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13,864 results for “staging”
Between a Pastoral and a Melodrama: Frances Burney and the Romantic Stage
<p>It is well known that the neglect of the dramatic works composed by Frances Burney (1752-1840) was largely caused by the unwavering opposition put up by her father, the famed musicologist Charles Burney, who shared the strong anti-theatrical prejudice that characterized the century as a whole. Paradoxically, this critical disregard has partly continued even after the watershed publication of Burney’s Complete Plays (Sabor ed.) in 1995. Although a number of interesting contributions have since reformulated Burney scholarship in terms of comedy (discussing, for instance, the comic elements in Evelina, or the genteel comedies The Witlings and A Busy Day), the tragic component of Burney’s opus remains one of the last frontiers of enquiry. My talk, "Between a Pastoral and Melodrama: Frances Burney and the Romantic Stage", offers a new dimension to the appraisal of Burney’s dramaturgy by focusing on 'Hubert De Vere, a Pastoral Tragedy,' written during Burney’s years at George III’s court (1786-1794). Despite the interest shown by John Philip Kemble, the greatest tragic actor of the age and the manager of Drury Lane Theatre, Hubert De Vere never reached the stage or, more surprisingly, the printed page, preordaining its subsequent critical eclipse.<br> <br> <br> This research is part of the Horizon 2020 project called "Opening Romanticism: Reimagining Romantic Drama for New Audiences"(OpeRaNew) ID 892230 within the ERC programme Horizon 2020 MSCA-IF-2019. The PI is Francesca Saggini. See CORDIS website at <a href="https://cordis.europa.eu/project/id/892230">https://cordis.europa.eu/project/id/892230</a></p>
Data files: Single-cell RNA sequencing of Plasmodium vivax sporozoites reveals stage- and species-specific transcriptomic signatures
<p>Scripts, preprocessed count matrices, single-cell data objects, and generated data (tables and .rds files) from the scRNA-seq analyses performed in <strong>“Single-cell RNA sequencing of Plasmodium vivax sporozoites reveals stage- and species-specific transcriptomic signatures".</strong></p> <p> </p>
Host developmental stages shape the evolution of a plant RNA virus
<p>Datasets used in the generation of figures 1 and 2 of:</p> <p>Melero, I., González, R., Elena, S.F. 2022. Host developmental stages shape the evolution of a plant RNA Virus. Philos. Trans. R. Soc. B doi: 10.1098/rtsb.2022.0005</p>
Generation time in stage-structured populations under fluctuating environments (Simulations)
<p>The study is about the computation of the generation time when individuals are classified based on their stage and the environment stochastically fluctuates with time. This folder contains simulation code in R to plot Figure 2 of the manuscript.</p>
Determination of traits responding to iron toxicity stress at different stages and genome-wide association analysis for iron toxicity tolerance in rice (Oryza sativa L.)
<p>This vcf file constitute underlying raw data material for the manuscript "Determination of traits responding to iron toxicity stress at different stages and genome-wide association analysis for iron toxicity tolerance in rice (Oryza sativa L.)". <br> The SNP genotype data came from a whole-genome resequencing and were called using the Nipponbare IRGSP 1.0 rice reference genome. SNPs with a miss rate greater than 30% and minor allele frequency (MAF) less than 5% were removed. Heterozygous alleles were also excluded. Finally, 160,498 SNPs were selected and used in the GWAS analysis. </p>
Text-fig. 13. Zoophycos isp. a: BK 17, Layer No. 6; b: BK 27, Layer No. 8; c: lateral tunnel continuing from spreite side to the surrounding rock, BK 28, Layer No. 23; d: BK 22, Layer No. 1; e: "juvenile" stage of the structure on a horizontal winding tunnel, BK 21, Layer No. 26; f: BK 24, Layer No. 17; g: broad winding tunnel adjacent to spreite, BK 26, Layer No. 6; h: BK 15, Layer No. 18; i: BK 23, Layer No. 2. Scale bar = 1 cm. in Early Complex Tiering Pattern: Upper Ordovician, Barrandian Area, The Czech Republic
Text-fig. 13. Zoophycos isp. a: BK 17, Layer No. 6; b: BK 27, Layer No. 8; c: lateral tunnel continuing from spreite side to the surrounding rock, BK 28, Layer No. 23; d: BK 22, Layer No. 1; e: "juvenile" stage of the structure on a horizontal winding tunnel, BK 21, Layer No. 26; f: BK 24, Layer No. 17; g: broad winding tunnel adjacent to spreite, BK 26, Layer No. 6; h: BK 15, Layer No. 18; i: BK 23, Layer No. 2. Scale bar = 1 cm.
