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113 results for “composer”
Controlled Comparison of a Traditional Dressing Versus a Biologic Dressing Composed of Fetal Fibroblasts and Keratinocytes in Association With a Collagen Matrix on Skin Donor Sites
ClinicalTrials.gov study NCT03334656. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Composed Pebbling PHP pyramid instances in OPB format
<p>Combinatorial instances composing pebbling and pigeonhole principle formulas over pyramid graphs in the pseudo-Boolean optimization OPB format.</p>
LTS Study - Composer Interviews
<p>This document contains a set of interviews that were conducted in textual form with composers and musicians who participated in the research project "Machine-Learning Assisted Music Composition". The participants were asked to use the machine-learning-based software "Latent Timbre Synthesis" to create a short musical composition. The interviews were conducted after the compositions had been created and served to purpose of evaluating how the software influences the compositional process. The project has been funded through the Scientific Exchanges program of the Swiss National Science Foundation (Grant number: IZSEZ0_190757).</p>
Gewandhaus repertoire levels for composers and works 1800–1895
<p>These datasets contain lists of composers and works that were part of the Leipzig Gewandhausorchestra's repertoire in the years 1800–1895. They have been ascribed to 5 different repertoire levels (core, 1, 2, 3, 4) on account of their appearance during each season. To gain comparability the evaluation period has been split up into two segments, before and after 1848.</p> <p>For instance: Beethoven's Eroica has been played in each season in the second half, therefore it is assigned the count "47".</p> <p>core (K): 43–47 (90–100 %)<br> 1: 33–42 (70–89 %)<br> 2: 19–32 (40–69 %)<br> 3: 6–18 (13–39 %)<br> 4: 1–5 (1–11 %)</p> <p>This dataset is used in the dissertation "Repertoire and canon", <<a href="https://nbn-resolving.org/urn:nbn:de:bsz:15-qucosa2-810514">https://nbn-resolving.org/urn:nbn:de:bsz:15-qucosa2-810514</a>>.</p>
Text-fig. 6. Quercus sp. Red Oak, UF 279-24550. a, b: Wood semi-ring-porous to diffuse-porous; vessels exclusively solitary; thinwalled tyloses in wide vessels; diffuse, diffuse-in-aggregates axial parenchyma; rays of two distinct sizes. TS. c: Rays of two distinct sizes, TLS. d: Vessel-vasicentric tracheid pitting, RLS. e: Vessel-ray parenchyma pitting with reduced borders, vertically elongate, RLS. f: Narrow rays 1-2 cells wide, TLS. g: Ray composed of procumbent cells, RLS. Scale bars: 200 µm in a, b, c; 50 µm in d, f, g; 20 µm in e. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 6. Quercus sp. Red Oak, UF 279-24550. a, b: Wood semi-ring-porous to diffuse-porous; vessels exclusively solitary; thinwalled tyloses in wide vessels; diffuse, diffuse-in-aggregates axial parenchyma; rays of two distinct sizes. TS. c: Rays of two distinct sizes, TLS. d: Vessel-vasicentric tracheid pitting, RLS. e: Vessel-ray parenchyma pitting with reduced borders, vertically elongate, RLS. f: Narrow rays 1-2 cells wide, TLS. g: Ray composed of procumbent cells, RLS. Scale bars: 200 µm in a, b, c; 50 µm in d, f, g; 20 µm in e.
◂Fig. 5 Cells of phylogenetically related strains (light microscopy). a Thecate cell in dorsal view. b Thecate cell in ventral view, note the sulcus extending onto the epitheca (arrow). c Putatively necrotic, thecate cell. d Thecate cell with one bulge on the epitheca (arrow), note that this was the only such cell among thousands of inspected cells. e, f Coccoid cells, apparently without thecae. g Two thecate cells enclosed in the parental theca. h Two connected, immotile cells enclosed in the parental thecae. j Lid of epitheca in dorsal-apical view (mirrored), composed of plates 2′‒4′, all intercalary plates and plates 2′′‒6′′. l‒m Same opened theca in ventral view (l) and dorsal view (m), note the sulcus extending onto the epitheca (arrow), the dorsal opening and all apical and all intercalary plates and plates 3′′‒5′′ remaining with the hypotheca. n Chloroplasts (as inferred from autofluorescence), note the space occupied by the nucleus. Plate labelling follows the Kofoidean notation, n′: apical plate; n′′: precingular plate; n′′′: postcingular plate; na: anterior intercalary plate. Scale= 10 µm in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)
◂Fig. 5 Cells of phylogenetically related strains (light microscopy). a Thecate cell in dorsal view. b Thecate cell in ventral view, note the sulcus extending onto the epitheca (arrow). c Putatively necrotic, thecate cell. d Thecate cell with one bulge on the epitheca (arrow), note that this was the only such cell among thousands of inspected cells. e, f Coccoid cells, apparently without thecae. g Two thecate cells enclosed in the parental theca. h Two connected, immotile cells enclosed in the parental thecae. j Lid of epitheca in dorsal-apical view (mirrored), composed of plates 2′‒4′, all intercalary plates and plates 2′′‒6′′. l‒m Same opened theca in ventral view (l) and dorsal view (m), note the sulcus extending onto the epitheca (arrow), the dorsal opening and all apical and all intercalary plates and plates 3′′‒5′′ remaining with the hypotheca. n Chloroplasts (as inferred from autofluorescence), note the space occupied by the nucleus. Plate labelling follows the Kofoidean notation, n′: apical plate; n′′: precingular plate; n′′′: postcingular plate; na: anterior intercalary plate. Scale= 10 µm
