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Geneseeq

Full company profile

uuid000215w

Namestring
Geneseeq
Legal namestring
Geneseeq Technology Inc.
Company typeenum
Private
Founded yearint
2008
Descriptiontext

Established in 2008, Geneseeq is an industry leader in Next-Generation Sequencing (NGS) fully committed to the research and clinical translation of NGS Genetic Sequencing in the field of personalized medicine. Geneseeq’s world-leading laboratories have successfully passed China’s National Center of Clinical Laboratories(NCCL) External Quality Assessment(EQA), College of American Pathologists(CAP) PT, European Molecular Genetics Quality Network(EMQN) PT, and received 3rd party medical laboratory and clinical PCR amplification laboratory qualifications.

Short descriptiontext

Geneseeq uses NGS technologies to help physicians make meaningful decisions for cancer treatment.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersToronto, Canada
HQ citystring
Toronto
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
NGS cancer diagnostics, precision oncology testing, companion diagnostic kits, liquid biopsy assays, minimal residual disease monitoring
Industry5 codes
1Genomic Profiling & Sequencing-Based Precision Medicine
CodeHLAAANAAPrimaryYes
2Genomics & Molecular Diagnostics (Trial Support)
CodeHLAGAEADPrimaryNo
3Genomics & Next-Generation Sequencing (NGS) Services
CodeHLAGANAAPrimaryNo
4Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics)
CodeHLAAALADPrimaryNo
5Molecular Diagnostics & Genomics Laboratories
CodeHLAFAMAEPrimaryNo
NAICS code4 codes
  • Medical Laboratories621511
  • In-Vitro Diagnostic Substance Manufacturing325413
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
SIC code3 codes
  • Services-Medical Laboratories8071
  • In Vitro & In Vivo Diagnostic Substances2835
  • Services-Commercial Physical & Biological Research8731
Product category
Precision Oncology Diagnostics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model5 records
1IVD Kit Sales
TypeOne Time License
Description

Sale of FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved NGS IVD kits (GENESEEQPRIME®, PanTRKare™, Essencare™, liquid biopsy kits) to oncology laboratories and hospitals for decentralized clinical testing.

na.geneseeq.com
2Central Laboratory Testing Services
TypeProfessional Services
Description

NGS-based genomic testing services offered through the company's CAP/CLIA-accredited central laboratory. Includes pan-cancer genetic testing, ctDNA liquid biopsy, and MRD monitoring for external clients including hospitals and biopharma companies.

na.geneseeq.com
3Research Services
TypeProfessional Services
Description

Genomic research services provided to biopharma companies and academic institutions, including DNA/RNA sequencing, project design, QC/QA, and data analysis. Geneseeq has 2000+ research projects with biopharma and research partners.

na.geneseeq.com
4Companion Diagnostic (CDx) Development Partnerships
TypeLicensing Royalties
Description

Co-development of CDx kits with pharmaceutical partners (e.g., Roche, HUTCHMED/AstraZeneca, Jiangsu Vcare PharmaTech) for patient selection in clinical trials and drug approvals. Revenue through development fees, milestone payments, and future kit sales.

prnewswire.com
5RUO Kit Solutions
TypeOne Time License
Description

Sale of Research Use Only (RUO) NGS kits to research institutions and biopharma for preclinical and translational research applications.

na.geneseeq.com
Marketing channels5 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, Technology or R&D, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 12 records shown
1GENESEEQPRIME
Description

NGS Tumor Profiling Assay for detecting gene alterations across 425 cancer-related genes in solid malignant neoplasms. FDA 510(k) cleared, CE-IVD marked, NMPA approved.

na.geneseeq.com
+11 more records
Core offering1 text field

Geneseeq develops and commercializes next-generation sequencing (NGS)-based genomic profiling products and services for precision oncology. Its offerings include FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved IVD kits (e.g., GENESEEQPRIME 425-gene assay, PanTRKare NTRK fusion CDx), CAP/CLIA-accredited central laboratory testing services, MRD monitoring (SHIELDING), multi-cancer early detection (CanScan), hematologic malignancy panels (Hemasalus), and contract research services for biopharma and academic institutions.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 9 values shown
  • CanScan® achieves 99% specificity and detects cancer tissue of origin with high accuracy, outperforming standard of care screening in prostate, lung, and liver cancers, and detecting cancer types without effective SOC screening such as esophageal, endometrial, gastric, pancreatic cancers and lymphoma.
+8 more records
Product overview1 text field

Geneseeq is a precision oncology company offering a comprehensive NGS-based genomic testing portfolio spanning products and services. The core offerings include GENESEEQPRIME (FDA 510(k)-cleared 425-gene tumor profiling assay), PanTRKare (China's first NGS-based pan-solid tumor CDx), CanScan (multi-cancer early detection with FDA Breakthrough Designation), SHIELDING (MRD monitoring), and Hemasalus (hematologic malignancies panels), all powered by the proprietary MERCURY multi-omics technology and GENESIS bioinformatics pipeline. Services include central lab testing, IVD kit solutions for decentralized deployment, and research services covering WGS, WES, RNA sequencing, and custom sequencing projects. The company operates CAP/CLIA-accredited facilities and holds regulatory approvals from FDA, CE-IVD, and NMPA.

