Technology

Nomic Omni 1000 — the nELISA proteomics platform

Synoptic's products are built on Nomic's nELISA technology: a service-lab, antibody-based multiplexed immunoassay delivering absolute quantification of ~1,000 plasma proteins per sample. This page describes the measurement architecture, platform positioning, sample collection strategy, lab infrastructure, and computational pipeline.

~1,000 proteins per sample · ~$50 per proteome · <10% CV, r > 0.95 vs Olink · 950,000+ samples processed commercially · Peer-reviewed: Nature Methods 2025
Nomic
Core Technology

nELISA — nano Enzyme-Linked Immunosorbent Assay

Nomic's nELISA is a direct sandwich immunoassay using dual-barcoded antibody pairs and flow cytometry readout — no proximity extension, no PCR amplification, no next-generation sequencing. Results are in absolute physical units (pg/mL), not relative log-scale scores.

Proteins quantified ~1,000 Absolute quantification (pg/mL) per sample
Analytical sensitivity ~0.1 pg/mL LOD range; 7 orders of magnitude dynamic range (xDR)
Precision / concordance <10% CV Median r > 0.95 vs Olink PEA across overlapping targets
Step 1 Collection
Sample collection — VAMS, DPS, or venipuncture
Whole blood collected via volumetric absorptive microsampling (VAMS) finger-stick or centrifuged as a dried plasma spot (DPS) — both ambient-stable for ≥14 days without cold chain. Standard EDTA venipuncture is also supported for clinical cohort studies. Dried microsamples are eluted at the processing lab before plating.
Step 2 Capture
CLAMP bead incubation — capture antibody barcoding
Eluted plasma is incubated with a panel of CLAMP (Color-barcoded Lanthanide-Antibody Multiplexing Particles) beads. Each bead carries a unique lanthanide barcode identifying the target protein, plus a capture antibody against that protein. Up to ~1,000 unique bead populations are pooled in a single well.
Step 3 Detection
emFRET detection — sandwich immunoassay signal generation
Detection antibodies conjugated to an emFRET (emission Förster Resonance Energy Transfer) fluorophore are added. When a target protein bridges the capture bead and detection antibody, proximity triggers fluorescent energy transfer — generating a signal proportional to protein concentration. No PCR amplification step. No proximity-extension dependency.
Step 4 Readout
Flow cytometry readout — absolute quantification
Beads are read on a high-throughput flow cytometer. Each bead is identified by its lanthanide barcode; signal intensity is converted to absolute concentration (pg/mL) via embedded calibration curves run in the same plate. Results are returned as a QC-flagged sample × protein matrix within 10–14 business days. No batch normalisation required for cross-run comparisons.
Peer-reviewed validation: The nELISA chemistry and flow cytometry architecture are described in Tosi L. et al. (Nomic Bio), Nature Methods, 2025 — "nELISA: a high-throughput, high-plex platform enables quantitative profiling of the inflammatory secretome." DOI: 10.1038/s41592-025-02861-6 · PDF ↗ — Note: this publication characterises a 191-plex inflammation panel — an earlier product configuration. The current Omni 1000 spans ~1,000 proteins and is not the subject of the paper. The publication should be read as independent methodological validation of the underlying assay chemistry; Omni 1000 performance claims in this document are from Nomic's commercial specification sheets.
Platform Comparison

nELISA vs Olink PEA vs SomaScan

The large-scale proteomics market is dominated by Olink's proximity extension assay (PEA) and SomaLogic's aptamer array. nELISA occupies a distinct position: direct antibody-based detection, absolute quantification, minimally invasive sample compatibility, and a cost structure that makes consumer-scale throughput viable.

Attribute Nomic Omni 1000
nELISA
Olink Explore 3072
Proximity Extension Assay
SomaScan v4.1
Aptamer array
Proteins per sample ~1,000 3,072 7,596
Quantification unitsabsolute vs relative Absolute (pg/mL) Relative (NPX log-scale) Relative (RFU)
Cost per sampleindicative ~$50 $200–$600+ $400–$800+
Sensitivity (LOD) ~0.1 pg/mL ~1–10 pg/mL ~1–100 pg/mL
Detection chemistry Dual-antibody sandwich Proximity extension + PCR Aptamer (off-target binding risk)
Batch-free longitudinal comparisons Embedded calibration curves Requires bridging normalisation Requires bridging normalisation
Minimally invasive sampleVAMS / DPS validated Validated Venipuncture preferred Venipuncture required
Capital equipment None — service-lab model Olink Insight instrument SomaLogic facility only
Commercial throughputsamples processed 950,000+ (150+ institutions) UKB-PPP (54K); research scale Limited; primarily academic
Concordance vs Olinkpublished r >0.95 (median) ~0.70–0.80
Olink and UKB-PPP figures from published literature and Olink commercial documentation. SomaScan concordance from published head-to-head comparisons. Nomic figures from nomic.bio and the Nature Methods 2025 paper. All figures approximate. Platform capabilities evolve; this table reflects specifications current as of Q1 2025.
Sample Collection

Minimally invasive, decentralised collection

Nomic Omni 1000 is validated for dried blood microsamples — removing the venipuncture requirement that confines most large-scale proteomics platforms to clinic settings. This is the enabling technology for SYN-WAVE's direct-to-consumer collection model.

