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887 results for “tunnels”

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zenodo36/100

Data for paper "Automated Structure Discovery for Scanning Tunneling Microscopy"

<p>Contents of the dataset:</p> <ul> <li>band.h5 -- keys are molecule indices, each molecule has the following keys:<br> <ul> <li>eigs: KS eigenvalues for each state</li> <li>coefs: KS eigenvectors for each basis set</li> <li>xyz: atomic positions</li> <li>Z: atomic species</li> <li>qs: mulliken point charges</li> </ul> </li> <li>rotations_210611.pickle -- keys train/val/test <ul> <li>Each set is a dict containing id -- rotation pairs</li> <li>rotations are 3x3 numpy arrays</li> </ul> </li> <li>disks.pt -- a pretrained model for Atomic Disks predictions</li> </ul>

opencc-by-4.0Feb 2024View details →
zenodo36/100

Reinforcing Tunnel Network Exploration in Proteins using Gaussian Accelerated Molecular Dynamics (parameters, trajectories)

<ul> <li>00_LinB-Wt.tar.gz - LinB-Wt simulation files:</li> </ul> <p>&nbsp; &nbsp; 1.cMD(Classical MD simulation):<br>&nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.<br>&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp;<br>&nbsp; &nbsp; 2.GaMD(Gaussian Accelerated MD simulation):&nbsp;<br>&nbsp; &nbsp; &nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.</p> <ul> <li>01_LinB-Open.tar.gz - LinB Open mutant simulation files:</li> </ul> <p>&nbsp; &nbsp; 1.cMD(Classical MD simulation):<br>&nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.<br>&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp;<br>&nbsp; &nbsp; 2.GaMD(Gaussian Accelerated MD simulation):&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.</p> <ul> <li>02_LinB-Closed.tar.gz - LinB Closed mutant simulation files:</li> </ul> <p>&nbsp; &nbsp; 1.cMD(Classical MD simulation):<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.<br>&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp;<br>&nbsp; &nbsp; 2.GaMD(Gaussian Accelerated MD simulation):&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; 1. Stripped parameter file *.parm7.<br>&nbsp; &nbsp; &nbsp; &nbsp; 2. Simulation file after removing ions and water and merging last 5us of production run in amber *.nc format.</p>

opencc-zeroApr 2024View details →
zenodo36/100

High-power in-phase and anti-phase mode emission from linear arrays of resonant-tunneling-diode oscillators in the 0.4-to-0.8-THz frequency range - data

<p>Experimental and simulation data from the paper "High-power in-phase and anti-phase mode emission from linear arrays of resonant-tunneling-diode oscillators in the 0.4-to-0.8-THz frequency range".</p>

opencc-by-4.0Dec 2023View details →
zenodo36/100

Wind tunnel experiments on wind turbine wakes in yaw

<p>This data set contains Laser Doppler Anemometer measurements in the wake behind two different model wind turbines, recorded in a wind tunnel campain at the NTNU in Trondheim. Full plane wake data were recorded, with a focus on the effect of yaw misalignment and inflow turbulence. Please refer to the documentation document for more information.</p>

opencc-by-nc-4.0Mar 2018View details →
zenodo36/100

Skeletomuscular adaptations of head and legs of Melissotarsus ants for tunnelling through living wood

