Bioinformatics CRO & consulting, based in France

Bioinformatics consulting for academic, clinical and biotech research

Vidya BioSeq turns complex omics data into actionable insights, including genomics, scRNA-seq, spatial transcriptomics, epigenetics, complex multi-omics projects, and custom analytical pipelines.

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Interactive bulk RNA-seq report: volcano plot, MA plot and heatmap of differentially expressed genes

What we do

Our Services

All our analyses

Bioinformatics Consulting

Independent advice to choose the right omics technology, design rigorous experiments, and validate or interpret existing analyses.

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Bulk RNA‑Seq Analysis

From raw FASTQ to differential expression, pathway enrichment and a complete interactive HTML report.

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Single-Cell RNA‑Seq Analysis

From 10x Chromium or Parse output to a fully annotated dataset: integration, clustering, cell types, trajectories and immune profiling.

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Genomics, Epigenetics and Spatial

Variant calling and interpretation, methylation and chromatin analyses, and spatial transcriptomics for academic, clinical and biotech projects.

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Custom Pipeline Development

Snakemake, Nextflow, R, Python, ML/AI: bespoke, reproducible workflows, plus review and optimisation of your existing scripts.

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AI Training for Biomedical Research

Training for research and R&D teams to use AI reliably, taught by bioinformaticians on real biological data.

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Our strengths

Why work with Vidya BioSeq

Advanced bioinformatics expertise

We specialise in cutting-edge omics data analysis. Our tailored pipelines deliver reproducible, publication-ready results across a wide range of biological questions.

Reliable and efficient turnaround

Optimised workflows and high-performance computing capacity allow us to deliver rigorous analyses without compromising on speed or quality.

Experimental design support

From study conception to data processing, we help you build robust analytical frameworks that maximise the value of your data before sequencing begins.

Publication-ready writing

We help you write clear, rigorous bioinformatics sections for your manuscripts: methods, results, figures and responses to reviewers.

Our approach

From experimental design to publication

Every dataset holds a question, whether biological, clinical or strategic. Our role is to help you answer it with rigour, clarity and a consistent commitment to reproducibility.

We don't stop at delivering results. Whether you're preparing a publication, informing a clinical decision or building the scientific case for an R&D asset, we work with you until your data has fully served its purpose.

Design

Choosing the right technology and a robust experimental design before sequencing begins.
Analysis

Reproducible pipelines, from raw data to rigorous, documented results.
Interpretation

Turning results into biological insight, with clear figures and interactive reports.
Publication

Methods, results, figures and responses to reviewers for your manuscripts.