Product and service14 records
1Hemasalus Hematologic Malignancies Panel
CategoryHematology NGS Panel
Description

NGS gene panel for hematologic malignancy genomic profiling and MRD monitoring. Used in the SCENT-2 trial for ENKTL patients. Covers pan-cancer and cancer-type-specific applications for blood cancers.

2GENESEEQPRIME NGS Tumor Profiling Assay
CategoryIn Vitro Diagnostic Kit
Description

FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved in vitro diagnostic test using next-generation sequencing to detect tumor gene alterations across 425 cancer-related genes in patients with solid malignant neoplasms. Sold as a ready-to-use IVD kit to oncology laboratories for decentralized implementation.

3Pan-Cancer Gene Panels (Solid Tumors)
CategoryNGS Test Panels
Description

Comprehensive pan-cancer NGS panels analyzing 400+ cancer-related genes across all solid tumor types and sample types, enabling comprehensive genomic profiling for treatment matching.

4Cancer Type-Specific Gene Panels (Solid Tumors)
CategoryNGS Test Panels
Description

Targeted NGS gene panels designed for individual solid tumor cancer types, enabling focused and efficient genomic profiling for specific malignancies.

5CanScan Multi-Cancer Early Detection
CategoryEarly Detection Test
Description

Blood-based multi-cancer early detection (MCED) solution utilizing low-depth whole-genome sequencing on circulating cell-free DNA. Achieves 99% specificity, predicts tissue of origin, and detects 13+ cancer types including those lacking effective standard-of-care screening (pancreatic, esophageal, gastric, endometrial, lymphoma).

6SHIELDING Minimal Residual Disease Monitoring
CategoryMRD Monitoring Test
Description

MRD monitoring product for early and mid-stage solid tumors using ctDNA liquid biopsy for post-surgical recurrence monitoring. ShieldingUltra variant integrates mutation, copy number variation, and fragmentomics analysis. Demonstrated median 5-month lead time over radiographic imaging.

7PanTRKare NTRK Gene Fusion Detection Kit
CategoryCompanion Diagnostic Kit
Description

NMPA-approved NGS-based pan-solid tumor companion diagnostic test for detecting NTRK1/NTRK2/NTRK3 gene fusions. Validated across 7 hospitals, 33 tumor types, and 2,400+ clinical samples detecting 200+ unique NTRK fusion variants. Approved as CDx for Roche's ROZLYTREK (entrectinib).

8Essencare EGFR/ALK/ROS1/BRAF/KRAS/HER2 Mutation Detection Kit
CategoryCompanion Diagnostic Kit
Description

NMPA-approved NGS-based CDx kit using reversible terminator technology for detecting actionable mutations in EGFR, ALK, ROS1, BRAF, KRAS, and HER2 across solid tumors.

9EGFR/KRAS/MET Gene Mutation Detection Kit (Liquid Biopsy)
CategoryLiquid Biopsy Kit
Description

NGS liquid biopsy kit that identifies mutations in multiple key tumor driver genes (EGFR, KRAS, MET) from circulating tumor DNA in a blood sample, eliminating the need for tumor tissue.

10Pulmocan Lung Cancer Panel
CategoryCancer-Specific NGS Panel
Description

Cancer type-specific 139-gene NGS panel for lung cancer genomic profiling used in MRD monitoring studies.

11PANCARNA Fusion Panel
CategoryFusion Detection Panel
Description

Targeted sequencing panel for comprehensive detection of cancer-related gene fusions across multiple cancer types.

12Radiotron Panel
CategoryMRD Research Panel
Description

474 cancer-related gene panel used in ctDNA MRD studies for chemoradiotherapy-treated inoperable NSCLC patients, with research published in Molecular Cancer.

13Central Lab Testing Service
CategoryLaboratory Testing Service
Description

NGS-based clinical genomic testing services performed through CAP/CLIA/ISO15189-accredited central laboratories in Canada and China. Includes pan-cancer genetic testing, ctDNA liquid biopsy, MRD monitoring, and turnaround times of 5 business days for external hospitals and biopharma clients.

14Research Services
CategoryResearch Service
Description

Comprehensive genomic research services for biopharma and academic institutions including DNA sequencing (WGS, WES, targeted panel, methylation, customer-made library), RNA sequencing (whole transcriptome, small RNA, circular RNA), project design, QC/QA, and data analysis. Over 2,000 research projects delivered.

