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1,737 results for “host data”
Data from: Spatial and host-related variation in prevalence and population density of wheat curl mite (Aceria tosichella) cryptic genotypes in agricultural landscapes
<p><strong>Filename: coord.csv</strong></p> <p>Names of the sampling locations and their geographic coordinates.</p> <ol> <li>Name - sampling locality identifier</li> <li>Lat - latitude</li> <li>Long - longitude</li> </ol> <p> </p> <p><strong>Filename: lineages.csv</strong></p> <ol> <li>id.sample - sample identifier</li> <li>host - host species (Arrela=<em>Arrhenantherum elatius</em>, Avesat=<em>Avena sativa</em>, Broine=<em>Bromus inermis</em>, Elyres=<em>Elymus repens</em>, Horvul=<em>Hordeum vulgaris</em>, Seccer=<em>Secale cereale</em>, Triaes=<em>Triticum aestivum</em>, Tririm=<em>Triticale rimpaui</em></li> <li>x, y - geodetic coordinates</li> <li>stems - no. of stems in a sample</li> <li>leaves - no. of leaves in a sample</li> <li>MT.01 to MT.27 - no. of mites belonging to each genetic lineage</li> </ol>
Accompanying data for the PhD thesis 'Nanomaterial safety for microbially-colonized hosts'
<p><strong>These files include all data presented in chapter 6 of the dissertation:</strong></p> <p><strong>"Nanomaterial safety for microbially-colonized hosts: microbiota-mediated physisorption interactions and particle-specific toxicity" by Bregje Brinkmann (2022).</strong></p> <p>The data presented in chapters 2-5 have previously been published elsewhere:</p> <ul> <li>Chapter 2: <em>Zenodo</em> (DOI: <a href="https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fdoi.org%2F10.5281%2Fzenodo.6800734&data=05%7C01%7Cb.w.brinkmann%40cml.leidenuniv.nl%7Cb5837fcc5a1b4cb5e88008da7615fe87%7Cca2a7f76dbd74ec091086b3d524fb7c8%7C0%7C0%7C637952134073527979%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=z4LB7Ziyiy%2BLXe0SllX67AJ%2F9zhfARBXp8QNzZsVg%2B4%3D&reserved=0">10.5281/zenodo.6800734</a>).</li> <li>Chapter 3: <em>Mendeley</em> <em>Data</em> (DOI: <a href="https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fdoi.org%2F10.17632%2F2d4hcr5cb5.1&data=05%7C01%7Cb.w.brinkmann%40cml.leidenuniv.nl%7Cb5837fcc5a1b4cb5e88008da7615fe87%7Cca2a7f76dbd74ec091086b3d524fb7c8%7C0%7C0%7C637952134073527979%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=x7LFz2OgiJ20%2BD18QlwR9qIwGH%2BCbju4BKqkUaqIoXs%3D&reserved=0">10.17632/2d4hcr5cb5.1</a>)</li> <li>Chapter 4: <em>Figshare</em> (DOI: <a href="https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fdoi.org%2F10.6084%2Fm9.figshare.c.4923261&data=05%7C01%7Cb.w.brinkmann%40cml.leidenuniv.nl%7Cb5837fcc5a1b4cb5e88008da7615fe87%7Cca2a7f76dbd74ec091086b3d524fb7c8%7C0%7C0%7C637952134073527979%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=n3wegOuHzKihCO%2FKbZhClnYHPyxWI0cALApBgLkUHnQ%3D&reserved=0">10.6084/m9.figshare.c.4923261</a>)</li> <li>Chapter 5: <em>Mendeley Data </em>(DOI: <a href="https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fdoi.org%2F10.17632%2F4nfg69v8hy.1&data=05%7C01%7Cb.w.brinkmann%40cml.leidenuniv.nl%7Cb5837fcc5a1b4cb5e88008da7615fe87%7Cca2a7f76dbd74ec091086b3d524fb7c8%7C0%7C0%7C637952134073527979%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=0A0ktYDmgfxwc7U%2BgzHzQUj8Q5wixi%2BUzoSzMctlbso%3D&reserved=0">10.17632/4nfg69v8hy.1</a>)</li> </ul> <p><br> <strong>1. Data presented in Figure 6.1:</strong> Survival_CFU_(...)