Text-fig. 2. Strobili of modern Equisetum hyemale L. in different stages of expansion/maturation. Living specimens from near Billerbeck in Westphalia, Germany. Scale bars 5 mm. in First Record Of Intact Equisetalean Strobili From The Wealden (Lower Cretaceous) Of The Isle Of Wight, Southern England
Text-fig. 2. Strobili of modern Equisetum hyemale L. in different stages of expansion/maturation. Living specimens from near Billerbeck in Westphalia, Germany. Scale bars 5 mm.
Figure 4 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 4. One percent agarose gel electrophoresis stained with Cyber Safe® showing 5.8S/ITS2 gene fragments amplified using Fanas/Ras for H. asiaticum with amplicon size 408 bp (100 bp DNA ladder). Numbers below bands representing location of collected specimens according to Fig. 4.
Figure 3 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 3. Immatures of Hyalomma asiaticum collected from Meriones persicus in western Iran (nymphal stage): left: dorsal and right: ventral views.
Figure 5 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 5. Phylogenetic tree of Hyalomma asiaticum ticks inferred from ITS2 sequence data constructed using Bayesian Inference (BI) method. Nodes indicated with posterior probability values. Branch lengths are proportional to evolutionary changes (substitutions/site). Tree was rooted by Rhipicephalus sanguineus.
Figure 1 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 1. Three rodent collection sites located in Lorestan province western Iran inlcuding: 1. Khorramabad-Kuhdasht road, Zamzam village; 2. Khorramabad-Tehran road, LUMS Campus; 3. Dorud-Azna road, Zarnan village.
Figure 2. A in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 2. A rodent specimen infested by a number of immature ticks (red arrow) (animal is restrained through the ear by forceps and treated by insecticied for killing of ectoparasites).
Text-fig. 1. a: Po Plain and foothills of the Northern Apennine in Northern Italy (inset) with the location of Oriolo (black star) and other Early and Middle Pleistocene plant localities, Enza and Stirone. Red lines indicate the frontal thrust arcs (modified from Martinetto et al. 2015). b: The "La Salita" section, Oriolo and chronology of the two "Sabbie gialle" cycles based on large mammals and palaeomagnetic correlation (modified from Toniato et al. 2017; IMMS 2020* [Italian Mediterranean Marine Stages] updated from Cohen and Gibbars 2020; GTS 2021* [Global Time Scale] updated from Head et al. 2021). c: Quarry "La Salita", Oriolo, in 1987. Main unconformities (U) separating the two "Sabbie gialle" cycles and terrestrial deposits on top are shown. Leaf symbols indicate the positions of some of the layers rich in fossil leaves (photo by G. B. Vai, modified). d: Surroundings of Faenza with the location of Oriolo and adjacent coeval sites yielding plant macrofossils. in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 1. a: Po Plain and foothills of the Northern Apennine in Northern Italy (inset) with the location of Oriolo (black star) and other Early and Middle Pleistocene plant localities, Enza and Stirone. Red lines indicate the frontal thrust arcs (modified from Martinetto et al. 2015). b: The "La Salita" section, Oriolo and chronology of the two "Sabbie gialle" cycles based on large mammals and palaeomagnetic correlation (modified from Toniato et al. 2017; IMMS 2020* [Italian Mediterranean Marine Stages] updated from Cohen and Gibbars 2020; GTS 2021* [Global Time Scale] updated from Head et al. 2021). c: Quarry "La Salita", Oriolo, in 1987. Main unconformities (U) separating the two "Sabbie gialle" cycles and terrestrial deposits on top are shown. Leaf symbols indicate the positions of some of the layers rich in fossil leaves (photo by G. B. Vai, modified). d: Surroundings of Faenza with the location of Oriolo and adjacent coeval sites yielding plant macrofossils.