Scale indicator18 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
1University Health Network (UHN) - Princess Margaret Cancer Centre
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-07-14
Description

Geneseeq Canada named first commercial genomic testing partner in UHN's SHERLOCK study, a large prospective cancer genomics and molecular residual disease (MRD) research initiative. The collaboration supports genomic profiling and MRD monitoring for approximately 1,000 of the study's expected 7,000 participants over five years, spanning solid tumours and hematologic malignancies. This partnership reflects growing collaboration between academic institutions, healthcare systems, and genomic testing companies in advancing precision oncology research in Canada.

oncodaily.com
2Roche
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-10
Description

Geneseeq's PanTRKare™ NTRK1/NTRK2/NTRK3 Gene Fusion Detection Kit received NMPA marketing authorization as companion diagnostic for Roche's ROZLYTREK® (entrectinib), making it China's first NGS-based pan-solid tumor companion diagnostic test. The assay was validated through a multi-center clinical study involving seven hospitals, 33 tumor types, and more than 2,400 clinical samples that detected over 200 unique NTRK fusion variants. This regulatory milestone represents a strategic collaboration between Geneseeq and Roche in China's precision oncology market.

prnewswire.com
3Jiangsu Vcare PharmaTech
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-07-03
Description

Partnership to develop a companion diagnostic (CDx) kit and advance the product launch of Vcare's pan-neurotrophic tyrosine receptor kinase (NTRK) inhibitor VC004 in China. VC004 is a highly selective next-generation NTRK inhibitor developed to overcome acquired resistance to first-generation NTRK inhibitors. Dr. Xiaonan Wang, Co-founder and CTO of Geneseeq, stated the aim to accelerate the development and clinical application of innovative drugs in China through this deep strategic collaboration.

na.geneseeq.com
4HUTCHMED
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-06-24
Description

Geneseeq served as the only designated NGS testing center in the NMPA approval process for savolitinib (developed by HUTCHMED and AstraZeneca) for NSCLC patients with MET exon 14 skipping alterations. Geneseeq, HUTCHMED, and AstraZeneca are collaborating on the potential development of a companion diagnostics kit for detecting MET mutations in lung cancer patients in China.

na.geneseeq.com
5AstraZeneca
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-06-24
Description

AstraZeneca partnered with Geneseeq and HUTCHMED in the MET inhibitor approval process for lung cancer patients in China. Geneseeq was the designated NGS testing center supporting the Phase II trial across 32 hospitals that led to the conditional approval of savolitinib by NMPA.

na.geneseeq.com
6Illumina
Strategic tierCoreTypeTechnology or IntegrationAnnounced on2018-12-01
Description

Collaboration between Geneseeq and Illumina to develop an oncogene detection kit for clinical diagnosis based on Illumina's sequencing technology. Both parties also conducted comprehensive cooperation in the promotion of high-throughput oncogene testing in China. At the time, Geneseeq's Multi-gene Detection Kit for Lung Cancer was entering CFDA's innovative approval green channel. This partnership leveraged Illumina's sequencing platforms and Geneseeq's assay development and regulatory expertise in China's NGS oncology market.

na.geneseeq.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
1Burning Rock Biotech
TypeDirect peer
Description

China-based NGS oncology company offering tumor profiling, liquid biopsy, and CDx services with multi-regional regulatory footprint. Most direct competitor in the China precision oncology market with overlapping CDx partnership model and NMPA-cleared panels.

2Guardant Health
TypeDirect peer
Description

US-based leader in liquid biopsy and genomic profiling for oncology, with FDA-approved Guardant360 CDx and active MRD/Early Detection programs. Compares to Geneseeq on NGS tumor profiling, liquid biopsy, and CDx strategy.

3Foundation Medicine
TypeBroad incumbent
Description

Roche subsidiary providing FoundationOne CDx and FoundationOne Liquid CDx for comprehensive genomic profiling. Serves as both a competitor and strategic benchmark for Geneseeq's CDx partnership with Roche for entrectinib.

4Tempus AI
TypeDirect peer
Description

US precision medicine company combining NGS tumor profiling, liquid biopsy, MRD, and AI-driven analytics with biopharma partnerships. Strong overlap with Geneseeq's central lab services and biopharma data offerings.

5Caris Life Sciences
TypeDirect peer
Description

US-based molecular profiling and AI company offering MI Profile for solid tumors and a growing liquid biopsy / MRD portfolio. Comparable NGS-based profiling offering for oncologists and biopharma partners.

6Personalis
TypeDirect peer
Description

US-based NGS company focused on tumor profiling (NeXT Personal) and MRD (NeXT Personal Dx). Direct competitor in NGS-based liquid biopsy and CGP for solid tumors, with biopharma CDx services.

