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Natera

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uuid0000cgg

Namestring
Natera
Legal namestring
Natera, Inc.
Websiteurl
natera.com
Company typeenum
Public
Founded yearint
2004
Descriptiontext

Natera, Inc. is a publicly traded (NASDAQ: NTRA) cell-free DNA (cfDNA) testing company founded in 2004 and headquartered in Austin, Texas, with operations in San Carlos, California and (via the Foresight Diagnostics acquisition) Boulder, Colorado. The company operates proprietary molecular and bioinformatics platforms built on multiplexed PCR and next-generation sequencing to detect and quantify circulating tumor DNA, donor-derived cfDNA, fetal cfDNA, and germline variants from a single blood draw. Flagship products include Signatera (tumor-informed, bespoke ctDNA minimal residual disease / MRD assay), Prospera (donor-derived cfDNA with the proprietary Donor Quantity Score algorithm for transplant rejection), Panorama (SNP-based non-invasive prenatal testing), Empower (hereditary cancer screening), Vistara (single-gene NIPT), and Zenith (whole-genome sequencing for rare disease). Natera runs ISO 13485, CAP, and CLIA-certified labs, holds SOC 2 Type II compliance, and is FDA-cleared for the Signatera CDx in muscle-invasive bladder cancer as of May 2026.

Natera generates revenue through clinical testing services billed to payors and health systems (with oncology ASP around $1,250 per Signatera test in Q1 2026), a dedicated BioPharma services unit that licenses Signatera MRD endpoints and provides real-world data access to trial sponsors, and licensing royalties following the April 2026 court award of a 30% royalty on infringing MRD products. Customers span five distinct segments: oncologists and cancer centers (over half of U.S. oncologists use Signatera), women's health providers (OB/GYNs and maternal-fetal medicine specialists), transplant centers, biopharma sponsors (including Allogene, Genentech, Diakonos, CytoDyn, and Purespring), and rare-disease patients via the Zenith platform. The go-to-market motion is direct enterprise field sales to clinicians and health systems, supplemented by channel partnerships (SRL Inc. in Japan, Pirche AG in transplant) and heavy clinical evidence generation that drives guideline inclusion.

The company has processed over 16 million cumulative tests, maintains a proprietary oncology database with 2M+ plasma timepoints, and reports approximately 50% market share in tumor-informed MRD testing. Investment in scientific marketing — 35 abstracts at ASCO 2026, 20 at AACR 2026, 21 at ATC 2026, and 400+ peer-reviewed publications — supports three NCCN guideline recommendations, including Category 1 for Signatera. Q1 2026 revenue of $696.6M (+38.8% YoY) implies TTM revenue of approximately $2.5B and FY2026 revenue in the $2.8B range, with gross margins near 65% and a market capitalization of approximately $30–31B. The announced Austin headquarters expansion (May 2026) will add roughly 400 new roles alongside the company's largest sequencing facility.

Short descriptiontext

Natera is a publicly traded cell-free DNA testing company that provides MRD oncology (Signatera), transplant rejection (Prospera), and reproductive health (Panorama) tests to clinicians, health systems, and biopharma partners, processing over 16 million cumulative tests across its CAP/CLIA-certified laboratories.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersSan Carlos, United States
HQ citystring
San Carlos
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cell-free DNA testing, molecular residual disease, non-invasive prenatal testing, transplant rejection monitoring, hereditary cancer screening
Product category
Molecular Diagnostics
GTM motion4 records

Each record includes

Type, Description, Source

Revenue model4 records
1Clinical diagnostic testing services
TypeUsage Based
Description

Revenue from running cell-free DNA tests (Signatera, Latitude, Altera, Empower, Prospera, Renasight, Panorama, Horizon, Vistara, Anora, Fetal Focus, Zenith) in CAP/CLIA-certified labs for clinicians, hospitals, health systems, and patients. ASPs in oncology testing were approximately $1,250 in Q1 2026, with 54-55% YoY oncology test volume growth.

natera.com:443
2Biopharma services and partnerships
TypeProfessional Services
Description

