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.
440
datasets available to search
ShareScore release 0.9.0
Dataset results
440 results for “potato”
FIGURE 14 in A new species of Longitarsus (Coleoptera: Chrysomelidae) feeding on Chinese potato, Plectranthus rotundifolius (Lamiaceae) in southern India
FIGURE 14. Leaves damaged by adults: (L to R) Plectranthus rotundifolius, P. amboinicus and P. scutellarioides.
FIGURES 2–10 in A new species of Longitarsus (Coleoptera: Chrysomelidae) feeding on Chinese potato, Plectranthus rotundifolius (Lamiaceae) in southern India
FIGURES 2–10. Longitarsus serrulatus sp. nov. 2. antenna; 3. male protarsus; 4. female protarsus; 5. metatibial spur; 6. last abdominal sternite of male (macerated specimen); 7. median lobe of aedeagus, ventral view; 8. median lobe of aedeagus, lateral view; 9. median lobe of aedeagus, dorsal opening; 10. tegmen.
Internal bruising in potatoes by biospeckle laser technique
<p>This research aimed at evaluating the applicability of the biospeckle laser technique in order to detect and predict the internal bruising in potatoes caused by mechanical impacts during the early stages where there is no visual perception of the injury.</p> <p>Published in https://academicjournals.org/journal/AJAR/article-abstract/6C3128356571</p> <p>Type of data: 130 images, 640x486 pixels, BMP, gray scale, of speckle images in a time rate of 12 frames per second</p> <p>The potatoes were submitted to mechanical impact and monitored regarding the biospeckle laser technique before and after the mechanical impact.</p> <p>Treatments:</p> <p>Before impact</p> <p>0h (Just after the impact)</p> <p>2h (after the impact)</p> <p>4h (after the impact)</p> <p>6h (after the impact)</p> <p>24h (after the impact)</p> <p>48h (after the impact)</p> <p>72h (after the impact)</p> <p> </p> <p>Each treatment has in a folder:</p> <p>5 replications and Control with 130 raw images of speckle</p> <p>Generalized Difference graphical outcome with the map of activity</p> <p> </p> <p>New version================</p> <p>Additional 15 replications of of: Before impact, 0h, 2h, (...), 72h</p> <p>The zip files of the additonal 15 replications are identified as *additnal_data.zip</p> <p>Observation: There isn't control data in the additional replications. One can use the data of "Before impact" as Control as well in all cases.</p> <p>=========================</p> <p> </p> <p>Summary: 20 replications in total using the same methodology and carried out at the same period.</p> <p> </p> <p>Funders: CNPq, CAPES and FAPEMIG</p>
Effects of Fertigation Treatment Using a Subsurface Drip System on Spring Potato (Solanum Tuberosum L.) Growth and Yield
Open the record for dataset details and reuse information.
GBS and phenotype data for MASPOT population, a panel of tetraploid potato clones
Open the record for dataset details and reuse information.
Differential gene expression table of the transcriptional response of Colorado potato beetle to aegerolysin-based complex
<p>The file in Excel format (xlsx) contains the results of differential gene expression analysis of a study with Colorado potato beetle larvae that explores the potential adaptive response of CPB larvae to feeding with feed complemented by the aegerolysin-based complex PlyA2/PlyB.</p> <p>Experimental design: Leptinotarsa decemlineata larvae fed on potato leaf disks supplemented with PlyA2/PlyB/buffer solution vs control larvae fed on leaves soaked in buffer. Whole larvae were sampled at 1 and 5 days post-treatment, and RNA was isolated and sequenced on an Illumina sequencing platform.</p>
Fig. 4 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 4. Transcript accumulation of genes associated with wound induced suberization. Transcript accumulation of known and putative genes encoding steps in suberin biosynthesis, from starch degradation to final assembly, over the wound-healing time course were retrieved from RNA-seq data. Heatmaps depict log2FPKM means for n = 3 biological replicates for each time point. Numbered pathway steps correspond to numbers in the suberin roadmap (Supplemental Fig. S4). Fumarase (step 63) is included as a step in the TCA pathway, but is shown in grey because its sequence did not have a corresponding PGSC gene identification number, and therefore transcript abundance could not be estimated in this study.
Fig. 6 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 6. Transcript accumulation of wound-induced CASP and GDSL genes. Transcript accumulation of known and putative CASP and GDSL genes, over the wound-healing time course were retrieved from RNA-seq data. Heatmaps depict log2FPKM means for n = 3 biological replicates for each time point.