<p>Micro-CT raw datasets (in DICOM format) used in &quot;Skeletomuscular adaptations of head and legs of&nbsp;Melissotarsus&nbsp;ants for tunnelling through living wood&quot;</p> <p>&nbsp;</p> <p><strong>Abstract:</strong></p> <p>Background:&nbsp;While thousands of ant species are arboreal, very few are able to chew and tunnel through living wood. Ants of the genus&nbsp;<em>Melissotarsus</em>&nbsp;(subfamily Myrmicinae) inhabit tunnel systems excavated under the bark of living trees, where they keep large numbers of symbiotic armoured scale insects (family Diaspididae). Construction of these tunnels by chewing through healthy wood requires tremendous power, but the adaptations that give&nbsp;<em>Melissotarsus</em>&nbsp;these abilities are unclear. Here, we investigate the&nbsp;morphology of the musculoskeletal system of&nbsp;<em>Melissotarsus</em>&nbsp;using histology, scanning electron microscopy, X-ray spectrometry, X-ray microcomputed tomography (micro-CT), and 3D modelling.</p> <p>Results:&nbsp;Both the head and legs of&nbsp;<em>Melissotarsus</em>&nbsp;workers contain novel skeletomuscular adaptations to increase their ability to tunnel through living wood. The head is greatly enlarged dorsoventrally, with large mandibular closer muscles occupying most of the dorsal half of the head cavity, while ventrally-located opener muscles are also exceptionally large. This differs from the strong closing: opening asymmetry typical of most mandibulated animals, where closing the mandibles requires more force than opening. Furthermore, the mandibles are short and cone-shaped with a wide articulatory base that concentrates the force generated by the muscles towards the tips. The increased distance between the axis of mandibular rotation and the points of muscle insertion provides a mechanical advantage that amplifies the force from the closer and opener muscles. We suggest that the uncommonly strong opening action is required to move away crushed plant tissues during tunnelling and allow a steady forward motion. X-ray spectrometry showed that the tip of the mandibles is reinforced with zinc. Workers in this genus have aberrant legs, including mid- and hindlegs with hypertrophied coxae and stout basitarsi equipped with peg-like setae, and midleg femura pointed upward and close to the body. This unusual design famously prevents them from standing and walking on a normal two-dimensional surface. We reinterpret these unique traits as modifications to brace the body during tunnelling rather than locomotion per se.</p> <p>Conclusions:&nbsp;<em>Melissotarsus</em>&nbsp;represents an extraordinary case study of how the adaptation to &ndash; and indeed engineering of &ndash; a novel ecological niche can lead to the evolutionary redesign of core biomechanical systems.</p>

opencc-by-4.0Dec 2017View details →
zenodo36/100

Magneto-Seebeck Tunneling on the Atomic Scale

<p>Data files for the figures in the&nbsp;publication &quot;Magneto-Seebeck Tunneling on the Atomic Scale&quot;.</p>

opencc-by-4.0Jan 2019View details →
zenodo36/100

Supplemental Material to Journal Article "Tunneling Crack Initiation in Trailing-Edge Bond Lines of Wind-Turbine Blades"

<p>This set supplements the figure data to the article &quot;Tunneling Crack Initiation in Trailing-Edge Bond Lines of Wind-Turbine Blades&quot;, DOI: <a href="http://doi.org/10.2514/1.J058179">10.2514/1.J058179</a>.</p>

opencc-by-4.0Jun 2019View details →
zenodo36/100

Dataset for Wenz et al. Phys. Rev. B 99, 201409(R) (2019), "Quantum dot state initialization by control of tunneling rates"

<p>Collection of the datasets used to generate the figures in the following journal paper:</p> <p>&quot;Quantum dot state initialization by control of tunneling rates&quot;<br> Tobias Wenz,&nbsp;Jevgeny Klochan,&nbsp;Frank Hohls,&nbsp;Thomas Gerster,&nbsp;Vyacheslavs Kashcheyevs,&nbsp;and Hans W. Schumacher<br> PHYSICAL REVIEW B 99, 201409(R) (2019)</p> <p>DOI:&nbsp;10.1103/PhysRevB.99.201409</p>

opencc-by-nc-nd-4.0Sep 2019View details →
zenodo36/100

Figure 3 in Do disturbed environments affect density of the tunnel-web spider Acanthogonatus centralis (Mygalomorphae: Nemesiidae) from native grasslands in Argentina?

Figure 3. Relationship between the density of potential shelters and the density of spiders.

opencc-by-4.0Nov 2018View details →
zenodo36/100

Additional information for Acidification from microbial oxidation of N, S, Fe and Mn as potential key mechanism for sprayed concrete deterioration in a subsea road tunnel

