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National Human Genome Research Institute

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uuid0006rgo

Namestring
National Human Genome Research Institute
Legal namestring
National Human Genome Research Institute
Websiteurl
genome.gov
Company typeenum
Public
Founded yearint
1990
Descriptiontext

The National Human Genome Research Institute (NHGRI) is a U.S. federal government research institute within the National Institutes of Health (NIH), itself an agency of the Department of Health and Human Services. Established in 1990 to lead the Human Genome Project, NHGRI's mission is to advance genomics research from basic science through clinical implementation. Its core activities include funding extramural research through competitive grants and contracts, conducting intramural research on the NIH campus in Bethesda, Maryland, and maintaining genomic data resources such as the Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL) and the dbGaP database of Genotypes and Phenotypes. The institute led the Telomere-to-Telomere Consortium, which released the first complete, gapless human genome sequence (T2T-CHM13) on March 31, 2022, adding approximately 200 million previously unread base pairs to the human reference.

NHGRI's portfolio of research programs spans functional genomics (ENCODE), tissue-specific gene expression (GTEx), cancer genomics (TCGA), polygenic risk methods in diverse populations (PRIMED), and clinical implementation networks (eMERGE, IGNITE, ClinGen, CSER, NSIGHT, UDN). It funds translational initiatives such as the Southeast Genomic Medicine Service (SE-GEMS) eConsult platform, ELSI (Ethical, Legal, and Social Implications) research, and SBIR grants to genomics startups. The institute also produces educational resources, fact sheets, and the GenomeTV lecture series for audiences ranging from K-12 educators and patients to physicians and policymakers.

As a government research institute rather than a commercial entity, NHGRI is funded through annual congressional appropriations distributed by NIH and does not generate commercial revenue. Its outputs — research funding, public-domain data resources, educational materials, and policy guidance — are provided free of charge to qualified recipients. Revenue streams consist of federal appropriations and the disbursement of research grants and multiyear awards (e.g., $7.87M to Vanderbilt Health and UAB; $3.2M to Feinstein Institutes; $2M SBIR to Dovetail Genomics). Its customer base is horizontal: scientists and academic researchers, healthcare providers, patients and the general public, educators, and policymakers.

Short descriptiontext

The National Human Genome Research Institute (NHGRI) is a U.S. federal research institute within NIH that funds and conducts genomics research, maintains public genomic data resources, and advances genomic medicine implementation for scientists, clinicians, patients, and the general public.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersBethesda, United States
HQ citystring
Bethesda
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
genomics research funding, human genome research, genomic medicine programs, genomics data resources, genomic science education
Industry4 codes
1Health Research Funding Agencies (Public/Quasi-Public)
CodeHLAJALABPrimaryYes
2Public Health Genomics & Sequencing (WGS/Metagenomics) Networks
CodeHLAJAIAKPrimaryNo
3Health Data, Vital Statistics & Population Health Informatics
CodeBPAIAJAMPrimaryNo
4Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics)
CodeHLAAALADPrimaryNo
NAICS code3 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
  • Research and Development in the Physical, Engineering, and Life Sciences54171
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Genomics Research
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Federal Appropriations
TypeLicensing Royalties
Description

NHGRI is funded through annual congressional appropriations to the National Institutes of Health. The institute receives a budget allocation from the NIH which is part of the U.S. Department of Health and Human Services. As a federal research institute, NHGRI does not generate commercial revenue but distributes funds through grants and contracts to support extramural and intramural genomics research.

genome.gov
2Research Grants and Awards
TypeManaged Services
Description

NHGRI issues multiyear awards and grants to external research institutions. Example: $7.87 million award to Vanderbilt Health and UAB for the Southeast Genomic Medicine Service (SE-GEMS) initiative. Funding supports genomic eConsult services, research projects, and training programs.

news.vumc.org
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components5 values
Personnel, Operations, Technology or R&D, Infrastructure, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