Revenue from biopharma customers using Signatera, CLARITY, and RenasightIQ for clinical trial MRD testing, molecular response analysis, real-world data access, and companion-diagnostic development (e.g., Diakonos, CytoDyn, Allogene, Genentech, Diakonos, Purespring/Travere collaborations).

ca.investing.com
3MRD patent licensing royalties
TypeLicensing Royalties
Description

Licensing royalties on MRD-related patents; a U.S. court awarded Natera a 30% ongoing royalty on revenues from infringing MRD-related products (including ArcherDx and Invitae product sales), establishing a recurring royalty revenue stream.

businesswire.com
4Renasight / RenasightIQ pharma research and clinical-trial services
TypeProfessional Services
Description

Revenue from genetic testing panels (Renasight kidney gene panel) and pharma research services that accelerate rare-disease and chronic kidney disease clinical trial recruitment (e.g., Alport, ADPKD, FSGS case studies).

natera.com:443
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels5 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 18 records shown
1Signatera
Description

Personalized, tumor-informed molecular residual disease (MRD) assay for cancer recurrence monitoring and treatment guidance.

natera.com:443
+17 more records
Core offering1 text field

Natera runs cell-free DNA (cfDNA) diagnostic tests in its ISO 13485/CAP/CLIA-certified laboratories, sold to clinicians, health systems, and biopharma customers. Its core franchise is Signatera, a personalized tumor-informed molecular residual disease (MRD) assay for cancer recurrence monitoring, complemented by Prospera dd-cfDNA transplant rejection tests (kidney, heart, lung), Panorama NIPT and women's health reproductive tests, Renasight kidney gene panels, and the Zenith whole-genome rare-disease platform.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 9 values shown
  • Signatera-positivity associated with HR 8.15 in adjuvant setting and HR 18.30 in surveillance across a meta-analysis of 18 studies, 3,000+ patients, 15 tumor types (ASCO 2026)
+8 more records
Product overview1 text field

Natera operates a platform-plus-modules architecture centered on its NateraCore laboratory services infrastructure and NateraConnect provider portal, with the test menu organized into four clinical franchises: (1) Oncology — anchored by Signatera (tumor-informed MRD) and Signatera Genome, complemented by Latitude (tissue-free MRD), Altera (tumor genomic profiling), Spectrum, Empower (hereditary cancer), and the acquired CLARITY MRD assay from Foresight Diagnostics; (2) Transplant — Prospera dd-cfDNA assessment for kidney, heart, and lung recipients; (3) Kidney genetics — Renasight and RenasightIQ panels; and (4) Reproductive health — Panorama NIPT, Vistara, Fetal Focus, Vasistera, Anora, and Horizon carrier screening. Beyond the clinical test menu, the Zenith whole-genome rare-disease platform, Annotation Platform, NEVA educational virtual assistant, ProReach services, and Constellation platform round out the broader offering.

Product and service17 records
1Signatera
CategoryOncology - Molecular Residual Disease (MRD)
2Signatera Genome
CategoryOncology - Molecular Residual Disease (MRD)
3Latitude
CategoryOncology - Molecular Residual Disease (MRD)
4Altera
CategoryOncology - Comprehensive Genomic Profiling
5Empower
CategoryOncology - Hereditary Cancer Testing
6Prospera
CategoryOrgan Health - Transplant Rejection Monitoring
7Renasight
CategoryOrgan Health - Kidney Genetics
8RenasightIQ
CategoryOrgan Health - Kidney Genetics
9Horizon
CategoryWomen's Health - Carrier Screening
10Panorama
CategoryWomen's Health - Non-Invasive Prenatal Testing
11Vistara
CategoryWomen's Health - Non-Invasive Prenatal Testing
12Fetal Focus
CategoryWomen's Health - Non-Invasive Prenatal Testing
13Vasistera
CategoryWomen's Health - Non-Invasive Prenatal Testing
14Anora
CategoryWomen's Health - Reproductive Genetics
15Zenith
CategoryRare Disease - Whole-Genome Sequencing
16CLARITY MRD Assay
CategoryOncology - Molecular Residual Disease (MRD)
17Spectrum
CategoryOncology - Tumor Molecular Characterization
Scale indicator16 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-06-24
Description

