“Their RNA-seq analysis turned a messy dataset into a clear biological story — every step handled systematically and explained clearly.”
— Dr. E**** C**** · PhD Researcher, University of Edinburgh
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.
“Their RNA-seq analysis turned a messy dataset into a clear biological story — every step handled systematically and explained clearly.”
— Dr. E**** C**** · PhD Researcher, University of Edinburgh
“They assembled a difficult non-model genome from long reads, polished it, and delivered annotation we could build on — with clear communication throughout.”
— Dr. K**** O**** · Postdoctoral Researcher, University of Oslo
“A reliable exome workflow with transparent variant annotation and interpretation. The documentation and data-quality focus gave us real confidence.”
— Dr. M**** T**** · Clinical Research Scientist, NUH Singapore
“They built a structured metagenomics workflow, interpreted the community patterns, and produced clear figures for our manuscript.”
— Prof. A**** H**** · Associate Professor, University of Toronto
“They screened our targets, ran the structural analysis, and prioritised candidates with clear rationale — saving weeks and sharpening our shortlist.”
— Dr. H**** S**** · Head of Computational Biology, Auronex Therapeutics
“They helped us choose the right methods, validate the analysis, and explain complex statistics clearly to experimental researchers.”
— Dr. P**** N**** · Research Fellow, University of Amsterdam
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 areaMetagenomics, microbiome profiling, eDNA biodiversity, and functional metagenomics across soil, water, sediment & marine systems.
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 quote for your project—or a formal SOW for institutional work.
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 pageCost depends on your data, analysis scope, and deliverables—so every project is quoted individually, never assumed. Here’s how engagements typically break down.
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.