br> "Shape analysis of railway ballast stones: curvature-based calculation of particle angularity"<br> <em>Scientific Reports, </em><strong>2020</strong><em>, 10</em>, 6045<br> DOI: https://doi.org/10.1038/s41598-020-62827-w</p> <p>A summary of several shape descriptors can be found in:<br> B. Suhr and K. Six:<br> "Simple particle shapes for DEM simulations of railway ballast -- influence of shape descriptors on packing behaviour"<br> Granular Matter, <strong>2020</strong><em>, 22</em><br> DOI: https://doi.org/10.1007/s10035-020-1009-0</p> <p><br> This data set is organised as follows:<br> 1_ScanMeshesCleaned<br> scanned meshes:<br> K_1.ply - K_25.ply Calcite (German: Kalzit)<br> KK_1.ply - KK_25.ply Kieselkalk<br> 2_CSE1 <br> simplifications of the scanned meshes, little simplifications, used in the detailed shape analysis<br> CSE1_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> 3_CSE2 <br> simplifications of the scanned meshes, more simplified, used in the detailed shape analysis<br> CSE2_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> 4_CSE3 <br> simplifications of the scanned meshes, even more simplified, used in the detailed shape analysis<br> CSE3_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> 5_CSE4 <br> simplifications of the scanned meshes, most simplified, used in the detailed shape analysis<br> CSE4_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> 6_RoundedMeshes<br> artificially rounded versions of the scanned ballast meshes, used in the detailed shape analysis<br> RoundedMeshes_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> 7_TestBodies <br> meshes of artificial test bodies, constructed for testing different angularity indices in the detailed shape analysis<br> TestBodies_AngInfo.csv: contains values of three different angularity indices used in the detailed shape analysis<br> scanMeshesInfo.csv: summary of several shape descriptors of the scanned meshes<br> README.txt </p> <p><br> Check the README.txt file for more information on the technical aspects of scanning.</p> <p> </p>
Data supplement for "Bifurcations of front motion in passive and active Allen-Cahn-type equations"
<p>This dataset contains the data and source files for figures 5 and 7-10 in the following publication: </p> <p>F. Stegemerten, S.V. Gurevich, U. Thiele</p> <p><em>'Bifurcations of front motion in passive and active Allen–Cahn-type equations' </em></p> <p>published in 2020 in CHAOS.</p> <p>Please follow the instructions given in 'Readme.txt'.</p>
Designing Types for R, Empirically (Dataset)
<p>This dataset is intended to accompany the paper "Designing Types for R, Empirically" (@ OOPSLA'20, <a href="https://2020.splashcon.org/details/splash-2020-oopsla/57/Designing-Types-for-R-Empirically">link to paper</a>). This data was obtained by running the Typetracer (aka propagatr) dynamic analysis tool (<a href="https://github.com/PRL-PRG/propagatr">link to tool</a>) on the test, example, and vignette code of a corpus of >400 extensively used R packages.<br> <br> Specifically, this dataset contains:</p> <ol> <li>function type traces for >400 R packages (raw-traces.tar.gz);</li> <li>trace data processed into a more readable/usable form (processed-traces.tar.gz), which was used in obtaining results in the paper;</li> <li>inferred type declarations for the >400 R packages using various strategies to merge the processed traces (see type-declarations-* directories), and finally;</li> <li>contract assertion data from running the reverse dependencies of these packages and checking function usage against the declared types (contract-assertion-reverse-dependencies.tar.gz).</li> </ol> <p> A preprint of the paper is also included, which summarizes our findings.</p> <p><strong>Fair warning Re: data size:</strong> the raw traces, once uncompressed, take up nearly 600GB. The already processed traces are in the 10s of GB, which should be more manageable for a consumer-grade computer.</p>
Effect of superparamagnetic iron oxide nanoparticles on glucose homeostasis on type 2 diabetes experimental model
