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29,145 results for “Association”
CARMEN immunopeptidomics publication associated dataset
<h1>CARMEN: CAnceR imMunopeptidogENomics</h1> <blockquote> <div>An immunopeptidomic dataset accompanying the publication "<a href="http://dx.doi.org/10.1101/2025.05.08.651510" target="_blank" rel="noopener">Expanding the definition of MHC Class I peptide binding promiscuity to support vaccine discovery across cancers with CARMEN</a>" containing peptides determined by mass-spectrometry associated with MHC Class I bindings from 72 publications (2323 samples).</div> </blockquote> <div> </div> <div> <p><strong>Authors:</strong> <a href="mailto:aleksander.palkowski@gmail.com" target="_blank" rel="noopener">Aleksander Palkowski</a>*, <a href="mailto:mwaleron@gmail.com" target="_blank" rel="noopener">Michal Waleron</a>*, <a href="mailto:emilia.daghir@gmail.com" target="_blank" rel="noopener">Emilia Daghir-Wojtkowiak</a>*, <a href="mailto:ashwinkallor@gmail.com" target="_blank" rel="noopener">Ashwin Adrian Kallor</a>*, <a href="mailto:javier.alfaro@proteogenomics.ca" target="_blank" rel="noopener">Javier Antonio Alfaro</a></p> <p>* <em>These authors contributed equally to this work</em></p> </div> <div> </div> <div>The entire dataset consist of four table files in the <a href="https://parquet.apache.org" target="_blank" rel="noopener">Apache Parquet</a> data file format:</div> <ul> <li>main</li> <li>mapped-protein-annotations-pogo</li> <li>mapped-protein-annotations-msfragger</li> <li>hla-sequences</li> </ul> <div> </div> <div><strong>Please refer to the README.md file for details.</strong></div> <div> </div>
The deployment of temporary nurses and its association with permanent nurses' outcomes in Swiss psychiatric hospitals: A secondary analysis.
<p>The objective of this analysis was to investigate the frequency of temporary nurses’ deployment and their association with nurse staffing levels and permanent nurses’ outcomes in Swiss psychiatric hospitals. The data is based on the Match<sup>RN</sup> Psychiatry study including 79 psychiatric units and 651 nurses and provides unit level frequency of temporary nurses’ deployment and individual nurse level data on staffing levels and permanent nurses’ outcomes namely job satisfaction, burnout, and intention to leave organization or profession. The data was collected in 2019 and 2020. We provide the unit and nurse-level dataset, a codebook and the r code to replicate the analyses of the paper. You can find the paper here: <a href="https://peerj.com/articles/15300/">https://peerj.com/articles/15300/</a> </p>
ClostriTof microflex Biotyper library plugin and associated raw Maldi spectra version 2.0
<p>This dataset contains the ClostriTof microflex Biotyper library plugin, an installation guide as well as the raw spectral data for all library and validation strains used to construct the ClostriTof library plugin.</p> <p>If you use this library for your research, please cite Asare et al., Frontiers in Microbiology, 2023; <a href="https://doi.org/10.3389/fmicb.2023.1104707">https://doi.org/10.3389/fmicb.2023.1104707</a></p> <p>We would like to thank Thomas Maier for his help with assembling version 2.0 of the ClostriTOF Database.</p>
Summertime methane and carbon dioxide emission rates and associated variables from a national-scale survey of 146 reservoirs in the United States, 2016-2023
Reservoirs are globally important sources of greenhouse gases, but the magnitude of their emissions is highly uncertain. Here we present data for 146 reservoirs from two surveys of reservoir methane and carbon dioxide emissions, one at the regional scale in the midwestern United States and one at the national scale in the conterminous United States, plus data from one reservoir in Washington and another in Puerto Rico. At all reservoirs, ebullitive and diffusive emissions and basic physiochemistry were measured at 15-70 locations during one 22 to 64-hour period during the summers of 2016-2023, with four reservoirs revisited a second time. Concomitant water chemistry measurements were also made at an index site. The dataset is comprised of two geospatial files and seven .csv files containing greenhouse gas emissions, water chemistry, morphology, and other relevant data. These data comprise the largest multi-reservoir emissions dataset ever assembled using consistent measurement methods.
Data associated with the FLooded Upland Dynamics EXperiment (FLUDEX), conducted at the IISD Experimental Lakes Area 1997 to 2003, investigating reservoir flooding impacts on ecosystems, particularly the release of mercury and greenhouse gases.
