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Figure 2 from: Bourassa S, Spence J, Hartley D, Lee S (2011) Wing-dimorphism and population expansion of Pterostichus melanarius (Illiger, 1798) at small and large scales in central Alberta, Canada (Coleoptera, Carabidae, Pterostichini). ZooKeys 147: 545-558. https://doi.org/10.3897/zookeys.147.2097
Figure 2 - Figure 2. Comparison of %LW in Pterostichus melanarius along an urban-rural gradient over the years 1998, 1999 and 2007. Error bars are ± 1 S.E of the mean.
Large scale expression and purification of full-length huntingtin Q54 with HAP40 from baculoviral expression system production in sf9 insect cells – 2018/08/04
<p><strong>Project</strong> - Huntingtin structure-function open lab notebook. </p> <p><strong>Rationale </strong>- Purified huntingtin samples with and without stabilising binding partners (HAP40) are required for use in structural and functional studies, in particular SAXS experiments. </p>
FIG. 1. — Souzalopesmyia polleti n in Souzalopesmyia Albuquerque, 1951 (Diptera: Muscidae): new species from South America with an updated phylogeny based on morphological evidence, in Touroult J. (ed.), "Our Planet Reviewed" 2015 large-scale biotic survey in Mitaraka, French Guiana.
FIG. 1. — Souzalopesmyia polleti n. sp.: A-D, ♂ holotype: head, anterior view (A); head, lateral view (B); lateral view (C); dorsal view (D); E-H, ♀ paratype: head anterior view (E); head lateral view (F); lateral view (G); dorsal view (H). Scale bars: 1.0 mm.
FIG. 4 in Souzalopesmyia Albuquerque, 1951 (Diptera: Muscidae): new species from South America with an updated phylogeny based on morphological evidence, in Touroult J. (ed.), "Our Planet Reviewed" 2015 large-scale biotic survey in Mitaraka, French Guiana.
FIG. 4. — Geographical distribution of the species of Souzalopesmyia Albuquerque,1951 from South America, with phylogenetic tree superimposed. Symbols: ●, S. sulina de Carvalho, 1999; ●, S. carioca Albuquerque, 1951; ●, S. singularis (Stein, 1911); ●, Souzalopesmyia polleti n. sp.; ●, S. paraensis de Carvalho, 1999; ●, S. amazonica Albuquerque, 1951;, Souzalopesmyia sp.
FIG. 3 in Souzalopesmyia Albuquerque, 1951 (Diptera: Muscidae): new species from South America with an updated phylogeny based on morphological evidence, in Touroult J. (ed.), "Our Planet Reviewed" 2015 large-scale biotic survey in Mitaraka, French Guiana.
FIG. 3. — Most parsimonious phylogenetic hypothesis obtained from the analysis of a morphological data set of the six species of Souzalopesmyia and the three outgroups species (Helina praecipua (Walker, 1853), Phaonia praesuturalis (Stein, 1904) and Dolichophaonia trigona (Shannon & Del Ponte, 1926)). All characters were given the same weight and treated as unordered. Tree length: 34, consistency index: 0.82, retention index: 0.84. Filled circles represent unique transforma- tion, and empty circles represent homoplastic character state transformation under fast optimization. Characters and character states: see Appendix.
Data files used in the paper "First Radar Evidence of Large-Scale Englacial Folding in the South Polar Layered Deposits (Ultimi Scopuli, Mars) and Possible Ice Sheet Flow Unveiled by MARSIS" By Guallini et al.