NHGRI is a U.S. federal research institute within the National Institutes of Health (NIH) that advances genomics research by funding extramural and intramural scientific programs, maintaining genomic data resources and bioinformatics infrastructure, and disseminating educational materials. It issues research grants and contracts to public and private research institutions worldwide and operates programs such as ENCODE, ClinGen, eMERGE, the Undiagnosed Diseases Network, and the Telomere-to-Telomere Consortium. It also provides public-facing tools including the genome.gov website, the Family Health History Tool, and the Genomic Medicine Meetings series.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • First complete human genome sequence completed with 200 million added base pairs
+1 more record
Product overview1 text field

The National Human Genome Research Institute (NHGRI) is a research institute within the NIH, not a commercial product company. Its offerings consist primarily of research programs, educational resources, and health information platforms rather than a unified commercial product. The genome.gov website serves as the primary public-facing platform, providing genomics education, research funding information, and health resources. NHGRI funds and coordinates numerous research programs including the Advancing Genomic Medicine Research (AGMR), Clinical Genome Resource (ClinGen), eMERGE Network, Undiagnosed Diseases Network (UDN), and the ENCODE Project. The institute also provides the Family Health History Tool for clinical use, supports the Southeast Genomic Medicine Service (SE-GEMS) eConsult platform for clinician guidance, and offers the ELSI Research Program addressing ethical, legal, and social implications of genomics. Training and fellowship programs like the NIH-ACMG Fellowship and educational resources for educators round out the portfolio.

Product and service1 record
1genome.gov Website Platform
Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership14 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-09
Description

Vanderbilt Health partnered with NHGRI-funded Southeast Genomic Medicine Service (SE-GEMS) initiative. The project is funded by a $7.87 million multiyear award from NHGRI to expand access to genomic medicine for clinicians and patients across the Southeast United States. The partnership creates a genomic eConsult service allowing clinicians to submit questions about genetic testing and receive guidance from genetics experts.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-09
Description

UAB partnered with Vanderbilt Health in the SE-GEMS initiative funded by a $7.87 million NHGRI award. The partnership initially focuses on general genetics, pharmacogenomics, prenatal genetics, and cancer genetics, with the goal of building a scalable model for broader regional and national implementation of genomic medicine services.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-10-23
Description

Feinstein Institutes received $3.2 million from NIH (including NHGRI) to fund research on polygenic embryo selection (PES) technology for evaluating embryos for disease risks during in vitro fertilization. Research involves collaborations with Baylor College of Medicine and Massachusetts General Hospital over four years.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-10-23
Description

Collaborator with Feinstein Institutes on NIH-funded polygenic embryo selection research. Part of a multi-institutional effort to assess scientific accuracy and ethical implications of PES technology.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-10-23
Description

Collaborator with Feinstein Institutes on NIH-funded polygenic embryo selection research. Part of multi-institutional effort to evaluate PES technology for disease risk assessment during IVF.

6Telomere-to-Telomere Consortium
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-03-31
Description

Consortium led by NHGRI with approximately 100 scientists that produced the first complete, gapless human genome sequence (T2T-CHM13). The consortium used Oxford Nanopore and PacBio long-read sequencing platforms to bridge repetitive sections that defeated earlier short-read methods. This achievement added nearly 200 million base pairs of previously unread sequence to the human reference genome.

spacedaily.com
7Human Microbiome Project (HMP)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Trans-NIH collaboration through the Common Fund. NHGRI collaborates with other NIH institutes on microbiome research as part of its cross-cutting activities in genomics and society.

genome.gov
Strategic tierCoreTypeStrategic or Co-development Partner
Description

International collaboration supporting genomics research in Africa. NHGRI participates as part of cross-NIH Common Fund projects to advance genomic research globally.

