Franklin
Genomic intelligence platform for precision medicine
Company profile
Company profile
Genoox is a precision medicine and genomics company that develops platforms for genomic data management and clinical interpretation. The company's flagship product, Franklin, serves as a comprehensive genomic analysis platform designed to help healthcare organizations, laboratories, and researchers interpret genetic variants and translate genomic data into actionable clinical insights. Genoox focuses on enabling precision medicine by providing tools that streamline the analysis of complex genomic information, support variant classification, and facilitate the integration of genomic findings into patient care pathways. The platform is designed to serve clinical geneticists, molecular pathologists, genetic counselors, and research scientists working across various medical specialties. By combining advanced bioinformatics with clinical decision support capabilities, Genoox aims to accelerate the adoption of genomic medicine in routine healthcare settings and support the growing demand for personalized treatment approaches based on individual genetic profiles.
Company description Genoox official website
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01 · Operating footprint
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02 · Flagship portfolio
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Genomic intelligence platform for precision medicine
03 · Research intelligence
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Research
Frontiers in public health · Jan 1, 2026
TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project.Orphanet journal of rare diseases · May 15, 2025
Defining and pursuing diversity in human genetic studies.Nature genetics · Oct 1, 2024
Applying data science methodologies with artificial intelligence variant reinterpretation to map and estimate genetic disorder prevalence utilizing clinical data.American journal of medical genetics. Part A · May 1, 2024
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels.Human genomics · Mar 28, 2023
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe.PloS one · Jan 1, 2023
Clinical validation
NCT06549218 · Sponsor · RECRUITING
Regulatory
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06 · Company updates
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Market context
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
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