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308 results for “coil”
Dataset for paper entitled "Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing"
<p>This dataset includes all results presented in the paper entitled "Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing", published in Advanced Materials Technologies, vol.5, 2000659, 2020<br> DOI: 10.1002/admt.202000659.<br> URL:<br> https://onlinelibrary.wiley.com/doi/full/10.1002/admt.202000659</p> <p>List of data in this dataset:<br> Fig.1-Theoretical Analysis and Basic characteristics.xlsx<br> Fig.2-Experimental results-Coil design.xlsx<br> Fig.3-Cyclic Bending and Folding.xlsx<br> Fig.4-Folding Angle Sensing Performance Evaluation.xlsx<br> Fig.5-Case studies.xlsx</p> <p>All the data included in this dataset were collected and processed by Dr. Hongbo Wang.</p> <p>Contact person:<br> Dr. Hongbo Wang, ustcwhb@gmail.com</p>
Data and scripts for the publication "Coil Optimization for Quasi-helically Symmetric Stellarator Configurations"
<p>Coils and VMEC configurations for the three stellarator configurations presented in "Coil Optimization for Quasi-helically Symmetric Stellarator Configurations", including the optimization scripts used to find the coils and plot scripts used to produce the figures in the text.</p>
Dataset for Gelatinous fibers develop asymmetrically to support bends and coils in common bean vines (Phaseolus vulgaris L., Fabaceae)
<ol> <li>Internode_lengths_AveragePerGroup_Stage5.csv = averaged internode lengths for each treatment groups at stage 5 (plastochron 9). Data represented in Appendix S2.</li> <li>Internode_lengths_Stage5.csv = data of all internodes lengths per individual plant at stage 5 (plastochron 9). Data represented in Appendix S2.</li> <li>InternodeLengths_allStages.csv = internode lengths through 5 stages (0-9 plastochon). Data represented in Appendix S1.</li> </ol> <p>Associated scripts: https://github.com/angelique-acevedo/Common-Bean-Analysis</p>
ODC mapper 7T surface coil
Open the record for dataset details and reuse information.
Temporal SNR optimization through RF coil combination in fMRI: The more, the better? - DATASET
Open the record for dataset details and reuse information.
Optimum spacing of thin rectangular magnetic field coils
<p>The data used to generate each of the figures in a pending submission to Reviews of Scientific Instruments.</p>
Dataset for Supporting Information of the paper entitled "Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing"
<p>This dataset includes all results presented in the "Supporting information" of the paper entitled "Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing", published in Advanced Materials Technologies, vol.5, 2000659, 2020<br> DOI: 10.5281/zenodo.4099806, DOI: <a href="https://doi.org/10.1002/admt.202000659">10.1002/admt.202000659</a><br> URL:<br> https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fadmt.202000659&file=admt202000659-sup-0001-SuppMat.pdf</p> <p>List of data in this dataset:<br> Fig.S1-Theoretical Analysis.xlsx<br> Fig.S5-LM Coils Folding-Exp and NA.xlsx<br> Fig.S6-CoilFoldingDataARC.xlsx<br> Fig.S7-Cyclic Bending-1000 cycles.xlsx<br> Fig.S8-Cyclic Folding of FPC and LM Coils.xlsx</p> <p>All the data included in this dataset were collected and processed by Dr. Hongbo Wang.</p> <p>Contact person:<br> Dr. Hongbo Wang, ustcwhb@gmail.com</p>
Supplementary Video: Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing
<p>Supplementary Video for Adv. Mater. Technol., DOI: 10.1002/admt.202000659<br> Folding and Bending Planar Coils for Highly Precise Soft Angle Sensing<br> H. Wang,* M. Totaro, S. Veerapandian,M. Ilyas, M. Kong, U. Jeong, L. Beccai*</p> <p>This video (.MP4) includes the following supporting movies:</p> <p>Movie S1. FE modeling of planar coil folding and bending<br> Movie S2. Numerical analysis of planar coil folding and bending<br> Movie S3. Dynamic bending test of FPC coil<br> Movie S4. Dynamic folding test of LM coil<br> Movie S5. Vibration detection with a folded FPC coil<br> Movie S6. Self-sensing origami<br> Movie S7. Sensorized soft pneumatic actuator<br> Movie S8. Wearable sensing</p> <p>Contact person:<br> Dr. Hongbo Wang, ustcwhb@gmail.com</p>
Figure 1 in Relationships of cochlear coiling shape and hearing frequencies in cetaceans, and the occurrence of infrasonic hearing in Miocene Mysticeti
Figure 1. Cochlear anatomy and visualization of methods. (a) Three-dimensional rendering of the cochlea (shown as right) of Balaenoptera acutorostrata in apical view. (b) Same, virtually transected along the modiolus (mod) showing the primary and secondary bony laminae (bl1 and bl2, respectively). (c) Radii ratio method as applied in this study: circles superimposed onto basal and apical turns of a 2-D projection of the path tracing the basilar membrane within the cochlea. Dots represent three points on each circle for calculation of the respective radius. (d) Landmark-based geometric morphometrics: 3-D resampled path with landmarks 1 to 40.
