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Proteomics for Genomic Analysis

Integrate proteomics and genomics for deeper biological insight with high-throughput protein profiling powered by SOMAmer™ proteomics.

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Why pair proteomic and genomic data?

Together, proteomics and genomics help researchers uncover causal biology, connect genotype to phenotype, and gain a more complete understanding of disease.

A broader view of biology

Understand disease more completely by combining genomic variation with direct measurements of protein abundance with direct protein measurements.

Deeper insight into disease mechanisms

Prioritize drug targets with greater confidence by linking genes, proteins, pathways, and phenotypes in a single discovery framework.

Stronger support for target discovery and prioritization

Advance high-throughput discovery at scale with proteomic profiling that complements sequencing-based research.

Proteins reveal biology in action

Proteomic data adds a dynamic, accessible layer of insight to genomic analysis, helping observe changes that may not be visible from DNA and RNA alone.

Proteins are dynamic

Proteins change with disease, treatment, environment, and time, offering a real-time view of biology in action.

Proteins are accessible

Many proteins circulate in blood and other biofluids, enabling minimally invasive sample collection for large discovery studies.

Proteins are measurable at scale

SOMAmer proteomics measures over 9,500 proteins across ~10 orders of magnitude, capturing high- and low-abundance signals for discovery research.

Not all protein measurements are the same

Most proteomic approaches force tradeoffs in sensitivity, reproducibility, and scalability

High-plex proteomics can be difficult to scale because researchers often have to compromise between sensitivity, reproducibility, and study throughput. These tradeoffs matter in genomic studies, where protein data must remain comparable across cohorts, sites, timepoints, and large sample sets.

Key challenges in high-plex proteomics

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Sensitivity

  • Limited sample volume
  • Proteome coverage, including low-abundance proteins

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Reproducibility

  • Data must be comparable across sites, cohorts, and time
  • Need for data lakes and unified datasets

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Scalability

  • Large studies require thousands to tens of thousands of samples
  • Precision retained as plex increases

SOMAmer proteomics is designed to eliminate those tradeoffs, delivering broad protein coverage, sensitive measurement, and reproducible data at scale.

Why SOMAmer proteomics?

Built for high-throughput proteomic discovery

SOMAmer proteomics gives geneticists a scalable way to add precise, reproducible protein measurements to large genomic discovery studies.

SOMAmer proteomics eliminates tradeoffs

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Sensitivity

~10,000 human proteins, >10 orders of magnitude (fM–µM)

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Reproducibility

Measure proteins consistently across cohorts, sites, and time with ~5% median CVs

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Scalability

Consistent performance across study size and multiplexing depth

With broad proteome coverage, low variability, and proven performance across population-scale research, SOMAmer proteomics is designed to generate data that can be trusted across cohorts, sites, and time.

Broad coverage
Specific
Reproducible
Scalable
Proven
Broad coverage

Broad Coverage

9,500+ proteins across ~10 orders of magnitude
Specific
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Synthetic affinity reagents chosen via SELEX* enrichment
Reproducible

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Low ~5% CV to detect subtle biological signals
Scalable

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Comparable data across studies, sites, and time
Proven

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1,800+ publications and 25+ consortia/biobanks

SOMAmer proteomics solutions for proteogenomic studies

SOMAmer proteomics enables high-throughput protein profiling in proteogenomic studies through flexible NGS-based or array-based readouts. Powered by SOMAmer Reagents—affinity reagents engineered for exceptional specificity—both assay formats deliver scalable, reproducible proteomic data that complement genomic insights.
Choose the approach that best fits your existing infrastructure and study design.

Illumina somaseq discovery

Illumina SomaSeq™ Discovery

An automated NGS-based proteomics solution

Explore SomaSeq Discovery

Illumina SomaScan™ Discovery

A high-throughput, array-based proteomics solution

Explore SomaScan Discovery

Illumina somascan discovery assay

Turn genetic associations into biological insight

SOMAmer proteomics adds a complementary protein layer that can help explain how genetic variation translates into biological function, strengthening genomic studies across:

  • pQTL discovery 
  • Genotype-to-phenotype research 
  • Pathway analysis 
  • Biomarker discovery 
  • Target prioritization 
  • Population-scale cohort studies

Research and resources

Population-scale proteogenomics

Large-scale plasma proteomics combined with genetic and phenotypic data can help connect sequence variation to disease biology and traits.

Read the Nature Genetics Study

pQTL discovery across diverse cohorts

Proteomic analysis across European and African ancestry cohorts identified protein quantitative trait loci (pQTLs) and supported models for proteome-wide association studies.

Read the Nature Genetics Study

pQTLs and the missing link between genes and disease

This white paper explains how pQTLs can help researchers connect genetic variants to protein biology, disease mechanisms, and potential therapeutic targets.

Download the pQTL white paper

Biobank-scale SOMAmer proteomics

Illumina announced a pilot program to analyze 50,000 UK Biobank samples with the SomaSeq Discovery assay, supporting population-scale proteomics that can be paired with genomic and phenotypic data.

Read the UK Biobank program announcement