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22,710 results for “Plant”
Medicinal Plants of the Guianas: Medical Guiana
Robert A. DeFilipps, Shirley L. Maina and Juliette Crepin. 2004. Medicinal Plants of the Guianas (Guyana, Surinam, French Guiana). Available online: <p></p>http://botany.si.edu/bdg/medicinal/index.html<p></p>Robert A. DeFilipps, Shirley L. Maina and Juliette Crepin. 2004. Medicinal Plants of the Guianas (Guyana, Surinam, French Guiana). Available online: <p></p>http://botany.si.edu/bdg/medicinal/index.html
Revealing real-time 3D in vivo pathogen dynamics in plants by label-free optical coherence tomography
<p>This repository contains all data and code underlying the publication: J. de Wit et al. "<em>Revealing real-time 3D in vivo pathogen dynamics in plants by label-free optical coherence tomography</em>" in Nature Communications (2024) (https://doi.org/10.1038/s41467-024-52594-x)</p> <p><strong>--------------Code description------------------</strong></p> <p>The set of scripts is largely organized around the figures. For each (sub)figure, also from supplementary materials, that involves data and plotting, there is a script that generates the plot from data that can be found in the different zip files that are present in the Zenodo repository under https://doi.org/10.5281/zenodo.11428245.</p> <p>The scripts use the data that is contained in the ZIP folders. The ZIP folders are organized by experiment (Experiment 1, including contrast optimization; Experiment 2), one for the other data (OtherData, the validation for with Trypan blue, and the Arabidopsis, Radish and nematode) and one as a smaller dataset to explain the method on a single B-scan (Example_Bscan_dynamicOCT).</p> <p>IMPORTANT: The folder where the ZIP files are unzipped should be put in the file '<em>basepath.txt</em>', such that the data can be automatically loaded.</p> <p>Besides the figures that mention 'MakeFig...' there are a few more scripts:</p> <ul> <li><em>pointcloud_generation_experiment1.py</em>: this file makes the point clouds from the dynamic OCT images as described in Fig 2b. The resulting data is saved as maximum intensity projections and axial sums(forming the basis for Fig S4, S6 and S7) and as voxel counts (forming the basis of Fig.2c and Fig S5)</li> <li><em>pointcloud_generation_timelapses.py</em>: this file does the segmentation for experiment 2 and saves the maximum intensity projections and axial sums of the different stages in the segmentation (forming the basis of Fig3a,d,e and FigS9a,b), and saves the point clouds of the data. These point clouds were refined manually in CloudCompare as described in methods. These segmented point clouds are contained in the data zip folder of experiment 2.</li> <li><em>StatisticalTests.R</em>: This R file calculates the statistical tests for Fig.2cd and Fig.S5d. Here the path is not automatically updated, and should be manually set. The input file is contained in "Experiment1/SegmentationData/segmentationdata_samples.csv" and the output of the file is "D:/DataZenodo/Experiment1/SegmentationData/data_combined_Rstats_output.csv"</li> <li><em>example_dynamic_Bscan.py</em>: This script gives an example of the dynamic OCT processing as proposed in this paper. First it shows the process from an OCT interference spectrum to a B-scan. Then it loads 100 B-scans and applies dynamic OCT, including normalization with histograms. Finally it gives a dynamic B-scan and plots this against the average normal OCT image. This script can be used with only the zip folder "Example_Bscan_dynamicOCT", which reduces the amount of data needed to download/unzip.</li> </ul> <p>The list of other script files to load the data and generate the figures (guiding to the path of uncropped figures) is:</p> <ul> <li><em>MakeFig1bce_Fig2e.py</em></li> <li><em>MakeFig1d.py</em></li> <li><em>MakeFig1agraphs_FigureS1.py</em></li> <li><em>MakeFig3acde_S9ab.py</em></li> <li><em>MakeFigS2_determine_dynamic_range_experiment1.py</em></li> <li><em>MakeFigS8.py</em></li> <li><em>MakeFigureS4-S6-S7.py</em></li> <li><em>MakeFigureS5.py</em></li> <li><em>MakeHistFig2b_makeFigS3b-e.py</em></li> <li><em>MakePlotsFig2ab.py</em></li> <li><em>MakePlotsFig2cd.py</em></li> </ul> <p>Code was all run in Python 3 using Anaconda Spyder.