Egg size and offspring phenotype data at early life stages in seven Arctic charr morphs
<p>Maternal effects have the potential to alter early developmental processes of offspring and contribute to adaptive diversification. Egg size is a major contributor to offspring phenotype, which can influence developmental trajectories and potential resource use. However, to what extent intraspecific variation in egg size facilitates evolution of resource polymorphism is poorly understood. We studied multiple resource morphs of Icelandic Arctic charr, ranging from an anadromous morph – with a phenotype similar to the proposed ancestral phenotype – to sympatric morphs that vary in their degree of phenotypic divergence from the ancestral anadromous morph. We characterised variation in egg size and tested whether egg size influenced offspring phenotype at early-life stages (i.e. timing of- and size at- hatching and first feeding [FF]). We predicted that egg size would differ among morphs and be less variable as morphs diverge away from the ancestral anadromous phenotype. We also predicted that egg size would correlate with offspring size and developmental timing. We found morphs had different egg size, developmental timing and size at hatching and FF. Egg size increased as phenotypic proximity to the ancestral anadromous phenotype decreased, with larger eggs generally giving rise to larger offspring, especially at FF, but egg size had no effect on developmental rate. The interaction between egg size and the environment may have a profound impact on offspring fitness, where the resulting differences in early-life history traits may act to initiate and/or maintain resource morphs diversification. </p>
Data and code for article "Nature reserve customized method of photo and video camera traps materials processing using two-stage neural network approach"
<p><strong>DESCRIPTION</strong> 📓</p> <p>"data" folder directory contains the datasets for classification and detection. </p> <ol> <li>The detection dataset has <strong>YOLOv5 format</strong> and contains three classes <strong>[tigers, leopards, empty]</strong>. The class empty is about <strong>10%</strong> of the total data. The leopard and tiger classes contain <strong>3500</strong> images each. The entire amount of data for the detection task is <strong>7600</strong> images.</li> <li>The classification dataset contains two classes <strong>[tigers, leopards]</strong>. Images for classification are cropped images from the detection task using bounding boxes. Each class has <strong>3500</strong> images</li> </ol> <p> </p> <p>The "weights" folder contains pretrained models for classification and detection tasks. </p> <ul> <li>The detector weights were pre-trained on <strong>231k</strong> images from camera traps located throughout Russia.</li> <li>The classifier weights were pre-trained on <strong>416k</strong> images that were cropped with <strong>bounding boxes</strong> from photographs for the detection task. Some of the images for the classification task were taken from the <strong>Internet</strong>. The classifiers were trained for <strong>29 classes</strong>.</li> <li>You can also find folder <strong>tigers_vs_leopards</strong> in both the detection and classification directory, where there are weights that have been trained on a part of the camera trap images available at the link below.</li> </ul> <p><em>Classification weights</em></p> <ol> <li>EfficientNetv2-M</li> <li><strong>ResNeSt-101e</strong> (🚀 RECOMMENDED)</li> <li>ResNet-101d</li> <li>ReXnet-100</li> <li>SeResNet-152d</li> </ol> <p><em>Detection weights</em></p> <ol> <li>YOLOR-W6-1280</li> <li>YOLOX-X-640</li> <li>YOLOv5-X-640</li> <li>YOLOv5-X-1280</li> <li>YOLOv5-M6-1280</li> <li><strong>YOLOv5-L6-1280</strong> (🚀 RECOMMENDED)</li> </ol> <p>Read README.md file for more details</p>
Annotation table - Whole body transcriptomes of the tick Ixodes ricinus at different stage and feeding conditions