9GTEx (Genotype-Tissue Expression Project)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Common Fund project studying relationship between genetic variation and gene expression across human tissues. NHGRI collaborates with other NIH institutes on this landmark project.

genome.gov
10CSER (Clinical Sequencing Evidence-Generating Research)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

NHGRI collaboration focused on generating evidence about the clinical use of genomic sequencing. Part of the Division of Genomics and Society's outreach activities.

genome.gov
11NSIGHT (Newborn Sequencing in Genomic Medicine and Public Health)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

NHGRI program exploring the implications of genomic sequencing in newborns. Collaborates across NHGRI divisions and with other NIH institutes.

genome.gov
12IGNITE (Implementing Genomics in Practice)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

NHGRI network focused on implementing genomic medicine in clinical practice. Supports pragmatic clinical trials and implementation research.

genome.gov
13eMERGE (Electronic Medical Records and Genomics) Network
Strategic tierCoreTypeStrategic or Co-development Partner
Description

NHGRI network combining DNA biobanks with electronic medical record systems for large-scale genomic research. Part of genomic medicine implementation efforts.

genome.gov
14ClinGen (Clinical Genome Resource)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

NHGRI-funded resource providing expert consensus on genes and variants relevant to disease. Part of clinical genome resources for genomic medicine.

genome.gov
Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Another major NIH institute focused on cancer research; like NHGRI it funds large extramural research programs, operates intramural labs, and convenes clinical networks (e.g., TCGA, which NHGRI co-leads). It is the closest functional peer within the federal genomics/biomedical ecosystem.

TypeDirect peer
Description

UK-based charitable foundation that funds genomics and biomedical research globally, including the Wellcome Sanger Institute, which produces large-scale genomic reference data (e.g., UK Biobank contributions). Most direct international peer to NHGRI's combination of research funding plus reference data stewardship.

TypeBroad incumbent
Description

Large, established genomics research organization operating major sequencing, computation, and disease-gene discovery programs. Comparable to NHGRI in scientific output and convening power, though private/non-profit and reliant on philanthropic and federal grants rather than direct congressional appropriation.

TypeDirect peer
Description

A sister NIH institute that funds basic biomedical research through grants and training programs. Directly comparable in operating model (federal institute, extramural grants, intramural research) though with a broader mandate than genomics.

TypeBroad incumbent
Description

Large private biomedical research organization supporting ~300 HHMI Investigators across U.S. universities. Comparable in funding scale, scientific prestige, and investigator-driven model, though broader than NHGRI's genomics-specific remit.

6European Molecular Biology Laboratory (EMBL-EBI)
TypeDirect peer
Description

Intergovernmental bioinformatics and genomics data institute operating major open data resources (Ensembl, ENA, EVA). Most direct international peer to NHGRI's data stewardship role (e.g., AnVIL/dbGaP).

TypeDirect peer
Description

Independent, nonprofit biomedical research institution specializing in mammalian genetics and genomics, operating research programs, genomic databases, and distributing mouse models. Closely comparable to NHGRI's intramural research and data resource mission.

TypeBroad incumbent
Description

Federal public health agency that operates genomic surveillance programs (e.g., PulseNet, AMD) and uses WGS for outbreak response. Overlaps with NHGRI in public-health-oriented genomic epidemiology but with a federal-regulatory rather than research-funding orientation.

TypeBroad incumbent
Description

Federal agency that funds basic scientific research across all disciplines, including genomics-adjacent computational biology. Comparable in funding-agency model and federal appropriations structure, though much broader in scope.

TypeEmerging player
Description

Private nonprofit research organization conducting large-scale scientific projects (brain science, cell science, immunology). Comparable as a mission-driven, large-scale research organization producing open data assets, though not genomics-focused.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

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Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

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

AI maturity
App detail

Has app

Feature4 records

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Core technology
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Profiles6 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

Each record includes

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

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

M&A

Each record includes

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

Investment19 records

Each record includes

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

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

National Human Genome Research Institute

Genomics Researchgenome.gov

The National Human Genome Research Institute (NHGRI) is a U.S. federal research institute within NIH that funds and conducts genomics research, maintains public genomic data resources, and advances genomic medicine implementation for scientists, clinicians, patients, and the general public.

What National Human Genome Research Institute does

The National Human Genome Research Institute (NHGRI) is a U.S. federal government research institute within the National Institutes of Health (NIH), itself an agency of the Department of Health and Human Services. Established in 1990 to lead the Human Genome Project, NHGRI's mission is to advance genomics research from basic science through clinical implementation. Its core activities include funding extramural research through competitive grants and contracts, conducting intramural research on the NIH campus in Bethesda, Maryland, and maintaining genomic data resources such as the Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL) and the dbGaP database of Genotypes and Phenotypes. The institute led the Telomere-to-Telomere Consortium, which released the first complete, gapless human genome sequence (T2T-CHM13) on March 31, 2022, adding approximately 200 million previously unread base pairs to the human reference.