SRL Inc. is Natera's exclusive business partner to commercialize Signatera in Japan following PMDA approval in colorectal cancer. Commercial launch planned by year-end 2026 with SRL supporting commercialization and access expansion across the country.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-19
Description

Pirche AG and Natera announced a strategic collaboration to advance transplant medicine by combining Pirche's TxPredictor pre-transplant immunological risk-stratification platform with Natera's Prospera dd-cfDNA post-transplant monitoring test. Joint launch planned at the 2026 American Transplant Congress.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-04
Description

Natera and CytoDyn announced a strategic collaboration to evaluate circulating tumor DNA (ctDNA) dynamics using Signatera on samples from CytoDyn's CLOVER Phase 2 study in metastatic colorectal cancer, plus access to Natera's proprietary oncology database (2M+ plasma timepoints) for molecular response analysis in leronlimab development.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-29
Description

Natera and Diakonos Oncology Corp. announced a collaboration for Signatera to assess molecular response in patients with refractory melanoma enrolled in Diakonos' DOC-RM Phase I/II trial evaluating DOC1021 (dubodencel), a personalized dendritic cell therapy with FDA Fast Track designation. Natera will perform serial ctDNA monitoring at multiple timepoints.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2026-05-29
Description

Natera partners with NVIDIA to enhance its AI models for cell-free DNA-based early cancer detection; Natera is cited as a leading example of a biotech that applies AI to cfDNA technology.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-15
Description

FDA approval of Genentech's Tecentriq / Tecentriq Hybreza as adjuvant treatment for muscle-invasive bladder cancer patients identified as ctDNA-MRD positive by Natera's Signatera CDx, supported by the IMvigor011 Phase III study (36% reduction in recurrence or death; 41% reduction in overall death).

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-04-29
Description

Natera collaborated on Purespring Therapeutics' publication in Kidney International Reports identifying NPHS2 variants as a significant under-recognised cause of adult-onset FSGS, informing development strategy for Purespring's PS-001 candidate treatment.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-27
Description

Strategic collaboration with BGI Genomics for developing NGS-based genetic testing assays, cited as a key partnership in stock analyses of Natera.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-13
Description

Natera's CLARITY MRD assay is being used to identify MRD-positive patients in Allogene Therapeutics' registrational ALPHA3 trial of cema-cel in first-line large B-cell lymphoma. Interim futility analysis showed 58.3% MRD clearance in the cema-cel arm vs. 16.7% observation.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-12
Description

Exclusive partnership with MyOme to develop Natera's Zenith whole-genome sequencing rare-disease platform, designed to shorten the 4-7 year diagnostic odyssey for rare disease patients.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Direct competitor in blood-based cancer diagnostics. Guardant360 (liquid biopsy CGP) and Guardant Reveal (tumor-naive MRD assay) overlap with Natera's Altera and Signatera franchises, targeting the same oncologists and biopharma partners.

TypeDirect peer
Description

Oncology diagnostics competitor with Cologuard (CRC screening), the Thrive/Earli detection platform, and Oncodetect MRD. Competes for the same clinician wallet and biopharma companion-diagnostic relationships as Natera's oncology franchise.

TypeDirect peer
Description

Competitor in MRD with the FDA-approved clonoSEQ assay for hematologic malignancies (ALL, MM, CLL). Also offers T-cell receptor immunodiagnostics. Direct overlap with Natera's hematology MRD work via CLARITY (acquired with Foresight).

TypeBroad incumbent
Description

Roche subsidiary and broad incumbent in comprehensive genomic profiling (FoundationOne CDx, FoundationOne Liquid CDx). Competes with Natera's Altera and Signatera within oncology workflows and has deep pharma/biopharma penetration.

TypeDirect peer
Description

Competitor in molecular profiling (MI Profile, MI Cancer Seek) and AI-driven multi-omics. Targets oncology clinicians and biopharma with similar use cases to Natera's Altera and CLARITY franchises.

TypeEmerging player
Description

AI-enabled precision medicine company offering genomic profiling, real-world data, and biopharma services. Adjacent competitor to Natera's biopharma services business, with overlapping pharma clients but a different technical foundation (DNA/RNA + imaging vs. cfDNA).