<p>Annotation table for a <em>de novo</em> assembled transcriptome of<em> Ixodes ricinus</em> in different stages and conditions.</p> <p>Description of the fields of each column (Trinotate results, and additionnal statistics):</p> <p>1. Contig_name: name of the contig (Trinity assembly)</p> <p>2. sprot_Top_BLASTX_hit: first hit of the blastx search against SwissProt (https://data.broadinstitute.org/Trinity/Trinotate v2.0 RESOURCES/)</p> <p>3. TrEMBL_Top_BLASTX_hit: first hit of the blastx search against Uniref90 (https://data.broadinstitute.org/Trinity/Trinotate v2.0 RESOURCES/)</p> <p>4. RNAMMER: identification of non-coding RNAs</p> <p>5. prot_id: identifier of the predicted protein (TransDecoder)</p> <p>6. prot_coords: coordinates (start, end and strand) of the predicted protein on the contig</p> <p>7. sprot_Top_BLASTP_hit: first hit of the blastp search between the predicted protein and SwissProt (https://data.broadinstitute.org/Trinity/Trinotate v2.0 RESOURCES/)</p> <p>8. TrEMBL_Top_BLASTP_hit: first hit of the blastp search between the predicted protein and Uniref90 (https://data.broadinstitute.org/Trinity/Trinotate v2.0 RESOURCES/)</p> <p>9. Pfam: result of the search against PfamA database</p> <p>10. SignalP: prediction of a signal peptide with SignalP</p> <p>11. TmHMM: prediction of a transmembrane domain with THMM</p> <p>12. eggnog: eggNOG database of orthologous genes (v3.0) assignation</p> <p>13. gene_ontology_blast: GO assignation based on blast results</p> <p>14. gene_ontology_pfam: GO assignation based on pfam results</p> <p>15. Contig_length: length of the contig in bp</p> <p>16. Busco_Id: name of the BUSCO (v1)</p> <p>17. Busco_status: status of the BUSCO (complete/fragmented/duplicated)</p> <p>18-32: Kallisto read counts for the 15 libraries</p> <p>A, B, C: unfed nymphs (replicates 1, 2, 3)</p> <p>D, E, F: partially fed nymphs (replicates 1, 2, 3)</p> <p>G, H, I: males (unfed) (replicates 1, 2, 3)</p> <p>J, K, L: unfed adult females (replicates 1, 2, 3)</p> <p>M, N, O: partially fed adult females (replicates 1, 2, 3)</p> <p>33. log2FoldChange_UnfedVsPartiallyFed: log fold change in base 2 of expression (comparison between "unfed" -including males- and "fed" ticks)</p> <p>34. pvalue_UnfedVsPartiallyFed: p-value of the comparison between "unfed" -including males- and "fed" ticks</p> <p>35. log2FoldChange_MaleVsFemale: log fold change in base 2 of expression (comparison between "males" and "females")</p> <p>36. pvalue_MaleVsFemale: p-value of the comparison between "males" and "females"</p> <p>37. log2FoldChange_NymphsVsAdults: log fold change in base 2 of expression (comparison between "nymphs" and "adults" -males and females-)</p> <p>38. pvalue_NymphsVsAdults: p-value of the comparison between "nymphs" and "adults" -males and females-)</p> <p> </p> <p> </p>
Carbon stock increase during post-agricultural succession in central France: no change of the superficial soil stock and high variability within forest stages
Open the record for dataset details and reuse information.
Fig. 3 in Description of the male and the larva of IxodES CollarIS Hornok, 2016 with drawings of all stages
Fig. 3 Drawings of Ixodes collaris male (a, dorsal view; b, ventral view) and female (c, dorsal view; d, ventral view)
Fig. 5 in Description of the male and the larva of IxodES CollarIS Hornok, 2016 with drawings of all stages
Fig. 5 Drawings of Ixodes collaris nymph (a, dorsal view; b, ventral view) and larva (c, dorsal view; d, ventral view)
Fig. 2 in Description of the male and the larva of IxodES CollarIS Hornok, 2016 with drawings of all stages
Fig. 2 Ventral views of male Ixodes vespertilionis (a, anterior part of the idiosoma; c, posterior part of the idiosoma) and I. collaris (b, anterior part of the idiosoma; d, posterior part of the idiosoma). The white dashed line indicates the second intercoxal space. The purple and red arrows show the genital aperture. The black and yellow arrows point to differences in the anterior part of the ivory coloration
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.