<p>The data correspond to figures in the paper by Ali, L.M.A. et al. Life Sciences 245 (2020) 117361. doi:10.1016/j.lfs.2020.117361.</p>
Activin A receptor, type I (ACVR1); A Target Enabling Package
<p>Germline gain of function mutations in the gene <em>ACVR1</em> encoding the BMP receptor ALK2 lead to the rare congenital syndrome FOP in which aberrant signalling through the BMP signalling pathway leads to progressive heterotopic ossification in muscle and connective tissue. Identical somatic mutations have been identified in 25% of cases of the childhood brain tumour DIPG. Both conditions affect young children and have no approved therapies. Highly selective ALK2 kinase inhibitors are therefore desirable to achieve chronic treatment of children with safety. We prepared recombinant ALK2 kinase domain and solved structures of ALK2 in complex with new ATP-competitive inhibitors. We identified a novel allosteric pocket in the ALK2 kinase domain and took advantage of these structures to perform crystallographic fragment screening (XChem) using both a standard poised fragment library and a new mini-fragment library. This work identified a poised fragment for development as an allosteric ALK2 inhibitor, as well as mini-fragments exploiting new areas of the ATP and substrate binding pockets. <em>In vitro</em> and cellular assays are available to advance these compounds for drug development in collaboration with patient groups.</p>
Data set for "Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing"
<p>Data set for: Gasselin C, Hohl B, Vernet A, Crochet C, Petersen CCH (2021) Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing. Neuron doi: 10.1016/j.neuron.2020.12.018</p> <p>There are 2 files in this upload:</p> <p>1. The file named "2021_Gasselin_Neuron.pdf" is the Open Access pdf of the online publication in Neuron.</p> <p>2. The file named "Gasselin_data_code.zip" (~9 GB) is a zipped version of a folder "Gasselin_data_code" (~13 GB), which contains the data analysed in the study along with the Matlab code used to generate the published figures. To access the data and the code, first unzip the file. Then add the folder with subfolders to the Matlab path and run the different codes. The current folder must be the main folder (‘Gasselin_data_code’). Each code computes and plots the results used in the corresponding figure. Figures and Tables are saved in the subfolder ‘Figures’.</p> <p>The subfolder ‘Functions’ contains functions called by the main codes.</p> <p>The main folder contains the following codes:</p> <p><em>Gasselin_Figure1: computes and plots the results for the panels D, E and F of figure 1.</em></p> <p><em>Gasselin_Figure2: computes and plots the results for the panels B and C of figure 2.</em></p> <p><em>Gasselin_Figure3: computes and plots the results for the panels B, C and D of figure 3.</em></p> <p><em>Gasselin_Figure4: computes and plots the results for the panels A, B and C of figure 4.</em></p> <p><em>Gasselin_FigureS1: computes and plots the results for the panels A, B and C of figure S1.</em></p> <p><em>Gasselin_FigureS2: computes and plots the results for the panels A and B of figure S2.</em></p> <p> </p> <p>The subfolder ‘Data’ contains the data structures used for the different figures:</p> <p><em>data_figure1.mat</em></p> <p><em>data_figure2.mat</em></p> <p><em>data_figure3.mat</em></p> <p><em>data_figure4_MECA.mat</em></p> <p><em>data_figure4_Activation.mat</em></p> <p><em>data_figure4_Inactivation.mat</em></p> <p><em>data_figureS2_Activation.mat</em></p> <p><em>data_figureS2_Inactivation.mat</em></p> <p><em>data_Axon.mat</em></p> <p> </p> <p>The data structures contain the following fields:</p> <p><em>Mouse_Name</em> : name of the mouse.</p> <p><em>Mouse_DateOfBirth</em>: date of birth of the mouse (YMD).</p> <p><em>Mouse_Sex</em>: sex of the mouse (F or M).</p> <p><em>Mouse_Genotype</em>: genotype of the mouse.</p> <p><em>Mouse_Drug</em>: experimental condition of the recording (control = ‘No Drug’; blockade of glutamatergic transmission = ‘CNQX_DAPV’; blockade of glutamatergic transmission and nicotinic receptors = ‘CNQX_DAPV_MECA’; blockade of nicotinic receptors only = ‘MECA’).