The data included in this repository were collected over the course of the FLooded Upland Dynamics Experiment (FLUDEX) conducted at the IISD Experimental Lakes Area (IISD-ELA) from 1997 to 2003. A plethora of data was collected over five years of flooding three upland reservoir sites, in order to examine the relationship between the amount of flooded, and thus decomposed, terrestrial organic matter and the production of methylmercury (MeHg), total mercury (THg), and greenhouse gases (GHGs) in the reservoirs. Findings from this experiment suggest that the amount of organic carbon stored in a flooded site does not directly influence the amount of THg, MeHg, and GHGs produced, but it does affect the persistence of mercury in the reservoir and food web. This version of the repository contains data collected on water chemistry, benthic invertebrate (chironomid) emergence, mercury and methylmercury concentrations in the water and food web, stable isotopes of carbon and nitrogen in emerging insects and zooplankton, and abundance and biomass of zooplankton, phytoplankton, and bacteria. This data package contains only some of the data from the FLUDEX project. IISD-ELA hopes to add more data in subsequent versions.
Langenheim Plant Species Data (1953) and Associated Resurvey Datasets (2014), Gunnison Basin, Colorado, USA
Quantitative plant abundance data were collected from the same 121 sites at two time periods separated by 65 years (1948-1952 and 2012-2014) in the Colorado Rocky Mountains to examine changes in plant community composition. The sites range in elevation from 2600m to 4100m. Approximately 30 sites were sampled from each of four habitat types: sagebrush (2528-3119m, n=27 sites), spruce-fir forest understory (3001-3520m, n=31 sites) , upland herb = montane meadow (3124-3850m, n=30 sites), and alpine (3549-4013m, n=33 sites). The earlier data set was collected by Jean H. Langenheim (1953, 1962) and consisted of counts of species occurrences along approximately 100m paced transects, noting species touching her boot tip every pace (n=100 sampled points per site). The later data set was collected by Stephanie D. Zorio (2015, 2016) consisting of counts of species occurrences every 1m along 300m transects (n=300 sampled points per site). The sites resurveyed by Zorio (2015, Zorio et al. 2016) were placed as close as possible to the original sites based on the written descriptions of Langenheim, but are only approximate. The GPS coordinates given for the resurveyed sites are the centerpoint of 2 perpendicular 150m transects, one across the slope and the other perpendicular to the slope. GPS coordinates for alpine sites along narrow ridges are the start and end points of three 100m transects along the ridge. Georeferenced localities and environmental site data are presented in Table 2: Lang Zorio Env Site Data. Langenheim’s original data were extracted from tables in her thesis (Langenheim 1953). These data omitted species that occurred in fewer than 14% of sites of a given habitat type (constancy). Species that occurred at very low frequencies (<1% per site) were only denoted as an x in the tables. Zorio converted these to frequencies of 0.5 for quantitative comparative purposes. This data set contains 157 species from 27 families across all sites and habitats. Species in seve
Phytoplankton, benthic algae, and associated environmental data from Lake Okeechobee, Florida, USA, August 2023 - November 2023
This data package contains phytoplankton, periphytometer, and environmental data collected from the South Florida Water Management District’s (SFWMD) Aquifer Storage and Recovery (ASR) monitoring sites and the Indian Prairie marsh during the 2023 rainy season. We collected phytoplankton from a surface water grab and benthic algae from artificial substrates (periphytometers) that were placed outside for three weeks. We also collected associated nutrient measurements and environmental data. Collections occurred twice from August to November 2023. Data were collected to better understand how phytoplankton and benthic algae differed in their responses to TN:TP ratios in a hypereutrophic lake known to have spatial differences in limiting nutrients. Data collection for this data package is complete.