TypeBroad incumbent
Description

Oncology-focused clinical laboratory services company offering CGP, MRD (RaDaR), and hematology testing. Competes with Natera in oncology hospital and biopharma channels; broader menu but less MRD-specific depth.

TypeDirect peer
Description

Genetic testing competitor with overlapping prenatal/women's health (Foresight, Prequel), hereditary cancer, and oncology products. Direct overlap with Natera's Panorama, Horizon, Empower, and Vistara franchises.

TypeDirect peer
Description

Direct competitor in transplant diagnostics with AlloSure (dd-cfDNA) for kidney and heart transplant monitoring. Competes head-to-head with Natera's Prospera in the same transplant centers and is also an active IP adversary.

TypeEmerging player
Description

Genomic diagnostics company focused on urology (Decipher Prostate), thyroid, and lung. Increasingly competing with Natera's oncology CGP and emerging MRD urology applications, with similar sales motion into specialist clinicians.

Market position
Strengths5 records

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Headline, Details, Source

Weaknesses5 records

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Headline, Details, Source

Competitive moat5 records

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Type, Details

Key risks6 records

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Key highlights7 records

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Headline, Details, Source

Customer concentration

Classification, Details

Segment5 records

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Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile5 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration1 record

Each record includes

Title, Type, Description, Source

AI capability9 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature8 records

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Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles21 records

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Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

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Name, Acquired on, Relationship type, Type, Business focus

Compliance6 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds14 records

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Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors13 records

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Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

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Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment2 records

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Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Natera

Molecular Diagnosticsnatera.com

Natera is a publicly traded cell-free DNA testing company that provides MRD oncology (Signatera), transplant rejection (Prospera), and reproductive health (Panorama) tests to clinicians, health systems, and biopharma partners, processing over 16 million cumulative tests across its CAP/CLIA-certified laboratories.

What Natera does

Natera, Inc. is a publicly traded (NASDAQ: NTRA) cell-free DNA (cfDNA) testing company founded in 2004 and headquartered in Austin, Texas, with operations in San Carlos, California and (via the Foresight Diagnostics acquisition) Boulder, Colorado. The company operates proprietary molecular and bioinformatics platforms built on multiplexed PCR and next-generation sequencing to detect and quantify circulating tumor DNA, donor-derived cfDNA, fetal cfDNA, and germline variants from a single blood draw. Flagship products include Signatera (tumor-informed, bespoke ctDNA minimal residual disease / MRD assay), Prospera (donor-derived cfDNA with the proprietary Donor Quantity Score algorithm for transplant rejection), Panorama (SNP-based non-invasive prenatal testing), Empower (hereditary cancer screening), Vistara (single-gene NIPT), and Zenith (whole-genome sequencing for rare disease). Natera runs ISO 13485, CAP, and CLIA-certified labs, holds SOC 2 Type II compliance, and is FDA-cleared for the Signatera CDx in muscle-invasive bladder cancer as of May 2026.

Natera generates revenue through clinical testing services billed to payors and health systems (with oncology ASP around $1,250 per Signatera test in Q1 2026), a dedicated BioPharma services unit that licenses Signatera MRD endpoints and provides real-world data access to trial sponsors, and licensing royalties following the April 2026 court award of a 30% royalty on infringing MRD products. Customers span five distinct segments: oncologists and cancer centers (over half of U.S. oncologists use Signatera), women's health providers (OB/GYNs and maternal-fetal medicine specialists), transplant centers, biopharma sponsors (including Allogene, Genentech, Diakonos, CytoDyn, and Purespring), and rare-disease patients via the Zenith platform. The go-to-market motion is direct enterprise field sales to clinicians and health systems, supplemented by channel partnerships (SRL Inc. in Japan, Pirche AG in transplant) and heavy clinical evidence generation that drives guideline inclusion.