Figure 3 in Relationships of cochlear coiling shape and hearing frequencies in cetaceans, and the occurrence of infrasonic hearing in Miocene Mysticeti
Figure 3. (a–g) Linear regressions for significant correlations of PC1 and PC2 with individual variables tested in this study.
Figure 2 in Relationships of cochlear coiling shape and hearing frequencies in cetaceans, and the occurrence of infrasonic hearing in Miocene Mysticeti
Figure 2. PCA plot of shape variation of cochlear coiling. Lines represent 95 % confidence ellipses for Mysticeti (red) and Odontoceti (blue). Shape change along the axes is shown as black landmark configurations against the average shape (in gray) in apical view and in profile. Known lowest hearing limits in Hz are given for extant cetaceans (see Table 2). Number in parentheses refers to a fetus. * denotes extinct mysticetes with presumed very low frequency hearing (50 Hz and below). ** denotes extinct mysticetes with presumed infrasonic hearing (below 20 Hz). Gray numbers represent identification numbers (ID) listed in Table 2. The specimens plotting outside of the ellipse are Megapteropsis robusta (ID12) and Eschrichtiidae indet. (ID6).
Evaluation of a Novel 8-Channel RX Coil for Speech Production at 0.55 T DATASET.
<p>This dataset contains raw imaging MRI data used in SNR evaluation for 4 subjects. For all scans, volumetric data of the upper airway was obtained using a 3D spoiled gradient echo sequence with either a speech coil, a head coil, or an integrated body coil. Imaging parameters were: flip angle = 10, TE = 5 ms, TR = 10 ms, FOV = 32x32x16 cm^3, resolution = 2.5 x 2.5 x 5 mm^3. Pre-scan noise information for each scan is also included.</p> <p> </p> <p> </p>
Localizing On-scalp MEG Sensors using an Array of Magnetic Dipole Coils
<p>Matlab scripts and data necessary to reproduce the results from the PLOS ONE paper. For more information see README.</p>
18X7 Human brain field maps for shim coil designs
<p>128 B0 field maps of head brains of 18 different healthy adult volunteers in seven different head positions.</p>
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass]. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass].
Fig. 3 in Taxonomic Revision Of Dyakia Janus From Peninsular Malaysia (Pulmonata: Dyakiidae), With Notes On Other Sinistrally Coiled Helicarionoids
Fig. 3. Genitalia, pallial system, caudal region, and radula morphology of Dyakia janus from Johor, Malaysia (CUMZ 4919). A. Whole genital organ. B. Internal wall sculpture of penis, amatorial organ and vagina. C. Left view of caudal region. D. Pallial system, lung cavity and ventral view of mantle edge. E. SEM image of radula; central tooth indicated by 'C'. Numbers indicate tooth order from lateral to marginal end.
Fig. 2 in Taxonomic Revision Of Dyakia Janus From Peninsular Malaysia (Pulmonata: Dyakiidae), With Notes On Other Sinistrally Coiled Helicarionoids
Fig. 2. Genitalia, mantle collar, and radula morphology of Nanina salangana Martens, 1883 from Songkhla, Thailand (CUMZ 4920). A. Whole genital organ. B. Internal wall sculpture of penis, vagina and amatorial organ. C. Ventral view of mantle collar region. D, E. SEM image of radula; central tooth indicated by 'C'. Numbers indicate tooth order from lateral to marginal end.
Fig. 1 in Taxonomic Revision Of Dyakia Janus From Peninsular Malaysia (Pulmonata: Dyakiidae), With Notes On Other Sinistrally Coiled Helicarionoids
Fig. 1. Shells of Dyakia species. A. Syntype of Dyakia hugonis (BMNH 1975118). B–F. Dyakia janus; B, neotype (BMNH 42.5.10.1463) from Malacca, Malaysia; C, examined specimen from Johor, Malaysia (CUMZ 4919); D, figures of "Helix janus bifron" after Chemnitz (1795, pl. 213, Figs. 3016, 3017); E, lectotype of Helix sannio Pfeiffer, 1854 (BMNH 20100242); and F, syntype of Nanina albersi Albers, 1864 (ZMB 57526). G. Syntype of Dyakia kintana (MNHN, 8 shells). H. Holotype of Dyakia lindstedti (BMNH).