Tree-Associated Fungal and Bacterial Communities at Harvard Forest 2021
Cities are investing in tree-planting initiatives to protect their citizens from climate change-related heat and pollution exposure, yet Boston’s street trees are growing nearly four times as fast and dying twice as young as Massachusetts’ rural forest trees. Our research aims to characterize the belowground variables and microbial community composition that might explain the differences in growth and mortality rates observed between urban and rural trees. In 2021, soil, leaf, and root samples were taken from 25 trees in Harvard Forest to use as a rural comparison to Boston’s street trees and trees in other forests along an urban-to-rural gradient from Boston into Western Massachusetts. At each tree, three 12” deep, 2.4-centimeter radius soil cores were taken within the drip line, and soil cores were divided into the top 6” and lower 6” of soil. Fine roots were picked from each soil core. Six leaf samples were taken from the mid-canopy of each tree, where possible. Soil variables including temperature, moisture, percent organic matter, soluble nitrogen availability, bulk density, and root biomass were measured. Thus far, we have found that urban trees have fewer roots than Harvard Forest trees (F1,252) = 10.88, p = 0.0011), and that urban trees establish more root biomass deeper into the soil than Harvard Forest trees (p = 4.84e-5).
Sap-flux and associated environmental data from ash tree monitoring at four urban parks in St. Paul, Minnesota, USA, from May to November of 2023.
We measured the sap flux density of eighteen ash trees (Fraxinus spp.) of varying health and canopy conditions across four urban parks in the City of St. Paul, MN, USA in summer 2023 with a low-cost, compact data logger system we designed in-house. Although many ash trees in the city have either been killed or removed to control the spread of Emerald Ash Borer, chemical insecticide treatments are available for trees that are in early stages infestation. The trees selected for the research have all been receiving insecticide treatment for a few years, but their health and canopy conditions vary. We also have collocated temperature, soil moisture, and precipitation measurements at the same site for summer 2023.
Oyster and associated fauna counts and lengths from restored and reference reefs in the coastal bays of Virginia, 2005-2019
This dataset has been superceded by Lusk, B., R. Smith, and M.C.N. Castorani. 2024. Oyster fauna lengths, counts, and biomass from restored and reference reefs in Virginia coastal bays, 2005-2023 ver 1. Environmental Data Initiative. https://doi.org/10.6073/pasta/d68de69f29cee5f737313a07f813f245 (Accessed 2024-02-22). which includes additional years and parameters. Oyster and associated reef fauna counts and lengths were sampled at 16 natural reference reefs and 61 restored shell plant reefs located at 18 sites in the Virginia Coast Reserve. Overfishing and disease decimated oyster reefs in the Virginia Coast Reserve in the 1900s. Reference reefs were defined as remnant reefs that naturally recovered in the early 2000s to develop the pronounced vertical structure and multiple oyster size classes that represent the desired endpoint of restoration efforts. Nearly every year since 2003, The Nature Conservancy and Virginia Marine Resource Commission have constructed oyster reefs in intertidal areas in the VCR. To construct the restored reefs, practitioners applied dredged, fossilized oyster shell to intertidal locations chosen for their bottom stability and accessibility (locations lacked oysters prior to construction). Whelk shell supplemented the oyster shell at 9 of the restored reefs.
Abundance and Size of Seagrass-Associated Fishes in the Virginia Coastal Lagoons, 2019-2024