<br> Tab-delimited file with zebrafish larvae survival, and the number of colony-forming units (CFUs) associated with zebrafish larvae, following exposure to silver nanoparticles (nAg) from 3-5 days-post fertilization (dpf):</p> <ul> <li><em>Concentration</em>: Nominal exposure concentration (mg nAg·L<sup>-1</sup>).</li> <li><em>Date</em>: The date at which the mortality was scored (Format: DD/MM/YYYY). </li> <li><em>Family</em>: A code referring to the aquarium of wildtype zebrafish (ABxTL) that were crossed to obtain the larvae for the experiment. </li> <li><em>Survival</em>: Percentage of larvae that had survived the treatment.</li> <li><em>CFU</em>: Number of colony-forming units that was isolated per larva</li> </ul> <p>The methodology for toxicity tests and the procedures to determine CFU counts, have been published in <em>Nanotoxicology</em>:</p> <p>Brinkmann BW, Koch BEV, Spaink HP, Peijnenburg WJGM, Vijver MG. 2020. Colonizing microbiota protect zebrafish larvae against silver nanoparticle toxicity. Nanotoxicology. 14: 725-739. DOI: <a href="http://doi.org/10.1080/17435390.2020.1755469">10.1080/17435390.2020.1755469</a></p> <p> </p> <p><strong>2. Data presented in Figure 6.2:</strong> ABs_DoseResponses_(...)<br> Tab-delimited file with zebrafish larvae mortality following a pretreatment of 0, 6 or 72 hours with an antibiotic and antifungal cocktail, and subsequent exposure to nAg from 3-5 dpf:</p> <ul> <li><em>Concentration</em>: Nominal exposure concentration (mg nAg·L<sup>-1</sup>). </li> <li><em>Mortality</em>: Percentage of larvae that had died.</li> <li><em>Date</em>: The date at which the mortality was scored (Format: DD/MM/YYYY).</li> <li><em>Family</em>: A code referring to the aquarium of wildtype zebrafish (ABxTL) that were crossed to obtain the larvae for the experiment. </li> <li><em>ABs</em>: Duration of the antibiotic/ antifungal pretreatment, either 0, 6 or 72 hours.</li> </ul> <p> </p> <p><strong>3. Data presented in Figure 6.3:</strong> il1beta_eGFP_(...)<br> Three folders comprising fluorescence microscopy images (TIFF format) of il1beta:eGFP reporter zebrafish larvae at 5 dpf:</p> <ul> <li><em>(...)_replicates1_20200226</em>: images for the first experimental replicate.</li> <li><em>(...)_replicates2_20200304</em>: images for the second experimental replicate.</li> <li><em>(...)_replicates3_20200318</em>: images for the third experimental replicate.</li> </ul> <p>For each of the replicates, the following images were acquired:</p> <ul> <li><em>nZnO_GFP</em>: GFP signal for larvae exposed to nZnO.</li> <li><em>Znion_GFP</em>: GFP signal for larvae exposed to zinc ions.</li> <li><em>nZnO_trans</em>: transmitted light images for larvae exposed to nZnO. </li> <li><em>Znion_trans</em>: transmitted light images for larvae exposed to zinc ions.