NHGRI's portfolio of research programs spans functional genomics (ENCODE), tissue-specific gene expression (GTEx), cancer genomics (TCGA), polygenic risk methods in diverse populations (PRIMED), and clinical implementation networks (eMERGE, IGNITE, ClinGen, CSER, NSIGHT, UDN). It funds translational initiatives such as the Southeast Genomic Medicine Service (SE-GEMS) eConsult platform, ELSI (Ethical, Legal, and Social Implications) research, and SBIR grants to genomics startups. The institute also produces educational resources, fact sheets, and the GenomeTV lecture series for audiences ranging from K-12 educators and patients to physicians and policymakers.

As a government research institute rather than a commercial entity, NHGRI is funded through annual congressional appropriations distributed by NIH and does not generate commercial revenue. Its outputs — research funding, public-domain data resources, educational materials, and policy guidance — are provided free of charge to qualified recipients. Revenue streams consist of federal appropriations and the disbursement of research grants and multiyear awards (e.g., $7.87M to Vanderbilt Health and UAB; $3.2M to Feinstein Institutes; $2M SBIR to Dovetail Genomics). Its customer base is horizontal: scientists and academic researchers, healthcare providers, patients and the general public, educators, and policymakers.

National Human Genome Research Institute firmographics

Firmographics
Name
National Human Genome Research Institute
Legal name
National Human Genome Research Institute
Website
https://genome.gov
Company type
Public
Founded year
1990
Operating status
Operating
Headcount range
501–1,000 employees
Short description
The National Human Genome Research Institute (NHGRI) is a U.S. federal research institute within NIH that funds and conducts genomics research, maintains public genomic data resources, and advances genomic medicine implementation for scientists, clinicians, patients, and the general public.
Ownership category
akta.pro rank

National Human Genome Research Institute industry classification

Industry
Product category
Genomics Research
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417), Research and Development in the Physical, Engineering, and Life Sciences (54171)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Health Research Funding Agencies (Public/Quasi-Public) (HLAJALAB)
akta.pro secondary industries
Public Health Genomics & Sequencing (WGS/Metagenomics) Networks (HLAJAIAK), Health Data, Vital Statistics & Population Health Informatics (BPAIAJAM), Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics) (HLAAALAD)

Keywords

  • Genomics research funding
  • Human genome research
  • Genomic medicine programs
  • Genomics data resources
  • Genomic science education

Where National Human Genome Research Institute is headquartered

Location

Headquarters

HQ city
Bethesda
HQ country
United States
HQ region
North America

Offices1 record

Markets served

National Human Genome Research Institute business model

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

Revenue model

  1. Federal Appropriations: NHGRI is funded through annual congressional appropriations to the National Institutes of Health. The institute receives a budget allocation from the NIH which is part of the U.S. Department of Health and Human Services. As a federal research institute, NHGRI does not generate commercial revenue but distributes funds through grants and contracts to support extramural and intramural genomics research.
  2. Research Grants and Awards: NHGRI issues multiyear awards and grants to external research institutions. Example: $7.87 million award to Vanderbilt Health and UAB for the Southeast Genomic Medicine Service (SE-GEMS) initiative. Funding supports genomic eConsult services, research projects, and training programs.

Go-to-market motion1 record

Distribution channels4 records

Marketing channels6 records

National Human Genome Research Institute product offering

Product offering

Core offering

NHGRI is a U.S. federal research institute within the National Institutes of Health (NIH) that advances genomics research by funding extramural and intramural scientific programs, maintaining genomic data resources and bioinformatics infrastructure, and disseminating educational materials. It issues research grants and contracts to public and private research institutions worldwide and operates programs such as ENCODE, ClinGen, eMERGE, the Undiagnosed Diseases Network, and the Telomere-to-Telomere Consortium. It also provides public-facing tools including the genome.gov website, the Family Health History Tool, and the Genomic Medicine Meetings series.