These data comprise annual summer estimates of the abundance (counts) and size (length) of fishes across restored seagrass meadows of the Virginia coastal lagoons. Fish were collected using a 25-ft (7.62-m) wide beach seine hauled by hand over a 25 m linear swath of the seafloor. Seine hauls were collected in June at 31 sites (1 haul per site). All fish caught in the seine were identified to lowest practical taxonomic level, counted, measured (total length), and released. Data collection began in June 2019 and continues annually (sampling was not carried out in 2020 due to logistical interruptions associated with the COVID-19 pandemic). Data on water temperature, salinity, and conductivity were collected while sampling occurred using a YSI 30 probe. Dissolved oxygen measurements were collected using a YSI ProODO probe. In 2019, these data were collected on at the top and bottom of the water column, but in 2021 and subsequent sampling only one observation (mid-water column) was made. To reconcile this difference for the combined data set, top and bottom environmental measurements from 2019 were averaged. Each fish collection site is co-located with a nearby synoptic site where long-term measurements of seagrass, sediments, and fauna are made. The relationship between site names and coordinates are given in Synoptic_fish_sites.csv. The sites where fish sampling occurred are different and are given by the "fish_sites" column, with coordinates for these sites under the "fish_longitude" and "fish_latitude" columns. Importantly, the coordinates of where sampling occurred will differ slightly between years without a change to the name of the site. Site geographic coordinates for individual years are in the PhysicalSamples.csv file. Sites are separated by at least 300 meters. In 2023, three new sites were added to represent unvegetated areas outside of but near the seagrass meadows. These sites are HI29, SPDR-bare, and SS-bare, and are designed to serve as references for se
Abundance, biomass, and length of seagrass-associated invertebrates in the Virginia coastal lagoons, 2019-2023
These data comprise annual summer estimates of the abundance (counts), biomass (dry mass), and individual lengths of infaunal and epifaunal invertebrates across restored seagrass meadows (eelgrass Zostera marina) of the coastal lagoons of Virginia, USA. Infauna were collected during low tide by hand using cylindrical benthic cores. Epifauna were collected during low tide using cubic weighted throw traps that were sampled with dip nets. Incidentally captured fishes are included in these data. In 2019-2022, 50 sites were sampled, using 3 replicates per sampling method per site. Beginning with 2023 sampling, two additional sites were added that are consistently bare of seagrass (unvegetated seafloor). At sites with patchy areas of seagrass and bare substrate, cores were collected within seagrass only and thus represent seagrass-associated fauna at those sites, rather than a spatially haphazard sample. At the few sites that lack seagrass, cores were collected in bare substrate. All cores were separated by 25 m. Regardless of substrate and seagrass conditions, throw traps were deployed haphazardly and separated by at least 10 m. In the laboratory, invertebrates were first sorted to broad taxonomic groups and later identified to lowest practical taxonomic level and enumerated. Most taxonomic groups were either dried and weighed by taxon or measured as individual length by specimen. Existing data include one table with counts and weights for broad taxonomic groups (2019-2023) and three tables related to lowest practical taxonomic identification (2019-2020), including one for counts and biomass, one for individual lengths, and one for taxonomic information. Data collection began in July 2019 and continues annually in June-July.
Unexplained Repeated Pregnancy Loss is Associated with Altered Perceptual and Brain Responses to Men’s Body-Odor
Open the record for dataset details and reuse information.
Stress-associated brain activation across the hormonal contraceptive cycle
Open the record for dataset details and reuse information.
Dataset for: Associating Mechano-electrochemical Phenomena to Stochastic Current Events in Micro-Electrochemical Cells Containing TiNb2O7 Particles
<p>This is the raw data used in a manuscript that will be submitted to ChemElectroChem. If you have any questions, please email the creators.</p>
Data associated with the following publication: Developing the Playground Play Value and Usability Audit Tool (PVUA): An Evaluation of Content Validity via an Expert Panel
<p>This data set contains the supporting data associated with the following publication:</p> <p>Morgenthaler, T., Loebach, J., Lynch, H., Pentland, D., Kottorp, A., & Schulze, C. (in press). Developing the Playground Play Value and Usability Audit Tool (PVUA): An Evaluation of Content Validity via an Expert Panel. Children, Youth and Environments. [DOI was not yet available when the data set was published]</p> <p>The data set includes the following files:</p> <ul> <li>read me file [contains all relevant information to understand and reuse this data set] </li> <li>13 additional files [for description, see read me file]</li> </ul> <p>For more information, please contact the lead researcher, Thomas Morgenthaler (tom.morgenthaler@gmail.com or 121101888@umail.ucc.ie)</p> <p> </p>