7Natera
TypeDirect peer
Description

US-based cell-free DNA testing company with Signatera MRD test as a flagship oncology product. Comparable in ctDNA-based MRD and tumor-informed testing strategy.

8NeoGenomics
TypeBroad incumbent
Description

US clinical oncology lab offering comprehensive solid tumor and hematologic profiling, including NGS panels and liquid biopsy. Broader portfolio but overlapping oncology testing and pharma services.

9Exact Sciences
TypeBroad incumbent
Description

US-based cancer diagnostics leader with Cologuard and Oncotype products, plus emerging MRD (Oncodetect) and multi-cancer efforts. Comparable in MRD and early detection strategy, though much larger and broader.

10Admera Health
TypeEmerging player
Description

US-based NGS lab offering genomic profiling and liquid biopsy services for oncology. Niche / emerging player with overlapping CGP and biopharma research services.

Market position
Strengths5 records

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Weaknesses5 records

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Competitive moat5 records

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Key risks5 records

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Key highlights7 records

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Named customers7 records

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Segment5 records

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Ideal customer profile3 records

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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

AI capability6 records

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Has app

Feature12 records

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Investors11 records

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

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

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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 →

Geneseeq

Precision Oncology Diagnosticsna.geneseeq.com

Geneseeq uses NGS technologies to help physicians make meaningful decisions for cancer treatment.

What Geneseeq does

Established in 2008, Geneseeq is an industry leader in Next-Generation Sequencing (NGS) fully committed to the research and clinical translation of NGS Genetic Sequencing in the field of personalized medicine. Geneseeq’s world-leading laboratories have successfully passed China’s National Center of Clinical Laboratories(NCCL) External Quality Assessment(EQA), College of American Pathologists(CAP) PT, European Molecular Genetics Quality Network(EMQN) PT, and received 3rd party medical laboratory and clinical PCR amplification laboratory qualifications.

Geneseeq firmographics

Firmographics
Name
Geneseeq
Legal name
Geneseeq Technology Inc.
Website
https://na.geneseeq.com
Company type
Private
Founded year
2008
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Geneseeq uses NGS technologies to help physicians make meaningful decisions for cancer treatment.
Ownership category
akta.pro rank

Geneseeq industry classification

Industry
Product category
Precision Oncology Diagnostics
NAICS
Medical Laboratories (621511), In-Vitro Diagnostic Substance Manufacturing (325413), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417)
SIC
Services-Medical Laboratories (8071), In Vitro & In Vivo Diagnostic Substances (2835), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Genomic Profiling & Sequencing-Based Precision Medicine (HLAAANAA)
akta.pro secondary industries
Genomics & Molecular Diagnostics (Trial Support) (HLAGAEAD), Genomics & Next-Generation Sequencing (NGS) Services (HLAGANAA), Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics) (HLAAALAD), Molecular Diagnostics & Genomics Laboratories (HLAFAMAE)

Keywords

  • NGS cancer diagnostics
  • Precision oncology testing
  • Companion diagnostic kits
  • Liquid biopsy assays
  • Minimal residual disease monitoring

Where Geneseeq is headquartered

Location

Headquarters

HQ city
Toronto
HQ country
Canada
HQ region
North America

Offices2 records

Markets served

Geneseeq business model

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

Revenue model

  1. IVD Kit Sales: Sale of FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved NGS IVD kits (GENESEEQPRIME®, PanTRKare™, Essencare™, liquid biopsy kits) to oncology laboratories and hospitals for decentralized clinical testing.
  2. Central Laboratory Testing Services: NGS-based genomic testing services offered through the company's CAP/CLIA-accredited central laboratory. Includes pan-cancer genetic testing, ctDNA liquid biopsy, and MRD monitoring for external clients including hospitals and biopharma companies.
  3. Research Services: Genomic research services provided to biopharma companies and academic institutions, including DNA/RNA sequencing, project design, QC/QA, and data analysis. Geneseeq has 2000+ research projects with biopharma and research partners.
  4. Companion Diagnostic (CDx) Development Partnerships: Co-development of CDx kits with pharmaceutical partners (e.g., Roche, HUTCHMED/AstraZeneca, Jiangsu Vcare PharmaTech) for patient selection in clinical trials and drug approvals. Revenue through development fees, milestone payments, and future kit sales.
  5. RUO Kit Solutions: Sale of Research Use Only (RUO) NGS kits to research institutions and biopharma for preclinical and translational research applications.

Go-to-market motion1 record

Distribution channels5 records

Marketing channels5 records

Geneseeq product offering

Product offering

Core offering

Geneseeq develops and commercializes next-generation sequencing (NGS)-based genomic profiling products and services for precision oncology. Its offerings include FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved IVD kits (e.g., GENESEEQPRIME 425-gene assay, PanTRKare NTRK fusion CDx), CAP/CLIA-accredited central laboratory testing services, MRD monitoring (SHIELDING), multi-cancer early detection (CanScan), hematologic malignancy panels (Hemasalus), and contract research services for biopharma and academic institutions.

