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605 results for “framing”
Figure 20. Consecutive frames from a 100 in Maratus playa, a new peacock spider in the fimbriatus group from Australia (Araneae: Salticidae: Euophryini)
Figure 20. Consecutive frames from a 100 fps video of courtship display by a male Maratus playa. White arrows indicate direction of movement by both legs I relative to the previous frame in this sequence (one cycle/step at ~11 Hz). Green arrows indicate movement of each pedipalp relative to the previous frame (several cycles at ~10 Hz).
Figure 17. Selected, sequential frames from a 25 in Maratus playa, a new peacock spider in the fimbriatus group from Australia (Araneae: Salticidae: Euophryini)
Figure 17. Selected, sequential frames from a 25 fps video of courtship display by a male Maratus playa. Arrows indicate the direction of movement (stepping or pivoting at ~2.2 Hz) relative to the previous position.
Figure 16. Selected, sequential frames from a 25 in Maratus playa, a new peacock spider in the fimbriatus group from Australia (Araneae: Salticidae: Euophryini)
Figure 16. Selected, sequential frames from a 25 fps video of courtship display by a male Maratus playa. Arrows indicate the direction of movement (stepping or pivoting at ~3 Hz) relative to the previous position.
Baroque Style Oil Painting Frame by JamesVTong
High poly baroque style oil painting frame, for constructing classical indoor scenes Orginal painting: River Landscape in the Late Afternoon Painting by Adriaen van de Source URL of the original painting : https://www.britannica.com/art/landscape-painting 3D modeler: JamesVTong 3D modeling software: Blender Uploaded on January 30, 2022 If you want more information about this product, please feel free to contact me at 1291477913t@gmail.com Source: Objaverse 1.0 / Sketchfab
Wmid-438e0c - Post Medieval buckle frame
An incomplete silvered white metal rectangular buckle frame of Post Medieval dating (AD 1690 to AD 1720). Less than 50% of the buckle frame is present, consisting of one loop. The front has been decorated with a ring and dot design in each surviving corner and one in between. Triangular knops are present on the corners. Crescents are present linking each ring and dot roundel. Rouletted grooves are present on the inner edges of the crescents. The reverse of the buckle frame is flat and undecorated. For more information, please visit the online database record available at: https://finds.org.uk/database/artefacts/record/id/1071859 Source: Objaverse 1.0 / Sketchfab
Framing the cross-border commuting literature: a systematic review and bibliographic analysis
<p>The dataset consist of the 134 publications selected for the systematic literature review on cross-border commuting. </p>
X-Rays micro-tomography of 54 Egyptian predynastic ceramic vessels from the MAN (Musée d'Archéologie Nationale-Domaine national du château de Saint-Germain-en-Laye, France) made in the frame of the project TECHNOPREGYPT 2021/43/P/HS3/03262. STACK DATA
<p><span>54 complete pots and sherds from the collection of the <span><span>Musée d’Archéologie Nationale-Domaine national du château de Saint-Germain-en-Laye, France, were scanned with X-Rays microtomography (CT-Scan) to carry out the technological analysis of the samples. The aim was to be able to see the internal structure of the ceramic vessels to reconstruct the manufacturing process. </span></span></span></p> <p><span>The scans are part of the project </span><span>TECHNOPREGYPT</span><em><span> <span>Ceramic technology and the socio-political environment of Predynastic Egypt</span></span></em><span><span> </span></span><span><span>2021/43/P/HS3/03262 directed by dr Jade BAJEOT. </span></span></p> <p><a title="TECHNOPREGYPT website" href="https://technopregypt.iksio.pan.pl/index.php/about-the-project"><span><span>TECHNOPREGYPT website</span></span></a></p> <p> </p> <p><strong>Funding</strong></p> <p><span>This research was led at the Institute of Mediterranean and Oriental Cultures, Polish Academy of Sciences and was </span><span>co-funded by the Polish National Science Centre and the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement no. 945339.</span><strong><span> </span></strong><span>For the purpose of Open Access, the author has applied a CC-BY public copyright license to any Author Accepted Manuscript (AAM) version arising from this submission.</span></p>
PRKN gene Introns in families from Order Primates show common Open Reading Frames
