This annotation schema is used to annotate data as part of the PINK project. It is based on DCAT for basic Accessibility and enhanced with domain and application specific terms. PINK Annotation Schema The Recommended Metadata for Biological Images (REMBI) are a set of guidelines developed by the bioimaging community as a framework for discussing different aspects of useful sharing of imaging data. In general, REMBI provides a way to explain how your images were generated, providing enough context to allow others to interpret them without reference to external sources. Recommended Metadata for Biological Images | REMBI A lightweight data-centric framework for semantic interoperability. DLite allows to represent data and metadata with simple, but formalised data models, making it possible to decouple the (meta)data from how it is serialised. It includes a rich and easy extendable plugin-system for loading/writing (meta)data to different storage backends (like JSON, BSON, YAML, RDF, MinIO, MongoDB, PostgreSQL, Redis, CSV/Excel, ...). DLite enhances the reusability of storage plugins by a clear separation between data transfer (protocol) and loading/writing. This makes it possible to use the same file-based storage plugin against for instance the local file system or an sftp or http server. Semantic interoperability and automated data transformations is achieved by mapping DLite data models and/or their properties of to classes defined in ontologies. By combining mappings with a library of reusable mapping functions, fully automated and very powerful data transformations and integrations can be achieved. DLite also include a collection of tools for e.g. validation of data models and generation of code for handling of i/o in C and Fortran programs. DLite is written in C, but includes bindings to Python and Fortran. It is commonly used from Python and available under a permissive MIT license. DLite: Lightweight data-centric framework for semantic interoperability Ontology based annotation schema used to annotate DYNCAT data and models. It is based on the Elementary Multiperspective Material Ontology and relevant doman ontologies. DYNCAT Annotation Schema Metadata schema for PEH research studies, developed for the processing of Personal Exposure and Health research data in the Partnership for the Assessment of Risks from Chemicals (PARC) Project. Personal Exposure and Health Metadata Schema (PEH Metadata Schema) Research Activity Identifier (RAiD) is an identifier mechanism designed for research projects and activities. It is persistent and connects existing PIDs for researchers, institutions, outputs and tools together to create a timeline of research activity which makes connecting digital infrastructure, reporting on impact and establishing data provenance clear and easy. RAiD is one of the Identifier Services owned and offered by the Australia Research Data Commons (ARDC), and can be accessed for machine-to-machine service by API integration, using a RAiD service point designated platform, or by manually minting via the RAiD user Dashboard. Research Activity Identifier | RAiD RO-Crate is a community effort to establish a lightweight approach to packaging research data with their metadata. It is based on schema.org annotations in JSON-LD. An RO-Crate is a structured archive of all the items that contributed to the research outcome, including their identifiers, provenance, relations and annotations. RO-Crate | Research Object Crate ToxTemp is a web-accessible template and database designed for documenting in vitro test methods while integrating different readiness levels and a structured review workflow. It was developed initially under the EU-ToxRisk and developed further under RISK-HUNT3R (both EC-funded Horizon 2020 projects). The test method template (ToxTemp) provides a standardized framework for documenting test methods and assessing their readiness status, guided by a structured questionnaire. By offering a user-friendly approach, ToxTemp helps test developers, especially those less familiar with regulatory requirements to describe their assays in sufficient detail. It also facilitates the comparison of different testing methods, including those targeting the same endpoint. Widespread adoption of ToxTemp could not only support test developers by providing clear documentation guidance but also drive a cultural shift toward more consistent and transparent method documentation. ToxTemp: A Standardized Framework and Database for Documenting and Assessing Readiness of In Vitro Test Methods 3.0.0 CodeMeta contributors are creating a minimal metadata schema for science software and code, in JSON and XML. The goal of CodeMeta is to create a concept vocabulary that can be used to standardize the exchange of software metadata across repositories and organizations. CodeMeta The Cell Annotation Platform (CAP) is a centralized, community-driven platform for the creation, exploration, and storage of cell annotations for single-cell RNA-sequencing (scRNA-seq) datasets. CAP enables scientists to upload their work to private collaborative workspaces, refine and visualize their annotations using the molecular data, and publish their findings with a citable DOI. Cell Annotation Platform 1.0.2 The Cell Annotation Platform (CAP) is a community-driven platform for creating, exploring, and storing cell annotations. It provides