Product overview

Geneseeq is a precision oncology company offering a comprehensive NGS-based genomic testing portfolio spanning products and services. The core offerings include GENESEEQPRIME (FDA 510(k)-cleared 425-gene tumor profiling assay), PanTRKare (China's first NGS-based pan-solid tumor CDx), CanScan (multi-cancer early detection with FDA Breakthrough Designation), SHIELDING (MRD monitoring), and Hemasalus (hematologic malignancies panels), all powered by the proprietary MERCURY multi-omics technology and GENESIS bioinformatics pipeline. Services include central lab testing, IVD kit solutions for decentralized deployment, and research services covering WGS, WES, RNA sequencing, and custom sequencing projects. The company operates CAP/CLIA-accredited facilities and holds regulatory approvals from FDA, CE-IVD, and NMPA.

Differentiator

Problem solved

Functional benefit

Brands

  • GENESEEQPRIME: NGS Tumor Profiling Assay for detecting gene alterations across 425 cancer-related genes in solid malignant neoplasms. FDA 510(k) cleared, CE-IVD marked, NMPA approved.
  • CanScan
  • SHIELDING
  • CALIBRATE
  • PanTRKare
  • Essencare
  • MERCURY
  • Hemasalus
  • Pulmocan
  • Radiotron
  • PANCARNA
  • GENESIS by GENESEEQ

Products and services

  • Hemasalus Hematologic Malignancies Panel NGS gene panel for hematologic malignancy genomic profiling and MRD monitoring. Used in the SCENT-2 trial for ENKTL patients. Covers pan-cancer and cancer-type-specific applications for blood cancers.
  • GENESEEQPRIME NGS Tumor Profiling Assay FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved in vitro diagnostic test using next-generation sequencing to detect tumor gene alterations across 425 cancer-related genes in patients with solid malignant neoplasms. Sold as a ready-to-use IVD kit to oncology laboratories for decentralized implementation.
  • Pan-Cancer Gene Panels (Solid Tumors) Comprehensive pan-cancer NGS panels analyzing 400+ cancer-related genes across all solid tumor types and sample types, enabling comprehensive genomic profiling for treatment matching.
  • Cancer Type-Specific Gene Panels (Solid Tumors) Targeted NGS gene panels designed for individual solid tumor cancer types, enabling focused and efficient genomic profiling for specific malignancies.
  • CanScan Multi-Cancer Early Detection Blood-based multi-cancer early detection (MCED) solution utilizing low-depth whole-genome sequencing on circulating cell-free DNA. Achieves 99% specificity, predicts tissue of origin, and detects 13+ cancer types including those lacking effective standard-of-care screening (pancreatic, esophageal, gastric, endometrial, lymphoma).
  • SHIELDING Minimal Residual Disease Monitoring MRD monitoring product for early and mid-stage solid tumors using ctDNA liquid biopsy for post-surgical recurrence monitoring. ShieldingUltra variant integrates mutation, copy number variation, and fragmentomics analysis. Demonstrated median 5-month lead time over radiographic imaging.
  • PanTRKare NTRK Gene Fusion Detection Kit NMPA-approved NGS-based pan-solid tumor companion diagnostic test for detecting NTRK1/NTRK2/NTRK3 gene fusions. Validated across 7 hospitals, 33 tumor types, and 2,400+ clinical samples detecting 200+ unique NTRK fusion variants. Approved as CDx for Roche's ROZLYTREK (entrectinib).
  • Essencare EGFR/ALK/ROS1/BRAF/KRAS/HER2 Mutation Detection Kit NMPA-approved NGS-based CDx kit using reversible terminator technology for detecting actionable mutations in EGFR, ALK, ROS1, BRAF, KRAS, and HER2 across solid tumors.
  • EGFR/KRAS/MET Gene Mutation Detection Kit (Liquid Biopsy) NGS liquid biopsy kit that identifies mutations in multiple key tumor driver genes (EGFR, KRAS, MET) from circulating tumor DNA in a blood sample, eliminating the need for tumor tissue.
  • Pulmocan Lung Cancer Panel Cancer type-specific 139-gene NGS panel for lung cancer genomic profiling used in MRD monitoring studies.
  • PANCARNA Fusion Panel Targeted sequencing panel for comprehensive detection of cancer-related gene fusions across multiple cancer types.
  • Radiotron Panel 474 cancer-related gene panel used in ctDNA MRD studies for chemoradiotherapy-treated inoperable NSCLC patients, with research published in Molecular Cancer.
  • Central Lab Testing Service NGS-based clinical genomic testing services performed through CAP/CLIA/ISO15189-accredited central laboratories in Canada and China. Includes pan-cancer genetic testing, ctDNA liquid biopsy, MRD monitoring, and turnaround times of 5 business days for external hospitals and biopharma clients.
  • Research Services Comprehensive genomic research services for biopharma and academic institutions including DNA sequencing (WGS, WES, targeted panel, methylation, customer-made library), RNA sequencing (whole transcriptome, small RNA, circular RNA), project design, QC/QA, and data analysis. Over 2,000 research projects delivered.