Product overview

The National Human Genome Research Institute (NHGRI) is a research institute within the NIH, not a commercial product company. Its offerings consist primarily of research programs, educational resources, and health information platforms rather than a unified commercial product. The genome.gov website serves as the primary public-facing platform, providing genomics education, research funding information, and health resources. NHGRI funds and coordinates numerous research programs including the Advancing Genomic Medicine Research (AGMR), Clinical Genome Resource (ClinGen), eMERGE Network, Undiagnosed Diseases Network (UDN), and the ENCODE Project. The institute also provides the Family Health History Tool for clinical use, supports the Southeast Genomic Medicine Service (SE-GEMS) eConsult platform for clinician guidance, and offers the ELSI Research Program addressing ethical, legal, and social implications of genomics. Training and fellowship programs like the NIH-ACMG Fellowship and educational resources for educators round out the portfolio.

Differentiator

Problem solved

Functional benefit

Products and services

  • genome.gov Website Platform

Quantifiable outcome

  • First complete human genome sequence completed with 200 million added base pairs
  • +1 more outcomes

Companies that use National Human Genome Research Institute

Customer profile

Named customers4 records

Segments5 records

Ideal customer profiles5 records

National Human Genome Research Institute technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

National Human Genome Research Institute partnerships and signals

Strategic signal

Partnerships

14 partnerships are on record, tiered core and major.

  • Vanderbilt HealthcoreStrategic or Co-development Partner · 9 June 2026Vanderbilt Health partnered with NHGRI-funded Southeast Genomic Medicine Service (SE-GEMS) initiative. The project is funded by a $7.87 million multiyear award from NHGRI to expand access to genomic medicine for clinicians and patients across the Southeast United States. The partnership creates a genomic eConsult service allowing clinicians to submit questions about genetic testing and receive guidance from genetics experts.
  • University of Alabama at Birmingham (UAB)coreStrategic or Co-development Partner · 9 June 2026UAB partnered with Vanderbilt Health in the SE-GEMS initiative funded by a $7.87 million NHGRI award. The partnership initially focuses on general genetics, pharmacogenomics, prenatal genetics, and cancer genetics, with the goal of building a scalable model for broader regional and national implementation of genomic medicine services.
  • Feinstein InstitutesmajorStrategic or Co-development Partner · 23 October 2025Feinstein Institutes received $3.2 million from NIH (including NHGRI) to fund research on polygenic embryo selection (PES) technology for evaluating embryos for disease risks during in vitro fertilization. Research involves collaborations with Baylor College of Medicine and Massachusetts General Hospital over four years.
  • Baylor College of MedicinemajorStrategic or Co-development Partner · 23 October 2025Collaborator with Feinstein Institutes on NIH-funded polygenic embryo selection research. Part of a multi-institutional effort to assess scientific accuracy and ethical implications of PES technology.
  • Massachusetts General HospitalmajorStrategic or Co-development Partner · 23 October 2025Collaborator with Feinstein Institutes on NIH-funded polygenic embryo selection research. Part of multi-institutional effort to evaluate PES technology for disease risk assessment during IVF.
  • Telomere-to-Telomere ConsortiumcoreStrategic or Co-development Partner · 31 March 2022Consortium led by NHGRI with approximately 100 scientists that produced the first complete, gapless human genome sequence (T2T-CHM13). The consortium used Oxford Nanopore and PacBio long-read sequencing platforms to bridge repetitive sections that defeated earlier short-read methods. This achievement added nearly 200 million base pairs of previously unread sequence to the human reference genome.
  • Human Microbiome Project (HMP)coreStrategic or Co-development PartnerTrans-NIH collaboration through the Common Fund. NHGRI collaborates with other NIH institutes on microbiome research as part of its cross-cutting activities in genomics and society.
  • H3Africa ProgramcoreStrategic or Co-development PartnerInternational collaboration supporting genomics research in Africa. NHGRI participates as part of cross-NIH Common Fund projects to advance genomic research globally.
  • GTEx (Genotype-Tissue Expression Project)coreStrategic or Co-development PartnerCommon Fund project studying relationship between genetic variation and gene expression across human tissues. NHGRI collaborates with other NIH institutes on this landmark project.
  • CSER (Clinical Sequencing Evidence-Generating Research)coreStrategic or Co-development PartnerNHGRI collaboration focused on generating evidence about the clinical use of genomic sequencing. Part of the Division of Genomics and Society's outreach activities.
  • NSIGHT (Newborn Sequencing in Genomic Medicine and Public Health)coreStrategic or Co-development PartnerNHGRI program exploring the implications of genomic sequencing in newborns. Collaborates across NHGRI divisions and with other NIH institutes.
  • IGNITE (Implementing Genomics in Practice)coreStrategic or Co-development PartnerNHGRI network focused on implementing genomic medicine in clinical practice. Supports pragmatic clinical trials and implementation research.
  • eMERGE (Electronic Medical Records and Genomics) NetworkcoreStrategic or Co-development PartnerNHGRI network combining DNA biobanks with electronic medical record systems for large-scale genomic research. Part of genomic medicine implementation efforts.
  • ClinGen (Clinical Genome Resource)coreStrategic or Co-development PartnerNHGRI-funded resource providing expert consensus on genes and variants relevant to disease. Part of clinical genome resources for genomic medicine.