</p> <p><em>Mouse_Virus</em>: virus injected if any.</p> <p><em>Cell_Counter</em>; cell recorded in a given mouse.</p> <p><em>Cell_Type</em>: type of the recorded cell based on 2P imaging. (EXC, VIP, PV, SST, 5HT3aR_non_VIP).</p> <p><em>Cell_Depth</em>: depth of the recorded cell relative to pia (µm).</p> <p><em>Cell_TargetedBrainArea</em>: cortical area targeted (C2 column of the barrel cortex = C2).</p> <p><em>Cell_Fluorescence</em>: expression of the genetically encoded fluorophore (FALSE or TRUE). A neuron recorded in a VIP_IRES_Cre x LSL_tdTomato (cf <em>Mouse_Genotype</em>) with <em>Cell_Fluorescence</em>=TRUE is considered as a VIP neuron (cf <em>Cell_Type</em>).</p> <p><em>Sweep_Counter</em>: number of the sweep recorded for a given neuron (data were acquired across successive continuous sweeps of 30-60 s).</p> <p><em>Sweep_Type</em>: experimental condition during that sweep (Only spontaneous whisking onset = ‘Onset’; Whisking onset and whisker stimulus = ‘Onset_Whisker_Stim’ ; Optogenetic stimulation = ‘Opto_Stim’; Optogenetic activation = ‘Opto_Activation’; Optogenetic inactivation = ‘Opto_Inactivation’; ).</p> <p><em>Sweep_Start_Time</em>: time at the beginning of the sweep recording (YMDHms).</p> <p><em>Sweep_WhiskerAngle</em>: C2 whisker angular position extracted from simultaneous high-speed video filming (deg).</p> <p><em>Sweep_WhiskerAngle_SamplingRate</em>: sampling rate of the whisker angle trace.</p> <p><em>Sweep_WhiskingOnset_Time</em>: time of identified whisking onset - excluding any whisker stimulus shortly before or after (s).</p> <p><em>Sweep_MembranePotential</em>: membrane potential recording (mV) after cutting of the APs.</p> <p><em>Sweep_MembranePotential_SamplingRate</em>: sampling rate of the membrane potential signal (pt.s<sup>-1</sup>).</p> <p><em>Sweep_CurrentInjected</em>: current injected into the cell (pA).</p> <p><em>Sweep_CurrentInjected_SamplingRate</em>: sampling rate of current signal (pt.s<sup>-1</sup>).</p> <p><em>Sweep_WhiskerStim_Name</em>: whisker to which the magnetic stimulus was applied to (C2 or B2&C2).</p> <p><em>Sweep_WhiskerStim_Time</em>: onset times of the whisker stimulus (s).</p> <p><em>Sweep_OptoStim_Power</em>: light power applied for optogenetic manipulations (% of the max power).</p> <p><em>Sweep_OptoStim_Time</em>: onset times of the light pulses for optogenetic manipulations (s).</p> <p><em>Cell_ID</em>: unique cell identifier (= <em>Mouse_Name</em>+<em>Cell_Counter</em>).</p> <p><em>SpikeThreshold</em>: spike threshold used to detect APs (mV).</p> <p><em>Trial_WhiskingOnset</em>: data structure containing the cut signals used to compute averaged responses around whisking onset times.</p> <p><em>Trial_WhiskerStim</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times.</p> <p><em>Trial_WhiskerStim_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without whisker movements.</p> <p><em>Trial_WhiskerStim_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with whisker movements.</p> <p><em>Trial_Opto</em>: data structure containing the cut signals used to compute averaged responses around optogenetic stimulus onset times.</p> <p><em>Trial_OptoAndWhisker_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with optogenetic manipulation and no whisker movements.</p> <p><em>Trial_OptoAndWhisker_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with optogenetic manipulation and with whisker movements.</p> <p><em>Trial_OnlyWhisker_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without optogenetic manipulation and without whisker movements.</p> <p><em>Trial_OnlyWhisker_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without optogenetic manipulation and with whisker movements.</p> <p><em>Trial_OnlyOpto</em>: data structure containing the cut signals used to compute averaged responses around optogenetic stimulus onset times in trials without whisker stimulus.</p>