VAMS — Volumetric Absorptive Microsampling
Mitra® tip device · Neoteryx
At-home
Absorbs exactly 10 µL of capillary whole blood from a finger-stick. The dried tip is ambient-stable for ≥14 days at room temperature — no cold chain required for shipping. Validated for 100+ biomarker panels. Preferred collection method for SYN-WAVE consumer kit. Hematocrit correction applied during processing.
DPS — Dried Plasma Spot
Filter card · plasma fraction
Research
Centrifuged plasma fraction spotted onto a standardised filter card. Provides a cleaner matrix than whole blood VAMS — eliminates hematocrit variability and red blood cell protein contamination. Preferred for longitudinal monitoring studies where within-subject consistency across timepoints is critical. Requires brief centrifugation step.
Standard Venipuncture
EDTA or serum tube · clinic / biobank
Clinical
Supported for clinical partner studies, hospital-based recruitment, and SYN-DROME clinical integration. Provides highest-quality plasma matrix and is fully compatible with existing biobank workflows — including UKB-PPP and EPIC cohort infrastructure. Required reference standard for VAMS/DPS equivalence validation studies.
Analytical equivalence: Published data from Nomic and independent groups demonstrate >0.90 Spearman correlation between VAMS-derived and venipuncture-derived proteomics profiles for the majority of analytes, following hematocrit correction. Protein-specific VAMS performance data are available in Nomic's assay validation reports on request.
Computational Pipeline

From proteomic profiles to interpretable health scores

Synoptic's analytical stack converts ~1,000-protein expression matrices into product-ready scores — trained on population-scale cohort reference data and validated against gold-standard clinical endpoints.

Product 1
SYN-WAVE — Organ Aging & Exposome
Multi-organ proteomic age scoring, benchmarked in the 54,306-participant UKB-PPP cohort

Organ-system biological age scores are derived by training regularised regression models (elastic net, gradient boosting) on proteomic age residuals — the deviation of each protein from its age-expected level — separately for each organ system. Architecture mirrors Oh et al., Nature 2023.

  • 11 organ systems scored independently (heart, adipose, liver, kidney, lung, brain, immune, musculoskeletal, endocrine, gut, vasculature)
  • Cross-validated against incident disease endpoints: CVD, CKD, liver disease, neurodegenerative markers
  • Exposome modules: lifestyle, dietary, environmental, and metabolic modifiers of proteomic age
  • Longitudinal drift detection for repeat-sample monitoring; change scores over time
  • Consumer report output: organ scores, percentile benchmarks, actionable lifestyle flags
Product 2
SYN-DROME — Disease Risk Assessment
Proteomic multi-disease risk stratification, calibrated in the 520,000-participant EPIC consortium

Disease-specific proteomic panels are identified from EPIC incidence data and integrated with polygenic risk scores (PRS) to produce multi-disease risk estimates. Architecture mirrors Carrasco-Zanini et al., Nature Medicine 2024.

  • PRS + proteomic biomarker interaction modelling; protein panels of 5–20 proteins per disease
  • Disease targets: T2D, CVD, CKD, dementia, selected cancers — curated by incidence power in EPIC
  • Bayesian posterior risk estimates with calibrated confidence intervals
  • Clinician-facing report: ICD-10 aligned, risk strata with actionable intervention thresholds
  • Patient-facing DTC variant with structured GP handoff pathway
Lab & Regulatory Infrastructure

CLIA/CAP-accredited processing pathway

Clinical-grade reporting requires certified laboratory infrastructure throughout the sample custody chain. Synoptic's two-lab model routes pre-analytical processing through a CLIA/CAP partner and measurement through Nomic's certified service lab.

Samples collected via VAMS or DPS are shipped to Biological Clinical Laboratories (BCL), Synoptic's designated CLIA/CAP partner for pre-analytical processing. BCL handles elution, quality control, and sample preparation before transferring eluates to Nomic for nELISA measurement.

This two-lab model separates pre-analytical sample custody from measurement — the standard architecture for multi-site clinical studies and laboratory developed test (LDT) pipelines. It enables Synoptic to add or switch measurement labs as throughput scales without re-validating consumer-facing collection protocols or BCL's CLIA certification.

SYN-WAVE's DTC reporting pathway operates under a wellness-use framing that does not require FDA clearance. SYN-DROME's clinical diagnostic reporting will require additional LDT validation studies under the FDA LDT framework — planned for Year 3–4 alongside regulatory pre-submission meetings.

CLIA Accreditation
Clinical Laboratory Improvement Amendments — federal certification for any test result reported to patients in the US.
Active · BCL
CAP Accreditation
College of American Pathologists — gold-standard voluntary quality program; proficiency testing, QC, and personnel requirements.
Active · BCL
Nomic Service Lab
Fee-for-service nELISA measurement. ISO-compliant QC. 950,000+ samples processed. Results in 10–14 business days.
Active · Nomic
FDA LDT Pathway
SYN-DROME clinical reports will be developed under the FDA laboratory developed test framework. Pre-submission meeting targeted for Year 3.
Planned · Y3
Atlas of Proteomic Technologies (APT)
Ignition Scientific's APT catalogues the global proteomics landscape. Synoptic uses APT to monitor platform positioning as the field evolves. apt.ignitionscientific.com ↗
Reference