</p> <p>Moreover, the zip file with the code contains the folder '<em>figures</em>' with all subfigures. Some of them are automatically saved from the scripts, others (like photos, icons, but also the Trypan blue microscopy figure) are added in the respective folder. The are logically organized by figure number.</p> <p><strong>--------------Dataset Description-----------------</strong></p> <p>As mentioned above, the data is organized in four zip folders for both experiments, the other data (validation with Trypan blue, other plant-pathogens) and one for the dynamic OCT B-scan example. The data contain the following:</p> <p><strong>Experiment 1: </strong></p> <ul> <li>DynamicOCTimages whose subfolders (organized by date) contain a folder per volume dataset in experiment 1 with a z-stack of .tif files that form the imaged volume. The lateral sampling is 3 um and the axial sampling is 1.37 um. </li> <li>ContrastOptimization: This folder contains <ul> <li><em>Bscans_with_segmentation</em>: segmented B-scans for contrast optimization (Fig S3)</li> <li><em>Bscan_figS1_fig1</em>: The B-scans and segementation for Figure S1.</li> <li><em>histogramdata_dynamicrange</em>: The histograms, bins and deducted reference data for determining the dynamic range per color channel for experiment 1 (Fig S2)</li> <li><em>logcompressed_3value_dOCT_example</em>: An example data stack for obtaining histograms (see script MakeFigS2_determine_dynamic_range_experiment1.py)</li> <li><em>overlaps_threshold-100-98-95-92-90-85-80-75-70-65-60-55-50-45perc_red-1_2_blue_-3_0_green1_filt.npy</em>: A file with intermediate data for the contrast optimization, which can also be generated with the script "<em>MakeHistFig2b_makeFigS3b-e.py</em>"</li> </ul> </li> <li>SegmentationData: This folder contains <ul> <li><em>MIP_segmentation_stages</em>: maximum intensityp projections and axial sums for all images at different stages in the segmentation (basis for Fig S4,6,7)</li> <li><em>processed_masks and StackMasks</em>: the manually obtained masks (segmented in StackMasks, made into masks in the folder 'processed_masks') for filtering out stomata, veins and artefacts.</li> <li><em>Unmasked_axialsum_th34_formanualsegmentation</em>: This folder contains the images of Fig.S4 and were used for the segmentation (we addes a small offset, such that the in segmentation we could set it to 0 and have a unique mask). </li> <li><em>overview_samples_bremiayn.csv</em>: A dataframe with the data for all the samples in experiment 1 that is used as input for the segmentation. It also contains the result of the manual check whether it has infection (Fig2c, left).</li> <li><em>segmentationdata_samples.csv</em>: This supplements the file of overview_samples_bremiayn.csv with the results from the segmentation and is output to script "<em>pointcloud_generation_experiment1.py</em>". It forms the basis of Fig.2a-c, and FigS5, as well as for the R-script to do the statistical testing.</li> <li><em>qPCR_dOCT.csv</em>: This script contains the qPCR data and is input to Fig2d. </li> </ul> </li> </ul> <p><strong>Experiment 2:</strong></p> <ul> <li><em>DynamicOCTimages</em>: This contains the z-stacks of .tif files of the volumes for experiment 2 (and one extra, where a z-slice is used in Fig.1b, bottom). Sampling step size is here again 3 um in lateral direction and 1.37 um in axial direction.</li> <li><em>.npy files </em>with the histograms (with same bins as Experiment 1), maxvalues and reference values for the dynamic range calculation.</li> <li><em>segmentation_data</em>: this folder contains: <ul> <li><em>quantification_volume_disc160_33_10.csv</em> and <em>quantification_volume_disc160_33_10.xlsx</em>: data from the manually segmented point clouds that form the basis of Fig.3c.