</li> </ul> <p>Additionally, the following images have previously been deposited to <em>Mendeley Data </em>(DOI: <a href="http://doi.org/10.1016/j.ecoenv.2022.113522">10.17632/4nfg69v8hy.1</a>):</p> <ul> <li><em>nAg_GFP</em>: GFP signal for larvae exposed to nAg.</li> <li><em>nAg_trans</em>: transmitted light images for larvae exposed to nAg.</li> <li><em>Agion_GFP</em>: GFP signal for larvae exposed to silver ions.</li> <li><em>Agion_trans</em>: transmitted light images for larvae exposed to silver ions.</li> <li><em>control_GFP</em>: GFP signal for control larvae that had not been exposed to silver ions or nAg</li> <li><em>control_trans</em>: transmitted light images for control larvae that had not been exposed to silver ions or nAg.</li> </ul> <p>All image processing steps have been published in <em>Ecotoxicology and Environmental Safety</em>:</p> <p>Brinkmann BW, Koch BEV, Peijnenburg WJGM, Vijver MG. 2022. Microbiota-dependent TLR2 signaling reduces silver nanoparticle toxicity to zebrafish larvae. Ecotox Environ Saf. 237: 113522. DOI: <a href="http://doi.org/10.1016/j.ecoenv.2022.113522">10.1016/j.ecoenv.2022.113522</a></p> <p> </p> <p><strong>Abbreviations:</strong></p> <ul> <li><em>ABs</em>: antibiotics</li> <li><em>CFU</em>: colony-forming units</li> <li><em>dpf</em>: days post-fertilization</li> <li><em>il1beta</em>: interleukin-1beta</li> <li><em>nAg</em>: silver nanoparticles (NM-300 K)</li> <li><em>nZnO</em>: zinc oxide nanoparticles (NM-110)</li> </ul>
CSM08 Small mammal host-parasite sampling data for 16 linear trapping transects located in 8 LTER burn treatment watersheds at Konza Prairie
Data set contains summaries (summer) of the number of individuals of each species of small mammal captured (relative abundance) on each transect. Each record contains date, treatment, transect, trap station, species, specimen number, recapture status, specimen disposition, external body measurements (where applicable), reproductive information, and miscellaneous associated comments. These sampling records are based on nightly captures during one 4-night trapping period in summer (June through August) for each of 16 permanent transects established on eight fire treatments (two transects per treatment). These treatments include two seasonal burn watersheds (SpB, SuB), two reversal burn watersheds (R1A, R20A), one annual burn watershed (1D), two 4-year burn watersheds (4B, 4F, and one 20-year burn watershed (20B). None of these treatments implement bison grazing.
Virgina Coast Reserve LTER Externally-hosted Models and Data
This dataset contains a listing of models and data associated with Virginia Coast Reserve Long-Term Ecological Research that are not otherwise available in the VCR/LTER data archive. It includes links to models and data that have been made available by researchers that are not in the VCR/LTER archive because they are deposited in a specialized system specifically tailored to a specific type (e.g. models) or in another archive due to requirements and constraints imposed by funders and journals. It takes the form of a spreadsheet including for each item the type (i.e., model or data), Internet link, name, brief description and optionally a link to a publication that used the data.