Data licences and organization type of contributors to the Global Biodiversity Information Facility as of 19 January 2016
<p>Data from the Global Biodiversity Information Facility were extracted using R (version 3.2.0) on 9 July 2015 using the rgbif package (version 0.9.0) (Chamberlain, S., Ram, K., Barve, V. & Mcglinn, D. (2015) Package ‘rgbif’: Interface to the Global 'Biodiversity' Information Facility 'API' http://cran.r-project.org/web/packages/rgbif/rgbif.pdf). The ‘rights’ statements was extracted for all occurrence datasets with one or more observations. A total of 12,458 datasets were extracted, but only about 11% of the datasets have an explicit data-useage-rights statement at the dataset level. However, some datasets use the occurrence level ‘rights’ and ‘accessRights’ fields. To extract these data the rights information was obtained from the first record of each dataset where a rights statement was missing at the dataset level.</p> <p>The datasets were categorized into 13 different types depending on the origin of the observations.</p> <ol> <li>Biodiversity Information Facility or data centre</li> <li>Botanical Garden or Herbarium</li> <li>Citizen science</li> <li>Commercial</li> <li>Data publisher</li> <li>Educational</li> <li>Government</li> <li>Museum</li> <li>Network</li> <li>Parks Authority or Nature Reserve</li> <li>Research institution</li> <li>Society</li> <li>Foundations</li> </ol>
Dataset: Finite groups of symplectic birational transformations of IHS manifolds of OG10 type
<p>Dataset for the finite symplectic birational actions on IHS manifolds of OG10 type.</p> <p>Contains the data related to the paper, a list of Jupyter notebooks for demonstrating some of the computations, two extra tables recording information about the entries of the dataset, and a file containing a list of exceptional lattices (in the wording of the paper). </p> <p>Read the README.md for more information.</p>
Type III interferons may suppress viral infections by triggering cell death -- Imaging Dataset
<p>This dataset accompanies the article "Type III interferons may suppress viral infections by triggering cell death". Earlier version is available as a preprint, <a href="https://doi.org/10.1101/2024.09.09.612051" target="_blank" rel="noopener">https://doi.org/10.1101/2024.09.09.612051</a>. The updated dataset includes quantifications for Figure 7C and Figure 7D.</p>
The data behind the ApJ article "Environmental Dependence of Type Ia Supernovae in Low-Redshift Galaxy Clusters"
<p>Data from "Environmental Dependence of Type Ia Supernovae in Low-Redshift Galaxy Clusters", <a href="https://ui.adsabs.harvard.edu/abs/2023arXiv230601088L/abstract">NASA ADS</a></p><p>inner_cluster_data.csv and outer_cluster_data.csv include the SALT3 mB, x1, and c parameter values, distance moduli and Hubble residuals (with _1 referring to Figure 9 and _2 referring to Figure 10), outlier designation from MCMC procedure, host cluster, host cluster redshift (with Hubble diagram version converted to frame of CMB), host cluster r500, projected separation from cluster center, NED Host galaxy name, photometrically-derived estimate for host mass, host or SN redshift used in analysis, and the Host SFR category (Q: quiescent, SF: star-forming, GV: green valley) for our cluster SNe Ia.</p><p>sf_field.csv and quiescent_field.csv contain SALT parameter values, distance moduli and Hubble residuals (from Figure 10), host galaxy sSFR and mass measurements, and host redshifts (all spectroscopic, also with Hubble diagram converted values) for SNe Ia in our field samples.</p><p>full_cluster.csv contains the data from the table in the appendix of the paper.</p><p>The inner_cluster_/outer_cluster_mcmc_samples.csv files contain the samples needed to reproduce the corner plot for Figure 10.</p><p>The Python scripts recreate the figures from the paper given the above data. The details for which columns and constraints needed to reproduce the figures are included in these files.</p>
BeBOD estimates of incidence, prevalence, and years lived with disability for 57 cancer types, 2004-2021