The company has processed over 16 million cumulative tests, maintains a proprietary oncology database with 2M+ plasma timepoints, and reports approximately 50% market share in tumor-informed MRD testing. Investment in scientific marketing — 35 abstracts at ASCO 2026, 20 at AACR 2026, 21 at ATC 2026, and 400+ peer-reviewed publications — supports three NCCN guideline recommendations, including Category 1 for Signatera. Q1 2026 revenue of $696.6M (+38.8% YoY) implies TTM revenue of approximately $2.5B and FY2026 revenue in the $2.8B range, with gross margins near 65% and a market capitalization of approximately $30–31B. The announced Austin headquarters expansion (May 2026) will add roughly 400 new roles alongside the company's largest sequencing facility.

Natera firmographics

Firmographics
Name
Natera
Legal name
Natera, Inc.
Website
https://natera.com
Company type
Public
Founded year
2004
Operating status
Operating
Headcount range
5,001–10,000 employees
Short description
Natera is a publicly traded cell-free DNA testing company that provides MRD oncology (Signatera), transplant rejection (Prospera), and reproductive health (Panorama) tests to clinicians, health systems, and biopharma partners, processing over 16 million cumulative tests across its CAP/CLIA-certified laboratories.
Ownership category
akta.pro rank

Where Natera is headquartered

Location

Headquarters

HQ city
San Carlos
HQ country
United States
HQ region
North America

Offices3 records

Markets served

Natera business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure

Revenue model

  1. Clinical diagnostic testing services: Revenue from running cell-free DNA tests (Signatera, Latitude, Altera, Empower, Prospera, Renasight, Panorama, Horizon, Vistara, Anora, Fetal Focus, Zenith) in CAP/CLIA-certified labs for clinicians, hospitals, health systems, and patients. ASPs in oncology testing were approximately $1,250 in Q1 2026, with 54-55% YoY oncology test volume growth.
  2. Biopharma services and partnerships: Revenue from biopharma customers using Signatera, CLARITY, and RenasightIQ for clinical trial MRD testing, molecular response analysis, real-world data access, and companion-diagnostic development (e.g., Diakonos, CytoDyn, Allogene, Genentech, Diakonos, Purespring/Travere collaborations).
  3. MRD patent licensing royalties: Licensing royalties on MRD-related patents; a U.S. court awarded Natera a 30% ongoing royalty on revenues from infringing MRD-related products (including ArcherDx and Invitae product sales), establishing a recurring royalty revenue stream.
  4. Renasight / RenasightIQ pharma research and clinical-trial services: Revenue from genetic testing panels (Renasight kidney gene panel) and pharma research services that accelerate rare-disease and chronic kidney disease clinical trial recruitment (e.g., Alport, ADPKD, FSGS case studies).

Go-to-market motion4 records

Distribution channels5 records

Marketing channels7 records

Natera product offering

Product offering

Core offering

Natera runs cell-free DNA (cfDNA) diagnostic tests in its ISO 13485/CAP/CLIA-certified laboratories, sold to clinicians, health systems, and biopharma customers. Its core franchise is Signatera, a personalized tumor-informed molecular residual disease (MRD) assay for cancer recurrence monitoring, complemented by Prospera dd-cfDNA transplant rejection tests (kidney, heart, lung), Panorama NIPT and women's health reproductive tests, Renasight kidney gene panels, and the Zenith whole-genome rare-disease platform.

Product overview

Natera operates a platform-plus-modules architecture centered on its NateraCore laboratory services infrastructure and NateraConnect provider portal, with the test menu organized into four clinical franchises: (1) Oncology — anchored by Signatera (tumor-informed MRD) and Signatera Genome, complemented by Latitude (tissue-free MRD), Altera (tumor genomic profiling), Spectrum, Empower (hereditary cancer), and the acquired CLARITY MRD assay from Foresight Diagnostics; (2) Transplant — Prospera dd-cfDNA assessment for kidney, heart, and lung recipients; (3) Kidney genetics — Renasight and RenasightIQ panels; and (4) Reproductive health — Panorama NIPT, Vistara, Fetal Focus, Vasistera, Anora, and Horizon carrier screening. Beyond the clinical test menu, the Zenith whole-genome rare-disease platform, Annotation Platform, NEVA educational virtual assistant, ProReach services, and Constellation platform round out the broader offering.

