Products

Omicost is the best way to monitor, analyze, and optimize your genomics workflows.

NRGene is a Genomics company that provides turn-key solutions to leading breeding companies. Using advanced algorithmics

DNAnexus Titan™ powers the future of genomics research and clinical pipelines with trusted, high-performance data analysis solutions.

Character Biosciences is a platform that merges genomics with clinical data and AI technology, focusing on patients affected by AMD.

Lantern Pharma is a clinical stage biopharma company developing precision oncology therapies leveraging A.I., machine learning, and genomics

Station X develops software for scientists and clinicians who work with human genomics data in either research or clinical settings.

Canomiks is the first technology company using Genomics, Bioinformatics, and an AI-based technology platform to test and certify biological efficacy and safety of ingredients and formulations.

BC Platforms is a world leader in providing powerful genomic data management and analysis solutions to address some of the biggest healthcare challenges today by leveraging the convergence of genomics and healthcare information technologies.

proprietary mitochondrial-based small molecule therapies and diagnostic biomarkers that offer genetic technologies, enabling the healthcare industry to harness the power of genomics for precise healthcare interventions and better overall well-being

EggNOG is an advanced AI-powered platform designed to streamline and enhance the process of protein sequence analysis and functional annotation. By leveraging a comprehensive database of orthologous groups, EggNOG enables researchers to predict gene functions, identify evolutionary relationships, and gain insights into the biological roles of proteins across various organisms. This tool is invaluable for bioinformatics studies, comparative genomics, and evolutionary biology research. Key Featur

VE3’s Genomix is a secure, cloud-based platform designed for clinical and research genomics. It supports NHS Secure Data Environments and global standards, combining data management, AI-driven insights, and flexible workflows in one place. From rare disease diagnostics to multi-omics research, Genomix helps teams work faster, smarter, and together.

VariantSpark is an advanced machine learning framework designed to analyze ultra-high dimensional datasets, particularly in genomics and clinical research. Built upon Apache Spark, it efficiently processes vast datasets containing millions of samples and features, enabling rapid and accurate insights into complex biological data. By leveraging the Random Forest algorithm, VariantSpark identifies intricate interactions between features, uncovering predictive markers that traditional methods might

Talus Bio is a biotechnology company specializing in the discovery and development of therapeutics targeting previously undruggable transcription factors—proteins that regulate gene expression and are implicated in various diseases, including cancer, diabetes, and neurological conditions. Founded in 2020 and based in Seattle, Talus Bio integrates advanced proteomics, synthetic chemistry, artificial intelligence, and computational biology to engineer and analyze drugs, proteins, and genomics at a

Noetik is an AI-native biotechnology company dedicated to revolutionizing cancer treatment through the discovery and development of precision immunotherapies. By integrating advanced machine learning techniques with extensive human multimodal data—including genomics, transcriptomics, and proteomics—Noetik aims to construct foundational models of cell and tissue biology. This innovative approach enables a deeper understanding of tumor-immune interactions, facilitating the identification of novel

BasePair is a SaaS platform for genomic data analysis and visualization that can be used for multitude of application areas across epigenetics, genomics, transcriptomics and others. Bioinformaticians can leverage the powerful CLI or APIs to scale and automate their validated workflows. The platform itself abstracts away the dev ops component of deploying NGS pipelines on AWS (security, access controls, audit trail, instance optimization etc), accelerating the migration and scaling of workflows

Owkin is a French-American startup that uses AI and machine learning to augment medical and biology research. Its proprietary platform, Owkin Socrates, uses machine learning technology to integrate biomedical images, genomics and clinical data to discover biomarkers and mechanisms associated with diseases and treatment outcomes. The company develops scientific collaborations with top-tier medical institutions and partners with leading pharmaceutical companies. Owkin has developed a state-of-the-

Introducing VIA – a complete and integrated solution for the visualization, interpretation and reporting of genomic variants. Existing data analysis solutions for genomics are laborious, time-consuming and incomplete. You have to manage various systems, navigate complex workflows and spend inordinate amounts of time hunting for annotations and creating data visualizations. Good news: those days are over. VIA software radically simplifies your sample-to-report workflow and empowers you to delive

We are all about innovation at Leap of Faith Technologies and are developing tools to help you develop and test your latest innovation in informatics. Our Genomic Archiving and Communication Systems (GACS) is available for you to use to speed the development of your latest innovation in genomics. Our GACS environment is cloud-hosted and has a fully functional FHIR API that can be used to support real clinical scenarios. The system includes a database of genomic and clinical resources that can be

Hugenomic Nanopolish is an accelerated software solution designed for ultra-fast signal-level analysis of large datasets from Oxford Nanopore sequencing. By leveraging FPGA technology, it significantly reduces computation times, enabling the processing of over 800,000 long reads in approximately three hours. Key Features and Functionality: - Accelerated Event Alignment: Utilizes FPGA acceleration to expedite the eventalign tool, transforming processes that traditionally took days into mere ho

Storm by Stanford is an advanced computational platform designed to facilitate the analysis and interpretation of complex genomic data. It offers researchers a suite of tools to process, visualize, and derive insights from large-scale genetic datasets efficiently. Key Features and Functionality: - Data Processing: Streamlines the handling of extensive genomic datasets, ensuring accurate and rapid analysis. - Visualization Tools: Provides interactive visual representations of genetic informatio