Scale indicators5 records

Recent moves7 records

Expansion highlights6 records

National Human Genome Research Institute competitors and assessment

Company assessment

Direct peers

  • National Cancer Institute (NCI): Another major NIH institute focused on cancer research; like NHGRI it funds large extramural research programs, operates intramural labs, and convenes clinical networks (e.g., TCGA, which NHGRI co-leads). It is the closest functional peer within the federal genomics/biomedical ecosystem.
  • Wellcome Trust / Wellcome Sanger Institute: UK-based charitable foundation that funds genomics and biomedical research globally, including the Wellcome Sanger Institute, which produces large-scale genomic reference data (e.g., UK Biobank contributions). Most direct international peer to NHGRI's combination of research funding plus reference data stewardship.
  • National Institute of General Medical Sciences (NIGMS): A sister NIH institute that funds basic biomedical research through grants and training programs. Directly comparable in operating model (federal institute, extramural grants, intramural research) though with a broader mandate than genomics.
  • European Molecular Biology Laboratory (EMBL-EBI): Intergovernmental bioinformatics and genomics data institute operating major open data resources (Ensembl, ENA, EVA). Most direct international peer to NHGRI's data stewardship role (e.g., AnVIL/dbGaP).
  • The Jackson Laboratory (JAX): Independent, nonprofit biomedical research institution specializing in mammalian genetics and genomics, operating research programs, genomic databases, and distributing mouse models. Closely comparable to NHGRI's intramural research and data resource mission.

Broad incumbents

  • Broad Institute of MIT and Harvard: Large, established genomics research organization operating major sequencing, computation, and disease-gene discovery programs. Comparable to NHGRI in scientific output and convening power, though private/non-profit and reliant on philanthropic and federal grants rather than direct congressional appropriation.
  • Howard Hughes Medical Institute (HHMI): Large private biomedical research organization supporting ~300 HHMI Investigators across U.S. universities. Comparable in funding scale, scientific prestige, and investigator-driven model, though broader than NHGRI's genomics-specific remit.
  • Centers for Disease Control and Prevention (CDC): Federal public health agency that operates genomic surveillance programs (e.g., PulseNet, AMD) and uses WGS for outbreak response. Overlaps with NHGRI in public-health-oriented genomic epidemiology but with a federal-regulatory rather than research-funding orientation.
  • National Science Foundation (NSF): Federal agency that funds basic scientific research across all disciplines, including genomics-adjacent computational biology. Comparable in funding-agency model and federal appropriations structure, though much broader in scope.

Emerging players

  • Allen Institute: Private nonprofit research organization conducting large-scale scientific projects (brain science, cell science, immunology). Comparable as a mission-driven, large-scale research organization producing open data assets, though not genomics-focused.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

National Human Genome Research Institute social profiles

Digital presence

National Human Genome Research Institute financial estimates

Financial estimate

Revenue estimate

Valuation estimate

National Human Genome Research Institute leadership team

Management profile

Number of profiles

Profiles6 records

National Human Genome Research Institute funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

National Human Genome Research Institute M&A and investment

M&A and investment

M&A

Investments19 records

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

Frequently asked questions about National Human Genome Research Institute

What does National Human Genome Research Institute do?

