OORT DataHub
Our decentralized platform streamlines AI data collection and labeling through a worldwide contributor network. By combining crowdsourcing with blockchain technology, we deliver high-quality, traceable datasets.
Platform Highlights:
Worldwide Collection: Tap into global contributors for comprehensive data gathering
Blockchain Security: Every contribution tracked and verified on-chain
Quality Focus: Expert validation ensures exceptional data standards
Platform Benefits:
Rapid scaling of data collection
Complete data providence tracking
Validated datasets ready for AI use
Cost-efficient global operations
Flexible contributor network
How It Works:
Define Your Needs: Create your data collection task
Community Activation: Global contributors notified and start gathering data
Quality Control: Human verification layer validates all contributions
Sample Review: Get dataset sample for approval
Full Delivery: Complete dataset delivered once approved
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Jama Connect
Jama Connect®, a product development platform, uniquely creates Living Requirements™. This digital thread is created through siloed, test, and risk activities to provide end to end compliance, risk mitigation, process improvement, and compliance. Companies creating complex products, systems, and software can now define, align, and execute on what they need. This reduces the time and effort required to prove compliance and saves on rework. You can be sure of success by choosing a solution that is easy-to-use, flexible, and offers support and services that are adoption-oriented.
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VarSeq
VarSeq is a user-friendly and efficient software designed for conducting variant analysis on gene panels, exomes, and complete genomes. This comprehensive software solution simplifies tertiary analysis, allowing users to effortlessly automate their workflows and examine variants across various genomic contexts. With VarSeq, the complexities of genomic data become more manageable, enabling researchers to easily navigate and interpret results. The software features a robust filtering and annotation system that helps users efficiently process extensive variant datasets. By employing a sequence of filters, you can swiftly refine your variant list to highlight those of greatest relevance. Once you establish effective parameters for your analysis, VarSeq allows you to save your filter configurations, facilitating the application of the same analytical approach to different datasets. This automated workflow can be consistently utilized across multiple sample batches, making VarSeq particularly suitable for high-throughput settings. Additionally, real-time filtering capabilities empower users to rapidly prototype and adjust analysis workflows according to their specific needs, enhancing the overall research experience. As a result, VarSeq significantly streamlines the variant analysis process for genetic studies.
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BioTuring Browser
Delve into a vast collection of meticulously curated single-cell transcriptome datasets, as well as your own, using dynamic visualizations and analytical tools. This software is versatile, accommodating multimodal omics, CITE-seq, TCR-seq, and spatial transcriptomics. Engage with the most extensive single-cell expression database globally, where you can access and extract insights from a repository featuring millions of fully annotated cells complete with cell type labels and experimental metadata. Beyond merely serving as a conduit to published research, BioTuring Browser functions as a comprehensive end-to-end solution tailored for your specific single-cell data needs. Easily import your fastq files, count matrices, or Seurat and Scanpy objects to uncover the biological narratives contained within. With an intuitive interface, you can access an extensive array of visualizations and analyses, transforming the process of extracting insights from any curated or personal single-cell dataset into a seamless experience. Additionally, the platform allows for the importation of single-cell CRISPR screening or Perturb-seq data, enabling users to query guide RNA sequences with ease. This functionality not only enhances research capabilities but also facilitates the discovery of novel biological insights.
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