Who we work with

overview

Enhancing discovery with bioinformatics enabling technologies and expertise

Our bioinformatics services and solutions empower academic and research institutions to maximize the value of their omics data; from experimental design support and sequencing to advanced data analysis, interpretation, and visualization.
We help researchers generate robust, reproducible, and insightful results, regardless of project scale, organism, or scientific domain.

Bioinformatics Consulting and Software for Academic Research Institutions

services

Our Services for Academic and Research Institutions

Whether you require tailored consulting, custom software development, or ready-to-use analysis solutions, our team provides the expertise and technology to support your research

Bioinformatics consulting

Maximize the value of your omics data through our bioinformatics expertise.

Custom software development

Tailored bioinformatics pipelines and data visualization dashboards designed to meet your specific needs.

Sequencing services

High-quality NGS data generation seamlessly integrated with downstream bioinformatics analysis.

Training programs

In-person or remote sessions designed to equip researchers with the skills and knowledge to manage and analyze omics data effectively.

propietary SOLUTIONS

Solutions for Academic and Research Institutions

GAIA

Universal Metagenomic Analysis

GAIA® is a cloud-based bioinformatics solution designed for fast and precise metagenomic analysis. It transforms complex sequencing data from any sample source into clear, actionable microbial insights.

AIR

RNA-Seq Expression Analysis

AIR® simplifies transcriptomic data analysis with an intuitive cloud-based platform that delivers accurate differential expression and functional enrichment results across any annotated species, enabling effortless access to advanced RNA-Seq insights.

GINO

Human Variant Interpretation

GINO™ performs secure, cloud-based genomic analyses, providing precise variant classification based on scientific evidence.

BATCHX

No-Code Bioinformatics Platform

BatchX™ is a cloud-based no-code platform that enables users to run, manage, and share bioinformatics tools and pipelines securely and at scale, eliminating infrastructure burdens and resource bottlenecks.

Explore all our cloud software solutions

Focus on breakthroughs, not bottlenecks. Harness Sequentia’s cloud-based omics solutions and streamline complex omics workflows into insights that drive innovation and real-world impact.

Case studies

Unlocking Human Embryo Development with Single-Cell Precision

The Need

New lab models of human embryonic development hold enormous promise for regenerative medicine and drug testing, but proving that these models truly reflect real human biology is a major challenge. Researchers generate vast amounts of complex data, yet often lack the time, tools, or expertise to fully interpret it. Without clear validation and insight, even the most innovative experimental approaches risk falling short of their potential.

The Solution

Sequentia Biotech helped turn complex data into clear biological confidence. By combining expert data analysis with intuitive data visualization and close scientific collaboration, we enabled researchers to scientifically validate their embryonic models and advance their work more quickly.

Revealing the Hidden Role of Astrocytes through a Multi-Species Brain Mapping Study

The Need

Astrocytes have long been overlooked in brain research, yet their role in information processing remains a mystery. Studying these delicate, complex cells across species and brain layers generates massive, high-dimensional datasets that are difficult to interpret without specialized expertise. Researchers needed a partner who could not only handle the technical challenges but also translate complex single-nuclei and spatial transcriptomics data into meaningful biological insights.

The Solution

Sequentia Biotech provided end-to-end bioinformatics expertise, transforming raw sequencing data into actionable discoveries. By integrating single nuclei and spatial transcriptomics, the team mapped astrocyte diversity, uncovered layer-specific roles, and revealed evolutionary patterns.

Speak to a specialist

Connect with our bioinformatics specialists to explore how our services and solutions can support your goals.