NHGRI is a U.S. federal research institute within the National Institutes of Health (NIH) that advances genomics research by funding extramural and intramural scientific programs, maintaining genomic data resources and bioinformatics infrastructure, and disseminating educational materials. It issues research grants and contracts to public and private research institutions worldwide and operates programs such as ENCODE, ClinGen, eMERGE, the Undiagnosed Diseases Network, and the Telomere-to-Telomere Consortium. It also provides public-facing tools including the genome.gov website, the Family Health History Tool, and the Genomic Medicine Meetings series.

Is National Human Genome Research Institute a public or private company?

National Human Genome Research Institute is a public company. It is classified as state government owned and is currently operating.

When was National Human Genome Research Institute founded?

National Human Genome Research Institute was founded in 1990. It employs 501 to 1,000 people.

Where is National Human Genome Research Institute based?

National Human Genome Research Institute is headquartered in Bethesda, United States, in the North America region.

How does National Human Genome Research Institute make money?

Two revenue lines are on record. Federal Appropriations are the primary driver. The others are research Grants and Awards.

Who are National Human Genome Research Institute's main competitors?

Direct peers on record are National Cancer Institute (NCI), Wellcome Trust / Wellcome Sanger Institute, National Institute of General Medical Sciences (NIGMS), European Molecular Biology Laboratory (EMBL-EBI) and The Jackson Laboratory (JAX). Broad incumbents are Broad Institute of MIT and Harvard, Howard Hughes Medical Institute (HHMI), Centers for Disease Control and Prevention (CDC) and National Science Foundation (NSF). Allen Institute is listed as an emerging player.

Does National Human Genome Research Institute have an API?

No public API is recorded for National Human Genome Research Institute.

What industry is National Human Genome Research Institute in?

National Human Genome Research Institute's product category is Genomics Research. Its primary akta.pro industry code is HLAJALAB, Health Research Funding Agencies (Public/Quasi-Public), with a secondary code of HLAJAIAK, Public Health Genomics & Sequencing (WGS/Metagenomics) Networks. Its NAICS code is 541714 and its SIC code is 8731.

