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11 results for “view cluster”
ELKI Multi-View Clustering Data Sets Based on the Amsterdam Library of Object Images (ALOI)
<p>These data sets were originally created for the following publications:</p> <p><em>M. E. Houle, H.-P. Kriegel, P. Kröger, E. Schubert, A. Zimek</em><br> <strong>Can Shared-Neighbor Distances Defeat the Curse of Dimensionality?</strong><br> In Proceedings of the 22nd International Conference on Scientific and Statistical Database Management (SSDBM), Heidelberg, Germany, 2010.</p> <p><em>H.-P. Kriegel, E. Schubert, A. Zimek</em><br> <strong>Evaluation of Multiple Clustering Solutions</strong><br> In 2nd MultiClust Workshop: Discovering, Summarizing and Using Multiple Clusterings Held in Conjunction with ECML PKDD 2011, Athens, Greece, 2011.</p> <p>The outlier data set versions were introduced in:</p> <p><em>E. Schubert, R. Wojdanowski, A. Zimek, H.-P. Kriegel</em><br> <strong>On Evaluation of Outlier Rankings and Outlier Scores</strong><br> In Proceedings of the 12th SIAM International Conference on Data Mining (SDM), Anaheim, CA, 2012.</p> <p> </p> <p>They are derived from the original image data available at <a href="https://aloi.science.uva.nl/">https://aloi.science.uva.nl/</a></p> <p>The image acquisition process is documented in the original ALOI work: <em>J. M. Geusebroek, G. J. Burghouts, and A. W. M. Smeulders</em>, <strong>The Amsterdam library of object images</strong>, Int. J. Comput. Vision, 61(1), 103-112, January, 2005</p> <p>Additional information is available at: <a href="https://elki-project.github.io/datasets/multi_view">https://elki-project.github.io/datasets/multi_view</a></p> <p>The following views are currently available:</p> <table> <tbody><tr> <th>Feature type</th> <th>Description</th> <th>Files</th> </tr> <tr> <td>Object number</td> <td>Sparse 1000 dimensional vectors that give the <em>true</em> object assignment</td> <td><a href="6355684/files/objs.arff.gz">objs.arff.gz</a></td> </tr> <tr> <td>RGB color histograms</td> <td>Standard RGB color histograms (uniform binning)</td> <td><a href="6355684/files/aloi-8d.csv.gz">aloi-8d.csv.gz</a> <a href="6355684/files/aloi-27d.csv.gz">aloi-27d.csv.gz</a> <a href="6355684/files/aloi-64d.csv.gz">aloi-64d.csv.gz</a> <a href="6355684/files/aloi-125d.csv.gz">aloi-125d.csv.gz</a> <a href="6355684/files/aloi-216d.csv.gz">aloi-216d.csv.gz</a> <a href="6355684/files/aloi-343d.csv.gz">aloi-343d.csv.gz</a> <a href="6355684/files/aloi-512d.csv.gz">aloi-512d.csv.gz</a> <a href="6355684/files/aloi-729d.csv.gz">aloi-729d.csv.gz</a> <a href="6355684/files/aloi-1000d.csv.gz">aloi-1000d.csv.gz</a></td> </tr> <tr> <td>HSV color histograms</td> <td>Standard HSV/HSB color histograms in various binnings</td> <td><a href="6355684/files/aloi-hsb-2x2x2.csv.gz">aloi-hsb-2x2x2.csv.gz</a> <a href="6355684/files/aloi-hsb-3x3x3.csv.gz">aloi-hsb-3x3x3.csv.gz</a> <a href="6355684/files/aloi-hsb-4x4x4.csv.gz">aloi-hsb-4x4x4.csv.gz</a> <a href="6355684/files/aloi-hsb-5x5x5.csv.gz">aloi-hsb-5x5x5.csv.gz</a> <a href="6355684/files/aloi-hsb-6x6x6.csv.gz">aloi-hsb-6x6x6.csv.gz</a> <a href="6355684/files/aloi-hsb-7x7x7.csv.gz">aloi-hsb-7x7x7.csv.gz</a> <a href="6355684/files/aloi-hsb-7x2x2.csv.gz">aloi-hsb-7x2x2.csv.gz</a> <a href="6355684/files/aloi-hsb-7x3x3.csv.gz">aloi-hsb-7x3x3.csv.gz</a> <a href="6355684/files/aloi-hsb-14x3x3.csv.gz">aloi-hsb-14x3x3.csv.gz</a> <a href="6355684/files/aloi-hsb-8x4x4.csv.gz">aloi-hsb-8x4x4.csv.gz</a> <a href="6355684/files/aloi-hsb-9x5x5.csv.gz">aloi-hsb-9x5x5.csv.gz</a> <a href="6355684/files/aloi-hsb-13x4x4.csv.gz">aloi-hsb-13x4x4.csv.gz</a> <a href="6355684/files/aloi-hsb-14x5x5.csv.gz">aloi-hsb-14x5x5.csv.gz</a> <a href="6355684/files/aloi-hsb-10x6x6.csv.gz">aloi-hsb-10x6x6.csv.gz</a> <a href="6355684/files/aloi-hsb-14x6x6.csv.gz">aloi-hsb-14x6x6.csv.gz</a></td> </tr> <tr> <td>Color similiarity</td> <td>Average similarity to 77 reference colors (not histograms) 18 colors x 2 sat x 