<p>This archive contains radargrams, geometric information and visualizations of a subset of MARSIS radar observations over Planum Australe, Mars. This archive contains everything needed to reproduce the results presented in the paper "Large-scale folds detected by MARSIS in the Southern ice sheet of Ultimi Scopuli (Mars)" by Guallini et al.</p> <p>Three types of MARSIS data files are contained in this archive:</p> <p>* orbit_XXXXX_frequency_Y_MHz_radargram.csv, where XXXXX is the orbit number, and Y the frequency at which the radar was operating, in MHz. The file contains an ASCII table of real numbers separated by commas. The table has as many columns as the number of radar echoes acquired during the orbit (usually 3200), and 980 lines, one for each echo sample. Values are samples of the uncalibrated echo voltage, without phase information (i.e. positive real numbers instead of complex echo samples). Echo samples are acquired every 0.3571 microseconds (2.8 MHz sampling rate). The first sample of an echo is located at a round-trip time corresponding to an altitude of 25 km above the Martian IAU ellipsoid.</p> <p>* orbit_XXXXX_frequency_Y_MHz_geometry.csv, where XXXXX is the orbit number, and Y the frequency at which the radar was operating, in MHz. The file contains an ASCII table of real numbers separated by commas. The table has as many rows as the number of radar echoes acquired during the orbit (usually 3200), and contains the following auxiliary parameters:</p> <p> - EPHEMERIS TIME - Number of seconds elapsed since Jan 1, 2000, 12:00 UTC corresponding to the time at which data collection for the current echo started.</p> <p> - MARS SOLAR LONGITUDE - Angle between the Mars-Sun line at the time corresponding to EPHEMERIS TIME and the Mars-Sun line at the vernal equinox, in degrees.</p> <p> - MARS SUN DISTANCE - Distance from the centre of Mars to centre of the Sun at the time corresponding to EPHEMERIS TIME, in Km.</p> <p> - SPACECRAFT ALTITUDE - Distance from the Mars Express spacecraft to the reference surface of the target body measured normal to the surface at the time corresponding to EPHEMERIS TIME, expressed in Km.</p> <p> - SUB-SPACECRAFT LONGITUDE - East longitude of the point on the target body that lies closest to the Mars Express spacecraft at the time corresponding to EPHEMERIS TIME, expressed in degrees and in the [ 0 -360 ] range.</p> <p> - SUB-SPACECRAFT LATITUDE - Planetocentric latitude of the point on the target body that lies directly beneath the Mars Express spacecraft at the time corresponding to EPHEMERIS TIME, expressed in degrees.</p> <p> - RADIAL VELOCITY - Radial component of the Mars Express spacecraft velocity vector in the reference frame of the target body at the time corresponding to EPHEMERIS TIME, expressed in Km/s.</p> <p> - TANGENTIAL VELOCITY - Tangential component of the Mars Express spacecraft velocity vector in the reference frame of the target body at the time corresponding to EPHEMERIS TIME, expressed in Km/s.</p> <p> - LOCAL TRUE SOLAR TIME - Angle between the extension of the vector from the Sun to Mars and the projection on Mars' ecliptic plane of a vector from the center of the target body and the point on the target body surface that lies directly beneath the Mars Express spacecraft at the time corresponding to EPHEMERIS TIME, expressed on a 24-hour clock with decimal fractions of the hour.</p> <p>* orbit_XXXXX_frequency_Y_MHz.png, where XXXXX is the orbit number, and Y the frequency at which the radar was operating, in MHz. The file is a visualization of the corresponding radargram, of the spacecraft ground track during the observation, and of surface and subsurface echo power.</p>
Text-fig. 34. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–h) images of "Paisia-like follicle"; Catefica locality, Portugal. a–d) Volume rendering of follicles in lateral (a, c) and ventral (b, d) views showing the decurrent stigmatic region that extends from base of the follicle to the apex; note papillate zone forming a probable stigma along the full length of the ventral suture; e) Longitudinal section (volume rendering cut at orthoslice yz0326) near the base of the follicle showing two ovules with a striate-reticulate surface (asterisks); note transverse fibers lining the inner follicle wall and large cells of the mesocarp; f) Transverse section (volume rendering cut at orthoslice xy2475) of follicle showing two rows of ovules borne on placentae on either side of the ventral suture (asterisks); note also the pronounced and densely-spaced papillae around the ventral suture; g) Transverse section (orthoslice xy1988) of follicle showing two ventral vascular bundles and one dorsal bundle (arrows) and ovules/seeds borne on two placentae, one on either side of the ventral suture; note the remains of the small thin-walled cells of the outer epidermis that cover the thicker-walled cells of the mesocarp; h) Transverse section (orthoslice xy2860) of follicle showing two ventral bundles and one dorsal bundle (arrows) and ovules/seeds in two rows on the placentae, one on either side of the ventral suture; note the remains of small epidermal cells and the large rounded cells of the mesocarp with thicker walls. Specimens, Catefica 49-S174916 (a, b), Catefica 49-S174917 (c–f, h), Catefica 50-S171525 (g). Scale bars = 300 Μm (a–d), 100 Μm (e–h). