Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
45
datasets available to search
ShareScore release 0.9.0
Dataset results
45 results for “human faces”
Data from: Distinctive microbial community and genome structure in coastal seawater from a human-made port and nearby offshore island in northern Taiwan facing the Northwestern Pacific Ocean
<p><span>Pollution in human-made fishing ports caused by petroleum </span><span>from</span><span> boats, dead fish, toxic </span><span>chemicals</span><span>, and effluent </span><span>poses</span><span> a challenge to the organisms in seawater. To decipher the impact of pollution on the microbiome, we collected surface water </span><span>from</span><span> a fishing port and a nearby offshore island in northern Taiwan facing the </span><span>Northwestern Pacific Ocean. By employing 16S </span><span>rRNA gene</span><span> amplicon sequencing and whole-genome shotgun sequencing, we discovered that </span><span>Rhodobacteraceae, Vibrionaceae, and Oceanospirillaceae emerged as the dominant species in the fishing port</span><span>,</span><span> where we found many genes harboring the functions of </span><span>antibiotic</span><span> resistance (</span><span>ansamycin, nitroimidazole, and aminocoumarin), metal tolerance (copper, chromium, iron and multimetal), virulence factors (chemotaxis, flagella, T3SS1), carbohydrate metabolism (biofilm formation and remodeling of bacterial cell </span><span>walls</span><span>), nitrogen metabolism (denitrification, N<sub>2</sub> fixation, and ammonium assimilation), and ABC transporters (phosphate, lipopolysaccharide, and branched-chain amino </span><span>acids</span><span>). The dominant bacteria at the nearby offshore island (</span><span>Alteromonadaceae, Cryomorphaceae, Flavobacteriaceae, Litoricolaceae, and Rhodobacteraceae) were partly similar to those in the South China Sea and the East China Sea. Furthermore, we inferred</span><span> that</span><span> the microbial community network of </span><span>the cooccurrence</span><span> of dominant bacteria </span><span>on the</span><span> offshore island was connected to dominant bacteria in </span><span>the </span><span>fishing port by mutual</span> <span>exclusion. By examining the assembled microbial genomes collected from the coastal seawater of the fishing port, we revealed four genomic islands containing large gene-containing sequences</span><span>,</span><span> including phage integrase, DNA</span> <span>invertase, restriction enzyme, DNA gyrase inhibitor, and antitoxin HigA-1.</span><span> In this study, </span><span>we provided </span><span>clues </span><span>for the possibility of genomic islands as the units of horizontal transfer and as the tools of microbes for facilitating adaptation in a human-made port environment.</span></p>
Video demonstration of the Looking at human face (behaviour element ID code: IILH); and Greeting sound (behaviour element ID code: IVGR) behaviour elements in the Interactive group for Korcsok and Korondi (2023), Biologia Futura
<p>The video demonstrates the behaviour elements: Looking at human face (behaviour element ID code: <strong>IILH</strong>); and Greeting sound (behaviour element ID code: <strong>IVGR</strong>) in the interactive experimental group, as exhibited by a social robot. The video is part of an ethogram cataloguing the behaviour elements of the robot, described in the publication: <em><strong>How do you do the things that you do? - Ethological approach to the description of robot behaviour</strong></em> submitted to Biologia Futura (2023) by Korcsok, B. and Korondi, P.</p>
Tusk, human face, caribou-Hot Springs Village AK
Walrus tusk with human face and two caribou heads. Probably a handle. Hot Springs Village, Port Moller, Alaska. Okada excavations HHU7. Hot Springs 2B 600-800 CE. The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
Data from: Distinctive microbial community and genome structure in coastal seawater from a human-made port and nearby offshore island in northern Taiwan facing the Northwestern Pacific Ocean
Open the record for dataset details and reuse information.
Data from: The morphometrics of “masculinity” in human faces
Open the record for dataset details and reuse information.
“Not only faces”: specialized visual representation of human hands revealed by adaptation
Open the record for dataset details and reuse information.