</li> <li><em>timelapse_sampleoverview.csv</em>: overview of the samples that is used as input in the file "<em>pointcloud_generation_timelapses.py</em>"</li> <li><em>pointclouds</em>: Folder with segmented point clouds for the three leaf discs. These files could be loaded in CloudCompare.</li> <li><em>overviewMIPs</em>: folder with overview maximum intensity projections for the different steps in segmentation, which also forms the input of Fig.3a, FigS9ab.</li> <li>rawpointclouds: folder with the automatically generated point clouds from file <em>pointcloud_generation_timelapses.py </em>which were imported into CloudCompare as the basis for the segmented point clouds.</li> </ul> </li> </ul> <p><strong>OtherData:</strong></p> <p>This folder contains the z-stacks of dynamic OCT tif images for Arabidopsis (here both a normal contrast and one that has been increased to only contain the original 0-180 range); nematodes, radish (called radijs_test_PP_py_0002), spores for Fig1c (SporesImaging) and the dynamic OCT image of Fig1d. </p> <p><strong>example_Bscan_dynamicOCT:</strong></p> <p>This folder contains data to run the script example_dynamic_Bscan.py to show the dynamic OCT imaging process from raw OCT spectra.</p> <ul> <li><em>raw_spectra_exampleframe:</em> contains interference spectra, a reference spectrum and interpolation grid to show how to get from a raw OCT spectrum to a normal single B-scan.</li> <li><em>abs_images:</em> contains 100 subsequent B-scans that can be used to generate a dynamic OCT image as done in example_dynamic_Bscan.py</li> </ul> <p> </p> <p> </p>
Projected distribution of invasive plant species in the tropical Andes under climate change
<p>Distribution maps of 11 invasive species now and in the future (2040-70). The projections were the result of the assembly of three algorithms: Adaptive Boosting (AdaBoost), Boosted Regression Trees (BRT), and Extreme Gradient Boosting (XGBoost). Future projections were made for three global circulation models and three climate change scenarios, each with low (SSP126), medium (SSP370), and high (SSP585) levels of carbon emission.</p> <p>Habitat suitability and presence/absence maps are also included. The threshold for establishing a species as present was determined to be the value that maximized the TSS. </p> <p>For more information, see the article accompanying the dataset by González-Trujillo et al. Mapping the threat: Projecting invasive plant distribution in the tropical Andes under climate change</p> <p>List of modeled invasive plant species and their known impacts in the tropics.</p> <table> <tbody> <tr> <td> <p><strong>Species </strong></p> </td> <td> <p><strong>Biogeographic origin</strong></p> </td> <td> <p><strong>Impacts </strong></p> </td> <td> <p><strong>References</strong></p> </td> <td> <p><strong>GBIF data (DOIs)</strong></p> </td> </tr> <tr> <td> <p><em>Acacia decurrens </em></p> </td> <td> <p>Australian</p> </td> <td> <p>Create regular layers of litter on the ground, inhibit or redirect successional processes, inhibit the expression of seed banks, and limit resource supply, leading to displacement of native plants and animals and increasing the frequency of fires.</p> </td> <td> <p> (Cárdenas López et al., 2017; Le Maitre et al., 2011)</p> </td> <td> <p>https://doi.org/10.15468/dl.mjyxhw</p> </td> </tr> <tr> <td> <p><em>Acacia melanoxylon</em></p> </td> <td> <p>Australian</p> </td> <td> <p>Alter the structure and function of their ecosystems, thereby displacing their native flora. It also causes soil erosion and alters hydrological cycles, negatively affecting agriculture.</p> </td> <td> <p>(Kumschick and Jansen, 2023; Le Maitre et al., 2011)</p> <p> </p> </td> <td> <p>https://doi.org/10.15468/dl.4cugnk</p> </td> </tr> <tr> <td> <p><em>Arundo donax</em></p> <p><em> </em></p> </td> <td> <p>Holarctic</p> </td> <td> <p>Alter<em> </em>the natural vegetation structure, outcompete native plant species and diminish the diversity and abundance of animals such as arthropods and birds. It also drives out soil, fuels forest fires, displaces native species, and increases the invasion of ticks that affect livestock.