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The Times of IndiaNot an animal, but one popular fruit shares 60% of human genes. Genetic expert says it’s not shocking: ‘There’s a lot of things we do the same way…'A study reported by Pfizer, discussed in an interview with HowStuffWorks, found that the banana genome has a recognisable homologue for over 60% of human genes, though the average protein similarity is about 40%. Researchers compared more than four million gene sequences, identifying roughly 7,000 strong matches. Genetics expert Dr Lawrence Brody of the National Human Genome Research Institute said the finding is less than popular estimates.Mirage NewsHuman Genome Breakthrough Paves Way for Custom GenomicsScientists from the Telomere-to-Telomere (T2T) Consortium, led by researchers at Johns Hopkins University, the National Human Genome Research Institute, and the National Institute of Standards and Technology, have reconstructed the first complete diploid human genome containing distinct chromosome sets from both parents, representing a major advancement over the consortium's 2022 work. The new approach reveals 15% more of the genome—including over 900 million previously inaccessible DNA letters—achieving near-perfect accuracy at approximately $5,000, compared to the original Human Genome Project's $5 billion cost. This breakthrough is expected to enable personalized genomics as routine medical care, significantly improving diagnosis of rare genetic diseases (currently unresolved in over half of cases) and enhancing prediction of risks for cancers, heart disease, immune disorders, and neuropsychiatric conditions.Alabama Political ReporterUAB receives NIH funding to expand genomic screening in primary careThe University of Alabama at Birmingham has received federal funding from the National Human Genome Research Institute to expand genomic screening into primary care settings through a multiyear initiative. The grant could total approximately $4.9 million through 2031, with UAB set to enroll 5,000 of the 20,000 participants planned nationally through the Population Genomic Screening Network. The project aims to identify actionable genetic risks for conditions like hereditary cancers and cardiovascular disease before symptoms develop, shifting from reactive care to proactive prevention.GenomeWebNHGRI-Funded Population Genomic Screening Network to Study 'Full Cycle of Implementation'The National Human Genome Research Institute is funding a five-year, $46.5 million initiative called the Population Genomic Screening Network to study the clinical implementation of genomic screening in primary care settings across the United States. Six clinical groups will enroll at least 30,000 patients to screen for actionable genetic conditions using whole-exome sequencing, with Baylor College of Medicine handling the sequencing and the University of Washington coordinating the network. The study aims to generate data on patient outcomes and clinical utility to influence future insurance reimbursement policies for preventive genomic interventions.MorningstarApertura Gene Therapy Announces Cooperative Research and Development Agreement with Institutes of the NIH to Test Investigational Gene Therapy for Niemann-Pick Disease Type C1Apertura Gene Therapy announced a CRADA with NICHD and NHGRI to test an investigational gene therapy for Niemann-Pick Disease Type C1 using its TfR1 CapX capsid. The Ara Parseghian Medical Research Fund will provide financial support. The agreement aims to advance preclinical development toward clinical testing.PR NewswireApertura Gene Therapy Announces Cooperative Research and Development Agreement with Institutes of the NIH to Test Investigational Gene Therapy for Niemann-Pick Disease Type C1Apertura Gene Therapy announced a CRADA with NICHD and NHGRI to test intravenous gene therapy for Niemann-Pick Disease Type C1 using its TfR1 CapX capsid. The Ara Parseghian Medical Research Fund will provide financial support. The agreement aims to advance preclinical development toward clinical testing.NatureA digital archive reveals how a funding agency cooperated with academics to support the nascent field of genomicsResearchers analyzed a digital archive of over 2 million pages assembled by the National Human Genome Research Institute (NHGRI) to understand how the agency cooperated with academic communities to develop genomics as a scientific field. The study found that NHGRI played a critical role in promoting genome-wide association studies (GWAS), working with a small group of academic experts through mechanisms like the "Kitchen Cabinet" to provide continuity between the Human Genome Project and subsequent genomics efforts. Machine learning models trained on archival data could accurately recapitulate how NHGRI and academics jointly decided which organisms' genomes to sequence, with the decisions aligning with the subsequent adoption of genomic approaches in research communities.STATAs dangerous eugenic ideas spread, NIH falls silentThe Trump administration has dismantled the communications and education offices at the National Human Genome Research Institute (NHGRI) through mass layoffs and restructuring, eliminating programs that had spent years building public outreach capacity to counter scientific racism and eugenic ideas. NIH communications output dropped 70-90% across most institutes in 2025 compared to the previous five years, with NHGRI losing its entire education branch, science writers, archivists, and public events team, while Genome.gov remains unupdated and archives are inaccessible to scholars. The timing is particularly consequential as eugenic ideologies resurface in political discourse and polygenic embryo selection companies backed by tech billionaires market genetic optimization services to prospective parents.EmerjBreaking Down AI’s Role in Genomics and Polygenic Risk PredictionEditorial Director Matthew DeMello spoke with Dr. Dan Elton, Staff Scientist at the National Human Genome Research Institute, on the 'AI in Business' podcast about how AI is transforming protein structure prediction and polygenic risk scoring. AlphaFold and similar AI-driven models now predict over 200 million protein structures from amino-acid sequences in minutes, slashing costs that previously averaged $150,000 per protein via X-ray crystallization. Elton noted that while neural networks can model nonlinear gene interactions for disease-risk predictions, they require massive datasets of 300,000 to 700,000 sequences, and for highly heritable traits like height, linear models already capture most genetic effects, limiting added value.ClinicalgenomeWelcome to ClinGenClinGen, a collaborative initiative founded by the National Human Genome Research Institute in 2013, is advancing genomic knowledge through global curation efforts involving over 2,700 contributors from more than 72 countries. The organization recently published methods for large-scale evidence-based curation in Genetics in Medicine and continues to recruit expert volunteers via surveys. It also provides access to curation files and API resources for its consortium.