Our bioinformatics consulting services support every step of the multiomics journey. Explore how we help teams move faster, smarter, and with complete analytical confidence.
Explore moreExplore how we support Pharma & Biotech companies in solving critical R & D challenges with bioinformatics.
View moreGAIA® demonstrates superior overall performance in taxonomic classification on long-read metagenomic datasets than alternative solutions.
Read WhitepaperHelping a leading European clinical diagnostics laboratory scale microbiome analysis.
View case studyGINOTM is a secure, cloud-based platform designed to transform NGS data into structured, interpretable results. It performs comprehensive genomic analysis and provides a flexible environment for data exploration and interpretation.
From DNA extraction to variants classification, GINOTM streamlines the entire workflow for genomes, exomes, and panels.
Annotates variants with gene-level functional context, predicted functional impact, population frequencies, and disease-associated variant databases, supporting ACMG-based prioritization.
Enables the creation of custom gene panels for focused analyses of specific genomic regions.
Easily assess variant recurrence across a single batch.
Includes phasing, ancestry inference, and integration with RNA-seq data for allele-specific expression, providing deeper biological context and insight.
Backed by Sequentia Biotech’s expertise in omics and commitment to scientific excellence, GINOTM is more than just a platform—it’s your partner in unlocking the full potential of human genomics.
Unlike other platforms that lock users into rigid workflows, GINO® is built with flexibility and scalability in mind. It evolves in tandem with the rapidly advancing field of genomics, ensuring that users always have access to the latest tools, methodologies, and databases.
Intuitive interface that requires no advanced computational expertise.
Cloud based, modular, and containerized for reproducibility and secure data management.
Designed to be compliant to ensure data privacy and security.
The complexity of genomes (human and non-human), which requires exceptional analytical power.
The heterogeneity and variable quality of omics data, along with the lack of standardized protocols.
The need for robust computational tools to process the sheer volume of data from high-throughput technologies.
The difficulty of translating complex data into applicable results tailored to each stakeholder’s unique needs, which demands the highest level of scientific and technical expertise.
This product is For Research Use Only (RUO). Not for use in diagnostic procedures.
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