</p> </td> <td> <p>(Cárdenas López et al., 2017; Girotto et al., 2021; Lambert et al., 2010)</p> </td> <td> <p>https://doi.org/10.15468/dl.bfep4t</p> </td> </tr> <tr> <td> <p><em>Genista monspessulana</em></p> </td> <td> <p>Holarctic</p> </td> <td> <p>Alter fire regime and nutrient cycling displace native species and decrease native diversity by forming dense monospecific stands. It also facilitates the establishment of other invasive species and produces seeds that are toxic to livestock and humans.</p> </td> <td> <p>(Cárdenas López et al., 2017; Herrera et al., 2016; Pauchard et al., 2008)</p> </td> <td> <p>https://doi.org/10.15468/dl.gyhnxh</p> </td> </tr> <tr> <td> <p><em>Hedychium coronarium </em></p> </td> <td> <p>Indo-Malesian</p> </td> <td> <p>Alter hydrological and nutrient cycles in soil. It forms thickets that suppress the successional and regeneration processes of native species, thus affecting the native flora and crops.</p> </td> <td> <p>(Cárdenas López et al., 2017; Costa et al., 2019)</p> </td> <td> <p>https://doi.org/10.15468/dl.6z2jgb</p> </td> </tr> <tr> <td> <p><em>Melinis minutiflora</em></p> </td> <td> <p>African</p> </td> <td> <p>Increases the occurrence of fires, displaces native species, and alters soil properties and decomposition. It also inhibits the growth of native species.</p> </td> <td> <p>(Cárdenas López et al., 2017; Nogueira et al., 2019; Sandoval et al., 2022)</p> </td> <td> <p>https://doi.org/10.15468/dl.fsqwsv</p> </td> </tr> <tr> <td> <p><em>Pteridium aquilinum</em></p> </td> <td> <p>Holarctic</p> </td> <td> <p>Alter vegetation success processes affect crops and cause livestock poisoning. It also produces acids that inhibit root growth in native and cultivated species.</p> </td> <td> <p> (Berget et al., 2015; Cárdenas López et al., 2017; Valdez-Ramírez et al., 2020)</p> <p> </p> </td> <td> <p>https://doi.org/10.15468/dl.sp4uuv</p> </td> </tr> <tr> <td> <p><em>Ricinus communis</em></p> </td> <td> <p>African</p> </td> <td> <p>Alter vegetation success processes affect crops and cause livestock poisoning. It also produces acids that inhibit root growth in native and cultivated species.</p> </td> <td> <p>(Cárdenas López et al., 2017; Sandoval et al., 2022; Silva and Fabricante, 2022)</p> </td> <td> <p>https://doi.org/10.15468/dl.dhbphb</p> </td> </tr> <tr> <td> <p><em>Senecio madagascariensis</em></p> </td> <td> <p>African</p> </td> <td> <p>Alter soil nutrient cycles, damage to agricultural crops, and outcompete native species. It also contains substances that are toxic to both animals and humans. </p> </td> <td> <p>(Wijayabandara et al., 2021)</p> </td> <td> <p>https://doi.org/10.15468/dl.7e8eyx</p> </td> </tr> <tr> <td> <p><em>Thunbergia alata</em></p> </td> <td> <p>African</p> </td> <td> <p>Displace native species and reduce habitat heterogeneity, thereby affecting the structure and function of native ecosystems.</p> </td> <td> <p>(Cárdenas López et al., 2017; Quijano-Abril et al., 2021)</p> </td> <td> <p>https://doi.org/10.15468/dl.g9zybc</p> </td> </tr> <tr> <td> <p><em>Ulex europeaus</em></p> </td> <td> <p>Holarctic</p> </td> <td> <p>Dry soil and increase the occurrence of fires. Inhibits vegetative growth, including pastures in agricultural and livestock lands.</p> </td> <td> <p>(Anderson and Anderson, 2009; Cárdenas López et al., 2017)</p> </td> <td> <p>https://doi.org/10.15468/dl.6642q9</p> </td> </tr> </tbody> </table>
First spectral Reflectance Dataset of Equisetum hyemale (Snake grass) Invasive Alien Plant
<p><em><span>This repository contains the first spectral reflectance dataset of <span>snakegrass</span> (Equisetum hyemale) invasive alien species recorded in South Africa. Spectral reflectance measurements were collected under lab conditions using the Spectral Evolution PSR-300 full-range spectrometer. Spectral pre-processing was performed in R statistical software to remove noisy spectra and regions and perform averaging per sample (code accessible: https://github.com/mkganyago/SpectralEvolutionFileReader).<br></span></em></p>