infrastructure to accumulate, share, and analyze annotation terms with associated molecular signatures to interpret cellular identities, encouraging researchers to converge on consensus nomenclature.The platform requires HDF5-backed AnnData files formatted according to a standard schema.The required fields are defined in CAP-AnnData-Schema. Data schema of Cell Annotation Platform 1.0.2 CELLxGENE aims to support the publication, sharing, and exploration of single-cell datasets. Building on those published datasets, CELLxGENE seeks to create references of the phenotypes and composition of cells that make up human tissues. CELLxGENE requires all datasets to adhere to the schema so that it can enable searching, filtering, and integration of datasets it hosts.The schema additionally describes how the dataset, genes, and cells are annotated to describe the biological and technical characteristics of the data. Single Cell Curation Schema 4.0.0 A general, open-standard schema for cell annotations and related metadata. This effort is part of scFAIR, an initiative to standardize single-cell genomics metadata. Cell Annotation Schema 1.1.0 Investigation Study Assay JSON (ISA-JSON) describes the ISA Abstract Model reference implementation specified using the JavaScript Object Notation (JSON) format, a text format for serializing structured data. The ISA model consists of three core entities to capture experimental metadata: investigation, study and assay. The extensible, hierarchical structure of this model enables the representation of studies employing one or a combination of technologies, focusing on the description of its experimental metadata (i.e. sample characteristics, technology and measurement types, sample-to-data relationships). Investigation Study Assay JSON | ISA-JSON This FER describes a metadata schema for the PRIDE Affinity Proteomics (PRIDE-AP) which is a new archive within the PRIDE repository dedicated to advancing the field of affinity proteomics (AP) by providing a centralised infrastructure for openly accessible datasets generated using AP platforms such as Olink and SomaLogic (the SomaScan platform). PRIDE-APM | PRoteomics IDEntifications database Affinity Proteomics metadata schema The OECD Omics Reporting Framework (OORF) was developed to increase transparency in the reporting of Omics data used in regulatory toxicology, and aid regulatory uptake while remaining sufficiently flexible to allow technologies to evolve. It is a harmonized combination of the Transcriptomics Reporting Framework (TRF) and a Metabolomics Reporting Framework (MRF), with four types of reporting modules: (i) The Study Summary Reporting Module (SSRM) provides a high-level overview of the regulatory toxicology and Omics experiment, (ii) The Toxicology Experiment Reporting Module (TERM) reports the key descriptors of the in vivo or in vitro toxicology study, (iii) Data Acquisition and Processing Reporting Modules (DAPRM) report descriptions of the Omics assays, data acquisition and associated data, (iv) Data Analysis Reporting Modules (DARM) describe the statistical analysis that has been undertaken in the Omics study. Guidance documents describe each of the reporting modules in detail alongside associated templates are available via the website. OECD Omics Reporting Framework | OORF A structured schema that defines tables, fields, data types, and relationships used in the ChEMBL database—a manually curated repository of bioactive, drug-like compounds with assay results and target bioactivities—ensuring consistent interpretation and interoperability across systems. ChEMBL Database Schema This document defines the core components of the Observation data model that are necessary to perform data discovery when querying data centers for astronomical observations of interest. It exposes use-cases to be carried out, explains the model and provides guidelines for its implementation as a data access service based on the Table Access Protocol (TAP). It aims at providing a simple model easy to understand and to implement by data providers that wish to publish their data into the Virtual Observatory. This interface integrates data modeling and data access aspects in a single service and is named ObsTAP. In this document, the Observation Data Model Core Components (ObsCoreDM) defines the core components of queryable metadata required for global discovery of observational data. It is meant to allow a single query to be posed to TAP services at multiple sites to perform global data discovery without having to understand the details of the services present at each site. It defines a minimal set of basic metadata and thus allows for a reasonable cost of implementation by data providers. Observation Data Model Core Components and its Implementation in the Table Access Protocol | ObsCoreDM MINSEQE describes the Minimum Information about a high-throughput nucleotide SEQuencing Experiment that is needed to enable the unambiguous interpretation and facilitate reproduction of the results of the experiment. By analogy to the MIAME guidelines for microarray experiments, adherence to the MINSEQE guidelines will improve integration of multiple experiments across different modalities, thereby maximising the value of high-throughput research. Metadata collection template includes critical information such as: 1) The description of the biological system, samples, and