Data Versioning Release Notes

August 2024

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies (listed below). In August 2024, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov for assistance.

Studies to be updated:

STUDY / CONSENT NAME
FULL STUDY NAME
BDC Version
Updating to:

AFLMU_HMB-IRB-PUB-COL-NPU-MDS

NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU

phs001543.v2.p1.c1

phs001543.v3.p1

EOCOPD_DS-CS-RD

NHLBI TOPMed - Boston Early-Onset COPD Study

phs000946.v5.p2.c1

phs000946.v6.p2

CAMP_DS-AST-COPD

NHLBI TOPMed - Childhood Asthma Management Program (CAMP)

phs001726.v2.p1.c1

phs001726.v3.p1

SARP_GRU

NHLBI TOPMed - Severe Asthma Research Program (SARP)

phs001446.v2.p2.c1

phs001446.v3.p2

SARP_DS-AAI-PUB

NHLBI TOPMed - Severe Asthma Research Program (SARP)

phs001446.v2.p2.c2

phs001446.v3.p2

GENAF_HMB-NPU

NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study

phs001547.v2.p1.c1

phs001547.v3.p1

EGCUT_GRU

NHLBI TOPMed - Early-Onset Atrial Fibrillation in the Estonian Biobank

phs001606.v2.p1.c1

phs001606.v3.p1

CCAF_GRU-IRB

NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study

phs001189.v4.p1.c1

phs001189.v5.p1

BioMe_HMB-NPU

NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai

phs001644.v2.p2.c1

phs001644.v3.p2

CHS_HMB-MDS

NHLBI TOPMed: Cardiovascular Health Study

phs001368.v3.p2.c1

phs001368.v4.p2

CHS_HMB-NPU-MDS

NHLBI TOPMed: Cardiovascular Health Study

phs001368.v3.p2.c2

phs001368.v4.p2

CHS_DS-CVD-MDS

NHLBI TOPMed: Cardiovascular Health Study

phs001368.v3.p2.c3

phs001368.v4.p2

CHS_DS-CVD-NPU-MDS

NHLBI TOPMed: Cardiovascular Health Study

phs001368.v3.p2.c4

phs001368.v4.p2

May 2024

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies (listed below). In May 2024, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov for assistance.

Studies to be updated:

STUDY / CONSENT NAME
FULL STUDY NAME
BDC Version
Updating to:

BioMe_HMB-NPU

NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai

phs001644.v1.p1.c1

phs001387.v2.p2

BioVU_AF_HMB-GSO

NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study

phs001624.v1.p1.c1

phs001624.v2.p2

CAMP_DS-AST-COPD

NHLBI TOPMed: Childhood Asthma Management Program (CAMP)

phs001726.v1.p1.c1

phs001726.v2.p1

CARE_BADGER_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Best ADd-on Therapy Giving Effective Response (BADGER)

phs001728.v1.p1.c2

phs001728.v2.p1

CARE_CLIC_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Characterizing the Response to a Leukotriene Receptor Antagonist and an Inhaled Corticosteroid (CLIC)

phs001729.v1.p1.c2

phs001729.v2.p1

CARE_PACT_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Pediatric Asthma Controller Trial (PACT)

phs001730.v1.p1.c2

phs001730.v2.p1

CARE_TREXA_DS-ASTHMA-IRB-COL

NHLBI TOPMed: TReating Children to Prevent EXacerbations of Asthma (TREXA)

phs001732.v1.p1.c2

phs001732.v2.p1

GCPD-A_DS-ASTHMA-GSO

NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A)

phs001661.v2.p1.c1

phs001661.v3.p1

GGAF_GRU

NHLBI TOPMed CCDG: Groningen Genetics of Atrial Fibrillation (GGAF) Study

phs001725.v1.p1.c1

phs001725.v2.p1

IPF_DS-ILD-IRB-NPU

NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing

phs001607.v2.p2.c1

phs001607.v3.p2

IPF_DS-LD-IRB-NPU

NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing

phs001607.v2.p2.c2

phs001607.v3.p2

IPF_DS-PFIB-IRB-NPU

NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing

phs001607.v2.p2.c3

phs001607.v3.p2

IPF_DS-PUL-ILD-IRB-NPU

NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing

phs001607.v2.p2.c4

phs001607.v3.p2

IPF_HMB-IRB-NPU

NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing

phs001607.v2.p2.c5

phs001607.v3.p2

LTRC_HMB-MDS

NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)

phs001662.v1.p1.c2

phs001662.v2.p1

OMG_SCD_DS-SCD-IRB-PUB-COL-MDS-RD

NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)