GO Term annotations for five plants species from Phytozome by FANTASIA
<p>This is the GO term annotation made with FANTASIA for five species (Arabidopsis thaliana, Oryza sativa, Zea mays, Populus trichocarpa, and Solanum lycopersicum) from the Phytozome 13 datasets as proof of concept for this tool.</p>
Data and code for "Negative effects of allelopathic plant invasion intensify as the growth season progresses"
<p>Initial release for TT23_ms_data.</p> <p>Repository contains data and code for "Negative effects of allelopathic plant invasion intensify as the growth season progresses" by Perkowski et al. (in prep). Manuscript plots and tables are also included in release.</p>
Data, Analytical Code, and Model Outputs From: "Green is the New Black: Outcomes of Post-Fire Tree Planting Across the Interior West, USA"
<p>This archive includes data (locations of tree plantings, one-year survival records, remotely sensed canopy cover change), statistical code, and model outputs from Rodman et al. (2024). For more information on specific information, processing methods, and data formats, see "README.md" or "README.html" files associated with this archive</p>
Plasmodesmata Act as Unconventional Membrane Contact Sites Regulating Inter-Cellular Molecular Exchange in Plants.
<p>This table contains peaks aera values from LC-MS for lipidomic quantification of PIP and PIP2. These data were used for Pérez-Sancho, Jessica and Smokvarska, Marija and Glavier, Marie and Sritharan, Sujith and Dubois, Gwennogan and Dietrich, Victor and Platre, Matthieu and Li, Ziqiang Patrick and Paterlini, Andrea and Moreau, Hortense and Fouillen, Laetitia and Grison, Magali S. and Cana-Quijada, Pepe and Moraes, Tatiana Sousa and Immel, Françoise and Wattelet, Valerie and Ducros, Mathieu and Brocard, Lysiane and Chambaud, Clément and Zabrady, Matej and Luo, Yongming and Busch, Wolfgang and Tilsner, Jens and Helariutta, Yrjö and Russinova, Jenny and Taly, Antoine and Jaillais, Yvon and Bayer, Emmanuelle, Plasmodesmata Act as Unconventional Membrane Contact Sites Regulating Inter-Cellular Molecular Exchange in Plants. </p>
Direct molecular evidence for an ancient, conserved developmental toolkit controlling post-transcriptional gene regulation in land plants
<p>In plants, miRNA production is orchestrated by a suite of proteins that control transcription of the pri-miRNA gene, post-transcriptional processing and nuclear export of the mature miRNA. Post-transcriptional processing of miRNAs is controlled by a pair of physically-interacting proteins, HYL1 and DCL1. However, the evolutionary history and structural basis of the HYL1-DCL1 interaction is unknown. Here we use ancestral sequence reconstruction and functional characterization of ancestral HYL1 <em>in vitro</em> and in <em>Arabidopsis thaliana </em>to better understand the origin and evolution of the HYL1-DCL1 interaction and its impact on miRNA production and plant development. We found the ancestral plant HYL1 evolved high affinity for both double-stranded RNA (dsRNA) and its DCL1 partner before the divergence of mosses from seed plants (~500 Ma), and these high-affinity interactions remained largely conserved throughout plant evolutionary history. Structural modeling and molecular binding experiments suggest that the second of two double-stranded RNA-binding motifs (DSRMs) in HYL1 may interact tightly with the first of two C-terminal DCL1 DSRMs to mediate the HYL1-DCL1 physical interaction necessary for efficient miRNA production. Transgenic expression of the nearly 200 Ma-old ancestral flowering-plant HYL1 in <em>A. thaliana</em> was sufficient to rescue many key aspects of plant development disrupted by HYL1<sup>-</sup> knockout and restored near-native miRNA production, suggesting that the functional partnership of HYL1-DCL1 originated very early in and was strongly conserved throughout the evolutionary history of terrestrial plants. Overall, our results are consistent with a model in which miRNA-based gene regulation evolved as part of a conserved plant ‘developmental toolkit’.</p>