the experimental variables being studied, 2) The sequence read data for each assay, 3) The ‘final’ processed (or summary) data for the set of assays in the study, 4) General information about the experiment and sample-data relationships, and 5) Essential experimental and data processing protocols. NOTE: The provided resource documentation at Zenodo contains version 1.0 of the MINSEQE guidelines, which originated from discussions at the March 2008 Functional Genomics Data (FGED) Society-hosted workshop held in Berkeley, CA, USA. The FGED Society was operational from 1999-2021. Minimal Information about a high throughput SEQuencing Experiment | MINSEQE Metadata schema defined in the framework of the European standard data model for sea surface current velocity data measured by High Frequency Radar (HFR) systems. The European standard data model specifies the structured representation of metadata and data for different levels of sea surface velocity data products for HFR data implementation in European marine data infrastructures, describing attributes of metadata and data in terms of semantics, syntax and optionality. The European standard data model also specifies the Quality control (QC) procedures to be applied to sea surface velocity data from HFR for enabling their distribution towards the marine data portals. EHN-HFRv-MS | European High Frequency Radar Node Metadata Schema for Sea Surface Current Velocity Data v2.0.0 The OceanGliders Metadata Schema specifies the file format for gliders data. It builds on and extends the EGO data model, promoting interoperability across global glider deployments. OceanGliders-MS | OceanGliders Metadata Schema v1.0.0 The U.S. IOOS National Glider Data Assembly Center Metadata Schema specifies the NetCDF file format specification used by the U.S. IOOS National Glider Data Assembly Center to archive and distribute real-time and delayed-mode glider data sets. IOOS-NGDAC-MS | U.S. IOOS National Glider Data Assembly Center Metadata Schema v2.0.0 The Attribute Convention for Data Discovery (ACDD) describes attributes recommended for describing a netCDF dataset to discovery systems such as Digital Libraries. THREDDS and other tools can use these attributes to extract metadata from datasets, and exporting to Dublin Core, DIF, ADN, FGDC, ISO 19115 and other metadata formats. This will help systems and users locate and use data efficiently. The NetCDF User Guide (NUG) provides basic recommendations for creating netCDF files; the netCDF Climate and Forecast Metadata Conventions (CF) provides more specific guidance. The ACDD builds upon and is compatible with these conventions; it may refine the definition of some terms in those conventions, but does not preclude the use of any attributes defined by the NUG or CF. ACDD | Attribute Convention for Data Discovery v1.3.0 NetCDF compliant with Climate and Forecasts (CF) Metadata Convention v1.10 NetCDF CF-1.10 EGO gliders Metadata Schema specifies the NetCDF file format of EGO-gliders that is used to distribute glider data, metadata and technical data. It documents the standards used therein; this includes naming conventions as well as metadata content. It was initiated in October 2012, based on OceanSITES, Argo and ANFOG user's manuals. EGO-GLIDER-MS | EGO gliders Metadata Schema v1.15.0 FAIR Digital Objects for images (iFDO) is a metadata schema aimed at creating standardized metadata for marine research images (photos and videos). The goal of this metadata schema is to enable all stakeholders to create iFDO files according to their research needs and use cases and to provide hints as to how the iFDO creation can be conducted by open source software. The application of iFDO results in metadata for image data sets that adheres to the international iFDO standard, that enables efficient analysis and browsing of large image data sets in tools like QGIS and BIIGLE. Achieving FAIRness and Openness of (marine) image data requires structured and standardised metadata on the image data itself and the visual and semantic image data content. This metadata shall be provided in the form of FAIR digital objects (FDOs). iFDOs consist of various metadata fields. Some are required, some are recommended, some are optional. The iFDOs standard aspires to be the most complete standard that allows to bridge between existing standards (like DublinCore, Audubon, SmartarID, PDS4) while filling gaps of those. All image metadata shall be stored in one image FAIR digital object (iFDO) file. This file shall contain all iFDO metadata fields. It does not contain the actual image data, only references to it through persistent identifiers. iFDO | FAIR Digital Objects for images v1.0.0 Fast Healthcare Interoperability Resources (FHIR) is a standardized framework developed by HL7 (Health Level Seven International) for exchanging, sharing, and integrating healthcare information. It enables interoperability between different healthcare systems by using modern web-based technologies like RESTful APIs, JSON, XML, and RDF. FHIR HL7 Standard 5.0.0 2.3.0 PAV is a lightweight ontology for tracking Provenance, Authoring and Versioning. PAV specializes the W3C provenance ontology PROV-O in order to describe authorship, curation and digital creation of online resources. This ontology describes the defined PAV properties and their usage. Note that PAV does not define any