<p>Here we include additional files for&nbsp;Karacic <em>et al</em>. <strong>Acidification from microbial oxidation of N, S, Fe and Mn as potential key mechanism for sprayed concrete deterioration in a subsea road tunnel</strong></p> <p>Metagenome reads and MAGs are avaliable in the NCBI BioProject PRJNA755678</p> <p>The following files are included here</p> <ul> <li><strong>MAGs_summary_Oslofjord.tsv</strong>: Information about the Oslofjord MAGs (GTDB R207 taxonomy, relative abundance, Completness, Contamination, NCBI accessions)</li> <li><strong>gtdbtk.ar53.summary.</strong> Output from GTDB-Tk v2.1.0 with GTDB R207_v2. Archaeal MAGs</li> <li><strong>gtdbtk.bac120.summary.tsv</strong>. Output from GTDB-Tk v2.1.0 with GTDB R207_v2. Bacterial MAGs</li> <li><strong>FeGenie-geneSummary.csv</strong>: Output from FeGenie</li> <li><strong>Annotations_1.tsv</strong> : Output from DRAM (215 MAGs)</li> <li><strong>Annotations_2.tsv</strong>: Output from DRAM (186 MAGs)</li> <li><strong>OFTMs_DRAM_genes.DiSCo.filtered.txt</strong>. Output from DiSCo</li> <li><strong>code_R.zip</strong>: R-code and additional files used for making MAGs figures</li> </ul> <p>This is version 2 of the dataset and it replaces version 1 (https://doi.org/10.5281/zenodo.5292093)&nbsp;</p>

opencc-by-4.0Jan 2024View details →
zenodo36/100

Figure 43. Cycloid teleost scale, hypotype UCMP 270032 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 43. Cycloid teleost scale, hypotype UCMP 270032.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 42 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 42. Thunnus vertebra, hypotype, UCMP 218506.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 41. Carcharhinus obscurus tooth, hypotype UCMP 218505 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 41. Carcharhinus obscurus tooth, hypotype UCMP 218505.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 40 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 40. Indeterminate barnacle. Hypotype from UCMP locality IP13002, UCMP 218825.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 36 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 36. Odontocete premaxilla, lateral view of hypotype, UCMP 269020.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 33. Indeterminate Actinopterygii fragments. Hypotype, UCMP 218647 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 33. Indeterminate Actinopterygii fragments. Hypotype, UCMP 218647.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 34 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 34. Mammalian rib fragment, hypotype, UCMP 270043.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 32 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 32. Balanidae indeterminate. Hypotype from UCMP locality IP13001, UCMP 218826.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 31 in Miocene marine macropaleontology of the fourth bore Caldecott Tunnel excavation, Berkeley Hills, Oakland, California, USA

Figure 31. Indeterminate crinoid stem. Hypotype from UCMP locality IP13001, UCMP 412360.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Impact of water models on structure and dynamics of enzyme tunnels