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 34. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–h) images of "Paisia-like follicle"; Catefica locality, Portugal. a–d) Volume rendering of follicles in lateral (a, c) and ventral (b, d) views showing the decurrent stigmatic region that extends from base of the follicle to the apex; note papillate zone forming a probable stigma along the full length of the ventral suture; e) Longitudinal section (volume rendering cut at orthoslice yz0326) near the base of the follicle showing two ovules with a striate-reticulate surface (asterisks); note transverse fibers lining the inner follicle wall and large cells of the mesocarp; f) Transverse section (volume rendering cut at orthoslice xy2475) of follicle showing two rows of ovules borne on placentae on either side of the ventral suture (asterisks); note also the pronounced and densely-spaced papillae around the ventral suture; g) Transverse section (orthoslice xy1988) of follicle showing two ventral vascular bundles and one dorsal bundle (arrows) and ovules/seeds borne on two placentae, one on either side of the ventral suture; note the remains of the small thin-walled cells of the outer epidermis that cover the thicker-walled cells of the mesocarp; h) Transverse section (orthoslice xy2860) of follicle showing two ventral bundles and one dorsal bundle (arrows) and ovules/seeds in two rows on the placentae, one on either side of the ventral suture; note the remains of small epidermal cells and the large rounded cells of the mesocarp with thicker walls. Specimens, Catefica 49-S174916 (a, b), Catefica 49-S174917 (c–f, h), Catefica 50-S171525 (g). Scale bars = 300 Μm (a–d), 100 Μm (e–h).
Large-scale demolitions in Brussels-Capital Region, 1987-2022
<p>This dataset contains the inventory of large scale demolition projects in Brussels, period 1987-2021. Only demolished buildings of more than 3000m² floorspace are included. The first version of the dataset includes the adress, function before demolition, function of the new building. </p>
Figure 2 in Large-scale snake genome analyses provide insights into vertebrate development
Figure 2. Evolutionary features of snake genomes (A) Chromosome evolution in snakes. A total of 23 proto-chromosomes of Serpentes were reconstructed using four lizards as outgroups (only eight species are shown here for clarity, with more species listed in Figure S2A). (B) Genome size, TE size, and TE type content in chicken, non-snake reptiles (four lizards, one turtle, and one crocodile), and snakes. (C) GC content and CpG island density of snake genomes.
Figure S4 in Large-scale snake genome analyses provide insights into vertebrate development
Figure S4. Genetic bases of snake limb loss, body elongation, lung asymmetry, and eye structure simplification, related to Figures 3 and 4 (A) Multiple alignments of PTCH1. Fish, mammals, frogs, birds, crocodiles, turtles, lizards, and snakes are indicated in different colors. (B) CPLANE1 multiple alignments. The gene structure is outlined by the black line with yellow blocks representing CDSs. The position span is obtained based on the European glass lizard reference genome. The ''378–381'' and ''473'' show the positions of snake-specific missing amino acids. The ''His472Try'' and ''Gln474Glu'' indicate the two snake-specific amino acid mutations. (C) Relative body mass and relative body length of WT mice and PTCH1-mutated mice with snake deletion. Mean ± SD is shown by error bar. (D) Microstructural characteristics of the proximal shinbone (colored in red) in 1-week-old WT mice and PTCH1-mutated mice with snake deletion. The trabecular bone volume (BV) and bone volume per tissue volume (BV/TV) of WT type and PTCH1-mutated mice. Significantly smaller *p <0.05 (independent Student's t test). Mean ± SD is shown by error bar. (E) Statistics of phalanx relative length (absolute length divided by body length) in WT mice and PTCH1-mutated mice with snake deletion. Mutated mice had significantly shorter fourth forelimb phalanx (n = 8, *p <0.05, independent Student's t test) and third hindlimb phalanx (n = 8, *p <0.05, independent Student's t test). Mean ± SD is shown by error bar. (F) Expressions of genes related to limb development in stage E11.5 forelimb bud (left) and hindlimb (right) of WT mice and PTCH1-mutated mice with snake deletion. (G) The 17-bp deletion of snake ZRS enhancer in our newly sequenced snakes. (H) Expression levels of somite development-related genes (under positive selection) in P. dhumnades (40 days post oviposition). (I) AP3B1 multiple alignments of snakes and outgroup. The gene structure is outlined by the black line with orange sticks representing CDSs and the numbers indicating the position span according to the European glass lizard reference genome. The positions of snake lost amino acids residues are indicated by the interval number ''796–800.''and number "802". (J) Example of differentially expressed genes (DEGs) between embryonic left and right lungs (40 days post oviposition) of P. dhumnades. The significance is indicated as *p <0.05, **p <0.01, or ***p <0.001. Mean ± SD is shown by error bar. (K) The SD-CNE located at ~13 kb downstream of YAP1. The identities (compared with the 31 reptile species ancestor sequence) of the SD-CNE were decreasing along the evolution of snakes. (L) A SSSV inserted to the 5 kb upstream of the TITF1 transcriptional start site. The SSSV was predicted to have one binding site of HOXA5 transcription factor. Heatmap (left) displays the expressions (log10(quantiled FPKMs)) of HOXA5 and TITF1 in lung, liver, heart, and muscle of green anole (Acar), keeled slug snake (Pber), and many-banded krait (Bmul). TITF1 and HOXA5 were highly expressed in the lung of all species but the expressions of TITF1 were significantly higher in the two snakes than in green anole (Student's t test p values: 0.0048 [Pber] and 0.0077 [Bmul]). (M) Snake-specific amino acid residues loss of CC2D2A. The black line layouts the gene structure with blue sticks representing CDSs and the numbers indicating the position span based on the European glass lizard reference genome. The interval number ''41–74'' points out the sites of lost amino acid residues in CC2D2A based on European glass lizard sequence. The lost amino acid residues were indicated in red on 3D structure.
Replication data for "Large-scale stability and the Greater Horn of Africa long and short rains"
<p>Replication data and code for Schwarzwald et al., "Large-scale stability and the Greater Horn of Africa long and short rains". All code needed to replicate this study is available at <a href="http://doi.org/10.5281/zenodo.8092685">https://doi.org/10.5281/zenodo.8092685</a>. The latest version of replication code and instructions for use of this dataset can be found at <a href="https://github.com/ks905383/gha_stability">https://github.com/ks905383/gha_stability</a>.</p> <p>The data in this repository allows for the replication of main text figures and analysis. All other data is available per request.</p> <p> </p>
INFLAMeR: a machine learning algorithm based on large-scale perturbation screening identified new lncRNAs regulating differentiation and survival of leukaemia cells
<p><strong>Abstract</strong></p> <p>Long non-coding RNAs (lncRNAs) are a diverse group of transcripts with poorly understood<br> functionality. To address this gap, we developed INFLAMeR, an advanced machine learning<br> model trained on CRISPRi screening data, to predict functional lncRNAs using comprehensive<br> genetic features. We experimentally validated the predictions by assessing their impact on cell<br> proliferation and anticancer drug resistance. Among the selected lncRNAs, 85% showed<br> significant effects upon knockdown, while low-scoring lncRNAs had no discernible impact.<br> Notably, our study elucidated the functional role of SNHG6 in hematopoietic differentiation.<br> INFLAMeR greatly enhances the prediction of functional lncRNAs, providing valuable insights<br> into their regulatory landscape. By integrating INFLAMeR with experimental validation, we can<br> identify and characterize functional lncRNAs in a cell-type-specific manner, contributing to a<br> deeper understanding of their involvement in cellular processes. Our findings revealed insights<br> into lncRNA biology and a framework for improving the identification of functional lncRNAs.</p>
1D-1V Vlasov-Poisson Simulations of Mutual Impedance Experiments in the presence of small-scale and large-scale plasma inhomogeneities - PART 2