explicit classes or domain/ranges, as every property is meant to be used directly on the described online resource. Provenance, Authoring and Versioning Ontology | PAV The Copernicus Marine In Situ TAC Metadata Schema specifies the NetCDF file format of Copernicus Marine In Situ TAC used to distribute ocean In Situ data and metadata. It documents the standards used herein; this includes naming conventions as well as metadata content. It was initiated in March 2019, based on OceanSITES and Argo user's manuals. CMS-INSTAC-MS | Copernicus Marine In Situ TAC Metadata Schema EMSO Metadata Specifications, which define how datasets should be structured to be compliant with EMSO's data policy. The specifications apply to both NetCDF files and datasets served through ERDDAP. EMSO Metadata Schema NetCDF compliant with Climate and Forecasts (CF) Metadata Convention v1.6 NetCDF CF-1.6 1.6.0 This is the template used when adding a Wordpress article. WP-MS | Wordpress Metadata Schema The FDSN StationXML schema defines an XML representation of the most important and commonly-used structures of SEED 2.4 metadata with enhancements. This format is intended primarily for the archival and exchange of seismological time series data and related metadata. The goal is to allow mapping between SEED 2.4 dataless SEED volumes and this schema with as little transformation or loss of information as possible, while at the same time simplifying station metadata representation when possible. Also, content and clarification has been added where lacking in the SEED standard. When definitions and usage are under-defined the SEED manual should be referred to for clarification. International Federation of Digital Seismograph Networks StationXML | FDSN StationXML Defined by the HBM4EU project to describe human biomonitoring metadata. The template is an extension of the IPCheM metadata schema which also covers environmental data. IPCheM metadata schema extension by HBM4EU Metadata schema used for measurements or modelling of air pollutant concentrations. EEA assessment methods metadata schema for air quality Metadata schema that archives genomics data submitted by the research community. GEODD | GEO DataSet descriptors Basic annotation schema used in Tripper for handling data and metadata in a knowledge base. Based on DCAT-AP, so compatible with all DCAT-aware services. Tripper Annotation Schema CLARIN offers a solution for the modelling, authoring and exploitation of metadata. This solution is implemented as a set of standards, registries, definitions and workflows which together form the Component Metadata Infrastructure (CMDI). The Component Metadata Infrastructure (CMDI) provides a standard for metadata within CLARIN. CMDI | The Component Metadata Infrastructure The OECD Harmonised Templates (OHTs) are standard data formats for reporting information on chemicals to determine their properties or effects on human health and the environment (e.g. toxicokinetics, skin irritation, repeated dose toxicity, biodegradation in soil, metabolism of residues in crops, etc.) and also to describe their use and related exposure to workers, consumers and the environment. Data and information on the use of and exposure to chemicals: 301 Use and exposure information: Manufacture. OHT-301 | OECD harmonised templates IGS Site Log v2.0 is the standard adopted by the International GNSS Service to exchange the history of GNSS site installation IGS-Site-Log-2.0 | International GNSS Service Site Information Form v2.0 Bioschemas aims to improve data interoperability in the life sciences. It does this by encouraging the use of Schema.org markup within web pages, so that their websites and services contain machine-processable metadata that is consistently structured. This structured information makes it easier to discover, collate and analyse distributed data. As well as extending Schema.org with life sciences specific types, the Bioschemas community has developed a group of specifications that provide guidelines to facilitate a more consistent adoption of Schema.org markup within the life sciences. Bioschemas Deploys PDBx/mmCIF is a dictionary of data archiving macromolecule crystallographic experiments and their results. macromolecular Crystallographic Information File | PDBx/mmCIF The BADM (Biological, Ancillary, Disturbance and Metadata) is a protocol standardized across eddy covariance networks (AmeriFlux, ICOS, Fluxnet and more) to report station characteristics, sensors' deployment and other metadata, as well as to submit discontinuous variables measured in dedicated campaigns not included in the main dataset. Many information are constrained on a vocabulary list. The information can be entered via an Excel spreadsheet, a csv file, and, in the ICOS context, an online tool, and they are exported to the user in a BIF (for BADM Interchange Format) format that enables the BADM data to be read programmatically. The BIF format consists of 5 columns: site ID, group ID, variable group name, variable name, and data value. A variable group is a set of variables that are reported together (e.g. a variable value, the date it was collected, and the method used to collect it). Sites may report multiple instances of the same variable group associated with different measurements collected over time, plant species, soil depths, collection methods, etc. The group ID uniquely identifies