Structure and composition and carbon Stocks of woody plant community in assisted and unassisted ecological succession in a Tamaulipan thornscrub, Mexico
<p>In November of 2017, the structure and composition of woody plant communities were investigated through a floristic composition and diversity evaluation on three areas: a control area, an assisted ecological succession area and an unassisted ecological succession area.</p>
Data from the National Prioritisation of Australian plant species after the 2019-2020 bushfires
<p>Data for 26,062 native Australian plant species assessed against ten post-fire recovery criteria. Details of criteria and methods available in Gallagher, R. V. (2020) <em>National prioritisation of Australian plants affected by the 2019–2020 bushfire season.</em> Report to the Commonwealth Dartement of Agriculture, Water and Environment. https://www.environment.gov.au/system/files/pages/289205b6-83c5-480c-9a7d-3fdf3cde2f68/files/final-national-prioritisation-australian-plants-affected-2019-2020-bushfire-season.pdf </p>
Resource use strategies, resistance and tolerance to aerial biomass removal in Argentina mid-west native plants
<p>Dataset of the PhD Thesis from Lucas D. Gorné:<br> - Gorné LD. 2018. Estrategias de uso de recursos, resistencia y tolerancia a la remoción de biomasa aérea en plantas nativas del centro-oeste de Argentina. Tesis del Doctorado en Ciencias Biológicas. Facultad de Ciencias Exactas, Físicas y Naturales. Universidad Nacional de Córdoba. Córdoba, Argentina. https://ri.conicet.gov.ar/handle/11336/87925.</p>
Seasonal trajectories of plant-pollinator interaction networks differ following phenological mismatches along an urbanization gradient - Data and code
<p>Dataset and code used in the article "Seasonal trajectories of plant-pollinator interaction networks differ following phenological mismatches along an urbanization gradient", by A. Fisogni et al., published in Landscape and Urban Planning (2022, 226:104512, <a href="https://www.sciencedirect.com/science/article/pii/S016920462200161X?via%3Dihub">https://doi.org/10.1016/j.landurbplan.2022.104512</a>)</p>
Dataset for "Fire disturbance promotes biodiversity of plants, lichens and birds in the Siberian subarctic tundra"
<p>Data that support the findings of the study "<strong>Fire disturbance promotes biodiversity of plants, lichens and birds in the Siberian subarctic tundra</strong>".</p>
Warming of experimental plant-pollinator communities advances phenologies, alters traits, reduces interactions, and depresses reproduction
<p>This is the data set supporting the analyses performed in the article entitled "Warming of experimental plant-pollinator communities advances phenologies, alters traits, reduces interactions, and depresses reproduction", by Natasha de Manincor, Alessandro Fisogni, and Nicole E. Rafferty, published in Ecology Letters (2023, 26:323-334, <a href="https://doi.org/10.1111/ele.14158">https://doi.org/10.1111/ele.14158</a>).</p> <p>The experiment has been performed in the greenhouse facilities at the University of California, Riverside, in 2021.</p> <p>The two treatments analyzed are ambient vs warmed (+ 4 °C), the focal pollinator species is <em>Osmia lignaria</em>, and the three focal plant species are <em>Collinsia heterophylla</em>, <em>Nemophila menziesii</em>, and <em>Phacelia campanularia</em>.</p> <p>Data are tab separated .txt files.</p>
Data from: Efficacy of labile carbon addition to reduce fast-growing, invasive non-native plants: A review and meta-analysis
<p>Data and analysis in R for the publication "Efficacy of labile carbon addition to reduce fast-growing, invasive non-native plants: A review and meta-analysis" by Ossanna & Gornish (2023), <em>Journal of Applied Ecology</em>, <em>60</em>(2), 218-228. <a href="http://doi.org/10.1111/1365-2664.14324">https://doi.org/10.1111/1365-2664.14324</a>.</p>