Differentiator

Problem solved

Functional benefit

Brands

  • Signatera: Personalized, tumor-informed molecular residual disease (MRD) assay for cancer recurrence monitoring and treatment guidance.
  • Latitude
  • Altera
  • Empower
  • Prospera
  • Renasight
  • Horizon
  • Panorama
  • Vistara
  • Anora
  • Vasistera
  • Fetal Focus
  • Zenith
  • Constellation
  • NateraConnect
  • NateraCore Services
  • NEVA for Empower
  • Spectrum

Products and services

  • Signatera
  • Signatera Genome
  • Latitude
  • Altera
  • Empower
  • Prospera
  • Renasight
  • RenasightIQ
  • Horizon
  • Panorama
  • Vistara
  • Fetal Focus
  • Vasistera
  • Anora
  • Zenith
  • CLARITY MRD Assay
  • Spectrum

Quantifiable outcome

  • Signatera-positivity associated with HR 8.15 in adjuvant setting and HR 18.30 in surveillance across a meta-analysis of 18 studies, 3,000+ patients, 15 tumor types (ASCO 2026)
  • +8 more outcomes

Companies that use Natera

Customer profile

Segments5 records

Ideal customer profiles5 records

Natera technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration1 record

AI capability9 records

Feature8 records

Natera partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered core and minor.

  • SRL Inc.coreChannel Partner/ Reseller/ Distributor · 24 June 2026SRL Inc. is Natera's exclusive business partner to commercialize Signatera in Japan following PMDA approval in colorectal cancer. Commercial launch planned by year-end 2026 with SRL supporting commercialization and access expansion across the country.
  • Pirche AGcoreStrategic or Co-development Partner · 19 June 2026Pirche AG and Natera announced a strategic collaboration to advance transplant medicine by combining Pirche's TxPredictor pre-transplant immunological risk-stratification platform with Natera's Prospera dd-cfDNA post-transplant monitoring test. Joint launch planned at the 2026 American Transplant Congress.
  • CytoDyn Inc.coreStrategic or Co-development Partner · 4 June 2026Natera and CytoDyn announced a strategic collaboration to evaluate circulating tumor DNA (ctDNA) dynamics using Signatera on samples from CytoDyn's CLOVER Phase 2 study in metastatic colorectal cancer, plus access to Natera's proprietary oncology database (2M+ plasma timepoints) for molecular response analysis in leronlimab development.
  • Diakonos Oncology Corp.coreStrategic or Co-development Partner · 29 May 2026Natera and Diakonos Oncology Corp. announced a collaboration for Signatera to assess molecular response in patients with refractory melanoma enrolled in Diakonos' DOC-RM Phase I/II trial evaluating DOC1021 (dubodencel), a personalized dendritic cell therapy with FDA Fast Track designation. Natera will perform serial ctDNA monitoring at multiple timepoints.
  • NVIDIAcoreTechnology or Integration · 29 May 2026Natera partners with NVIDIA to enhance its AI models for cell-free DNA-based early cancer detection; Natera is cited as a leading example of a biotech that applies AI to cfDNA technology.
  • Genentech (Tecentriq)coreStrategic or Co-development Partner · 15 May 2026FDA approval of Genentech's Tecentriq / Tecentriq Hybreza as adjuvant treatment for muscle-invasive bladder cancer patients identified as ctDNA-MRD positive by Natera's Signatera CDx, supported by the IMvigor011 Phase III study (36% reduction in recurrence or death; 41% reduction in overall death).
  • Purespring Therapeutics (with Bristol Renal / Genescape / Travere Therapeutics)minorStrategic or Co-development Partner · 29 April 2026Natera collaborated on Purespring Therapeutics' publication in Kidney International Reports identifying NPHS2 variants as a significant under-recognised cause of adult-onset FSGS, informing development strategy for Purespring's PS-001 candidate treatment.
  • BGI Genomics Co., Ltd.coreStrategic or Co-development Partner · 27 April 2026Strategic collaboration with BGI Genomics for developing NGS-based genetic testing assays, cited as a key partnership in stock analyses of Natera.
  • Allogene TherapeuticscoreStrategic or Co-development Partner · 13 April 2026Natera's CLARITY MRD assay is being used to identify MRD-positive patients in Allogene Therapeutics' registrational ALPHA3 trial of cema-cel in first-line large B-cell lymphoma. Interim futility analysis showed 58.3% MRD clearance in the cema-cel arm vs. 16.7% observation.
  • MyOmecoreStrategic or Co-development Partner · 12 March 2026Exclusive partnership with MyOme to develop Natera's Zenith whole-genome sequencing rare-disease platform, designed to shorten the 4-7 year diagnostic odyssey for rare disease patients.