<ul> <li>1-initial_topologies_coordinates.tar.gz <ul> <li>primary input coordinates and parameter-topology files of all initial systems (LinBwt, LinB32, and Linb86 variants of haloalkane dehalogenase) in OPC and TIP3P water models</li> <li>prepared with the tleap module of AMBER18 package</li> <li>parm7 and crd formatted</li> </ul> </li> <li>2-cap_domain_gate_distances.tar.gz <ul> <li>datasets with minimum distance calculation between Asp146 and Leu176</li> <li>calculated by CPPTRAJ module of AMBER 18 for each performed simulation</li> <li>plain text formatted</li> </ul> </li> <li>3-protein_trajectories-linbwt.tar.gz <ul> <li>three replicated 400 ns (20,000 frames, i.e., every second frame) dry production phase trajectories of LinBwt in OPC and Tip3P water models with corresponding parameter-topology files</li> <li>produced by pmemd.cuda module of AMBER 18</li> <li>netcdf and parm7 formatted</li> </ul> </li> <li>3-protein_trajectories-linb32-closed.tar.gz <ul> <li>two replicated 400 ns (20,000 frames, i.e., every second frame) dry production phase trajectories of closed state LinB32 in OPC and Tip3P water models with corresponding parameter-topology files</li> <li>produced by pmemd.cuda module of AMBER 18</li> <li>netcdf and parm7 formatted</li> </ul> </li> <li>3-protein_trajectories-linb32-open.tar.gz <ul> <li>two replicated 400 ns (20,000 frames, i.e., every second frame) dry production phase trajectories of open state LinB32 in OPC and Tip3P water models with corresponding parameter-topology files</li> <li>produced by pmemd.cuda module of AMBER 18</li> <li>netcdf and parm7 formatted</li> </ul> </li> <li>3-protein_trajectories-linb86-closed.tar.gz <ul> <li>&nbsp;two replicated 400 ns (20,000 frames, i.e., every second frame) dry production phase trajectories of closed state LinB86 in OPC and Tip3P water models with corresponding parameter-topology files</li> <li>produced by pmemd.cuda module of AMBER 18</li> <li>netcdf and parm7 formatted</li> </ul> </li> <li>3-protein_trajectories-linb86-open.tar.gz <ul> <li>two replicated 400 ns (20,000 frames, i.e., every second frame) dry production phase trajectories of open state LinB86 in OPC and Tip3P water models with corresponding parameter-topology files</li> <li>produced by pmemd.cuda module of AMBER 18</li> <li>netcdf and parm7 formatted</li> </ul> </li> <li>4-basic_analyses.tar.gz <ul> <li>datasets on RMSF, RMSD, RoG, and RDF from the CPPTRAJ module of AMBER 18</li> <li>for selected replicas 3x LinBwt, 2x LinB32-closed, 2x LinB32-open, 2x LinB86-closed and 2x LinB86-open</li> <li>plain text and PDB formatted</li> </ul> </li> <li>5-caver_analyses.tar.gz <ul> <li>results of tunnel analyses for two replicas of open &amp; closed state each for LinB32 &amp; LinB86 in OPC and TIP3P, and three replicas of LinBWT in OPC and TIP3P</li> <li>generated by CAVER 3.0 using "Divide-and-conquer approach" (MethodsX, 10, 2023, 101968)</li> <li>comprising csv and pdb formatted: tunnel_profiles.csv and bottlenecks.csv, stripped_system.10001.pdb, v_origins.pdb</li> <li>For this and following analyses, the names of the trajectories were modified as follows: <ul> <li>linbwt_opc1_2 = md1_opc_linbwt; linbwt_opc2_2 = md2_opc_linbwt; linbwt_opc3_2 = md3_opc_linbwt;</li> <li>linbwt_tip3p1_2 = md1_tip3p_linbwt; linbwt_tip3p2_2 = md2_tip3p_linbwt; linbwt_tip3p3_2 = md3_tip3p_linbwt;</li> <li>linb32-closed_opc1_2 = md1_closed_opc_linb32; linb32-closed_opc2_2 = md2_closed_opc_linb32;</li> <li>linb32-open_opc1_2 = md1_open_opc_linb32; linb32-open_opc2_2 = md2_open_opc_linb32;</li> <li>linb32-closed_tip3p1_2 = md1_closed_tip3p_linb32; linb32-closed_tip3p2_2 = md2_closed_tip3p_linb32;</li> <li>linb32-open_tip3p1_2 = md1_open_tip3p_linb32; linb32-open_tip3p2_2 = md2_open_tip3p_linb32;</li> <li>linb86-closed_opc1_2 = md1_closed_opc_linb86; linb86-closed_opc2_2 = md2_closed_opc_linb86;</li> <li>linb86-open_opc1_2 = md1_open_opc_linb86; linb86-open_opc2_2 = md2_open_opc_linb86;</li> <li>linb86-closed_tip3p1_2 = md1_closed_tip3p_linb86; linb86-closed_tip3p2_2 = md2_closed_tip3p_linb86;</li> <li>linb86-open_tip3p1_2 = md1_open_tip3p_linb86; linb86-open_tip3p2_2 = md2_open_tip3p_linb86.</li> </ul> </li> </ul> </li> <li>6-transport_tools_analyses.tar.gz <ul> <li>results of comparative analyses for all simulations generated in 5-caver_analyses.tar.gz</li> <li>generated by TransportTools 0.9.3</li> <li>comprising csv, pdb, plain text and py formatted: configuration file (config_TT.ini), tunnel_profiles (data folder) for all filtered tunnels and bottlenecks (data folder) for all filtered tunnels, statistics (statistics folder) and visualization (visualization folder)<br>&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;</li> </ul> </li> </ul> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-zeroSep 2024View details →

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