TNT file for phylogenetic analysis of the moss class Polytrichopsida composed of morphological and sequence level characters
<p>PREMISE OF THE STUDY: When fossils are sparse in morphologically divergent lineages, phylogenetic analyses based on morphology may support hypotheses of relationships incongruent with those supported by gene sequence data. Integration of morphological and sequence data from conservative gene regions may reconcile such situations by circumscribing the search space of combined analyses.</p> <p>METHODS: We revisited the phylogeny of Polytrichopsida, a highly divergent group of mosses, in parsimony analyses. We supplemented the existing morphological matrix with sequence data of four genes (nt 18S, cp rbcL & rps4, mt nad5) commonly used in mosses; we included both fossils and extant terminals that lack sequence data.</p> <p>KEY RESULTS: We recovered patterns of relationships largely congruent with those supported by analyses of sequence data from a higher number of terminals. Analyses including all terminals recovered one optimal tree with Alophosia and the fossil Meantoinea forming a clade sister to the rest of the ingroup. Outgroup sampling experiments produced congruent topologies for most ingroup relationships.</p> <p>CONCLUSIONS: The potential of total-evidence analyses sampling conservative genes to alleviate conflict with morphology-based hypotheses should be tested in groups with denser fossil record. Although bryophyte fossils have been deemed fragmentary, it was recently shown that integrating fossils in total-evidence analyses may not reduce phylogenetic resolution. Therefore, total-evidence analyses incorporating fossils bear promise for clarifying bryophyte phylogenetic relationships. In Polytrichopsida, a group with a long evolutionary history, we cannot assume, a priori, that currently known fossils, which date back to only c. 140 Ma ago, represent the oldest lineages.</p>
Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a–d) Volume renderings of abraded seeds in ventral (a), lateral (b, d) and apical (c) views showing the slightly protruding chalaza (arrows) and dense longitudinal grooves with shallow pits in the surface of the endotesta; e) Transverse section of seed (orthoslice xy0665) showing the irregular grooved surface of the endotesta (oi-en) and the tegmen comprised of two layers of thick-walled cells that surround the cells of the prominent endothelium (asterisk); f) Longitudinal section (orthoslice xz1195) through seed showing the thin-walled endothelium cells (asterisk) surrounded by the thicker cells of the outer tegmen and endotesta; g) Longitudinal section (orthoslice yz0727) through seed showing outlines of angular crystals evenly distributed in cells of the endotesta (oi-en); note the outer epidermis of the tegmen (ii-o) composed of thick-walled cells; h) Longitudinal section (orthoslice xz0940) of seed showing details of the chalazal region with course of the vascular bundle (vb), cells of the prominent endothelium (asterisk), crystalliferous endotesta of the outer integument (oi-en) and the distinct thick walled cells of the outer cells of the tegmen (ii-o); i) Longitudinal and tangential section (orthoslice yz0542) through the endotesta (oi-en) showing the outlines of densely spaced crystals. Specimens, Catefica 242-S175178 (a–c, e–h), Catefica 49-S175179 (d, i). Scale bars = 300 Μm (a–d), 100 Μm (e, f, h, i), 50 Μm (g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a–d) Volume renderings of abraded seeds in ventral (a), lateral (b, d) and apical (c) views showing the slightly protruding chalaza (arrows) and dense longitudinal grooves with shallow pits in the surface of the endotesta; e) Transverse section of seed (orthoslice xy0665) showing the irregular grooved surface of the endotesta (oi-en) and the tegmen comprised of two layers of thick-walled cells that surround the cells of the prominent endothelium (asterisk); f) Longitudinal section (orthoslice xz1195) through seed showing the thin-walled endothelium cells (asterisk) surrounded by the thicker cells of the outer tegmen and endotesta; g) Longitudinal section (orthoslice yz0727) through seed showing outlines of angular crystals evenly distributed in cells of the endotesta (oi-en); note the outer epidermis of the tegmen (ii-o) composed of thick-walled cells; h) Longitudinal section (orthoslice xz0940) of seed showing details of the chalazal region with course of the vascular bundle (vb), cells of the prominent endothelium (asterisk), crystalliferous endotesta of the outer integument (oi-en) and the distinct thick walled cells of the outer cells of the tegmen (ii-o); i) Longitudinal and tangential section (orthoslice yz0542) through the endotesta (oi-en) showing the outlines of densely spaced crystals. Specimens, Catefica 242-S175178 (a–c, e–h), Catefica 49-S175179 (d, i). Scale bars = 300 Μm (a–d), 100 Μm (e, f, h, i), 50 Μm (g).