A biodiversity dataset graph: Biological Associations in TaxonWorks hash://sha256/e4a47c067d6c125da60c9a1b92b5eecdea539cb8666cd3aed99db347ae5b8ed0 hash://md5/686007de79cc2a49ab23fd3debe56e3f
<p>The intended use of this archive is to facilitate (meta-)analysis of Biological Associations captured in TaxonWorks [1]. TaxonWorks is an integrated web-based workbench for taxonomists and biodiversity scientists. It allows you to capture, organize, and enrich your data; share it with collaborators; and package it for analysis and publication. </p> <p>This dataset provides versioned snapshots of the TaxonWorks network as tracked by Preston [2,3,4] during 2024-05-07 using:</p> <pre><code>preston track -u https://sfg.taxonworks.org</code></pre> <p>. In addition, this dataset provides a processed version of the biological associations using the "preston tw-stream" command as generated by the following bash script:</p> <pre><code>#!/bin/bash # # Generates GloBI interaction JSON Lines from provided provenance log as generated by preston tw-stream. # /usr/local/bin/preston cat hash://sha256/c1b081afa6ea0f60570c24cca85c4d9acd91eeefe36b9cacd1fe53b6893ea154\ | /usr/local/bin/preston tw-stream </code></pre> <p><br>The script itself was executed using:</p> <pre><code>cat transform.sh | preston bash </code></pre> <p>The execution of this transform.sh script (with content id hash://sha256/6dfe3c4ebf877bed73aebbe88c7d388bf894c569578ed7b28ca68e57a6afe43b), as well as their results, is captured within this datasets also. A rdf/quads formatted machine readable version of the workflow execution description can be found via:</p> <pre><code>preston cat hash://sha256/e4a47c067d6c125da60c9a1b92b5eecdea539cb8666cd3aed99db347ae5b8ed0 </code></pre> <p>And, the resulting JSON Lines file has content id (or signature) hash://sha256/4c2b8642251ced5985660d63c565efa6e5a9bf3d12b3b0c0d9ac577905f5e897 and is also included as interactions.json to facilitate access. </p> <p>The first json record can be generated using:</p> <pre><code>preston cat hash://sha256/4c2b8642251ced5985660d63c565efa6e5a9bf3d12b3b0c0d9ac577905f5e897\ | head -n1\ | jq . </code></pre> <p>or, provided that the interactions.json has content id starting with hash://sha256/4c2b86...</p> <pre><code>cat interactions.json\ | head -n1\ | jq . </code></pre> <p>This produces the following (formatted) json object:</p> <pre><code>{<br> "http://www.w3.org/ns/prov#wasDerivedFrom": "hash://sha256/fdbf13dc5f3d9c5afbc03db62699e2ce2724c499b7d91d8b0bf31e39409b153a",<br> "http://www.w3.org/1999/02/22-rdf-syntax-ns#type": "application/vnd.taxonworks+json",<br> "referenceId": "https://sfg.taxonworks.org/api/v1/sources/213218",<br> "interactionId": "https://sfg.taxonworks.org/api/v1/biological_associations/227664",<br> "taxonRootsResolved": 2,<br> "referenceResolved": true,<br> "referenceCitation": "@article{213218,\n author = {Monzen, Kota},\n journal = {Annual Report of the Gakugei Faculty of the Iwate University},\n pages = {24-38},\n title = {Revision of the Japanese gall wasps with the descriptions of new genus, subgenus, species and subspecies (II). Cynipidae (Cynipinae) Hymenoptera.},\n volume = {6},\n year = {1954}\n}\n",<br> "interactionTypeId": "gid://taxon-works/BiologicalRelationship/69",<br> "interactionTypeName": "gall",<br> "sourceTaxonName": "Neuroterus hakonensis",<br> "sourceTaxonId": "gid://taxon-works/TaxonName/1174121",<br> "sourceTaxonRank": "species",<br> "sourceTaxonAuthorship": "Ashmead, 1904",<br> "sourceTaxonPath": "Root | Cynipidae | Neuroterus | Neuroterus hakonensis",<br> "sourceTaxonPathIds": "gid://taxon-works/TaxonName/623170 | gid://taxon-works/TaxonName/1170060 | gid://taxon-works/TaxonName/1170097 | gid://taxon-works/TaxonName/1174121",<br> "sourceTaxonPathNames": "nomenclatural rank | family | genus | species",<br> "targetTaxonName": "Quercus",<br> "targetTaxonId": "gid://taxon-works/TaxonName/1173543",<br> "targetTaxonRank": "genus",<br> "targetTaxonAuthorship": "",<br> "targetTaxonPath": "Root | Fagaceae | Quercus",<br> "targetTaxonPathIds": "gid://taxon-works/TaxonName/623170 | gid://taxon-works/TaxonName/1173542 | gid://taxon-works/TaxonName/1173543",<br> "targetTaxonPathNames": "nomenclatural rank | family | genus"<br>}<br></code></pre> <p>In this example, a claim is made that, according to https://sfg.taxonworks.org/api/v1/sources/213218 [6] Neuroterus hakonensis (a gall wasp) has a primary host in the genus of Quercus (oak tree). </p> <p>In total, 237,068 such claims can be found in the generated resource with alias interactions.json and content id starting with hash://sha256/4c2b86... .