the data belonging to the same instance of a reported variable group. The variable names and data value provide the details of the reported data within a variable group. BADM | Biological, Ancillary, Disturbance and Metadata protocol NetCDF compliant with Climate and Forecasts (CF) Metadata Convention v1.11 NetCDF CF-1.11 NetCDF compliant with Climate and Forecasts (CF) Metadata Convention v1.7 NetCDF CF-1.7 Metadata schema for nanosafety NanoSSch | Nanosafety Metadata schema The specification defines the architecture, metadata structure and schema, API and validation rules for a FAIR Data Point. FDPspec | FAIR Data Point specification A template that captures detailed information about reagents used in experiments, such as Image Histology and Metabolomics Mass Spectrometry. It includes multiple tabs in the reagents.xlsx file to accommodate platform-specific details, addressing the varying reagent requirements across platforms. It is used to define and annotate reagents not covered by other reagent templates. This same template also appears on the web with other names like 'Other Reagents'. ImmPort Reagents Template Version 3.36 A template that captures information on samples, reagents, and results from HLA typing experiments, linking samples, experiments, and assay results by defining and annotating the assay data for each sample. Supports the description of new experiments and biological samples or the integration of new assay results with existing ImmPort content. Requires experiment sample IDs to be unique and not already stored in ImmPort. This same template also appears on the web with other names like 'HLA Experiment' and 'HLA Experiment Sample(s)'. ImmPort HLA Typing Experiment Sample Template Version 3.36 An optional template designed to document groups of reagents used collectively in assays. It enables researchers to define and organize reagents as sets, streamlining reference and documentation processes for assay workflows. This same template also appears on the web with other names like 'Reagent Sets' and 'Reagent Set'. ImmPort Reagents Set Template Version 3.36 A template that captures samples, reagents, and results from RNA sequencing experiments. Links samples, experiments, and assay results, supporting the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Requires experiment sample IDs to be unique and not previously stored in ImmPort. This same template also appears on the web with other names like 'RNA Sequencing Transcripts Results Experiment Sample(s)'. ImmPort RNA Sequencing Experiment Sample Template Version 3.36 A template that documents in vitro modifications applied to samples, including the addition of molecules, temperature adjustments, and treatment durations. It supports three types of treatments: amount of agent, duration, and temperature. Treatments are required for experiment samples and optional for biological samples. ImmPort Treatments Template Version 3.36 A template that captures samples, reagents, treatments, and results from MBAA experiments. It defines and annotates assay platforms, including a row for each analyte assayed by the MBAA array. ImmPort Multiplex Bead Array Assays Reagents Template Version 3.36 A template that records detailed information about human subjects from whom samples are collected for analysis. It defines and annotates key elements, including demographics and subject-arm links within a study. This same template also appears on the web with other names like 'Subject Humans' and 'Subject Human'. ImmPort Human Subjects Template Version 3.36 A template that defines and annotates key study subject elements, including demographics and subject-arm links within a study. This same template also appears on the web with other names like 'Subject Animals' and 'Subject Animal'. ImmPort Animal Subjects Template Version 3.36 A template that structures and annotates standard curves for interpretation within ImmPort, linking control sample concentrations and MFI to analyte concentrations in experiment samples. Standard curves must always be new and unique, while the associated experiment may be new or pre-defined. This template facilitates searching and display of results. ImmPort Standard Curves Template Version 3.36 A template that captures detailed information about the reagents used in a PCR experiment. This same template also appears on the web with other names like 'PCR Reagent'. ImmPort PCR Reagents Template Version 3.36 A template that captures detailed information about the reagents used in a HAI assays. These include the cell type used. The viral stain and concentration would be defined in the treatments.txt template. This same template also appears on the web with other names like 'HAI Reagent'. ImmPort Hemaglutinnation Inhibition Reagents Template Version 3.36 A template that captures detailed information about the reagents used in a HLA typing experiment. This same template also appears on the web with other names like 'HLA Typing System Reagents'. ImmPort HLA Typing Reagents Template Version 3.36 A template that defines and annotates assay platforms for KIR typing and captures detailed information about the reagents used, which are linked to KIR experiment sample records. This same template also appears on the web with other names like 'KIR Typing System Reagents'. ImmPort KIR Typing Reagents Template Version 3.36 A template that defines and