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21 results for “Character Animation”
VR-Together Pilot 1: 3D Animated Character Meshes
<p>This dataset contains the 3D Animated Characters as used for the Pilot 1 experience of the VR-Together project. The animated characters come as a set of FBX files with associated diffuse and normal maps. </p>
VR-Together Pilot 3: 3D Character Models and Animation Data
<p>VR-Together Pilot 3 Character and Animation Dataset.</p> <p>This dataset contains the 3D characters and animations as used in <a href="https://vrtogether.eu/about-vr-together/pilots/pilot3/">Pilot 3 of the VR-Together project</a>. It contains the 4 characters of the associated experience and their post-processed motion capture animation data in the FBX format, as well as the texture data in the PNG format. </p> <p>The data contained in this dataset was prepared for the Unity game engine, but should be usable in other content creation systems without issue. </p> <p>VR-Together has been funded by the European Commission as part of the H2020 program, under the grant agreement 762111.</p>
Data from: Morphological characters can strongly influence early animal relationships inferred from phylogenomic data sets
<p>There are considerable phylogenetic incongruencies between morphological and phylogenomic data for the deep evolution of animals. This has contributed to a heated debate over the earliest-branching lineage of the animal kingdom: The sister to all other Metazoa (SOM). Here we use published phylogenomic datasets (∼45,000-400,000 characters in size with ∼15-100 taxa) that focus on early metazoan phylogeny to evaluate the impact of incorporating morphological datasets (∼15-275 characters). We additionally use small exemplar datasets to quantify how increased taxon sampling can help stabilize phylogenetic inferences. We apply a plethora of common methods, i.e. likelihood models and their "equivalent" under parsimony: character weighting schemes. Our results are at odds with the typical view of phylogenomics, i.e., that genomic-scale datasets will swamp out inferences from morphological data. Instead, weighting morphological data 2-10× in both likelihood and parsimony can in some cases "flip" which phylum is inferred to be the SOM. This typically results in the molecular hypothesis of Ctenophora as the SOM flipping to Porifera (or occasionally Placozoa). However, greater taxon sampling improves phylogenetic stability, with some of the larger molecular datasets (>200,000 characters and up to ∼100 taxa) showing node stability even with ≧100× up-weighting of morphological data. Accordingly, our analyses have three strong messages. A) The assumption that genomic data will automatically "swamp out" morphological data is not always true for the SOM question. Morphological data have a strong influence in our analyses of combined datasets, even when outnumbered thousands of times by morphological data. Morphology therefore should not be counted out a priori. B.) We here quantify for the first time how the stability of the SOM node improves for several genomic datasets when the taxon sampling is increased. C.) The patterns of "flipping points" (i.e., the weighting of morphological data it takes to change the inferred SOM) carry information about the phylogenetic stability of matrices. The weighting space is an innovative way to assess comparability of datasets that should be developed into a new sensitivity analysis tool.</p>
Japanese Visual Media Graph - Anime Characters Database Ontology
<p>This group of files represents the RDF ontology used in the Japanese Visual Media Graph for the Anime Characters Database. Included in the upload are an explanatory PDF, the ontology in the Turtle serialization, and an HTML visualization of the ontology.</p>
Data from: The relationship between microbial community succession, decay, and anatomical character loss in non-biomineralized animals
Open the record for dataset details and reuse information.
Data from: Morphological characters can strongly influence early animal relationships inferred from phylogenomic data sets
Open the record for dataset details and reuse information.
FIGURE 7. Bornella hermanni Angas, 1864. A–F, Living animals. A-E, Specimens from New South Wales. A in Systematics and preliminary phylogeny of Bornellidae (Mollusca: Nudibranchia: Dendronotina) based on morphological characters with description of four new species
FIGURE 7. Bornella hermanni Angas, 1864. A–F, Living animals. A-E, Specimens from New South Wales. A, Photo: J. Wyche (AM C. 126475); B, Photo: W.B. Rudman (AM C. 152056); C, Photo: W.B. Rudman (AM C. 138000); D, Photo: J. Fields (AM C. 113793); E, Photo: J. Fields (AM C. 108069). F. Marshall Islands, Photo: S. Johnson (CASIZ 175404).
FIGURE 16. Living animals. A–B in Systematics and preliminary phylogeny of Bornellidae (Mollusca: Nudibranchia: Dendronotina) based on morphological characters with description of four new species
FIGURE 16. Living animals. A–B, Bornella pele sp. nov. A, Hawaii, Kahoolawe Island, Halona Point, Photo: P. Fiene. B, Specimen from Japan, Photo: J. Imamoto. C–D, Bornella valdae sp. nov. South Africa, Natal, Oslo Beach. C, Photo: V. Fraser. D, Photo: L. Warren. E–F, Bornella johnsonorum sp. nov. Marshall Islands, Oceanside Ennubuj-Ennylabegan reef, Kwajalein Atoll, Photo: J. Johnson. G–H, Pseudobornella orientalis Baba, 1932. China, Luoyuan Bay, Photo: S. Xikum.
