Bioinformatics consulting for academic, clinical and biotech research

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

Explore our services

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 Services

Genomic Data Analysis

Preprocessing, variant calling, annotation and clinical or research interpretation for academic, clinical and biotech projects.

Genomics

Single-Cell and Spatial Transcriptomics

scRNA-seq, multimodal integration and exploration of cellular and tissue heterogeneity at unprecedented resolution.

Transcriptomics

Custom Pipeline Development

Snakemake, Nextflow, R, Python, ML/AI: bespoke analytical solutions built around your specific research workflows.

Workflow

Our approach

Every dataset holds a question — 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.

Selected publications from our scientists

Neurodevelopmental Disorder Caused by Deletion of CHASERR, a lncRNA Gene

The New England Journal of Medicine
October 2024

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Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders

Journal of Medical Genetics
July 2023

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Integrative analysis of miRNA expression profiles reveals distinct and common molecular mechanisms underlying broad diagnostic groups of severe mental disorders

Molecular Psychiatry
April 2025

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A perfused iPSC-derived proximal tubule model for predicting drug-induced kidney injury

Toxicology in Vitro
May 2025

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Single cell profiling of circulating autoreactive CD4 T cells from patients with autoimmune liver diseases suggests tissue imprinting

Nature Communications
January 2025

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Neutrophil-derived extracellular vesicles induce endothelial inflammation and damage through the transfer of miRNAs

Journal of Autoimmunity
May 2022

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Ready to get more from your data?

Get in touch to discuss how our bioinformatics expertise can support your research — from exploratory analysis to publication.