annotates microarrays assay platforms, capturing detailed information about the reagents used in Gene Expression and Genotyping experiments. This same template also appears on the web with other names like 'Array Reagent'. ImmPort Array Reagents Template Version 3.36 A template that captures captures detailed information about the reagents used in RNA sequencing experiments and defines and annotates the assay platforms utilized for sequencing. This same template also appears on the web with other names like 'Sequencing Reagent'. ImmPort RNA Sequencing Reagents Template Version 3.36 A template that captures detailed information about the antibody reagents used in flow cytometry experiments, defining and annotating their usage. This same template also appears on the web with other names like 'Flow Cytometry Reagent'. ImmPort Flow Cytometry Reagents Template Version 3.36 A template that captures detailed information about the reagents used in neutralizing antibody titer experiments. It defines and annotates reagents, including cell types and antibodies, particularly for experiments employing an ELISA approach. This same template also appears on the web with other names like 'Neutralizing Antibody Titer Reagent'. ImmPort Neutralizing Antibody Titer Reagents Template Version 3.36 A template that defines and annotates detailed information about the mass tagged antibody reagents used in a CyTOF (Mass cytometry) experiment. This same template also appears on the web with other names like 'Mass Cytometry Reagent'. ImmPort CyTOF Reagents Template Version 3.36 A template that lists and annotates protocols associated with lab tests, which may include PDF, Word, Excel, or other file types. It links protocol documents to studies, subjects, biological samples, or experiments. This same template also appears on the web with other names like 'Protocol'. ImmPort Protocols Template Version 3.36 A template that defines and annotates the antibody reagents assay platforms for ELISA experiment. This same template also appears on the web with other names like 'ELISA Reagent'. ImmPort ELISA Reagents Template Version 3.36 A template that lists and annotates results associated with experiments, including assay outcomes linked to samples and experiments. Results can be in various file formats, such as PDF, Word, or Excel. This same template also appears on the web with other names like 'RNA Sequencing Transcripts Results'. ImmPort RNA Sequencing Results Template Version 3.36 A template that captures information on public repository names and accessions, allowing one or more to be linked to an experiment sample. This same template also appears on the web with other names like 'Public Repositories'. ImmPort Public Repository Template Version 3.36 An optional template that enables updates to a study's design after the initial design is uploaded, including adding files, publications, or subjects. It defines and annotates study elements, such as weblinks and publications, that can be modified or added later. This same template also appears on the web with other names like 'Study Design Edit'. ImmPort Edit Study Design Template Version 3.36 A template that captures samples, reagents, and results from QRT-PCR experiments. It links samples, experiments, and assay results, supporting multiple analyte results per sample by duplicating columns like 'Entrez Gene ID' and 'Threshold Cycles (Ct).' The template allows for the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort, with required details provided for any new biological samples or experiments. ImmPort Quantitative PCR Experiment Sample Template Version 3.36 A template that captures samples, reagents, and results for experiment types not characterized by other ImmPort templates. It links samples, experiments, and assay results, supporting the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort, with required details provided for any new biological samples or experiments. This template ensures flexibility when no specific experiment template is available. This same template also appears on the web with other names like 'Other' and 'Other Experiment Sample'. ImmPort Experiment Sample Template Version 3.36 A template that captures samples, reagents, and results from neutralizing antibody titer experiments. It links samples, experiments, and assay results, supporting multiple analyte results per sample by duplicating relevant columns such as 'Virus Strain' and 'Titration Dilution Value.' The template accommodates new experiments and biological samples or integrates assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort, with required details provided for any new biological samples or experiments. ImmPort Neutralizing Antibody Titer Experiment Sample Template Version 3.36 A template that describes Multiplex Bead Array Assays (MBAA) results in a structure that can be interpreted by ImmPort to facilitate searching and display of results. ImmPort Multiplex Bead Array Assays Results Template Version 3.36 A template that captures samples, reagents, treatments, and results from Multiplex Bead Array Assays (MBAA) experiments. It links samples, experiments, and assay results, supporting the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort. If the biological sample or experiment is new, required details must be provided, ensuring flexibility in linking new and existing content. ImmPort