Retinotopic localizer with embedded dynamic macaque faces and walking humans
<p>Retinotopic localizer with embedded dynamic macaque faces and walking humans. From Zhu, Q., & Vanduffel, W. (2019). Submillimeter fMRI reveals a layout of dorsal visual cortex in macaques, remarkably similar to New World monkeys. <em>Proceedings of the National Academy of Sciences of the United States of America</em>, <em>116</em>(6), 2306–2311. http://doi.org/10.1073/pnas.1805561116</p>
Assessing carnivore spatial co-occurrence and temporal overlap in the face of human interference in a semi-arid forest
<p>Apex predators drive top-down effects in ecosystems and the loss of such species can trigger mesopredator release. This ecological process has been well documented in human-modified small areas, but for management and conservation of ecological communities, it is important to know which human factors affect apex predator occurrence and which mediate mesopredators release at large scales. We hypothesized that mesopredators would avoid spatial and temporal overlap with the apex predator, the puma; but that human perturbations (i.e. cattle raising and trophy hunting) would dampen top-down effects and mediate habitat use. We installed 16 camera traps in each of 45, 10x10-km grid cells in the Caldén forest region of central Argentina resulting in 706 total stations covering 61,611km<sup>2</sup>. We used single-season occupancy and two-species co-occurrence models and calculated the species interaction factor (SIF) to explore the contributions of habitat, biotic, and anthropic variables in explaining co-occurrence between carnivore pairs. We also used kernel density estimation techniques to analyze temporal overlap in activity patterns of the carnivore guild. We found that puma habitat use increased with abundance of large prey and with proximity to protected areas. Geoffroy's cats and skunks spatially avoided pumas and this effect was strong and mediated by distance to protected areas and game reserves, but pumas did not influence pampas fox and pampas cat space use. At medium and low levels of puma occupancy, we found evidence of spatial avoidance between 3 pairs of mesocarnivores. All predators were mostly nocturnal and crepuscular across seasons and mesopredators showed little consistent evidence of changing activity patterns with varying levels of puma occupancy or human interference. We found potential for mesopredator release at large scale, especially on the spatial niche axis. Our results suggest that a combination of interacting factors, in conjunction with habitat features and intervening human activities, may make mesopredator release unlikely or difficult to discern at broad scales. Overall, we believe that promoting the creation of new protected areas linked by small forest patches would likely lead to increased predator and prey abundances, as well as the interactions among carnivores inside and outside of protected areas.</p>
Bridging the Gap: Using Video Art to Document the Human Face of Disease & Predict Quality of Life Assessments in Brain Tumor Patients
ClinicalTrials.gov study NCT02890940. IPD Sharing: NO. Countries: 0. Publications: 3.
Data from: A face-selective ventral occipito-temporal map of the human brain with intracerebral potentials
Open the record for dataset details and reuse information.
Assessing carnivore spatial co-occurrence and temporal overlap in the face of human interference in a semi-arid forest
Open the record for dataset details and reuse information.
Data from: Eye coding mechanisms in early human face event-related potentials
Open the record for dataset details and reuse information.
Data from: Human face structure correlates with professional baseball performance: insights from professional Japanese baseball players
Open the record for dataset details and reuse information.
Mir-130a potentiates the reparative properties of human endothelial colony forming cells facing hypoxia via VEGFR2 and STAT3
GEO Series GSE142123. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Data from: Face-selective neurons in the vicinity of the human Fusiform Face Area
No abstract entered
Dehydrated Human Amnion/Chorion Membrane (dHACM) for Recovery After Fractionated Ablative CO2 Laser Resurfacing of the Face
ClinicalTrials.gov study NCT01995604. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Face Anthropometric Pattern Recognition Technology for Computer Aided Diagnosis of Human Genetic Disorders.
ClinicalTrials.gov study NCT00705055. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Data from: Face-selective neurons in the vicinity of the human Fusiform Face Area
Open the record for dataset details and reuse information.
Sentinel flaps recapitulate key inflammatory aspects of human face transplant rejection
GEO Series GSE313108. Homo sapiens. 28 samples. Type: Expression profiling by array.
U2-90 Human Face, Bone, hot Springs Village, AK
Human Face. Sea Mammal Bone. Hot Springs Village, Alaska, Alaska. U2-90 Okada Excavations. HHU2 Level 2B, 600-800 BCE The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
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.