Exploring Data Evaluation Strategies for Enhanced Identification of Host Cell Proteins in Drug Products of Therapeutic Antibodies and Fc-Fusion Proteins
<p>This data repository contains all previously unpublished raw data files for the manuscript “Exploring Data Evaluation Strategies for Enhanced Identification of Host Cell Proteins in Drug Products of Therapeutic Antibodies and Fc-Fusion Proteins” by Wolfgang Esser-Skala, Marius Segl, Therese Wohlschlager, Veronika Reisinger, Johann Holzmann, and Christian G. Huber. See <em>readme.md</em> for further information.</p>
A dissymmetric [Gd2] coordination molecular dimer hosting six addressable spin qubits. Open data sets
<p>Includes data relevant for publication with DOI <a href="https://doi.org/10.1038/s42004-020-00422-w">10.1038/s42004-020-00422-w</a> plus a table with information about how the data were obtained and processed.</p>
Data from: Choosy beetles: how host trees and southern boreal forest naturalness may determine dead wood beetle communities
<p>See methods section of paper for detailed information on dataset and sources; briefly, these .csv files includes numbers of each beetle species captured at all sites used in the project, as well as information about each site and about each species.</p> <p> </p> <p>Data from:</p> <p><strong>Choosy beetles: how host trees and southern boreal forest naturalness may determine dead wood beetle communitie</strong><strong>s</strong></p> <p>Ryan C. Burner, Tone Birkemoe, Jörg G. Stephan, Lukas Drag, Jörg Muller, Otso Ovakainen, Mária Potterf, Olav Skarpaas, Tord Snall, Anne Sverdrup-Thygeson</p> <p>Forest Ecology and Management, 2021</p> <p> </p> <p>From abstract of paper:</p> <p>Wood-living beetles make up a large proportion of forest biodiversity, and contribute to important ecosystem services, including decomposition. Beetle communities in managed southern boreal forests are less species rich than in natural and near-natural forest stands. In addition, many beetle species rely primarily on specific tree species. Yet, the associations between individual beetle species, forest management category, and tree species are seldom quantified, even for red-listed beetles. We compiled a beetle capture dataset from flight intercept traps placed in Norway spruce (<em>Picea abies</em>), oak (<em>Quercus sp.</em>), and Eurasian aspen (<em>Populus tremulae</em>) trees in 413 sites in mature managed forest, near-natural forest, and clear-cuts in southeastern Norway. We used joint species distribution models to estimate the strength of associations for 368 saproxylic beetle species (including 20 vulnerable, endangered, or critical red-listed species) for each forest management category and tree species. Tree species on which traps were mounted had the largest effect on beetle communities; oaks had the most highly associated beetle species, including most of the red-listed species, followed by Norway spruce and Eurasian aspen. Most beetle species were more likely to be captured in near-natural than in mature managed forest. Our estimated associations were compatible – for many species – with categorical classifications found in several existing databases of saproxylic beetle preferences. These quantitative beetle-habitat associations will improve future analyses that have typically relied on categorical classifications. Our results highlight the need to prioritize conservation of near-natural forests and oak trees in Scandinavia to protect the habitat of many red-listed species in particular. Furthermore, we underline the importance of carefully considering the species of trees on which traps are mounted in order to representatively sample beetle communities in forest stands.</p>
Supplementary data for Willemsen et al., 2024 "Novel high-quality amoeba genomes reveal widespread codon usage mismatch between giant viruses and their hosts".
<p>Supplementary data for Willemsen et al., 2024 "Novel high-quality amoeba genomes reveal widespread codon usage mismatch between giant viruses and their hosts". The data set consists of five folders: “Codon_usage_amoebae_and_viruses”, "Genome_annotations_amoebae", "Phylogenetic_trees_18S_amoebae", “Phylogenomic_trees_amoebae”, and "Viral_integration_detection_amoebae". The “Codon_usage_amoebae_and_viruses” folder contains for each amoeba host the calculated codon usage tables in the subfolder "codon_usage_table_host", the calculated codon usage preferences using different scores in the subfolder "codon_usage_scores_host", and the calculated codon usage preferences of giant viruses versus each host in the subfolder "codon_usage_scores_viruses_vs_host". The giant viruses in the subfolder "codon_usage_scores_viruses_vs_host" are organised by viral family and genus in separate sub-subfolders. The "Genome_annotations_amoebae" folder contains the generated genome annotations in different formats and the manually curated mitochondrial genome annotations for each amoeba host. The "Phylogenetic_trees_18S_amoebae" contains for the eukaryotic phyla <em>Discosea</em>, <em>Heterolobosea</em>, and <em>Tubulinea, </em>the 18S rRNA nucleotide alignments, distance matrices, and computed phylogenetic trees. The folder "Phylogenomic_trees_amoebae" contains for the eukaryotic clades <em>Amoebozoa</em> and <em>Discoba, </em>the protein alignment matrices and computed phylogenomic trees. The folder "Viral_integration_detection_amoebae" contains the MCP databases used (fasta file, alignment file, HMM profile and DIAMOND BLASTX database) and the MCP sequences detected in this study and the blast results of these. </p>