Multiplex Bead Array Assays Experiment Sample Template Version 3.36 A template that structures proteomics mass spectrometry assay results for interpretation, searching, and display within ImmPort. It links samples, experiments, and results, supporting multiple intensity results per assayed sample. This same template also appears on the web with other names like 'Mass Spectrometry Proteomic Results' and 'Proteomics Mass Spectrometry Assays Results'. ImmPort Proteomics Mass Spectrometry Results Template Version 3.36 A template that captures samples, reagents, and results from proteomics mass spectrometry experiments. It links samples, experiments, and assay results, enabling the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort. If the biological sample or experiment is new, required details must be provided, ensuring flexibility in linking new and existing content. This same template also appears on the web with other names like 'Mass Spectrometry Experiment Sample'. ImmPort Proteomics Mass Spectrometry Experiment Sample Template Version 3.36 A template that captures samples, reagents, and results from metabolomics mass spectrometry experiments. It links samples, experiments, and assay results, allowing for the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not previously stored in ImmPort. If the biological sample or experiment is new, required details must be provided, ensuring flexibility in linking new and existing content. This same template also appears on the web with other names like 'Mass Spectrometry Experiment Sample'. ImmPort Metabolomics Mass Spectrometry Experiment Template Version 3.36 A template that describes Metabolomics Mass Spectrometry Assay results in a structure that can be interpreted by ImmPort to facilitate searching and display of results. This same template also appears on the web with other names like 'Mass Spectrometry Metabolomic Results'. ImmPort Metabolomics Mass Spectrometry Results Template Version 3.36 A template that defines and annotates the lab test panels, the lab tests and results. This template combines the functions of the legacy lab test panels and lab test results templates into a single template. The biological sample and the lab test panel can be either new or pre-defined in this template. Any combination is acceptable. The only restriction is that the biological sample is the key to template and must be unique within the template. This same template also appears on the web with other names like 'Lab Tests'. ImmPort Clinical Lab Test Template Version 3.36 A template to describe KIR typing results in a format to facilitate sharing of results. This same template also appears on the web with other names like 'KIR Typing'. ImmPort KIR Typing Results Template Version 3.36 A template that captures samples, reagents, and results from KIR experiments. It links samples, experiments, and assay results, supporting the description of new experiments and biological samples or the integration of assay results with existing ImmPort content. Experiment sample IDs must be unique and not already stored in ImmPort. If the biological sample or experiment is new, required details must be provided, ensuring flexibility in linking new and existing content. ImmPort KIR Experiment Template Version 3.36 A template to capture and annotate the results of an ELISA (Enzyme-Linked Immunosorbent Assay) experiment, linking the biological samples, experiments, and assay results together. This template allows users to describe new experiments and biological samples or link existing ones in ImmPort with their respective assay results. Multiple analyte results can be reported for each assayed sample by duplicating the necessary columns, such as 'Analyte', 'Calculated Concentration Value', and 'Calculated Concentration Unit', to describe each result. Each experiment sample entry must have a unique ID that is not already stored in ImmPort. ImmPort ELISA Experiment Sample Template Version 3.36 A template that defines and annotates the assay results for a sample by linking sample, experiment, and results together. More than one analyte's results per assayed sample may be reported by copying the group of columns 'Analyte', 'Number Of Spots Per Well', and 'Cell number per well Value', 'Cell number per well Unit' needed to describe each assay result. The experiment samples template allows you to describe to ImmPort new experiments and biological samples or link experiments and biological samples stored in ImmPort with assay results. All of the experiment sample IDs in the template must always be unique in the template and must not already be stored in ImmPort. The biological sample and the experiment in the template may be new or they both may be new. ImmPort ELISPOT Experiment Sample Template Version 3.36 A template to describe and annotate the results of CyTOF (Cytometry by Time-of-Flight) experiments, linking biological samples, experimental details, and assay outcomes in the ImmPort system. The template provides a flexible way to either document new experiments and biological samples or connect existing ones with new assay results. Each experiment sample entry must have a unique ID, ensuring that it is not already stored in ImmPort. ImmPort CyTOF Experiment Sample Template Version 3.36 A template that captures the study indicated interventions, concomitant medications, and substance use for subjects