Quantifiable outcome

  • CanScan® achieves 99% specificity and detects cancer tissue of origin with high accuracy, outperforming standard of care screening in prostate, lung, and liver cancers, and detecting cancer types without effective SOC screening such as esophageal, endometrial, gastric, pancreatic cancers and lymphoma.
  • +8 more outcomes

Companies that use Geneseeq

Customer profile

Named customers7 records

Segments5 records

Ideal customer profiles3 records

Geneseeq technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability6 records

Feature12 records

Geneseeq partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core.

  • University Health Network (UHN) - Princess Margaret Cancer CentrecoreStrategic or Co-development Partner · 14 July 2026Geneseeq Canada named first commercial genomic testing partner in UHN's SHERLOCK study, a large prospective cancer genomics and molecular residual disease (MRD) research initiative. The collaboration supports genomic profiling and MRD monitoring for approximately 1,000 of the study's expected 7,000 participants over five years, spanning solid tumours and hematologic malignancies. This partnership reflects growing collaboration between academic institutions, healthcare systems, and genomic testing companies in advancing precision oncology research in Canada.
  • RochecoreStrategic or Co-development Partner · 10 November 2025Geneseeq's PanTRKare™ NTRK1/NTRK2/NTRK3 Gene Fusion Detection Kit received NMPA marketing authorization as companion diagnostic for Roche's ROZLYTREK® (entrectinib), making it China's first NGS-based pan-solid tumor companion diagnostic test. The assay was validated through a multi-center clinical study involving seven hospitals, 33 tumor types, and more than 2,400 clinical samples that detected over 200 unique NTRK fusion variants. This regulatory milestone represents a strategic collaboration between Geneseeq and Roche in China's precision oncology market.
  • Jiangsu Vcare PharmaTechcoreStrategic or Co-development Partner · 3 July 2024Partnership to develop a companion diagnostic (CDx) kit and advance the product launch of Vcare's pan-neurotrophic tyrosine receptor kinase (NTRK) inhibitor VC004 in China. VC004 is a highly selective next-generation NTRK inhibitor developed to overcome acquired resistance to first-generation NTRK inhibitors. Dr. Xiaonan Wang, Co-founder and CTO of Geneseeq, stated the aim to accelerate the development and clinical application of innovative drugs in China through this deep strategic collaboration.
  • HUTCHMEDcoreStrategic or Co-development Partner · 24 June 2021Geneseeq served as the only designated NGS testing center in the NMPA approval process for savolitinib (developed by HUTCHMED and AstraZeneca) for NSCLC patients with MET exon 14 skipping alterations. Geneseeq, HUTCHMED, and AstraZeneca are collaborating on the potential development of a companion diagnostics kit for detecting MET mutations in lung cancer patients in China.
  • AstraZenecacoreStrategic or Co-development Partner · 24 June 2021AstraZeneca partnered with Geneseeq and HUTCHMED in the MET inhibitor approval process for lung cancer patients in China. Geneseeq was the designated NGS testing center supporting the Phase II trial across 32 hospitals that led to the conditional approval of savolitinib by NMPA.
  • IlluminacoreTechnology or Integration · 1 December 2018Collaboration between Geneseeq and Illumina to develop an oncogene detection kit for clinical diagnosis based on Illumina's sequencing technology. Both parties also conducted comprehensive cooperation in the promotion of high-throughput oncogene testing in China. At the time, Geneseeq's Multi-gene Detection Kit for Lung Cancer was entering CFDA's innovative approval green channel. This partnership leveraged Illumina's sequencing platforms and Geneseeq's assay development and regulatory expertise in China's NGS oncology market.