</p> <p>In addition, the archive preston.tar.gz to allow for batch download. The archive contains three types of files: index files, provenance logs and data files. In addition, index files have been individually included in this dataset publication to facilitate remote access. Index files provide a way to links provenance files in time to establish a versioning mechanism. Provenance files describe how, when, what and where the TaxonWorks content was retrieved. For more information, please visit https://preston.guoda.bio or https://doi.org/10.5281/zenodo.1410543 . </p> <p>To retrieve and verify the downloaded TaxonWorks biodiversity dataset graph, download preston.tar.gz. Then, extract the archive into a "data" folder. Alternatively, you can use the preston[2] command-line tool to "clone" this dataset using:</p> <pre><code>java -jar preston.jar clone --remote https://zenodo.org/record/11151783/files </code></pre> <p>After that, verify the index of the archive by reproducing the following provenance log history:</p> <pre><code> java -jar preston.jar history --log tsv</code></pre> <p>to be:</p> <pre><code>hash://sha256/e4a47c067d6c125da60c9a1b92b5eecdea539cb8666cd3aed99db347ae5b8ed0 http://www.w3.org/ns/prov#wasDerivedFrom hash://sha256/c1b081afa6ea0f60570c24cca85c4d9acd91eeefe36b9cacd1fe53b6893ea154 </code><br><code>hash://sha256/c1b081afa6ea0f60570c24cca85c4d9acd91eeefe36b9cacd1fe53b6893ea154 http://www.w3.org/ns/prov#wasDerivedFrom hash://sha256/a4d651aac5220487835e6178511886e98b845b2d98cb7c5447fb2b042e0654d2hash://sha256/a4d651aac5220487835e6178511886e98b845b2d98cb7c5447fb2b042e0654d2 http://www.w3.org/ns/prov#wasDerivedFrom hash://sha256/ab7550368905e7c919e70a306efbb97719a1edbba2cfe4c4515f635ebc0be4bb hash://sha256/a4d651aac5220487835e6178511886e98b845b2d98cb7c5447fb2b042e0654d2 http://www.w3.org/ns/prov#wasDerivedFrom hash://sha256/ab7550368905e7c919e70a306efbb97719a1edbba2cfe4c4515f635ebc0be4bb</code><br><code>hash://sha256/ab7550368905e7c919e70a306efbb97719a1edbba2cfe4c4515f635ebc0be4bb http://www.w3.org/ns/prov#wasDerivedFrom hash://sha256/ff5e709305e593c87711e897b6341b94e775e2f312aa6d4ae5ed6120babd6f5e urn:uuid:0659a54f-b713-4f86-a917-5be166a14110 http://purl.org/pav/hasVersion hash://sha256/ff5e709305e593c87711e897b6341b94e775e2f312aa6d4ae5ed6120babd6f5e </code></pre> <p><br>To check the integrity of the extracted archive, confirm that each line produce by the command "preston verify" produces lines as shown below, with each line including "CONTENT_PRESENT_VALID_HASH". Depending on hardware capacity, this may take a while.</p> <pre><code>java -jar preston.jar verify</code></pre> <p>Note that a copy of the java program "preston", preston.jar, is included in this publication. The program runs on java 8+ virtual machine using "java -jar preston.jar", or in short "preston". </p> <p>Files in this data publication:</p> <p>--- start of file descriptions ---</p> <p>-- description of archive and its contents (a rendition of this file) --<br>README</p> <p>-- biological associations indexed from TaxonWorks expressed in a GloBI [5] compatible JSON Lines file --<br>interactions.json</p> <p>-- first 10 biological associations indexed from TaxonWorks expressed in a GloBI [5] compatible JSON Lines file --<br>interactions-10.json</p> <p>-- executable java jar containing preston [2,3,4] v0.8.5-SNAPSHOT. --<br>preston.jar</p> <p>-- preston archive containing TaxonWorks data files, associated provenance logs and a provenance index --<br>preston.tar.gz</p> <p>-- individual provenance index files --</p> <p>1fed32bf78298d7ecc3d9f36d106f1d7d7773a8b9a5e47af6632f36c1f82adb5<br>29306c5c144c3d7fd21be344d8b6b554b6f6efa3b8f8f5c0b27cdf0e88785652<br>2a5de79372318317a382ea9a2cef069780b852b01210ef59e06b640a3539cb5a<br>d31ff1ef1dea88c5952181a4f30e7ea7862873aa5f66430451275aa6d08d329e<br>deb84d69224af488da585186f88cafc58e978db5f9897de624cc9b02c0c83742<br>e9c34683f1e826f68f841f3419bd5ee9c0fa18be04713a6fd3364f226c7c5f2f<br>f98d36a9dc7bd833c93b3b61130865628f7bc2f7bb0920e95afcd16fba3dc6a8<br>ffb41d48979ceb964fbfbeb68cb60b584b759950087fdcc012521b866249bc39</p> <p>--- end of file descriptions ---</p> <p>This work is funded in part by grant NSF OAC 1839201, NSF DBI 1901932, NSF DBI 1901926, and NSF DBI 2102006 from the National Science Foundation.<br> </p>