<p><strong>Belgian National Burden of Disease Study</strong></p><p><strong>Estimates of the morbidity burden of disease for 57 cancer sites</strong></p><p><i>Incidence</i></p><p>Data on new cancer cases in Belgium are collected by the <a href="https://kankerregister.org/Annual%20Tables">Belgian Cancer Registry</a> (BCR). For the current study, we selected 80 ICD-10 (C00.0-96.9 and chronic myeloid neoplasms) codes resulting in 57 cancer sites. Data were extracted by year (from 2004 to 2021), age group (5-years), sex and region (N=3). We excluded "Respiratory system and intrathoracic organs, NOS (not otherwise specified)" from further analyses because of too few cases.</p><p><i>Prevalence</i></p><p>Prevalence estimates were estimated using the above-described incidence estimates and the survival estimates also provided by BCR, derived from linkage with the Belgian Crossroads Bank for Social Security. We used a 10-year prevalence perspective meaning that from the year 2013 onwards, we were able to define the prevalence in a given year as the sum of person-months spent in the different health states. Specifically, we used a microsimulation approach to simulate future health states for each year-, age-, sex-, region- and cancer-specific cohort of incident cases.</p><p>See for more details: <a href="https://doi.org/10.1186/s12885-021-09109-4">https://doi.org/10.1186/s12885-021-09109-4</a></p><p><i>Years Lived with Disability</i></p><p>Years Lived with Disability (YLDs) were calculated using both an incidence and prevalence perspective as a measure of morbidity. YLDs are calculated as the product of the number of prevalent cases with the disability weight (DW), averaged over the different health states of the disease. The DWs reflect the relative reduction in quality of life, on a scale from 0 (perfect health) to 1 (death). We calculate YLDs using the Global Burden of Disease DWs.</p>
BK Channels activation by N-type Ca2+ channels in the dendrites of neocortical pyramidal neurons
<p>This dataset contains imaging and whole-cell electrophysiological recordings from neocortical layer-5 pyramidal neuron dendrites in brain slices of the mouse.</p><p>Somatic electrophysiological and dendritic imaging recordings were done at 20 kHz. Imaging recordings were done with ~2.5 µm nm pixel resolution. These correspond to:</p><ul><li>Voltage imaging (Figures 1 and 7)</li><li>Calcium imaging (Figures 2,3 and 4).</li></ul><p>This dataset is used in the paper:</p><p>Blömer LA, Giacalone E, Abbas F, Filipis L, Migliore M, Canepari M. Kinetics and functional consequences of BK Channels activation by N-type Ca2+ channels in the dendrite of mouse neocortical layer-5 pyramidal neurons. bioRxiv, 2023 (https://www.biorxiv.org/content/10.1101/2023.10.26.564136v1).</p>
Redistribution of the Natura 2000 habitat map of Flanders, partim habitat type 3260 (version 2023)
<p>This is a redistribution of a subdataset of the data source '<a href="https://www.vlaanderen.be/datavindplaats/catalogus/biologische-waarderingskaart-en-natura-2000-habitatkaart-toestand-2023">Biologische Waarderingskaart en Natura 2000 Habitatkaart - Toestand 2023</a>', originally published by the Research Institute for Nature and Forest (INBO) and distributed by 'Digitaal Vlaanderen' under a CC-BY compatible license. It is redistributed for reproducible, analytical workflows on Flemish Natura 2000 habitats and regionally important biotopes.</p><p>The subdataset is a shapefile of line segments of the Natura 2000 habitat type 3260 (Watercourses of plain to montane levels with the <i>Ranunculion fluitantis</i> and <i>Callitricho-Batrachion</i> vegetation) that correspond with its presence in watercourses in the Flemish Region, identical to the shapefile Hab3260 in the original data source.</p><p>The data source is produced, owned and administered by the Research Institute for Nature and Forest (INBO, Department of Environment of the Flemish government).</p>
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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.