2 bri + 5 grey values (incl. white, black)</td> <td><a href="6355684/files/aloi-colorsim77.arff.gz">aloi-colorsim77.arff.gz</a> (feature subsets are meaningful here, as these features are computed independently of each other)</td> </tr> <tr> <td>Haralick features</td> <td>First 13 Haralick features (radius 1 pixel)</td> <td><a href="6355684/files/aloi-haralick-1.csv.gz">aloi-haralick-1.csv.gz</a></td> </tr> <tr> <td>Front to back</td> <td>Vectors representing front face vs. back faces of individual objects</td> <td><a href="6355684/files/front.arff.gz">front.arff.gz</a></td> </tr> <tr> <td>Basic light</td> <td>Vectors indicating basic light situations</td> <td><a href="6355684/files/light.arff.gz">light.arff.gz</a></td> </tr> <tr> <td>Manual annotations</td> <td>Manually annotated object groups of semantically related objects such as cups</td> <td><a href="6355684/files/manual1.arff.gz">manual1.arff.gz</a></td> </tr> </tbody></table> <p><strong>Outlier Detection Versions</strong></p> <p>Additionally, we generated a number of subsets for outlier detection:</p> <table> <tbody><tr> <th>Feature type</th> <th>Description</th> <th>Files</th> </tr> <tr> <td>RGB Histograms</td> <td>Downsampled to 100000 objects (553 outliers)</td> <td><a href="6355684/files/aloi-27d-100000-max10-tot553.csv.gz">aloi-27d-100000-max10-tot553.csv.gz</a> <a href="6355684/files/aloi-64d-100000-max10-tot553.csv.gz">aloi-64d-100000-max10-tot553.csv.gz</a></td> </tr> <tr> <td> </td> <td>Downsampled to 75000 objects (717 outliers)</td> <td><a href="6355684/files/aloi-27d-75000-max4-tot717.csv.gz">aloi-27d-75000-max4-tot717.csv.gz</a> <a href="6355684/files/aloi-64d-75000-max4-tot717.csv.gz">aloi-64d-75000-max4-tot717.csv.gz</a></td> </tr> <tr> <td> </td> <td>Downsampled to 50000 objects (1508 outliers)</td> <td><a href="6355684/files/aloi-27d-50000-max5-tot1508.csv.gz">aloi-27d-50000-max5-tot1508.csv.gz</a> <a href="6355684/files/aloi-64d-50000-max5-tot1508.csv.gz">aloi-64d-50000-max5-tot1508.csv.gz</a></td> </tr> </tbody></table>
Text-fig. 2. SEM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in oblique lateral view showing remains of calyx and slightly semi-inferior ovary with elongated apical style (a); note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities and the stomata-like secretory structures on the upper portion of the ovary (arrows) that are interpreted as nectariferous (b). c: Detail of ovary surface showing secretory stomata-like structures (arrows). d: Flower in lateral view showing fragmentary calyx and broken slightly semi-inferior ovary with secretory stomata-like structures; note the point of attachment of the central placenta (pl). e: Cluster of seeds removed from the ovary in (d) showing reticulate surface. f: Outer (abaxial) surface of calyx lobe showing the slightly pointed papillae and scattered, fine trichomes (arrows). g: Triaperturate pollen grains from the ovary surface. Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c), Mira 100-S101266 (d, e), Mira 105-S100732 (f), Mira 100-S170125 (g). Scale bars = 600 µm (a, b, d), 300 µm (f), 100 µm (c, e), 10 µm (g). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications
Text-fig. 2. SEM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in oblique lateral view showing remains of calyx and slightly semi-inferior ovary with elongated apical style (a); note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities and the stomata-like secretory structures on the upper portion of the ovary (arrows) that are interpreted as nectariferous (b). c: Detail of ovary surface showing secretory stomata-like structures (arrows). d: Flower in lateral view showing fragmentary calyx and broken slightly semi-inferior ovary with secretory stomata-like structures; note the point of attachment of the central placenta (pl). e: Cluster of seeds removed from the ovary in (d) showing reticulate surface. f: Outer (abaxial) surface of calyx lobe showing the slightly pointed papillae and scattered, fine trichomes (arrows). g: Triaperturate pollen grains from the ovary surface. Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c), Mira 100-S101266 (d, e), Mira 105-S100732 (f), Mira 100-S170125 (g). Scale bars = 600 µm (a, b, d), 300 µm (f), 100 µm (c, e), 10 µm (g).