<p>Supplementary material:</p> <p><strong>01 Supplementary material. </strong>Contains Table 1, named: “<u>PRKN</u><em> gene determined in Primates in Gene database NCBI. Supplementary material</em>”. Data are shown for the primate species identified for this study. In addition, a Folder with title “<em>PRKN</em> database”, that contains the subfolders of the 34 primate species for which the <em>PRKN</em> gene was reported until April 2023. Species used for this study are indicated with the title “0 Selected-species”, and those not used only with the species name. In turn, all have four subfolders:</p> <ul> <li><strong>01 <em>PRKN</em> gene and mRNA variants-Fasta format</strong>: contains the sequences of the mRNA variants in FASTA format and of the <em>PRKN</em> gene.</li> <li><strong>02 Alignment <em>PRKN</em> gene and mRNA variants</strong>: contains the <em>PRKN</em> gene and mRNA sequences in FASTA format and the result of the alignment between the gene and the variants. Additionally, a Word document with the manual verification of the previous result. This document is not included in the primate species folders that were not used in this study.</li> <li><strong>03 <em>PRKN</em> aminoacid variants-Fasta format: </strong>contains the amino acid sequences of the <em>PRKN </em>gene variants in FASTA format.</li> <li><strong>04 PRKN Protein variants domains</strong>: contains documents with the graphical representation of the PRKN isoform domains, in Scalable Vector Graphic (SVG) format.</li> </ul> <p><strong>02 Supplementary material.</strong> Table 2 in Excel document containing the positions of the introns and exons of <em>PRKN </em>gene the 16 primate species used in this study. The first sheet contains the size of the introns/exons and their location by species. In the following sheets, the species name, intron/exon position and size are indicated.</p> <p><strong>03 Supplementary material. </strong>Contains two files:</p> <ul> <li><strong>Figure 1.</strong> Document with the alignments of the Primate PRKN proteins encoded by each mRNA variant. Also, are indicated the amino acids whose codons contain the intron with their respective phase.</li> <li><strong>Table 3, named “<em>Intron Phase for </em>PRKN<em> gene</em>”</strong>, in Excel document containing the phases, codons, their respective amino acids and the location of the introns of the primate <em>PRKN</em> gene. The first sheet contains the consensus data for each species, grouped according to families. In the following sheets, the species name, the Phases, the codon and the respective amino acid for each intron are indicated. Phases 0, 1, and 2 are indicated in purple, red, and green letters, respectively. To Phases 1 and 2, the position of the intron in the codon is indicated with a vertical bar, whereas, for Phase 0, each codon is in separate boxes. The mRNA variants that showed loss or fusion of introns are indicated as “Non determine”. Variants with alternatively spliced mRNA and phase change are indicated in yellow boxes.</li> </ul> <p><strong>04 Supplementary material. </strong>Contains two Excel documents and a subfolder with the putative <em>PRKN</em> introns Open Reading Frame (ORF):</p> <ul> <li><strong>Excel file: Table 4, named “<em>Positive ORFs</em>”</strong>. The first sheet contains the general data of 5’-3’ and 3’-5’ ORFs, characterized for each species by intron and organized by families. The second sheet corresponds to the total number of exons determined for each ORF, with the previously mentioned organization. The additional sheets are divided by intron and the species are organized by families along with the different characterized ORFs.</li> <li><strong>Excel file: Table 5 named “<em>ORFs Introns</em>”</strong>. In the first sheet, the number of ORFs of the introns is indicated, according to the grouping performed in this study. The other Sheets correspond to both unique and common ORFs determined for each species per intron, organized by family.</li> <li><strong>Subfolder named “<em>ORFs alignments</em>”</strong>: Contains the alignments between the ORFs of each intron by species. Exclusive and common ORFs are also indicated.</li> </ul> <p><strong>05 Supplementary material.</strong> Contains two Excel documents with putative functional sites of PRKN introns ORFs protein:</p> <ul> <li><strong>Excel file: Table 6 named “<em>Family Common Functional Sites</em>”</strong>. The first sheet contains the general information of the functional sites characterized in the ORFs, determined in the introns of each species ordered by family. Also, the total count of ORFs per family. The other sheets correspond to the categories of cellular processes. Within these are the functional site according to the species that presented it, ordered by family and the total count of each site.</li> <li><strong>Excel file: Table 7 named “<em>Protein Domain ORFs</em>”</strong>. Functional sites determined only for ORFs common to two or more species are found. The position of each functional site is indicated according to the amino acid sequence and in relation to each species.