Ango Hub
Ango Hub is an all-in-one, quality-oriented data annotation platform that AI teams can use. Ango Hub is available on-premise and in the cloud. It allows AI teams and their data annotation workforces to quickly and efficiently annotate their data without compromising quality.
Ango Hub is the only data annotation platform that focuses on quality. It features features that enhance the quality of your annotations. These include a centralized labeling system, a real time issue system, review workflows and sample label libraries. There is also consensus up to 30 on the same asset.
Ango Hub is versatile as well. It supports all data types that your team might require, including image, audio, text and native PDF. There are nearly twenty different labeling tools that you can use to annotate data. Some of these tools are unique to Ango hub, such as rotated bounding box, unlimited conditional questions, label relations and table-based labels for more complicated labeling tasks.
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SKUDONET
SKUDONET provides IT leaders with a cost effective platform that focuses on simplicity and flexibility. It ensures high performance of IT services and security.
Effortlessly enhance the security and continuity of your applications with an open-source ADC that enables you to reduce costs and achieve maximum flexibility in your IT infrastructure.
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Geneyx
Geneyx Analysis offers an all-encompassing solution for managing next-generation sequencing (NGS) data, efficiently transforming FASTQ files into clinical reports tailored for both hospital and commercial laboratories. This cutting-edge platform incorporates machine learning and artificial intelligence capabilities to uncover new biomedical insights, enhancing diagnostic efficiency and reducing turnaround times. By delivering a fully transparent and user-friendly interface, Geneyx Analysis empowers clinicians and researchers with complete control over data interpretation and simplifies the challenges associated with managing in-house bioinformatics workflows. Users can customize protocols to suit various gene panels, exomes, and genomes, while our extensive annotation engine facilitates the analysis of all genetic variants, including structural and copy number variations, as well as regulatory elements. In combination, Geneyx Analysis streamlines the diagnostic journey from sequencer output to finalized report, while also serving as a valuable resource for the discovery of novel variants. This platform not only enhances clinical capabilities but also paves the way for groundbreaking research in genomics.
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Emedgene
Emedgene optimizes the workflows involved in tertiary analysis for rare disease genomics and various germline research endeavors. It is specifically built to enhance the speed and reliability of interpreting, prioritizing, curating, and generating research reports for user-defined variants. By incorporating explainable AI (XAI) and automation, Emedgene boosts efficiency across diverse analysis workflows, including genomes, exomes, virtual panels, and targeted panels. The platform facilitates the integration of laboratory processes and NGS instruments with IT systems, streamlining and securing the entire workflow. With continuous advancements in science, technology, and demand, Emedgene empowers users to stay current by offering cutting-edge knowledge graph features, curation tools, and expert support throughout their research journey. Furthermore, it allows laboratories to increase their throughput without the need for additional personnel, thanks to XAI and automated processes. Ultimately, Emedgene enables the deployment of high-throughput workflows for whole genome sequencing (WGS), whole exome sequencing (WES), virtual panels, or targeted panels that seamlessly fit into the digital framework of any lab. This comprehensive approach ensures that researchers can focus on their discoveries while relying on robust technological support.
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