<p>PART 1 IS FOUND AT <strong>https://doi.org/10.5281/zenodo.8118023</strong></p> <p> </p> <p> </p> <p>=====================================================================================================<br> Author : L. Bucciantini<br> Date : 05/07/2023<br> Laboratory : CNRS-LPC2E, Orléans (France)<br> =====================================================================================================</p> <p>Dear reader, we thank you for your interest in our dataset. In this document, we describe what you will<br> find in it.</p> <p>In case you need help with using the dataset, or if you are interested in mutual impedance experiments,<br> do not hesitate to contact our team in Orléans (pierre.henri@cnrs-orleans.fr, pierre.henri@oca.eu)</p> <p>=====================================================================================================<br> Topic:<br> This dataset contains the outputs of numerical simulations performed to assess<br> the impact of plasma inhomogeneities on the diagnostic performance<br> of mutual impedance experiments.</p> <p><br> Numerical model:<br> The outputs are obtained from a numerical model based on the solution of the 1D-1V Vlasov-Poisson<br> system of equations. The scheme used to solve the model is the one developed<br> by Mangeney et al. (2002), A Numerical Scheme for the Integration of the Vlasov-Maxwell System of Equations. Journal of Computational Physics, (doi: https://doi.org/10.1006/jcph.2002.7071).<br> The 1D-1V Vlasov-Poisson version of this model is described in Henri, et al. (2010), Vlasov-Poisson<br> simulations of electrostatic parametric instability for localized Langmuir wave packets in the solar wind,<br> Journal of Geophysical Research (Space Physics), 115, 6106 (2010)<br> -----------------------------------------------------------------------------------------------------<br> What is inside the dataset:</p> <p>The dataset is composed of 7 different mutual impedance measurements, each corresponding to one<br> directory (see below). The measurements (i.e. directory) correspond to small-scale plasma inhomogeneities at different<br> positions with respect to the mutual impedance antennas, or to a large-scale plasma inhomogeneity.</p> <p>Each directory contains a number of folders. Each folder corresponds to the emission of a signal at<br> different frequency.<br> -----------------------------------------------------------------------------------------------------<br> List of directories:</p> <p>(Note : each directory corresponds to one mutual impedance measurement)</p> <p>L : These outputs correspond to one mutual impedance measurement in<br> small antenna emission amplitude, which corresponds to a linear<br> plasma response to the emission.</p> <p>s_xx : Each of these outputs corresponds to one mutual impedance measurement in correspondance of<br> a small-scale plasma inhomogeneity at xx Debye lengths of distance from the emitting antenna<br> </p> <p>-----------------------------------------------------------------------------------------------------<br> List of folders inside the directories:</p> <p>Folders begin with the name "000" and have increasing index. Inside the same directory, each folder<br> represents a different simulation used to build the same mutual impedance measurement.</p> <p>------------------------------------------------------------------------------------------------------<br> List of files inside the folders:</p> <p>density_e.npz : electron density inside the box, in function of time (tempo)</p> <p>density_p.npz : ion density inside the box, in function of time (tempo)</p> <p>E.npz : electric field in the box, in function of time (tempo)</p> <p>qrho.npz : electric potential in the box, in function of time (tempo)</p> <p>qrho_imposed.npz : electric charge imposed at the emitting antennas, in function of time (tempo)</p> <p>tempo.npz : time-vector for density, electric field, electric potential and charge vectors</p> <p>TEST_Luca.dat : parameters describing the characteristics of the simulated plasma box</p> <p><br> [<br> Note : the previous files can be opened as follows</p> <p>import numpy as np</p> <p>vector_file_name = np.load('file_name.npz') # Use these for the .npz files<br> characteristics_of_the_box = np.genfromtxt('TEST_Luca.dat',skip_header=1)</p> <p>]</p> <p><br> -------------------------------------------------------------------------------------------------------<br> Characteristics of the simulated plasma box (TEST_Luca.dat)</p> <p>nx : amount of spatial grid points</p> <p>xl : physical size of the spatial box, expressed in Debye length</p> <p>tt_w : time resolution for ion and electron density, electric field, electric potential and charge</p> <p>rap_m : ion-to-electron mass ratio</p> <p>R_p : ion-to-electron temperature ratio</p> <p>dt : time step used to evolve in time the numerical simulation</p> <p>emission : emission frequency</p> <p>power : amplitude of the electric charge imposed at the emitting antennas</p> <p><br> (Note : all parameters not listed here but present inside the TEST_Luca.dat file correspond to additional<br> functionalities of the model. For the use of this dataset, they can be discarded.)</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