CryoEM Maps and Associated Data Submitted to the 2015/2016 EMDataBank Map Challenge
<p>Files and metadata associated with the EMDataBank/Unified Data Resource for 3DEM 2015/2016 Map Challenge hosted at challenges.emdatabank.org are deposited.</p> <p>All members of the Scientific Community--at all levels of experience--were invited to participate as Challengers, and/or as Assessors.</p> <p>Seven benchmark raw image datasets were selected for the challenge. Six are selected from recently described single particle structure determinations with image data collected as multi-frame movies; one is based on simulated (in silico) images. All of the raw image datasets are archived at pdbe.org/empiar.</p> <p>27 Challengers created 66 single particle reconstructions from the targets, and then uploaded their results with associated details. 15 of the reconstructions were calculated using the SDSC Gordon supercomputer.</p> <p>This map challenge was one of two community-wide challenges sponsored by EMDataBank in 2015/2016 to critically evaluate 3DEM methods that are coming into use, with the ultimate goal of developing validation criteria associated with every 3DEM map and map-derived model.</p> <p> </p>
Genome-wide association summary statistics for human blood plasma glycome
<p>The dataset contains results of genome-wide association study of human blood plasma glycome. The 113 files contain association summary statistics for 113 glycome traits, of which 36 were directly measured by UPLC technology and 77 were derived glycome traits. Description of each glycome trait can be found in the <strong>Additional notes</strong> section. This dataset is also available for graphical exploration in the genomic context at <a href="http://gwasarchive.org">http://gwasarchive.org</a>. </p> <p>The data are provided on an "AS-IS" basis, without warranty of any type, expressed or implied, including but not limited to any warranty as to their performance, merchantability, or fitness for any particular purpose. If investigators use these data, any and all consequences are entirely their responsibility. By downloading and using these data, you agree that you will cite the appropriate publication in any communications or publications arising directly or indirectly from these data; for utilisation of data available prior to publication, you agree to respect the requested responsibilities of resource users under 2003 Fort Lauderdale principles; you agree that you will never attempt to identify any participant. This research has been conducted using the UK Biobank Resource and the use of the data is guided by the principles formulated by the UK Biobank.</p> <p><strong>When using downloaded data, please cite corresponding paper and this repository:</strong></p> <ol> <li>Sharapov, S. Z., Tsepilov, Y. A., Klaric, L., Mangino, M., Thareja, G., Shadrina, A. S., … Aulchenko, Y. (2019). Defining the genetic control of human blood plasma N-glycome using genome-wide association study. <em>Human Molecular Genetics</em>. http://doi.org/10.1093/hmg/ddz054</li> <li>Sodbo Sharapov, Yakov Tsepilov, Lucija Klaric, Massimo Mangino, Gaurav Thareja, Mirna Simurina, Concetta Dagostino, Julia Dmitrieva, Marija Vilaj, FranoVuckovic, Tamara Pavic, Jerko Stambuk, Irena Trbojevic-Akmacic, Jasminka Kristic, Jelena Simunovic, Ana Momcilovic, Harry Campbell, Malcolm Dunlop, Susan Farrington, Maria Pucic-Bakovic, Christian Gieger, Massimo Allegri, Edouard Louis, Michel Georges, Karsten Suhre, Tim Spector, Frances MK Williams, Gordan Lauc, Yurii Aulchenko. (2018). Genome-wide association summary statistics for human blood plasma glycome (Version 1) [Data set]. Zenodo. http://doi.org/10.5281/zenodo.1298406</li> </ol> <p><strong>Funding</strong></p> <p>This work was supported by the European Community’s Seventh Framework Programme funded project PainOmics (Grant agreement # 602736) and by the European Structural and Investments funding for the "Croatian National Centre of Research Excellence in Personalized Healthcare" (contract #KK.01.1.1.01.0010).