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Spatial Proteomics Patents: Who Leads, Where the Gaps Are 2026

Spatial Proteomics Patents: Who Leads, Where the Gaps Are 2026
https://www.patsnap.com/resources/blog/rd-blog/spatial-proteomics-and-multiplexed-staining-patent-landscape/ · Patsnap · data cut-off 2026-07-31 · downloaded from the live page
Patent Landscape · Spatial Proteomics & Multiplexed Staining
Spatial Proteomics and Multiplexed Staining Patents: Who Holds the Core Claims
  • Filing peaked in 2021 at 63 records, then eased to 53 by 2024 — a -16% shift over that span, not a collapsing field.
  • Five assignees hold 51.5% of all 297 records, and the top ten hold 76.8% — concentration that starts early and stays tight.
  • G01N material analysis touches 46.5% of records, while image processing under G06T and G06V sits far lower, near 12% each.
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297
Published Records
52%
Top-5 Share of All Records
-16%
Filing Growth 2021→2024
US
Leading Jurisdiction

Filing growth compares 2021 (63 records) with 2024 (53) — a three-year span. 2024 is the most recent year we treat as complete: publication lags filing by roughly 18 months, so 2025 onwards are still filling in and any growth rate that ends there would understate the field. Top-5 share is the combined record count of the five largest assignees divided by all 297 records in scope (CR5), not by the ranked leaders only.

Published byPatsnap Research··7 min readSourced from Patsnap Eureka
Field Overview

What's being claimed, and by whom

Spatial proteomics and multiplexed staining sit at the intersection of tissue biology and instrumentation: methods for imaging mass cytometry, cyclic staining, and antibody panel validation that let researchers map dozens of protein markers onto a single tissue section without destroying it. The patent record in scope spans 297 published records filed between 2015 and mid-2026, concentrated around problems that are easy to state and hard to solve cleanly — signal spillover between channels, metal isotope tag design, and batch normalization across imaging runs.

The filing curve shows a field that grew fast, cycled through a peak, and has since settled rather than stalled. Because publication lags filing by roughly 18 months, the most recent one to two years in any chart will always look thinner than they eventually turn out to be — read the tail with that in mind, not as a signal of declining interest.

Filing activity by year, 2017–2026
  1. 1AMBERGEN INC41
  2. 2SINGULAR GENOMICS SYSTEMS INC29
  3. 3MASSACHUSETTS INST OF TECH29
  4. 4THE BROAD INST INC27
  5. 5EVELO BIOSCIENCES INC27
  6. 6DANA FARBER CANCER INSTITUTE INC21
  7. 7BOSTONGENE CORP16
  8. 8UNIVERSITY OF ZURICH15
  9. 9THE GENERAL HOSPITAL CORP12
  10. 10TEMPUS AI INC11
Source: Patsnap Eureka. Assignee ranking and totals. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP

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The Numbers

Filing trend and technology composition

Two views of the same 297 records: how filings moved year over year, and which IPC subclasses carry the claim density.

A peak in 2021, then a manageable pullback

Filings rose from zero in 2017 to a peak of 63 in 2021, then eased to 53 by 2024 — a -16% change over that three-year span. That is a normalization after a surge, not evidence of a shrinking field; 2025 and 2026 figures will keep revising upward as publication catches up with filing.

A peak in 2021, then a manageable pullback02040608002017201820192020632021202220232024202522026Most recent year is partial — publication lag means later filings are not yet visible.

Material analysis dominates; image processing lags

G01N (material analysis & testing) appears on 46.5% of the 297 records, well ahead of C12Q (28.3%) and A61K (21.5%). Image-side classes — G06T image processing and G06V image recognition — sit at 12.1% and 11.8% respectively, notably lower than the wet-lab and assay classes despite spatial proteomics being fundamentally an imaging problem.

Material analysis dominates; image processing lagsG01N · Material analysis & testing13846.5%C12Q · Measuring & testing involving …8428.3%A61K · Medicinal preparations6421.5%A61P · Therapeutic activity of compou…5618.9%G16B · Bioinformatics3913.1%G06T · Image data processing & genera…3612.1%C12N · Microorganisms & genetic engin…3511.8%G06V · Image/video recognition3511.8%Other14448.5%

Shares are the percentage of the 297 records in scope. A patent can carry several IPC classes, so the shares add up to more than 100%.