FIGURE 1. Living animals. A–B in Systematics and preliminary phylogeny of Bornellidae (Mollusca: Nudibranchia: Dendronotina) based on morphological characters with description of four new species
FIGURE 1. Living animals. A–B, Bornella stellifer (Adams and Reeve in Adams, 1848); A, Malaysia, Malay Peninsula, South China Sea, Photo: T.M. Gosliner. B, Papua New Guinea, north coast, Madang, Photo: R.C. Willan. C–D, Bornella calcarata Mörch, 1863; C, Brazil, Photo: C.M. Cunha. D, Guarapi, Espiritu Santo, Brazil, Photo: J.P. Cauduro Filho. E, Bornella sarape Bertsch, 1980, Pacific coast of Mexico, Photo: A. Hermosillo. F, Bornella anguilla Johnson, 1984, Japan, Ryukyu Island, Okinawa, Photo: R.F. Bolland. G, Bornella irvingi Edmunds and Preece, 1996, Pitcairn Islands, Photo: J. Jamieson. H, Bornella dotoides sp. nov. Papua New Guinea, north Madang, "The Quarry", Photo: T.M. Gosliner.
FIGURE 11 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 11: Naticid egg masses collected on Giglio Island. A/a, Neverita josephinia (Campese Bay); B/b, probably Tectonatica rizzae (Pt. delle Secche); C/c, Notocochlis dillwynii (Pt. delle Secche); D/d, Notocochlis dillwynii (Cala dell´Allume); E/e, Notocochlis dillwynii (Fenaio); F/f, Tectonatica sagraiana (Campese Bay); G/g, Naticarius hebraeus (Pt. del Morto); H-I, egg capsules in egg masses of T. sagraiana (10 days old); J-K, egg capsules in egg masses of N. josephinia (1 day old).
FIGURE 7 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 7: Photos of the holotype of Natica sagraiana Orbigny, 1842 (A–C, F), held at the Natural History Museum, London, BM(NH)#1854.10.4.228, including its labels (G, H), and figured specimen (D, E) of Natica sagraiana Orbigny, 1842 (Orbigny in Sagra 1842, Mollusques, vol. 2, pl. 17, page 34). A, apertual view; B, dorsal view; C, umbilical view; F, apical view; G, BM(NH) label of holotype; H, original labels of Orbigny, indicating the type locality to be Cuba. The figured specimen (D, E) appears to represent the holotype (A-C, F). Scale bars represent 0.5 cm.
FIGURE 3 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 3: Photos of all egg masses used for molecular analysis (see Figure 1) in this study. For details concerning collection sites and the sequences amplified see Table 2. The pictures were taken immediately after the collars has been collected. DNA samples from egg masses were marked with C followed by a reference number when DNA was extracted directly from an egg mass; they were marked with L followed by a reference number if DNA extraction was performed from hatched larvae. Scale bars represent 0.5 cm.
FIGURE 2 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 2: Apertual views of all adult naticid specimens used for molecular analysis (see Figure 1) in this study. For more details concerning collection sites and the sequences amplified see Table 2. Scale bars represent 0.5 cm.
FIGURE 10 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 10: A, Payraudeautia intricata (Donovan, 1804); B, Neverita josephinia (Risso, 1826). Further details as in Figure 3. Scale bars represent 0.5 cm.
FIGURE 8 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 8: A, Tectonatica sagraiana (Orbigny, 1842); B, Tectonatica rizzae (Philippi, 1844). Further details as in Figure 3. Scale bars represent 0.5 cm.
FIGURE 9 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 9: A, Euspira nitida (Donovan, 1804); B, Euspira macilenta (Philippi, 1844). Further details as in Figure 3. Scale bars represent 0.5 cm.
FIGURE 4 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 4: Schematic map of Giglo Island, Grosseto County, Tuscany, Italy (42°21.000´´N 10°54.000´´E), including all collecting sites with naticid occurence: 1, Campese Bay; 2, Pt. del Faraglione; 3, Pt. delle Secche; 4, Cala dell´Allume; 5, Pt. del Corvo; 6, Pt. del Morto; 7, Pt. della Campana; 8, Cannelle Bay; 9,´Swiss House´; 10, Pt. del Fenaio. Pure shallow sandy sites are Campese Bay, Pt. del Faraglione, and Canelle Bay, while the remaining sites are bluffs with rocks, coarse sand flats, and sea weeds. The circular charts show the material (A, living specimens; E, egg masses; S, empty shells) collected at each site in a qualitative manner. N. dillwynii is distributed widest. Collected egg masses listed here were included in the molecular analysis.
FIGURE 6 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 6: A, Naticarius hebraeus (Martyn, 1786); B, Notocochlis dillwynii (Payraudeau, 1826). Further details as in Figure 3. Scale bars represent 0.5 cm.
FIGURE 1 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 1: Phylogenetic tree based on an analysis of the entire data set (H3, COI, 16S, and 18S sequences) of all specimens listed in Table 2. The phylogenetic model (GTR+I+G) was estimated by MrModeltest (Nylander 2004) performed with Paup*4.0b10 (Swofford 2003). Protein coding data sets were coded as "CODON". Based on different base compositions (chi-square test) in each of the single data sets, all parameters were defined as unlinked. Paup*4.0b10 tree characteristics: RI=0.851, CI=0.579. 325 positions were parsimony-informative, 76 were parsimony-uninformative, and 1141 were constant (1542 bp). Tonna cerevisina (Hedley, 1919) and Cypraea annulus (Linnaeus, 1758) were used as outgroup.
FIGURE 5 in The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses
FIGURE 5: A, Sparsely dotted form of Naticarius stercusmuscarum (Gmelin, 1791); B, Naticarius stercusmuscarum (Gmelin, 1791). All specimens are shown in four standardized views (dorsal, apertural, apical, umbilical) as well as alive. The pictures of living specimens were taken in an aquarium with a black bottom. Scale bars represent 0.5 cm.
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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.