BRAIN Journal-Redesigning a Flexible Material Master Data Application with Language Dependency-Figure 7. Dialog structure of the View Cluster
<p>Field dependency has been generated automatically and as a result the following desired structure has been achieved (figure 7). After populating the database tables with data in different languages with the help of the view cluster, the popup has been adapted in order to support the translation of the tabs and areas. Supplementary internal tables have been defined in the function module POPUP_FLEX, in order to copy data from the translation tables. The corresponding SELECT statements have been embedded in TRY-CATCH blocks, in order to prevent short dumps due to faulty selection processes.</p>
BRAIN Journal-Redesigning a Flexible Material Master Data Application with Language Dependency-Figure 6. View cluster TAFC
<p>For all these tables and views, table maintenance generators have been created and activated, in order to have the possibility to manage individual datasets in every table and view. The corresponding names of those function groups for the table maintenance generators are the same names as those for the views. The purpose of these maintenance views is only to take care of the input data more efficiently. These views will be used later in the view cluster, which ensures a hierarchical order of the data. Therefore, the maintenance views will also include the predecessor, in order to facilitate linking in the field dependency tab of the view cluster (Swapna, 2007). These three maintenance views are embedded in the following view cluster (figure 6)</p>
Text-fig. 1. Scanning electron micrographs of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). a) Flower in oblique lateral view showing numerous broad tepals, numerous inwardly curved stamens and the flat floral receptacle with a conical gynoecial region; b–c) Flower in two different oblique apical views showing numerous broad laminar tepals and inwardly curved stamens surrounding the carpels; note cellular differences between outer (op) and inner (in) perianth parts, as well as bases of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads); d) Detail of flower showing a cluster of poorly differentiated carpels in the center surrounded by elongated stamens; note grooves in the dorsal surface of the stamens indicating the position of the pollen sacs; e) Detail of flower showing the broad bases of the laminar tepals, rhomboidal stamen bases and poorly differentiated carpels; f) Detail of flower showing inwardly arched stamens and poorly differentiated carpels. Scale bars = 1 mm (a–c), 200 µm (d–f). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 1. Scanning electron micrographs of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). a) Flower in oblique lateral view showing numerous broad tepals, numerous inwardly curved stamens and the flat floral receptacle with a conical gynoecial region; b–c) Flower in two different oblique apical views showing numerous broad laminar tepals and inwardly curved stamens surrounding the carpels; note cellular differences between outer (op) and inner (in) perianth parts, as well as bases of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads); d) Detail of flower showing a cluster of poorly differentiated carpels in the center surrounded by elongated stamens; note grooves in the dorsal surface of the stamens indicating the position of the pollen sacs; e) Detail of flower showing the broad bases of the laminar tepals, rhomboidal stamen bases and poorly differentiated carpels; f) Detail of flower showing inwardly arched stamens and poorly differentiated carpels. Scale bars = 1 mm (a–c), 200 µm (d–f).