Scale indicators16 records

Recent moves7 records

Expansion highlights6 records

Natera competitors and assessment

Company assessment

Direct peers

  • Guardant Health: Direct competitor in blood-based cancer diagnostics. Guardant360 (liquid biopsy CGP) and Guardant Reveal (tumor-naive MRD assay) overlap with Natera's Altera and Signatera franchises, targeting the same oncologists and biopharma partners.
  • Exact Sciences: Oncology diagnostics competitor with Cologuard (CRC screening), the Thrive/Earli detection platform, and Oncodetect MRD. Competes for the same clinician wallet and biopharma companion-diagnostic relationships as Natera's oncology franchise.
  • Adaptive Biotechnologies: Competitor in MRD with the FDA-approved clonoSEQ assay for hematologic malignancies (ALL, MM, CLL). Also offers T-cell receptor immunodiagnostics. Direct overlap with Natera's hematology MRD work via CLARITY (acquired with Foresight).
  • Caris Life Sciences: Competitor in molecular profiling (MI Profile, MI Cancer Seek) and AI-driven multi-omics. Targets oncology clinicians and biopharma with similar use cases to Natera's Altera and CLARITY franchises.
  • Myriad Genetics: Genetic testing competitor with overlapping prenatal/women's health (Foresight, Prequel), hereditary cancer, and oncology products. Direct overlap with Natera's Panorama, Horizon, Empower, and Vistara franchises.
  • CareDx: Direct competitor in transplant diagnostics with AlloSure (dd-cfDNA) for kidney and heart transplant monitoring. Competes head-to-head with Natera's Prospera in the same transplant centers and is also an active IP adversary.

Broad incumbents

  • Foundation Medicine: Roche subsidiary and broad incumbent in comprehensive genomic profiling (FoundationOne CDx, FoundationOne Liquid CDx). Competes with Natera's Altera and Signatera within oncology workflows and has deep pharma/biopharma penetration.
  • NeoGenomics: Oncology-focused clinical laboratory services company offering CGP, MRD (RaDaR), and hematology testing. Competes with Natera in oncology hospital and biopharma channels; broader menu but less MRD-specific depth.

Emerging players

  • Tempus AI: AI-enabled precision medicine company offering genomic profiling, real-world data, and biopharma services. Adjacent competitor to Natera's biopharma services business, with overlapping pharma clients but a different technical foundation (DNA/RNA + imaging vs. cfDNA).
  • Veracyte: Genomic diagnostics company focused on urology (Decipher Prostate), thyroid, and lung. Increasingly competing with Natera's oncology CGP and emerging MRD urology applications, with similar sales motion into specialist clinicians.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Natera social profiles

Digital presence

Natera compliance and trust

Trust signal

Compliance6 records

Natera financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Natera leadership team

Management profile

Number of profiles

Profiles21 records

Natera subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Natera funding detail

Funding detail

Funding overview

Funding rounds14 records

Investors13 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Natera M&A and investment

M&A and investment

M&A1 record

Investments2 records

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Frequently asked questions about Natera

What does Natera do?

Natera runs cell-free DNA (cfDNA) diagnostic tests in its ISO 13485/CAP/CLIA-certified laboratories, sold to clinicians, health systems, and biopharma customers. Its core franchise is Signatera, a personalized tumor-informed molecular residual disease (MRD) assay for cancer recurrence monitoring, complemented by Prospera dd-cfDNA transplant rejection tests (kidney, heart, lung), Panorama NIPT and women's health reproductive tests, Renasight kidney gene panels, and the Zenith whole-genome rare-disease platform.

Is Natera a public or private company?

Natera is a public company. It is classified as public and is currently operating.

When was Natera founded?

Natera was founded in 2004. It employs 5,001 to 10,000 people.

Where is Natera based?