A large-scale serological survey in pets from October 2020 through June 2021 in France shows significantly higher exposure to SARS-CoV-2 in cats
<p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can infect many animals, including pets such as dogs and cats. Many studies have documented infection in companion animals by bio-molecular and serological methods. However, only a few have compared seroprevalence in cats and dogs from the general population, and these studies were limited by small sample sizes and collections over short periods. Our goal was to obtain a more accurate evaluation of seroprevalence in companion animals in France and to determine whether cats and dogs differ in their exposure to SARS-CoV-2. For this purpose, we conducted an extensive SARS-CoV-2 serological survey of 2036 cats and 3577 dogs sampled by veterinarians during medical examinations in clinics throughout France. Sampling was carried out from October 2020 through June 2021, a period encompassing the second and third waves of SARS-CoV-2 infections in humans in the country. Using a microsphere immunoassay targeting receptor binding domain and trimeric spike protein, we found 7.1% seroprevalence in pets, in a subset of 308 seropositive samples, 26.3% had neutralizing antibodies. We found that cats were significantly more likely to test positive than dogs, with seropositivity rates of 9.3% and 5.9% in cats and dogs, respectively. Finally, data for both species showed that seroprevalence was lower in older animals and was not associated with the date of sampling or the sex of the animal. Our results show that cats are significantly more sensitive to SARS-CoV-2 than dogs, in line with experimental studies showing that cats are more susceptible than dogs. This study reinforces that pets are commonly infected or exposed to SARS-CoV-2, emphasizing the importance of a One-Health approach to the SARS-CoV-2 pandemic and raising the question of vaccination of companion animals in close contact with humans.</p>
Supplementary material 1 from: Shaffer JA, Parks D, Campbell K, Moragne A, Hueske B, Adams P, Bauman JM (2023) Coastal beaver, Chinook, coho, chum salmon and trout response to nearshore changes resulting from diking and large-scale dam removals: synergistic ecosystem engineering and restoration in the coastal zone. Nature Conservation 53: 61-83. https://doi.org/10.3897/natureconservation.53.85421
Mean woody plant abundance surveyed from the riparian and shrub-emergent marsh vegetation
Preparatory Process in Advance of Runaway Fault Rupture through Fluid Injection observed in Laboratory Experiments using a Large Specimen of Sub-meter scale
<p>Fault slip is initiated by locally applied fluid pressure, and it can expand unstably over a wide area causing elastic waves having magnitudes that induce felt or destructive earthquakes. Thus, it is important to examine the unstable expansion of initial slips. However, it is hard to reproduce the process by general setup of laboratory experiment such as triaxial loading tests on cylindrical specimens with inclined faults. In this study, we prepared a cubic specimen of sub-meter scale, which was separated into two triangular prisms by a model fault. The specimen was subjected to bi-axial compressions with different magnitudes. A 2D array of strain gauges was embedded beneath the fault plane to measure the changes in shear strain with the fault slip driven by fluid injection. Based on the experimental results, we discussed the features of fault slips that lead to injection-induced earthquake. The dataset obtained by the experiments were presented in the current data repository.</p>
Wednesday 6 May: Large-scale studies using Netarkivet's HPC, Janne Nielsen, Aarhus University
<p>Wednesday 6 May: Large-scale studies using Netarkivet's HPC, Janne Nielsen, Aarhus University</p>
The structural landscape of the immunoglobulin fold by large-scale de novo design
<p>Dataset for the high-quality immunoglobulin designs.</p>
FiN-2: Larg-Scale Powerline Communication Dataset (Pt.4)
<p>See <a href="https://zenodo.org/record/8328113">https://zenodo.org/record/8328113</a> for more information.</p> <p> </p>
FiN-2: Larg-Scale Powerline Communication Dataset (Pt.2)
<p>See <a href="https://zenodo.org/record/8328113">https://zenodo.org/record/8328113</a> for more information.</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.