Scale indicators18 records

Recent moves6 records

Expansion highlights6 records

Geneseeq competitors and assessment

Company assessment

Direct peers

  • Burning Rock Biotech: China-based NGS oncology company offering tumor profiling, liquid biopsy, and CDx services with multi-regional regulatory footprint. Most direct competitor in the China precision oncology market with overlapping CDx partnership model and NMPA-cleared panels.
  • Guardant Health: US-based leader in liquid biopsy and genomic profiling for oncology, with FDA-approved Guardant360 CDx and active MRD/Early Detection programs. Compares to Geneseeq on NGS tumor profiling, liquid biopsy, and CDx strategy.
  • Tempus AI: US precision medicine company combining NGS tumor profiling, liquid biopsy, MRD, and AI-driven analytics with biopharma partnerships. Strong overlap with Geneseeq's central lab services and biopharma data offerings.
  • Caris Life Sciences: US-based molecular profiling and AI company offering MI Profile for solid tumors and a growing liquid biopsy / MRD portfolio. Comparable NGS-based profiling offering for oncologists and biopharma partners.
  • Personalis: US-based NGS company focused on tumor profiling (NeXT Personal) and MRD (NeXT Personal Dx). Direct competitor in NGS-based liquid biopsy and CGP for solid tumors, with biopharma CDx services.
  • Natera: US-based cell-free DNA testing company with Signatera MRD test as a flagship oncology product. Comparable in ctDNA-based MRD and tumor-informed testing strategy.

Broad incumbents

  • Foundation Medicine: Roche subsidiary providing FoundationOne CDx and FoundationOne Liquid CDx for comprehensive genomic profiling. Serves as both a competitor and strategic benchmark for Geneseeq's CDx partnership with Roche for entrectinib.
  • NeoGenomics: US clinical oncology lab offering comprehensive solid tumor and hematologic profiling, including NGS panels and liquid biopsy. Broader portfolio but overlapping oncology testing and pharma services.
  • Exact Sciences: US-based cancer diagnostics leader with Cologuard and Oncotype products, plus emerging MRD (Oncodetect) and multi-cancer efforts. Comparable in MRD and early detection strategy, though much larger and broader.

Emerging players

  • Admera Health: US-based NGS lab offering genomic profiling and liquid biopsy services for oncology. Niche / emerging player with overlapping CGP and biopharma research services.

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Frequently asked questions about Geneseeq

What does Geneseeq do?

Geneseeq develops and commercializes next-generation sequencing (NGS)-based genomic profiling products and services for precision oncology. Its offerings include FDA 510(k)-cleared, CE-IVD-marked, and NMPA-approved IVD kits (e.g., GENESEEQPRIME 425-gene assay, PanTRKare NTRK fusion CDx), CAP/CLIA-accredited central laboratory testing services, MRD monitoring (SHIELDING), multi-cancer early detection (CanScan), hematologic malignancy panels (Hemasalus), and contract research services for biopharma and academic institutions.

Is Geneseeq a public or private company?

Geneseeq is a private company. It is classified as venture growth investor backed and is currently operating.

When was Geneseeq founded?

Geneseeq was founded in 2008. It employs 501 to 1,000 people.

Where is Geneseeq based?

Geneseeq is headquartered in Toronto, Canada, in the North America region.

How does Geneseeq make money?

Five revenue lines are on record. IVD Kit Sales are the primary driver. The others are central Laboratory Testing Services, research Services, companion Diagnostic (CDx) Development Partnerships and RUO Kit Solutions.

Who are Geneseeq's main competitors?

Direct peers on record are Burning Rock Biotech, Guardant Health, Tempus AI, Caris Life Sciences, Personalis and Natera. Broad incumbents are Foundation Medicine, NeoGenomics and Exact Sciences. Admera Health is listed as an emerging player.

Does Geneseeq have an API?

No public API is recorded for Geneseeq.

What industry is Geneseeq in?

Geneseeq's product category is Precision Oncology Diagnostics. Its primary akta.pro industry code is HLAAANAA, Genomic Profiling & Sequencing-Based Precision Medicine, with a secondary code of HLAGAEAD, Genomics & Molecular Diagnostics (Trial Support). Its NAICS code is 621511 and its SIC code is 8071.