Source: Patsnap Eureka. Filing trend and technology composition. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.

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Key Patents

The most-cited records in this space

Representative Record
US20220336058A12022-10-20

Analysis methods for multiplex tissue imaging including imaging mass cytometry data

CEDARS-SINAI MEDICAL CENTER

The invention relates to methods for multiplex tissue imaging by methods such as imaging mass cytometry (IMC) and methods for analysis of imaging mass cytometry data. In various embodiments, methods are provided of cell-of-origin analysis and mutational analysis, coupled with spatial parameters derived from tumor clusters in the tumor microenvironment; which reveals signature marker profiles and therapeutic targets for treating cancers including diffuse large B cell lymphoma.Filed by Cedars-Sinai Medical Center, published 2022-10-20 as US20220336058A1.

US20220336058A1 — patent drawing 1US20220336058A1 — patent drawing 2
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Highly-cited records in scope
#Publication no.Patent titleCitations
1US20210090694A1Data based cancer research and treatment systems and methods712
2WO2021091611A1Spatially-tagged analyte capture agents for analyte multiplexing153
3US20220326251A1Spatially-tagged analyte capture agents for analyte multiplexing124
4US11592447B2Spatially-tagged analyte capture agents for analyte multiplexing101
5US20230228762A1Spatially-tagged analyte capture agents for analyte multiplexing83
6US20190347557A1Generalizable and Interpretable Deep Learning Framework for Predicting MSI from Histopathology Slide Images76
7US11808769B2Spatially-tagged analyte capture agents for analyte multiplexing64
8WO2019070755A1Methods and compositions for detecting and modulating an immunotherapy resistance gene signature in cancer61
9US20220367053A1Multimodal fusion for diagnosis, prognosis, and therapeutic response prediction57
10US20240053351A1Spatially-tagged analyte capture agents for analyte multiplexing53

Citation counts favour older records inside any searched corpus — read them as a signal of influence on later filings, not as a ranking of current technical importance.

Each row carries its publication number; clicking a row searches Eureka by that number.

Source: Patsnap Eureka. Citation counts and representative records. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
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Insights

What the data means for a filing decision

Three patterns worth acting on before drafting the next claim set in this space.

Concentration
51.5% of 297
held by top 5 assignees

The top of the field is dense, not diffuse

Five assignees hold more than half of all 297 records in scope, and the top ten hold 76.8%. New entrants filing broad method claims on core imaging-mass-cytometry workflows are filing into occupied ground; differentiation has to come from a specific application, marker panel, or normalization step, not from the general workflow.

Based on the assignee ranking of 297 records.
Growth signal
63 → 53
peak-year filings, 2021 to 2024

A peak, then a settle — not a decline

Filing rose to a peak of 63 records in 2021 before easing to 53 by 2024, a -16% change. Given the roughly 18-month lag between filing and publication, 2025-2026 figures are still incomplete; treat the recent dip as a return to a steadier baseline rather than as evidence the field has stalled.

2021 and 2024 are the two years directly cited in the underlying trend.
Claim geography
46.5% vs 12.1%
G01N share vs G06T share of 297 records

Wet-lab assay claims outweigh image-processing claims

G01N material analysis appears on nearly half of all records, while the two image-side classes, G06T and G06V, sit near 12% each. For a field built on multiplexed imaging, the algorithmic layer — segmentation, spillover correction, batch normalization software — looks comparatively lightly claimed relative to the assay and reagent side.

IPC shares are measured against the same 297-record denominator; a record can carry multiple classes.
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Eureka can read the same corpus for gaps instead of for coverage: under-claimed branches adjacent to spatial proteomics and multiplexed staining, with the prior art for and against each one.

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Source: Patsnap Eureka. Co-assignee relationships and derived observations. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
Who's Filing

The assignee landscape

73 companies and institutions make up the full ranking returned for this dataset — not a top-50 or top-100 cut, but the entire ranked list for these 297 records. Filing is led by a mix of instrument makers, cancer research institutes and diagnostics companies, with academic-industry co-assignee pairs appearing repeatedly near the top.