</li> </ul> <p><strong>06 Supplementary material. </strong>Contains two subfolders that comprise BLAST and Protein Data Bank search from mRNA and PRKN ORF intron proteins:</p> <ul> <li><strong>BLAST subfolder comprises a Word document and 7 plain text documents. </strong>The Word document corresponds to the sequences reported in the Transcriptome Shotgun Assembly protein (tsa_nr) and Expressed sequence tags (est) databases, for ORFs that are common between Homo sapiens and the other species, according to the intron. The plaintext-like documents correspond to BLAST analyses that yielded more than six sequences similar to the reference ORF. The documents are named according to the sequences analyzed: the ORF name and database (Protein or Nucleotide).</li> <li><strong>Protein Data Bank subfolder. </strong>Contains 6 files in .PDF format, that correspond to protein structures that showed similarities with human ORFs 32 and 11, from Introns 6 and 9, respectively. Each document contains the protein structure information indicated in the Protein Data Bank (PDB) and the amino acid alignment between the Intron ORF sequence and the PDB protein sequence. The documents are named according to the protein ID obtained in the PDB and the respective ORF.</li> </ul>
Data for the paper "Computing MHD equilibria of stellarators with a flexible coordinate frame"
<p>Data for the revised paper "<span>Computing MHD equilibria of stellarators with a </span><span>flexible coordinate frame"</span></p> <p>Thetitle has changed from the submission title: "A generalized Frenet frame for computing MHD equilibria in stellarators"</p> <p>We provide the input and output files for all GVEC simluations presented at the "JOINT VARENNA - LAUSANNE INTERNATIONAL WORKSHOP: THEORY OF FUSION PLASMAS, 2024" and to be published in PPCF.</p> <p>An ipython script that generates the postprocessing /plots is also provided.</p> <p>New content computing the frame from a boundary surface obtained from quasr is now also part of this compilation.</p> <p>See the README.md file for details.</p>
Figure 26. Four frames from a in Neurobiology and vision of jumping spiders (Araneae: Salticidae)
Figure 26. Four frames from a video of an adult female Colonus sylvanus in Greenville County, South Carolina. The transparency of the prosoma allowed a direct view of the movements of the AME. 1, This spider faced a Leucauge venusta (Araneae: Tetragnathidae) suspended under a nearby grass blade. The axis of the prosoma (blue line) and the optical axes of the AME (red lines) faced the prey directly. 2, The eye tube of the right AME moved to the left, shifting the axis of that eye to face the stem that would serve as an indirect route of access to that prey. 3-4, The spider slowly turned to the right, lowering its profile in the prey direction (upper left), and faced that access route. Subsequently, this Colonus slowly climbed the nearby stem, then moved under the attached grass blade to approach its prey, which was then captured with an upside-down jump. Active movement of the two AME tends to be loosely coupled, but each eye can also be moved independently a shown in (2).
Ultimate load of randomly sampled stainless steel frames under gravity plus wind loads
<p>Data was generated using the general purpose finite element software ABAQUS and performing advanced nonlinear analyses. The database is comprised of ultimate load factors corresponding to different random samples of six different nominal stainless steel frames under gravity and wind load combinations. The values of the random variable assignments are given for each case.</p> <p>The full details of the finite element model can be found in: Arrayago, I.; Rasmussen, K.J.R.; Zhang, H. System-based reliability analysis of stainless steel frames subjected to wind loads. "Structural Safety", July 2022, vol. 97, art. No. 102211.</p> <p>DOI: https://doi.org/10.1016/j.strusafe.2022.102211</p>
Figure 20. Selected sequential frames from a 25 in Maratus candens, a new peacock spider in the linnaei group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 20. Selected sequential frames from a 25fps video of the Fan dance of a male Maratus candens. As in Figure 16, green arrows indicate the lower positions of the opisthosoma, touching the underlying surface at least once per cycle (4 down+up cycles/16.08s or 0.25Hz). Movement of the opisthosoma is not completely smooth, but includes some low-amplitude waving or bobbing (Figure 22). The attentive female (♀ #1) can be seen in the foreground.
Figure 13. Serial frames from a 120 in Maratus pinniger, a new peacock spider in the vespa group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 13. Serial frames from a 120fps video of courtship display by a male Maratus pinniger. Lateral movement of the elevated fan relative to the preceding frame is indicated with an arrow. Movement was fairly constant, at a rate of ~4.3Hz (12.5 left-right cycles in 2.9s). There was little movement of the extended legs III, or the pedipalps, during this display. For each numbered frame (1-25) in this series (and in other series shown below), the sequential frame number (f), time elapsed since the previous frame (+), and the total elapsed time is shown.