</p> <p>The work of SSh was supported by the Russian Ministry of Science and Education under the 5-100 Excellence Programme.</p> <p>The work of YT was supported by the Federal Agency of Scientific Organizations via the Institute of Cytology and Genetics (project #0324-2018-0017).</p> <p>Karsten Suhre and Gaurav Thareja are supported by ‘Biomedical Research Program’ funds at Weill Cornell Medicine - Qatar, a program funded by the Qatar Foundation. We thank all staff at Weill Cornell Medicine - Qatar and Hamad Medical Corporation, and especially all study participants who made the QMDiab study possible.</p> <p>The SOCCS study was supported by grants from Cancer Research UK (C348/A3758, C348/A8896, C348/ A18927); Scottish Government Chief Scientist Office (K/OPR/2/2/D333, CZB/4/94); Medical Research Council (G0000657-53203, MR/K018647/1); Centre Grant from CORE as part of the Digestive Cancer Campaign (<a href="http://www.corecharity.org.uk">http://www.corecharity.org.uk</a>).</p> <p>TwinsUK is funded by the Wellcome Trust, Medical Research Council, European Union, the National Institute for Health Research (NIHR)-funded BioResource, Clinical Research Facility and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London.</p> <p><strong>Column headers:</strong></p> <ol> <li>SNP: SNP rsID</li> <li>CHR: chromosome</li> <li>POS: position (GRCh37 build) </li> <li>OTHER_ALLELE: reference allele (coded as "0")</li> <li>EFFECT_ALLELE: effective allele (coded as "1")</li> <li>EAF: effective allele frequency </li> <li>N: sample size</li> <li>BETA: effect size of effective allele</li> <li>SE: standard error of effect size</li> <li>PVAL: P-value of association (without GC correction)</li> <li>IMPUTATION: imputation quality</li> </ol>
Genome-wide association summary statistics for human healthspan
<p>The dataset contains genome-wide association summary statistics computed for heathspan. The UKB sub-population of 300,447 genetically Caucasian, British individuals were analyzed. For more details see [1].</p> <p>The data are provided on an "AS-IS" basis, without warranty of any type, expressed or implied, including but not limited to any warranty as to their performance, merchantability, or fitness for any particular purpose. If investigators use these data, any and all consequences are entirely their responsibility. By downloading and using these data, you agree that you will cite the appropriate publication in any communications or publications arising directly or indirectly from these data; for utilisation of data available prior to publication, you agree to respect the requested responsibilities of resource users under 2003 Fort Lauderdale principles; you agree that you will never attempt to identify any participant. This research has been conducted using the UK Biobank Resource and the use of the data is guided by the principles formulated by the UK Biobank.</p> <p><strong>When using downloaded data, please cite corresponding paper and this repository:</strong></p> <ol> <li>Zenin, A., Tsepilov, Y., Sharapov, S., Getmantsev, E., Menshikov, L. I., Fedichev, P. O., & Aulchenko, Y. (2019). Identification of 12 genetic loci associated with human healthspan. <em>Communications Biology</em>, <em>2</em>(1), 41. http://doi.org/10.1038/s42003-019-0290-0</li> <li>Aleksandr Zenin, Yakov Tsepilov, Sodbo Sharapov, Evgeny Getmantsev, Leonid Menshikov, Peter Fedichev, & Yurii Aulchenko. (2018). Genome-wide association summary statistics for human healthspan (Version 1) [Data set]. Zenodo. http://doi.org/10.5281/zenodo.1302861</li> </ol> <p><strong>Funding</strong></p> <p>The work was supported by Russian Ministry of Science and Education under 5-100 Excellence Programme. <br> The work was supported by the Federal Agency of Scientific Organizations via the Institute of Cytology and Genetics (project #0324-2018-0017). <br> This research has been conducted using the UK Biobank Resource. <br> The study has been funded by Gero LLC.</p> <p><strong>Column headers:</strong></p> <ol> <li>SNPID - SNP rsID</li> <li>chr - chromosome</li> <li>pos - position (GRCh37 build / hg19)</li> <li>EA - effective allele (coded as "1")</li> <li>RA - reference allele (coded as "0")</li> <li>EAF - effective allele frequency</li> <li>beta - effect size of effective allele</li> <li>se - standard error of effect size</li> <li>Z - Z-value of association</li> <li>-log10(p-value) - minus log10(P-value) of association</li> </ol>
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.