Data for: Prior exposure of a fungal parasite to cyanobacterial extracts does not impair infection of its Daphnia host
<p>This dataset supports the findings of the study 'Prior exposure of a fungal parasite to cyanobacterial extracts does not impair infection of its <em>Daphnia</em> host', published in Hydrobiologia (https://doi.org/10.1007/s10750-022-04889-7)</p>
Data for: Polystyrene nanoplastics differentially influence the outcome of infection by two microparasites of the host Daphnia magna
<p>This dataset supports the findings of the study 'Polystyrene nanoplastics differentially influence the outcome of infection by two microparasites of the host <em>Daphnia magna</em>', published in Philosophical Transactions of the Royal Society B (https://doi.org/10.1098/rstb.2022.0013).</p>
Data files: Single-cell RNA profiling of Plasmodium vivax-infected hepatocytes reveals parasite- and host- specific transcriptomic signatures and therapeutic targets
<p>Scripts, preprocessed count matrices, and single-cell data objects generated in <strong>“Single-cell RNA profiling of <em>Plasmodium vivax</em><em>-</em>infected hepatocytes reveals parasite- and host- specific transcriptomic signatures and therapeutic targets” </strong></p>
Data and code for: Habitat preference of an herbivore shapes the habitat distribution of its host plant
<p>Initial release of analysis and code for:</p> <p>Alexandre, N. M., P. T. Humphrey, A. D. Gloss, J. Lee, J. Frazier, H. A. Affeldt III, and N. K. Whiteman. 2018. Habitat preference of an herbivore shapes the habitat distribution of its host plant. Ecosphere 00(00):e02372. (full citation pending)</p> <p>Release published to accompany corrected proofs on 2018-Jul-26.</p>
Data and code for: Genomic changes underlying host specialization in the bee gut symbiont Lactobacillus Firm5
<p>This dataset contains data and code underlying the comparative genomics, amplicon sequencing, and statistical analysis of the research article "Genomic changes underlying host specialization in the bee gut symbiont Lactobacillus Firm5”. Genome sequences and short read datasets are available under NCBI Bioproject accession PRJNA392822.</p> <p>The dataset contains tar-balls for the main workflows of the analysis. Dowload and unpack to view the contents (tar -zxvf filename.tar.gz). For each tar-ball, a README.txt file describes the contents of the directory. The analyses require certain open-source software packages to be installed. These are not provided here.</p>
Catalog Data for Prior-Informed AGN-Host Spectral Decomposition Using PyQSOFit
<p>This catalog contains 76,565 AGN-host decomposed spectral measurements for all quasars with z<0.8 in SDSS DR16Q. Our prior-informed decomposition method significantly improved the decomposition success rate from less than 60% to 94%. For the first time, we perform the AGN-host spectral decomposition on survey scale catalog.</p> <p>Our spectral decomposition results are highly consistent to those of HSC image decomposition. Our catalog suggests that an average host galaxy contribution at 5100A is 38.8%, which would lead to an overestimation of 0.215 dex in L5100 and 0.219 dex in black hole mass if the host is not removed. The Dn4000 and stellar velocity dispersion measurements from the decomposed host galaxy spectra are also provided.</p> <p>Please read this paper for more techinique details: <a href="https://arxiv.org/abs/2406.17598">arXiv: 2406.17598</a></p>
Geographic range size and species morphology determines the organization of sponge host-guest interaction networks across tropical coral reefs (Raw data)
<p>Datasets for the analysis developed in the Article "<em><strong>Geographic range size and species morphology determines the organization of sponge host-guest interaction networks across tropical coral reefs</strong></em>". For more information, please refer to the original publication.</p> <p>Network_Structural_Index_&_SpogeTraits.csv <- Structural Index for the sponge-dwelling fauna network, sponge accumulated area and sponges’ morphology.</p> <p>NWTA_CoralReefs_Sponges_ interactions.csv <- Relationship between host sponges and guest fauna in the Northwester Atlantic coral reefs</p> <p>NWTA_CoralReefs_Sponge_reacords.csv <- Sponge species incidence records in the Northwester Atlantic coral reefs</p> <p>sponges_morphological_description.csv <- Sponge morphological standardization</p> <p>Network.html <- Interactive sponge-dwelling fauna network</p> <p>Enjoy!<br> </p>
Code and data for manuscript: Incorporating environmental heterogeneity and observation effort to predict host distribution and viral spillover from a bat reservoir.
