Platforms & Technologies
Every platform below runs on documented protocols with QC at every step. Book a single category directly, combine several into one project, or draw on a named partner for a specific technique.
One category, one deliverable: sample prep through exosomes, booked individually.
Tier 2 · Multi-OmicsTwo or more of our own platforms run as one coordinated project, one dataset.
Tier 3 · ComboBuilt together with an academic or industry partner around a specific technique.
Already an approved client, ordering a routine service? Extraction, QC, PCR, qPCR, dPCR and Sanger sequencing are available at catalogue price in our online shop, straight from your client area. No quote round-trip.
Not sure where to start?
A quick keyword match against our catalogue (single-omics, multi-omics or combo), not a substitute for talking to our team, but a fast first pointer.
Try: "extracellular vesicles from plasma", "SNP genotyping", "gut microbiome + host RNA", "whole genome and RNA-seq together"…
Not every project starts with a clear parameter list. Our scoping service pairs you with our scientific team for a structured study of your question (bibliography, one or more scientific meetings, and a written protocol & parameter definition) before any platform below is booked.
A structured review of relevant published work framing your question and prior approaches.
One or more working sessions with our scientific team to discuss feasibility, options and trade-offs.
A written definition of experimental parameters, sample requirements and the platform combination suited to your project.
A written document you keep, usable to move forward with us, or elsewhere.
A paid, bookable service, reserved like a platform slot. If the resulting project is booked with us, the scoping fee may be credited toward it: case by case, confirmed when you book. For a fuller engagement with a dedicated project lead through to publication, see GenXMap's Collaborative Research program.
Book a scoping sessionDNA, cfDNA, RNA, small RNA, cfRNA and protein extraction, with documented QC on arrival, after extraction and before library preparation. Every batch ships with its QC report.
High yield and purity across blood, tissue, cells, FFPE, saliva, plasma, stool and bacteria.
Fluorometric quantification (Qubit) plus 260/280 and 260/230 ratio assessment.
Bioanalyzer / TapeStation electrophoresis for RIN/DIN scoring.
Documented chain-of-custody from intake to storage, with long-term traceable biobanking for archival and re-analysis.
Platform sheet (PDF)Sourcing of qualified human material through our partner biobanks, on request.
Sequencing and targeted quantification, from whole genome to a single gene target: genomics, transcriptomics, metagenomics and PCR-based assays, run on documented protocols with QC at every step.
Whole genome and exome sequencing, plus targeted panels for biomarkers, variants and disease gene sets.
Genome-wide profiling, or deep coverage of coding regions, delivered as quality-controlled FASTQ.
Focused panels for biomarkers, variants and disease gene sets.
Secure, fast and reliable data delivery via cloud.
Bulk, small RNA and single-cell sequencing for expression profiling and cellular heterogeneity.
Transcriptome-wide profiling on total or poly-A selected RNA, stranded libraries.
miRNA and other small RNA profiling, with dedicated library chemistry.
Single-cell resolution for cellular heterogeneity and rare populations.
16S and shotgun sequencing for microbial community profiling and host-microbiome studies.
Taxonomic profiling of bacterial communities.
Whole-community sequencing for strain-level resolution and functional potential.
Host transcriptomics and microbiome profiling on the same samples.
See our Infectious Diseases & Microbiome industry page for applications.
Platform sheet (PDF)PCR, qPCR, RT-qPCR and dPCR for absolute and relative quantification on a defined set of targets.
Relative and absolute quantification with high reproducibility, including targeted pathogen detection assays.
Absolute quantification for rare targets and low-abundance variants.
Platform sheet (PDF)SNP genotyping and copy-number assays.
Book this assay →Targeted validation of key transcripts from sequencing data.
Targeted and untargeted protein analysis for expression profiling and biomarker work.
Untargeted proteome profiling and label-free quantification.
Proximity extension assay for targeted protein quantification and validation, with MIPP.
Mass-spectrometry proteomics runs in-house. Biomarker panels are delivered with our specialized partner, MIPP: same single point of contact, same QC standards.
Book this platform Platform sheet (PDF)Cargo profiling: RNA and protein content of isolated vesicles, for biological signature and biomarker discovery.
Ultracentrifugation, precipitation and size-exclusion chromatography protocols.
Nanoparticle tracking analysis (NTA) and marker validation by Western blot.
RNA and protein content of isolated vesicles, for biological signature and biomarker discovery.
Combine two or more services into a single coordinated project, with every layer generated from the same extraction batch. The examples below are starting points, and any combination can be scoped.
Whole-genome or exome sequencing paired with RNA-seq on the same DNA and RNA extractions, for studies linking sequence variation to its expression consequences.
Draws on: NGS & Molecular Biology (Genomics + Transcriptomics) Enquire about this packageRNA-seq paired with mass-spectrometry proteomics on matched samples, for studies where transcript levels alone don't predict protein abundance.
Draws on: NGS & Molecular Biology (Transcriptomics) + Proteomics Enquire about this packageRNA-seq on a discovery cohort, followed by RT-qPCR or dPCR validation of selected targets on the full sample set.
Draws on: NGS & Molecular Biology (Transcriptomics, RT-qPCR & dPCR) Enquire about this packageExamples above are illustrative starting points, not a fixed menu: tell us your project and we'll scope the right combination. Need the whole scientific project designed and run, not just the platforms booked: protocol design, connecting the right platforms, multi-omics data integration, through to publication? That's GenXMap's Collaborative Research program, with a dedicated PhD-level project lead as your single point of contact.
For projects where the biomarker is the deliverable, not the data. The platform combination is defined by the question rather than fixed in advance, and can draw on our own platforms, GenXMap's Computational Biology & AI, and our partner network.
Built for biomarker discovery projects. When the question calls for it, this package mobilizes the full range of resources available (OMICS4's own platforms, GenXMap's Computational Biology & AI layer, and our partner network), scoped and delivered as one coordinated project with unified sample tracking.
Draws on: OMICS4 platforms, GenXMap Computational Biology & AI and our partner network, as required Scope a biomarker discovery projectEach joint platform began as a need, and became a workflow we built with our partners, bringing together complementary expertise and equipment. Distinct from our own Multi-Omics packages, which combine our categories in-house, each combo platform draws on one of our 4 categories, plus the dedicated expertise and equipment of one or more named partners.
You send the molecule, we return the readout. With our partners, we select the human cell or tissue model, apply your compound and run the treatment. We then proceed with extraction, QC and transcriptomic profiling. One project, one point of contact, from compound to expression data.
Draws on: NGS & Molecular Biology Enquire about this platformA dedicated exosome/EV characterization workflow combining OMICS4's isolation and cargo-analysis capacity with the Faculté de Pharmacie de Marseille's specialized nanoparticle-characterization equipment, built for higher-resolution EV sizing, count and marker validation than either partner runs alone.
Draws on: Exosomes & EVs Enquire about this platformThree views of the same transcriptome, on one design and one sample set. Bulk RNA-seq runs on our own platforms and tells you what changed; single-cell with Parean Biotechnologies tells you in which cells; spatial transcriptomics with Explicyte tells you where in the tissue. Bought separately the three rarely line up. Run together they are interpreted as one reading rather than three reports to reconcile.
Draws on: NGS & Molecular Biology (Transcriptomics) Enquire about this platformThe scientific detail is on genxmap.com.
Not sure which platform fits your project?