Text-fig. 18. Scanning electron microscope (SEM) images of a fruit of Canrightia sp. with associated pollen; Torres Vedras locality, Portugal. a) Fruit in lateral view showing prominent cavities in the fruit wall formed by the scattered oil bodies and the broad hypanthium fused to the base of the fruit (arrowhead); b) Fruit surface showing epidermal cells and the scattered oil cells embedded in the fruit wall (arrowheads); c) Cluster of monocolpate pollen grains in the probable stigmatic region of the fruit; d) Pollen grains showing the long colpus and semitectate-reticulate pollen wall; e) Pollen wall showing the reticulum with large and small lumina, and scattered, compressed columellae supporting the smooth muri. Specimen, TV142-S170213. Scale bars 300 Μm (a), 100 Μm (b), 30 Μm (c), 6 Μm (d), 1 Μm (e). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 18. Scanning electron microscope (SEM) images of a fruit of Canrightia sp. with associated pollen; Torres Vedras locality, Portugal. a) Fruit in lateral view showing prominent cavities in the fruit wall formed by the scattered oil bodies and the broad hypanthium fused to the base of the fruit (arrowhead); b) Fruit surface showing epidermal cells and the scattered oil cells embedded in the fruit wall (arrowheads); c) Cluster of monocolpate pollen grains in the probable stigmatic region of the fruit; d) Pollen grains showing the long colpus and semitectate-reticulate pollen wall; e) Pollen wall showing the reticulum with large and small lumina, and scattered, compressed columellae supporting the smooth muri. Specimen, TV142-S170213. Scale bars 300 Μm (a), 100 Μm (b), 30 Μm (c), 6 Μm (d), 1 Μm (e).
Text-fig. 45. Scanning electron microscope (SEM) images of "Staminate structure"; Catefica locality, Portugal. a–c) Staminate structure in oblique apical (a), oblique basal (b) and lateral (c) views showing distinct stalk and head with a cluster of about 20 stamens; note bracts at the base of the structure (asterisks) and probable secretory openings in the anther tissues (arrows). Specimen, Catefica 358-S135451 (a–c). Scale bars = 600 Μm (a–c). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 45. Scanning electron microscope (SEM) images of "Staminate structure"; Catefica locality, Portugal. a–c) Staminate structure in oblique apical (a), oblique basal (b) and lateral (c) views showing distinct stalk and head with a cluster of about 20 stamens; note bracts at the base of the structure (asterisks) and probable secretory openings in the anther tissues (arrows). Specimen, Catefica 358-S135451 (a–c). Scale bars = 600 Μm (a–c).
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).
ESFRI thematic cluster view on EOSC
<p>The illustration visualizes the view of the five ESFRI cluster projects EOSC-Life, ENVRI-FAIR, SSHOC, PANOSC and ESCAPE on the emerging European Open Science Cloud. Particular focus is put on the three building layers of consolidated e-infrastructures, open science, and scientific communities' content and users which the ESFRI cluster projects bring to the EOSC. The three layers identified by the cluster projects provide an "alternative" interpretation of the acronym EOSC.</p>
Deep Clustering Representation for Spatially Resolved Transcriptomics Data via Multi-view Variational Graph Auto-Encoders with Consensus Clustering
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Dataset for "Decomposing God Header File via Multi-View Graph Clustering"
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