Native and exotic plants play different roles in urban pollination networks across seasons
<p>Datasets for 'Native and exotic plants play different roles in urban pollination networks across seasons' by Zaninotto et al. (2023) in Oecologia.</p>
Restriction of access to the central cavity is a major contributor to substrate selectivity in plant ABCG transporters
<p>The input and main output files used for the paper <em><strong>"Restriction of access to the central cavity is a major contributor to substrate selectivity in plant ABCG transporters"</strong></em> are separated in the different tar files depending the MD stage they belong to.</p> <p><strong>Content</strong></p> <p>00_AlphaFold2: The models predicted from AlphaFold2</p> <p>01_build_system: The parameters for ATP and the initial pdb file used to build each system</p> <p>02_minimization: Minimization input files for each variant</p> <p>03_equilibration: Equilibration input files for each variant</p> <p>04_long_equilibration: ATP restrained equilibration input files for each variant</p> <p>05_free_equilibration: Free equilibration input files for each variant</p> <p>06_production: Free production input files for each variant</p> <p>07_caver: Caver calculations for each variant and replica</p> <p>08_transport_tools: Analysis of tunnel networks using TransportTools software</p> <p>09_tunnel_selection: Selection of the tunnels with widest bottleneck radius to perform CaverDock experiments</p> <p>10_caverdock: CaverDock calculations for each variant and for each ligand tested</p> <p>11_membrane_patch: MD simulations for liquiritigenin and POPC membrane only</p> <p>12_MD_analysis: Calculations of RMSD, RMSF of each system. Calculation of helical parameters for trans-membrane helices 2, 5, 8 and 11 (not for APO). Calculation of X1 and X2 angles for residue N1331 in each variant (not for APO)</p> <p>13_US_closed_to_open: Umbrella Sampling simulations to obtain the inward facing (IF) open state of each variant. Not used for PMF analysis.</p> <p>14_US_opening_energy: Umbrella Sampling simulations to obtain the Potential of Mean Force for the transition from IF-closed to IF-open conformations.</p> <p>15_US_equilibration: Equilibration input files for WT and F562L variants in IF-open states.</p> <p>16_US_production: Production input files for WT and F562L variants in IF-open states.</p> <p>17_US_caver: Caver calculations for WT and F562L variants in IF-open states.</p> <p>18_US_transport_tools: Analysis of tunnel networks using TransportTools software of WT and F562L variants in IF-open states.</p> <p>19_US_tunnel_selection: Selection of the tunnels with widest bottleneck radius to perform CaverDock experiments for WT and F562L variants in IF-open states.</p> <p>20_US_caverdock: CaverDock calculations for WT and F562L variants in IF-open states.</p> <p>21_US_MD_analysis: Calculations of RMSD, RMSF of each system. Calculation of helical parameters for trans-membrane helices 2, 5, 8 and 11.</p> <p>ABC_Sequences.fasta: Sequences from 1KP analysis</p>
Reproducibility package for Using root economics traits to predict biotic plant soil-feedbacks
<p>Using root economics space to predict biotic plant soil-feedbacks presents a novel framework linking below ground ecological theory to plant soil feedback effects. We show how to calculate root functional distance and location of two plant species in root economics space and how these measures can help to predict the strength and direction of the plant soil feedback between them. </p> <p>Contains data and scripts to reproduce analysis and figures for the manuscript (https://github.com/ggpmrutten/linkingRES-PSF)</p>
Tea bag index (TBI) for a pot trial with five plant species in Trani (Apulia, Italy)
<p>The file contains mean k and S value per GPS location, with as meta-data the starting date, duration and biome of the study.</p>
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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.