<p>This is the source code and data required to reproduce data analysis and figures from the manuscript, "Incorporating environmental heterogeneity and observation effort to predict host distribution and viral spillover from a bat reservoir". </p>
Data from: Deciphering host-parasitoid interactions and parasitism rates of crop pests using DNA metabarcoding
Open the record for dataset details and reuse information.
CSM09 Small mammal host-parasite sampling data associated with the Consume herbivore exclusion plots across two burned and native-grazed watersheds at Konza Prairie
Data set contains summaries of the number of individuals of each species of small mammal captured (relative abundance) on each trapping grid. Each record contains date, treatment, grid, trap station, species, specimen number, recapture status, specimen disposition, external body measurements (where applicable), reproductive information, and miscellaneous associated comments. These sampling records are based on nightly captures during one 4-night trapping period in fall (October concurrent with annual bison roundup activites) for each of 4 permanent trapping grids established on two fire/grazing treatments (two grids per treatment). These treatments are both grazed by native grazers (bison) and include one treatment burned annually (N1A) and one treatment burned every 4 years (N4B). In each treatment, sampling grids are arranged as 5 x 10 permanent stakes spaced 10m apart and labeled numerically between 1-50 for grid A and 51-100 for grid B. One grid per treatment (grid A) is sampled using capture-mark-release methods and the other grid in each treatment (grid B) is sampled using specimen removal and subsequent whole body processing and curation.
Data from: Can the genomics of ecological speciation be predicted across the divergence continuum from host races to species? A case study in Rhagoletis
<p>Studies assessing the predictability of evolution typically focus on short-term adaptation within populations or the repeatability of change among lineages. A missing consideration in speciation research is to determine whether natural selection predictably transforms standing genetic variation within populations into differences between species. Here, we test whether host-related selection on diapause timing anticipates genome-wide differentiation during ecological speciation by comparing ancestral hawthorn and newly formed apple-infesting host races of <i>Rhagoletis pomonella </i>to their sibling species <i>R. mendax</i> that attacks blueberries. The responses of 57,857 single nucleotide polymorphisms in a diapause study on the hawthorn race strongly predicted the direction and magnitude of genomic divergence among the three flies at a field site in Fennville, Michigan, USA. As anticipated, the apple race and <i>R. mendax</i> show parallel changes in the frequencies of putative inversions on three chromosomes associated with the earlier fruiting times of apples and blueberries compared to hawthorns. A diapause experiment on <i>R. mendax</i> revealed compensatory mutations throughout the genome accounting for the earlier eclosion of blueberry, but not apple flies. Thus, a degree of predictability, although not complete, exists in the genomics of diapause across the ecological speciation continuum in <i>Rhagoletis</i>. The generality of this result is placed in the context of other similar systems.</p>
Tara Pacific 18S-based coral host genetic analysis data release version 1
<p>This dataset contains 4 tables and 3 sets of figures related to the primary analysis of the 18S metabarcoding sequencing output. This dataset is only concerned with the identity of the coral host (i.e. not additional protist diversity). The samples included in this dataset have a 'sample-material_label' value of 'CORAL' and 'sampling-protocol_label' value of 'SEQ-CS4L'. They represent the coral samples collected at all 32 of the islands visited in the Tara Pacific expedition.</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.