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Live signals
PR NewswirePanTRKare™ Officially Approved as the Companion Diagnostic for VELMARTO® (Eratrectinib)The National Medical Products Administration (NMPA) approved Geneseeq's PanTRKare™ kit as the companion diagnostic for Vcare PharmaTech's VELMARTO® (Eratrectinib). This regulatory milestone validates the testing method for identifying patients with NTRK fusion-positive solid tumors, facilitating precise clinical treatment and market adoption of the drug.PR Newswire APACPanTRKare™ Officially Approved as the Companion Diagnostic for VELMARTO® (Eratrectinib)On August 6, the NMPA granted approval to Geneseeq's PanTRKare™ NTRK1/2/3 Gene Fusion Detection Kit as a companion diagnostic for VELMARTO® (Eratrectinib), a TRK inhibitor developed by Vcare PharmaTech. This approval supports the identification and treatment of patients with NTRK fusion-positive solid tumors, enhancing the clinical application of Eratrectinib. The partnership between Geneseeq and Vcare is expected to improve patient access to targeted therapies in the oncology space.OncoDailyGeneseeq Canada Joins UHN’s SHERLOCK Study as First Genomic Testing PartnerGeneseeq Canada has been named the first commercial genomic testing partner in the SHERLOCK study, a large prospective cancer genomics and molecular residual disease research initiative led by University Health Network's Princess Margaret Cancer Centre. The collaboration will support genomic profiling and molecular residual disease monitoring for approximately 1,000 of the study's expected 7,000 participants over five years across solid tumours and hematologic malignancies. The partnership reflects growing collaboration between academic institutions, healthcare systems, and genomic testing companies in advancing precision oncology research in Canada.PR NewswireGeneseeq Canada Named First Genomic Testing Partner in UHN's SHERLOCK StudyGeneseeq Canada announced its support for the SHERLOCK study at University Health Network, providing genomic testing and molecular residual disease monitoring for about 1,000 patients. The study expects to enroll 7,000 patients over five years across solid tumors and hematologic malignancies. Geneseeq will use its GeneseeqPrime, Shielding Ultra, and Hemasalus assays for selected participants.Chinaventure终于又有NGS企业准备IPO了Nanjing Shihe Gene resubmitted an IPO application to the Sci-Tech Innovation Board in June 2026, ending a two-year silence in tumor NGS IPOs. Previous applicants like Burning Stone and PanGene failed or privatized, and Zhenhe Technology's Hong Kong applications were rejected. The resubmitted prospectus may signal changes in the company's story, performance, and compliance.BioSpaceGeneseeq Receives NMPA Approval for PanTRKare™ - China’s First NGS-Based Pan-Solid Tumor Companion Diagnostic Kit for NTRK Gene FusionsGeneseeq Technology Inc. received marketing authorization from China's National Medical Products Administration for its PanTRKare™ NGS-based companion diagnostic kit, the first of its kind approved in China for detecting NTRK gene fusions. The test is designated as a companion diagnostic for Roche's entrectinib and was validated through clinical studies involving over 2,400 samples across 33 tumor types. This approval enables clinicians in China to accurately identify patients with rare NTRK mutations for targeted therapy.PR NewswireGeneseeq Receives NMPA Approval for PanTRKare™ - China's First NGS-Based Pan-Solid Tumor Companion Diagnostic Kit for NTRK Gene FusionsGeneseeq Technology Inc. announced that its PanTRKare™ NTRK1/NTRK2/NTRK3 Gene Fusion Detection Kit received marketing authorization from China's National Medical Products Administration (NMPA), making it China's first next-generation sequencing (NGS)-based pan-solid tumor companion diagnostic test. The assay is approved as a companion diagnostic for Roche's ROZLYTREK® (entrectinib) and was validated through a multi-center clinical study involving seven hospitals, 33 tumor types, and more than 2,400 clinical samples that detected over 200 unique NTRK fusion variants. The company stated it will continue advancing precision oncology diagnostics through global regulatory collaborations and biopharma partnerships.Clinical Lab ProductsFDA Clears Tumor Profiling Assay that Analyzes 425 Cancer-Related GenesThe FDA has granted 510(k) clearance to Geneseeq Technology Inc's GENESEEQPRIME NGS Tumor Profiling Assay, an in vitro diagnostic test that uses next-generation sequencing to detect tumor gene alterations across 425 cancer-related genes in patients with solid malignant neoplasms. Analytical and clinical validation studies conducted across multiple US clinical laboratories demonstrated high sensitivity, specificity, and reproducibility. The clearance follows previous CE-IVD marking in Europe and NMPA approval in China, completing a multi-regional regulatory strategy that enables the company to support clinical trials, biomarker-driven drug development, and companion diagnostic strategies globally.DelveinsightGeneseeq Technology, Medtronic, CorNeat VisionThe article reports on multiple medical device and diagnostics companies achieving regulatory milestones or launching products, including Geneseeq receiving FDA clearance for its oncology assay and Medtronic securing FDA approval to expand its MiniMed system integration with Abbott's sensor. Additionally, CorNeat Vision announced successful vision restoration using its artificial cornea, while SprintRay acquired EnvisionTEC's dental portfolio and Olympus launched a new imaging platform in the U.S.PR NewswireGeneseeqPrime® Gains FDA 510(k) ClearanceGeneseeq Technology Inc. announced that the U.S. Food and Drug Administration has granted 510(k) clearance for its GENESEEQPRIME® NGS Tumor Profiling Assay, an in vitro diagnostic test kit that uses next-generation sequencing of DNA from tumor tissue to detect gene alterations across 425 cancer-related genes in patients with solid malignant neoplasms. The ready-to-use IVD kit enables decentralized implementation in oncology laboratories while maintaining globally harmonized standards, and is paired with the company's proprietary bioinformatics pipeline GENESIS by GENESEEQ®. This milestone positions Geneseeq as a globally compliant precision oncology company, following prior regulatory achievements including CE-IVD marking in Europe and NMPA approval in China.