Collaborate with experienced bioinformatics scientists for RNA-seq, single-cell, genomics, transcriptomics, proteomics, and multi-omics analysis—from your raw sequencing data to publication-ready results.
Trusted by researchers at institutions including:
Journals & databases our clients’ work appears in and draws on:
From PhD students defending their thesis to clinical teams submitting to high-impact journals — in their own words.
“They built my entire Seurat pipeline, annotated every cell cluster, and delivered figures that went straight into my thesis. My supervisor called it my strongest chapter.”
— Dr. S. P****l · PhD Graduate, Oncology & Cancer Biology, University of Manchester
“Reviewer three demanded a full reanalysis with new normalisation and batch correction. InSilicoNext turned it around in five days, and the paper was accepted.”
— Prof. M. R****d · Principal Investigator, Immunogenomics Lab, King’s College London
“We needed publication-grade genomics for our Series A but couldn’t justify a full-time hire. They delivered a multi-omics target report, under NDA, on time and on budget.”
— Dr. L. K****s · Chief Scientific Officer, PrecisionOmics Therapeutics, Budapest
“Our postdoc left mid-project and took the knowledge with them. They audited what existed, finished the metagenomics pipeline in three weeks, and wrote our methods section.”
— Dr. C. O*****r · Associate Professor, Microbiology & Infectious Disease, University of Lagos
“Two weeks before my viva I couldn’t explain my GWAS pipeline. Their 30-minute walkthrough covered every analytical decision, and I passed without corrections.”
— R. F*******z · PhD Candidate, Human Genetics & Population Genomics, University of Barcelona
“We needed a partner who understood both the science and data governance. They signed our data agreement, processed our WES cohort with a full audit trail, and delivered a genuinely usable report.”
— Dr. A. N*****n · Clinical Research Lead, Genomic Medicine Unit, Singapore General Hospital
Organized by what you need run, not by research trend. Every service follows the same rigor: documented methods, reproducible pipelines, reviewer-ready output.
WGS/WES, variant calling and annotation, clinical genomics, and long-read data analysis (ONT/PacBio).
Explore serviceBulk RNA-seq, single-cell RNA-seq, and spatial transcriptomics, from FASTQ to figure.
Explore serviceChIP-seq, ATAC-seq, and DNA methylation analysis mapped to regulatory function.
Explore serviceGenomic, transcriptomic, proteomic, and metabolomic data layered into one coherent model, including CITE-seq.
Explore serviceCommunity composition, diversity metrics, and functional profiling from shotgun or amplicon data.
Explore serviceStructure prediction (incl. AlphaFold), docking context, and phosphoproteomic signaling analysis.
Explore serviceCandidate biomarker discovery and validation, including low-frequency liquid biopsy/ctDNA calling.
Explore serviceBespoke, versioned pipelines for recurring analysis needs — including RWE/EHR genomics workflows.
Explore serviceStatistical design, power analysis, and publication-grade figures that hold up under review.
Explore servicePPI, gene-regulatory, and co-expression networks, module detection, and pathway topology.
Explore serviceMethods sections, results narrative, and revision support aligned to your target journal.
Explore serviceStudy design, pipeline audits, and second-opinion review before you commit budget or samples.
Explore serviceWe go deep in a focused set of therapeutic and scientific areas rather than spreading thin across everything.
Tumor genomics, liquid biopsy, and immuno-oncology analysis across solid and liquid tumors.
Explore areaImmune repertoire profiling, from TCR/BCR sequencing data to treatment-response modeling.
Explore areaNeurogenomics and brain-organoid bioinformatics for CNS disease and development research.
Explore areaPathogen genomics, outbreak tracking, and infectious-disease surveillance pipelines.
Explore areaAgricultural genomics, comparative genomics, and eDNA/biodiversity analysis.
Explore areaAI-assisted target identification, pharmacogenomics, and cell & gene therapy bioinformatics.
Explore areaeDNA and metabarcoding biodiversity, marine metagenomics, population genomics, and aquaculture.
Explore areaTell us about your data and your question. We scope the analysis and flag anything that needs attention before it starts.
You receive a written scope, timeline, and price — public pricing for individual and university work, or a formal SOW for institutional projects.
Data moves under NDA via encrypted transfer. Nothing starts until a signed agreement is in place.
An analyst runs the pipeline, documents every step, and validates outputs against QC benchmarks before delivery.
You receive a full report, figures, and methods text — plus revision support through journal review.
Not a spreadsheet dump — a structured deliverable your co-authors and reviewers can actually use.
Every engagement starts with an NDA. Data is transferred and stored under encryption, and our workflows are documented for audit and reproducibility.
Read our Compliance & Data Security pageIndividual and university pricing is public. Institutional work is scoped and quoted — never assumed.
For PhD students and independent researchers
For labs and research groups
For biotech, pharma & clinical teams
Answers to what most researchers and project leads ask before starting.
Tell us what you're working with — we'll scope it honestly, including if we're not the right fit.