High-throughput event-based and frame-based convolutions for event-cameras
<p>Event cameras are promising sensors for on-line and real-time vision tasks, due to their high temporal resolution, low latency and the elimination of redundant static data. Many vision algorithms use some form of spatial convolution (i.e. spatial pattern detection) as a fundamental component, but additional consideration must be taken for event cameras, as the visual signal is asynchronous and sparse. While elegant methods have been proposed for event-based convolutions, they are unsuitable for real scenarios due to their inefficient processing pipeline, and subsequent low event-throughput. This paper presents an efficient implementation based on decoupling the event-based computations from the computationally heavy convolution ones, increasing the maximum event processing rate by 15.92x, to over 10 million events/second, while still maintaining the event-based paradigm of asynchronous input and output. Results on public datasets with modern 640x480 event-camera recordings show that the proposed implementation achieves real-time processing with minimal impact in the convolution result, while the prior state-of-the-art results in latency of over 1 second per-event.</p>
Figure 16. Sequential frames from a 120 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 16. Sequential frames from a 120 fps video of a male Maratus nubilis displaying in front of a female. This advertisement or tentative display included extension of one leg III (frames 1, 19) and slow, low amplitude left-to
DATASET: Palaeoenvironmental framing of the O Areal Roman saltworks and related anthropogenic activities in north-western Iberia
<p>Palynological and geochemical dataset of two pedo-sedimentary profiles (P3-6-I and P3-6-II) of the manuscript: <em>Palaeoenvironmental framing of the O Areal Roman saltworks and related anthropogenic activities in north-western Iberia</em>.</p>
Prediction Result of Next Monochrome Ionogram frame using LSTM-CNN Model
<p>Video of next frame ionogram prediction result using simple LSTM-CNN model</p> <p>Paper published in The 9Th International Seminar on Aerospace Science and Technology ISAST 2022</p>
Generating spatiotemporal patterns of linearly polarised light at high frame rates for insect vision research
<p><strong>Electrophysiology dataset for the work presented in:</strong></p> <p>Supple et al., (2022) Generating spatiotemporal patterns of linearly polarised light at high frame rates for insect vision research. J. Exp. Biol. 225, jeb244087. doi:10.1242/jeb.244087</p> <p><strong>Analysis code available at:</strong> https://github.com/jacksupple/Supple22_JEB_PolDevice_DataAnalysisScripts</p> <p>Download, select all, and extract files. Navigate to the assembled folder to re-run the analysis code.</p> <p><em>Argynnis paphia</em> butterfly intracellular photoreceptor traces are located in "\Photoreceptor_data". Results of the analysed data are found in "\photoreceptor_results"</p> <p><em>Calliphora vicina</em> blowfly extracellular lobula plate tangential cell (LPTC) recordings are located in "\LPTC_data". Results of the analysed data are found in "\LPTC_results".</p> <p>"\DualDLP_Stim" contains parameter files for the rotating dot stimuli, which are used during analysis.</p>
Simulations of Single Molecule Localization Microscopy frames with scattered single emitters
<p>Datasets used in the work "Combining deep learning with SUPPOSe and Compressed Sensing for SNR-enhanced localization of overlapping emitters".</p> <p>The file <strong>Sample dataset.zip</strong> contains simulated images of frames of Single-Molecule Localization Microscopy. In the directory structure, Q is the number of emitters, d is the emitter distance (in pixels), imax is the image maximum intensity and i indexes different noise realizations. There are three images within each folder: <strong>X</strong> is a noiseless image, <strong>Y</strong> is the image with noise and background and <strong>Z</strong> is a denoised image predicted using a convolutional neural network.</p> <p>The file <strong>Train dataset.zip</strong> contains 5000 simulated pairs of images of single emitters distributed randomly that were used to train a convolutional neural network for denoising. The folder <strong>X</strong> contains noiseless images and the folder <strong>Y</strong> contains the corresponding images with noise and background.</p> <p>In all cases, a Gaussian PSF with size <span class="math-tex">\(\sigma = 3\)</span> px was used as the PSF of the imaging system, Noise is modeled as a Poisson process with a dark signal <span class="math-tex">\(i_{dark} = 10\)</span>.</p> <p>Corresponding author: Axel M. Lacapmesure (alacapmesure@fi.uba.ar)</p> <p> </p> <p><strong>CHANGELIST</strong></p> <ul> <li>Version 2: corrected all file extensions in "Train dataset.zip" that were wrong.</li> </ul>
Figure 94. Sequential but not consecutive frames from a 25 in Five new peacock spiders from eastern Australia (Araneae: Salticidae: Euophryini: Maratus Karsch 1878 and Saratus, new genus)
Figure 94. Sequential but not consecutive frames from a 25fps video of a male Saratus hesperus displaying in front of a female. 1-2, Sudden movement or pivot to one side with the fan elevated. 3-4, Bobbing the depressed opisthosoma, followed by extension of legs III. 5-10, Consecutive frames (0.04s/frame) showing rapid, continuous up-and-down vibration of the extended legs III as the opisthosoma was depressed. 12-19, Successive positions assumed during intermittent (staccato or interrupted) pivoting and stepping to one side (12-17) and then to the other side (18-19) with the fan elevated.
ScienceDex guides
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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.