Natera is headquartered in San Carlos, United States, in the North America region.

How does Natera make money?

Four revenue lines are on record. Clinical diagnostic testing services are the primary driver. The others are biopharma services and partnerships, MRD patent licensing royalties and renasight / RenasightIQ pharma research and clinical-trial services.

Who are Natera's main competitors?

Direct peers on record are Guardant Health, Exact Sciences, Adaptive Biotechnologies, Caris Life Sciences, Myriad Genetics and CareDx. Broad incumbents are Foundation Medicine and NeoGenomics. Emerging players are Tempus AI and Veracyte.

Does Natera have an API?

No public API is recorded for Natera.

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Live signals
YahooNatera (NTRA) Could Be 33% Undervalued Following FDA Breakthrough Device DesignationThe FDA granted Breakthrough Device designation to Natera's multi-cancer early detection blood test. The company's shares have gained 75.10% year-to-date, and a DCF model values them at $599.47, implying a 33% discount. Risks include tighter reimbursement rules and high R&D spending.American Banking and Market NewsNatera, Inc. (NASDAQ:NTRA) Stock Has Average Target Price of $353.45Natera reported Q2 EPS of -$0.47, beating estimates of -$0.49, with revenue of $752.75 million, up 37.7% year-over-year. Analysts give an average Moderate Buy rating with a $353.45 price target. The stock opened at $400.71, trading above its 50-day moving average.YahooWhy Natera (NTRA) Stock Is Up TodayNatera shares rose 1.7% after the FDA granted Breakthrough Device designation to its blood-based multi-cancer early detection assay. The decision followed evaluation of performance data across 12 cancer types. The stock is trading at $400.22, up 2.2% from the previous close.MarketBeatNatera, Inc. (NASDAQ:NTRA) Stock Has Average Target Price of $353.45 According to AnalystsAnalysts rate Natera a Moderate Buy with an average price target of $353.45. The company reported Q2 EPS of -$0.47, beating estimates, and revenue of $752.75 million, up 37.7% year-over-year. Insiders sold 52,985 shares in the last three months.MarketScreenerNatera, Inc. Receives FDA Breakthrough Device Designation for Its Multi-Cancer Early Detection AssayNatera's multi-cancer early detection assay received FDA Breakthrough Device designation. The FDA assessed data from 12 cancer types, considering sensitivity, specificity, and cancer signal origin. The designation aims to speed up development and review for premarket approval.FinancialContent Business PageWhy Natera (NTRA) Stock Is Up TodayShares of genetic testing company Natera rose approximately 2% after the U.S. Food and Drug Administration granted Breakthrough Device designation to its blood-based multi-cancer early detection assay. This regulatory decision follows an evaluation of the test's sensitivity, specificity, and ability to pinpoint cancer origin across 12 different cancer types. The market reaction suggests investors view the approval as significant but not enough to fundamentally alter their long-term perception of the business.American City Business JournalsNatera, PPD top list of Austin life science companiesThe top five life science companies in the Austin area each reported at least 100 employees. Texas State University's endowment grew 839% since 2019 to $2.11 billion, and the University of Texas at Austin has the largest endowment in the region.AdvfnNatera Receives FDA Breakthrough Device Designation for Multi-Cancer Early Detection Blood TestNatera received FDA Breakthrough Device Designation for its multi-cancer early detection blood test after an assessment of clinical performance data covering 12 cancer types. The designation grants access to an accelerated regulatory review framework but does not constitute approval. The company will need further clinical evidence and regulatory submissions before marketing the test.Markets DailyBiotech Stocks To Keep An Eye On – October 6thMarketBeat's stock screener highlights Moderna, Natera, and AbbVie as biotech stocks to watch on October 6th, citing their highest dollar trading volume in recent days. The companies are described with their product portfolios, including vaccines, diagnostics, and pharmaceuticals.FinancialContent Business Page3 Market-Beating Stocks with Competitive AdvantagesDatadog, Brinker International, and Natera are highlighted as market-beating stocks with five-year returns of 93.8%, 281%, and 246% respectively. The article cites rising sales, expanding margins, and increasing returns on capital as key traits, and notes their forward price-to-sales multiples.