Text-fig. 23. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Longitudinal section (orthoslice yz0827) showing fruitlet with apical stigmatic region and a single seed enclosed within the fruitlet wall that has a thick epidermal cuticle; note the tiny embryo (emb) internal to the micropyle (mi) and oriented toward the base of the fruitlet; b) Transverse section through apical part of two fruitlets (orthoslice xy0810) showing the fruitlet wall (fr) composed of small thin-walled cells covered by an epidermis of isodiametric cells (ep) with a thick outer cuticle (cu); c) Longitudinal section (orthoslice xz0370) through basal part of fruitlet perpendicular to section in (a) showing the micropyle (mi), embryo (emb) composed of tiny cells, and the thick cuticle (cu) covering the bulging cells of the fruitlet epidermis. Specimen, Catefica 50-S174907 (a–c). Scale bars = 300 Μm (a–c). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 23. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Longitudinal section (orthoslice yz0827) showing fruitlet with apical stigmatic region and a single seed enclosed within the fruitlet wall that has a thick epidermal cuticle; note the tiny embryo (emb) internal to the micropyle (mi) and oriented toward the base of the fruitlet; b) Transverse section through apical part of two fruitlets (orthoslice xy0810) showing the fruitlet wall (fr) composed of small thin-walled cells covered by an epidermis of isodiametric cells (ep) with a thick outer cuticle (cu); c) Longitudinal section (orthoslice xz0370) through basal part of fruitlet perpendicular to section in (a) showing the micropyle (mi), embryo (emb) composed of tiny cells, and the thick cuticle (cu) covering the bulging cells of the fruitlet epidermis. Specimen, Catefica 50-S174907 (a–c). Scale bars = 300 Μm (a–c).
COMPOSED FAULT DATASET (COMFAULDA)
<p>The measurement and diagnosis of the severity of failures in rotating machines allow the execution of predictive maintenance actions on equipment. These actions make it possible to monitor the operating parameters of the machine and to perform the prediction of failures, thus avoiding production losses, severe damage to the equipment, and safeguarding the integrity of the equipment operators. This paper describes the construction of a dataset composed of vibration signals of a rotating machine. The acquisition has taken into consideration seven distinct operating scenarios, with different speed values. Unlike the few datasets that currently exist, the resulting dataset contains simple and combined faults with several severity levels. The considered operating setups are normal condition, unbalance, horizontal misalignment, vertical misalignment, unbalance combined with horizontal misalignment, unbalance combined with vertical misalignment, and vertical misalignment combined with horizontal misalignment. The dataset described in this paper can be utilized by machine learning researchers that intend to detect faults in rotating machines in an automatic manner. In this context, several related topics might be investigated, such as feature extraction and/or selection, reduction of feature space, data augmentation methods, and prognosis of rotating machines through the analysis of failure severity parameters.</p>
Prenatal Listening to Songs Composed for Pregnancy and Symptoms of Anxiety and Depression: a Pilot Study
ClinicalTrials.gov study NCT02776293. IPD Sharing: NO. Countries: 0. Publications: 1.
TNT file for phylogenetic analysis of the moss class Polytrichopsida composed of morphological and sequence level characters
Open the record for dataset details and reuse information.
Data from: The genetic structure of a Venturia inaequalis population in a heterogeneous host population composed of different Malus species
Open the record for dataset details and reuse information.
Whole-blood transcriptional signatures composed of erythropoietic and Nrf2-regulated genes differ between cerebral malaria and severe malarial anemia
GEO Series GSE117613. Homo sapiens. 46 samples. Type: Expression profiling by array.
Analysis of the Activity and Regulon of the Two-component Regulatory System Composed by Cjj1484 and Cjj1483 of Campylobacter jejuni
GEO Series GSE66942. Campylobacter jejuni. 18 samples. Type: Expression profiling by array.
single-cell ATAC-sequencing of human aortic media that was composed by vascular smooth muscle cells
GEO Series GSE286575. Homo sapiens. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Therapeutic targets of a new treatment for osteoarthritis composed by curcuminoids extract, hydrolyzed collagen and green tea extract
GEO Series GSE75181. Homo sapiens. 48 samples. Type: Expression profiling by array.
Gene expression profile of 3D liver organoids composed of hepatocyte and Kupffer cells exposed to nanoparticles.
GEO Series GSE201500. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Neuroblastoma is composed of two super enhancer-associated differentiation states
GEO Series GSE91028. Homo sapiens. 31 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Response to lupus antibodies of a human cardiac tissue model composed of cardiomyocytes and myofibroblasts
GEO Series GSE227571. Homo sapiens. 42 samples. Type: Expression profiling by high throughput sequencing.
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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.