Fig. 3. Network modules for suberin-associated metabolism genes. Expression profiles for 317 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 3. Network modules for suberin-associated metabolism genes. Expression profiles for 317 wound-induced and suberin-associated genes encompassing primary carbohydrate metabolism and the formation of suberin phenolic and aliphatic monomers were subjected to WGCNA. Genes belonging to carbohydrate (C), tricarboxylic acid cycle (TCA), shikimate pathway (S), phenolic metabolism (P), phenolic assembly (PA), fatty acid biosynthesis (FAB), fatty acid modification (FAM) and aliphatic assembly (AA) are colour-coded (see legend). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 2. Gene set enrichment analysis (GSEA) of biological processes across differentially expressed genes (DEGs). Time point comparison panels represent a union parametric analysis of gene set enrichment (PAGE) of biological process (BP) categorized gene ontology (GO) terms. Nodes represent gene sets and their size represents a range from 5 to 464 genes, and edges show overlapping genes between sets, with width representing ranges from 5 to 149 genes. Blue sets are downregulated, red are up-regulated, and grey nodes denote terms that were not detected as significantly differentially regulated (i.e. enriched) at that time point comparison. Labels denote assigned node numbers that correspond to Table 1 with associated GO ID, GO term and regulation overview. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 1. Global overview of the wound-healing transcriptome. A. Principle component analysis (PCA) of RNA-seq libraries. Colours represent biological replicate libraries generated from the same time point (gene log2FPKM space with scaling). B. Differentially expressed genes (DEGs) across time point comparisons. Genes were considered significantly up- or down-regulated if they met p ≤ 0.01 and |log2 (fold change)| (| LFC|) ≥ 2 significance cut-offs. Lists of significantly DEGs were generated using voom by applying these parameters with the Benjamini-Hochberg procedure to TMM-normalized HT-Seq count data. C. Venn diagram of DEGs significantly up- (red) or down-regulated (blue) over the wound-healing time course. Genes were considered significantly up- or down-regulated if they met p ≤ 0.01 and |LFC| ≥ 2 significance cut-offs. Lists of significantly DEGs were generated using voom by applying these parameters with the Benjamini-Hochberg procedure to TMM-normalized HT-Seq count data. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 5. Transcript accumulation of genes associated with wound induced ABA biosynthesis and degradation. Transcript accumulation of known and putative genes encoding steps in ABA biosynthesis and degradation, over the wound-healing time course were retrieved from RNA-seq data. Heatmaps depict log2FPKM means for n = 3 biological replicates for each time point. Numbered pathway steps correspond to numbers in the ABA metabolism pathway (Supplemental Fig. 6).
Fig. 7 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 7. RT-qPCR validation of select wound-induced genes. Gene expression values for 14 genes from RT-qPCR (ΔΔCq) and RNA-seq (CPM) analyses were normalized to 0 dpw values, then log2-transformed to generate log2 (foldchange) values. Pearson's correlation coefficients were calculated for log2 (foldchange) values from the two experimental procedures, with α = 0.05 (Supplemental Table 9). The 95% confidence interval was calculated and plotted as 95% confidence bands.
Images of flowers and tubers produced by potato recombinant inbred lines
<p>Recombinant inbred line (RIL) populations are powerful mapping tools in many crops but have not yet been created using cultivated potato germplasm. We crossed the doubled monoploid cultivated clone DM 1-3 with the self-compatible diploid inbred wild clone M6 to create a diploid F1 hybrid. One F1 plant was self-pollinated to generate a phenotypically diverse F2 population, which was selfed to create 87 RILs. This is the first report of a RIL population developed from a cultivated x wild hybrid in potato. Poor fertility was a significant challenge in creating RILs. Nevertheless, we generated inbred lines that ranged from high to low fertility, vigor, and tuber production. F6 RILs ranged from 98% to 68% homozygosity, based on 2884 SNP markers. Considering the phenotypic variability between the two parents and among the RILs, we expect the RIL population to be valuable for mapping traits important to the potato industry.</p>
Figure 5 in Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae)
Figure 5. Lectotype specimen of Solanum andigenum Juz. & Bukasov (Solanum tuberosum L. Andigenum group) held in LE. Reproduced with permission of the V. L. Komarov Botanical Institute.
Figure 4 in Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae)
Figure 4. Lectotype specimen of Solanum tuberosum L. (Chilotanum group) held in LINN (LINN 248.12). Reproduced with permission of the Linnean Society of London.
Figure 1 in Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae)
Figure 1. Lectotype specimen of Solanum ajanhuiri Juz. & Bukasov held in WIR (note spelling of specific epithet on this sheet, see text). Reproduced with permission of the N. I. Vavilov Institute of Plant Industry.
Figure 3 in Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae)
Figure 3. Lectotype specimen of Solanum juzepczukii Bukasov held in WIR (WIR-36897). Reproduced with permission of the N. I. Vavilov Institute of Plant Industry.
Figure 2 in Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae)
Figure 2. Lectotype specimen of Solanum curtilobum Juz. & Bukasov held in LE. Reproduced with permission of the V. L. Komarov Botanical Institute.
FIGURE 8 in A new species of Epicaerus Pascoe, 1881 (Coleoptera: Curculionidae: Entiminae: Geonemini) associated with potato cultivars in Tierras Altas de Chiriquí, Panama
FIGURE 8. Specimens of Epicaerus nr. inaequalis from El Zamorano, El Paraíso Department, Honduras: A–C, H female (ASUCOB0019961), D–G, I male (ASUCOB0019962). A, D dorsal view (black arrow in A pointing straight apical fifth of elytral outline), B, E lateral view, C, F ventral view, G dorsal view of head, H, I posterior view (black arrows pointing costate odd-numbered elytral interstriae). Scale bars for A–F: 2 mm.
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.