Leader
41
records

A single leader well ahead of the field

The top-ranked assignee holds 41 records, noticeably ahead of fifth place at 27 and tenth place at 11 — the drop-off from first to fifth is steep, then flattens into a longer tail.

Counted in records across the 73-assignee ranking.
Co-filing
23
shared records, strongest pair

Academic-institute pairs file together repeatedly

Ten co-assignee pairs appear in the data, with the strongest research-institute pairing sharing 23 records and a second pairing sharing 19 — a pattern consistent with grant-funded, multi-institution cancer research programs rather than single-company R&D.

Ten identified co-assignee pairs across the corpus.
Momentum
-100% YoY
for several prior leaders

Several early leaders show no recent-year filings

A number of assignees that were active earlier in the dataset show zero filings in the latest year, including multiple research institutes with -100% year-on-year change. That does not necessarily mean exit — it is consistent with the publication lag — but it does mean recent competitive attention has shifted toward whoever is still filing.

Momentum figures compare each assignee's latest-year count to the prior year.
🔍
Under-claimed sub-areas worth watching
Branches where filing density is thin relative to the core assay and reagent claims
Spillover-correction algorithmsAutomated antibody panel design toolsCross-platform batch normalizationMetal isotope tag chemistry variantsCyclic staining tissue-preservation methods
Rank all filers by momentum →
Recent-year filing momentum by assignee
AssigneeRecent yearYoY
Singular Genomics Systems Inc1-80%
AmberGen Inc0-100%
Massachusetts Institute of Technology0
Evelo Biosciences Inc0
The Broad Institute Inc0-100%
Dana-Farber Cancer Institute Inc0-100%
BostonGene Corp0-100%
University of Zurich0
Source: Patsnap Eureka. Assignee-level momentum. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
What's Next

Where to take this next

The dataset points to a few concrete next steps depending on what you're trying to decide.

Check freedom-to-operate against the top 10

With 76.8% of records held by ten assignees, any new filing in core imaging-mass-cytometry or cyclic-staining methods should be checked against that group's claim scope before drafting.

Run a freedom-to-operate search →

Look at the image-processing gap

G06T and G06V classes sit far below the assay-side classes in share of records, suggesting the algorithmic layer of spatial proteomics is less densely claimed than the wet-lab side.

Explore the IPC breakdown →

Track the co-filing institutions

Repeated academic co-assignee pairs suggest active, ongoing research programs; watching their newest filings is a reasonable proxy for where the science is heading next.

See assignee momentum →
Source: Patsnap Eureka. Forward-looking reading of the same dataset. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
FAQ

Common questions about this landscape

Answers are grounded in the same dataset. Derived from a Patsnap search on Spatial Proteomics and Multiplexed Staining covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP

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Disclaimer. This page is generated from Patsnap Eureka data drawn from a limited snapshot of global patent and scientific-literature records, and is provided for general information and reference only.

Patent data carries inherent limitations: recent filings (typically the most recent 18–24 months) are under-counted due to standard publication lag; counts may be reported at either a patent-family or a patent-record basis and are not always directly comparable; classification, applicant-name, and citation data may contain errors, duplicates, or omissions; and the underlying search query defines and constrains the scope shown. As a result, the analysis may be incomplete or inaccurate and may not reflect the full technology landscape.

Nothing on this page constitutes an exhaustive prior-art, novelty, freedom-to-operate, or validity search, nor does it constitute legal, financial, investment, or professional advice, and it should not be relied upon as such. Any patent, commercial, or strategic decision should be verified independently and reviewed with qualified patent, legal, and domain professionals. Patsnap makes no warranties, express or implied, as to the accuracy, completeness, or fitness for any particular purpose of the information presented.

Machine translation. Assignee and organisation names originally recorded in Chinese, Japanese or Korean have been rendered into English by an AI translation step so that the tables stay readable. These renderings are best-effort and may not match a company’s registered English name; the original name is what the underlying patent record carries, and it is what any Eureka query launched from this page uses.

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