Text-fig. 20. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a) and scanning electron microscope (SEM, b–h) images of fruits of Appomattoxia sp. (a–d) and anther and pollen of Goczania rugosa (e–h); Catefica locality, Portugal. a) Surface rendering of fruit in lateral view showing densely spaced hairs, some with delicate coiled tips; b) Fruit in lateral view showing short, densely spaced hairs and apical stigmatic region; c, d) Detail of fruit surface and hairs from fruit in (b); e) Fragmentary anther showing four pollen sacs; f) Proximal view of pollen grains from an abraded anther showing microechinate surface of pollen wall and clusters of small, spiny orbicules; g, h) Proximal (g) and distal (h) views of pollen grains from an isolated pollen sac, showing short colpus (h), tectate pollen wall and microechinate surface ornamentation. Specimens, Catefica 49-S174913 (a), Catefica 49-S107794 (b–d), Catefica 50-S170391 (e), Catefica 49-S170138 (f), Catefica 49-S170143 (g, h). Scale bars = 300 Μm (a, b, e), 100 Μm (c), 50 Μm (d), 6 Μm (f–h). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 20. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a) and scanning electron microscope (SEM, b–h) images of fruits of Appomattoxia sp. (a–d) and anther and pollen of Goczania rugosa (e–h); Catefica locality, Portugal. a) Surface rendering of fruit in lateral view showing densely spaced hairs, some with delicate coiled tips; b) Fruit in lateral view showing short, densely spaced hairs and apical stigmatic region; c, d) Detail of fruit surface and hairs from fruit in (b); e) Fragmentary anther showing four pollen sacs; f) Proximal view of pollen grains from an abraded anther showing microechinate surface of pollen wall and clusters of small, spiny orbicules; g, h) Proximal (g) and distal (h) views of pollen grains from an isolated pollen sac, showing short colpus (h), tectate pollen wall and microechinate surface ornamentation. Specimens, Catefica 49-S174913 (a), Catefica 49-S107794 (b–d), Catefica 50-S170391 (e), Catefica 49-S170138 (f), Catefica 49-S170143 (g, h). Scale bars = 300 Μm (a, b, e), 100 Μm (c), 50 Μm (d), 6 Μm (f–h).
Text-fig. 4. Taphonomic features of the studied localities of ammonoids. a: Sandstone slab with fragmentary remains of productid and spiriferid brachiopods, orthocerids, coiled nautiloids and ammonoids (stratigraphic level No. 3). b: Shell debris cluster and fragment of crushed ammonoid conch (stratigraphic level No. 1). c: Epibionts on the surface of an ammonoid conch (stratigraphic level No. 5). d: Cluster of bivalves, gastropods and cephalopods remains in a siderite nodule (stratigraphic level No. 5). e: Fragment of an ammonoid conch (stratigraphic level No. 3). f: Fragment of an ammonoid conch (?) with terminal aperture and brachiopod valve (stratigraphic level No. 3). g: Specimen of?Anthracoceratites sp. with conch injuries (shown by arrows) (stratigraphic level No. 8). h, i: Bioerosion trace fossils Cyclopuncta girtyi ELIAS, 1958 on the fragments of cephalopod conchs (stratigraphic level No. 5). j: Limonitized conchs of the ammonoid (stratigraphic level No. 7). k: Fragment of an ammonoid conch (stratigraphic level No. 5). Scale bars 10 mm. in Late Bashkirian Ammonoids From The Mospyne Formation Of The Donets Basin, Ukraine
Text-fig. 4. Taphonomic features of the studied localities of ammonoids. a: Sandstone slab with fragmentary remains of productid and spiriferid brachiopods, orthocerids, coiled nautiloids and ammonoids (stratigraphic level No. 3). b: Shell debris cluster and fragment of crushed ammonoid conch (stratigraphic level No. 1). c: Epibionts on the surface of an ammonoid conch (stratigraphic level No. 5). d: Cluster of bivalves, gastropods and cephalopods remains in a siderite nodule (stratigraphic level No. 5). e: Fragment of an ammonoid conch (stratigraphic level No. 3). f: Fragment of an ammonoid conch (?) with terminal aperture and brachiopod valve (stratigraphic level No. 3). g: Specimen of?Anthracoceratites sp. with conch injuries (shown by arrows) (stratigraphic level No. 8). h, i: Bioerosion trace fossils Cyclopuncta girtyi ELIAS, 1958 on the fragments of cephalopod conchs (stratigraphic level No. 5). j: Limonitized conchs of the ammonoid (stratigraphic level No. 7). k: Fragment of an ammonoid conch (stratigraphic level No. 5). Scale bars 10 mm.
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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.