in a study. ImmPort Intervention Template Version 3.36 A template that captures samples, reagents, and results from image histology experiments. It links samples, experiments, and assay results, supporting the description of new or existing experiments and biological samples. Experiment sample IDs must be unique and not already stored in ImmPort. ImmPort Image Histology Experiment Sample Template Version 3.36 A template that reports adverse events recorded for subjects in a study. ImmPort Adverse Events Template Version 3.36 A template that captures and annotates assay results from HLA typing experiments by linking samples, reagents, and results to experiments. This same template also appears on the web with other names like 'HLA Typing'. ImmPort HLA Typing Results Template Version 3.36 A template that defines and annotates assessment panels and their components, which represent responses or results recorded in Case Report Forms (CRFs) linked to a study. It captures essential fields, including Subject ID, Panel ID, User Defined ID, Planned Visit ID, Component Name, and Study Day, allowing users to define both panels and components in a single form. Panels can be new or pre-defined, with any combination allowed as long as the Assessment Panel ID is unique within the template. ImmPort Assessment Template Version 3.36 A template that captures essential details for assessment components, including User Defined ID, Assessment Panel ID, Subject ID, Planned Visit ID, Name, and Study Day. Assessments can be new or pre-defined, with any combination allowed, provided the Assessment Panel ID is unique within the template. ImmPort Assessment Component Template Version 3.36 A template that captures the User Defined ID, Study ID, and Name for assessment panels, allowing panels to be new or pre-defined in any combination. The only requirement is that the Assessment Panel ID must be unique within the template. ImmPort Assessment Panel Template Version 3.36 A template that describes a study’s essential elements, including title, goals, endpoints, criteria for participation, subject grouping (arms or cohorts), personnel, planned visits, and protocols, all within a single worksheet. It defines key aspects such as purpose, grouping, schedule of events, and references. After defining a study in ImmPort, additional details can be added using the study_design_edit template. The Basic Study Design template is organized into several sections or compound templates to comprehensively capture study design and protocol information. ImmPort Basic Study Design Template Version 3.36 A legacy template that defines and annotates the types of samples derived from study subjects and when during the study schedule the sample was derived. The function of this template is also captured in the experiment samples template. This template will continue to be supported for the foreseeable future to support backward compatibility. ImmPort Biological Samples Template Version 3.36 A template defines and annotates control samples used in MBAA assays. It specifies that control samples, which are not assumed to be of biological origin, must always be new, while the associated experiment can be new or pre-defined. Each control sample serves as a unique key within the template. This same template also appears on the web with other names like 'Control Sample'. ImmPort Control Samples Template Version 3.36 A legacy template that defines and annotates the mechanistic assays performed on samples, by describing the type of experiment, measurement technique and protocols used in the experiment. The function of this template is also captured in the experiment samples template. This template will continue to be supported for the foreseeable future to support backward compatibility. ImmPort Experiments Template Version 3.36 A template that defines and annotates the antibody reagents assay platforms for ELISPOT experiment. This same template also appears on the web with other names like 'ELISPOT Reagent'. ImmPort ELISPOT Reagents Template Version 3.36 A template that captures and annotates the assay results for a sample by linking sample, experiment, and interpreted results together. It allows users to describe CyTOF (Mass Cytometry) results in a format to facilitate sharing of results. ImmPort CyTOF Derived Data Template Version 3.36 A template that captures and annotates assay results for a sample by linking the sample, experiment, and interpreted results, providing a standardized format to facilitate the sharing of flow cytometry results. ImmPort Flow Cytometry Derived Data Template Version 3.36 A template that captures and annotates samples, reagents, and results from flow cytometry experiments by linking samples, experiments, and assay results. This template supports describing new experiments and biological samples or connecting existing ImmPort experiments and biological samples to assay results. It offers flexibility in linking new and existing ImmPort content, with key guidelines to follow: all experiment sample IDs in the template must be unique and not already stored in ImmPort. Both the biological sample and the experiment in the template can be new, or either one can already exist in ImmPort. This same template also appears on the web with other names like 'Flow Cytometry Experiment Samples'. ImmPort Flow Cytometry Experiment Sample Template Version 3.36