phs001608.v1.p1.c1

phs001608.v2.p1

PIMA_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Pathways to Immunologically Mediated Asthma (PIMA)

phs001727.v1.p1.c2

phs001727.v2.p1

PUSH_SCD_DS-SCD-IRB-PUB-COL

NHLBI TOPMed: Pulmonary Hypertension and the Hypoxic Response in SCD (PUSH)

phs001682.v1.p1.c1

phs001682.v2.p1

Walk_PHaSST_SCD_DS-SCD-IRB-PUB-COL-NPU-MDS-RD

NHLBI TOPMed: Walk-PHaSST Sickle Cell Disease (SCD)

phs001514.v1.p1.c2

phs001514.v2.p1

Walk_PHaSST_SCD_HMB-IRB-PUB-COL-NPU-MDS-GSO

NHLBI TOPMed: Walk-PHaSST Sickle Cell Disease (SCD)

phs001514.v1.p1.c1

phs001514.v2.p1

April 2024

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies. In April 2024, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov before April 5, 2024 for assistance.

Studies to be updated:

STUDY / CONSENT NAME
FULL STUDY NAME
BDC Version
Updating to:

AFLMU_HMB-IRB-PUB-COL-NPU-MDS

NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU

phs001543.v1.p1.c1

phs001543.v2.p1

AustralianFamilialAF_HMB-NPU-MDS

NHLBI TOPMed: Australian Familial Atrial Fibrillation Study

phs001435.v1.p1.c1

phs001435.v2.p1

CCDG_PMBB_AF_HMB-IRB-PUB

NHLBI TOPMed - NHGRI CCDG: Penn Medicine BioBank Early Onset Atrial Fibrillation Study

phs001601.v1.p1.c1

phs001601.v2.p2

ChildrensHS_GAP_GRU

NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)

phs001602.v1.p1.c1

phs001602.v2.p1

ChildrensHS_IGERA_GRU

NHLBI TOPMed: Children's Health Study (CHS) Integrative Genomics and Environmental Research of Asthma (IGERA)

phs001603.v1.p1.c1

phs001603.v2.p1

ChildrensHS_MetaAir_GRU

NHLBI TOPMed: Children's Health Study (CHS) Effects of Air Pollution on the Development of Obesity in Children (Meta-AIR)

phs001604.v1.p1.c1

phs001604.v2.p1

CHIRAH_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Chicago Initiative to Raise Asthma Health Equity (CHIRAH)

phs001605.v1.p1.c2

phs001605.v2.p1

DECAF_GRU

NHLBI TOPMed: Determining the association of chromosomal variants with non-PV triggers and ablation-outcome in AF (DECAF)

phs001546.v1.p1.c1

phs001546.v2.p1

EGCUT_GRU

NHLBI TOPMed: Early-onset Atrial Fibrillation in the Estonian Biobank

phs001606.v1.p1.c1

phs001606.v2.p1

GALA_DS-LD-IRB-COL

NHLBI TOPMed: Genetics of Asthma in Latino Americans (GALA)

phs001542.v1.p1.c2

phs001542.v2.p1

GENAF_HMB-NPU

NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study

phs001547.v1.p1.c1

phs001547.v2.p1

GeneSTAR_DS-CVD-IRB-NPU-MDS

NHLBI TOPMed: Genetic Study of Atherosclerosis Risk (GeneSTAR)

phs001218.v2.p1.c2

phs001218.v3.p1

GenSalt_DS-HCR-IRB

NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)

phs001217.v2.p1.c1

phs001217.v3.p1

HCHS-SOL_HMB

NHLBI TOPMed - NHGRI CCDG: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

phs001395.v1.p1.c2

phs001395.v2.p1

HCHS-SOL_HMB-NPU

NHLBI TOPMed - NHGRI CCDG: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

phs001395.v1.p1.c1

phs001395.v2.p1

HyperGEN_GRU-IRB

NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy

phs001293.v2.p1.c1

phs001293.v3.p1

INSPIRE_AF_DS-MULTIPLE_DISEASES-MDS

NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry

phs001545.v1.p1.c1

phs001545.v2.p1

JHU_AF_HMB-NPU-MDS

NHLBI TOPMed - NHGRI CCDG: The Johns Hopkins University School of Medicine Atrial Fibrillation Genetics Study

phs001598.v1.p1.c1

phs001598.v2.p1

Mayo_VTE_GRU

NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)

phs001402.v2.p1.c1

phs001402.v3.p1

MGH_AF_DS-AF-IRB-RD

NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study

phs001062.v4.p2.c2

phs001062.v5.p2

MGH_AF_HMB-IRB

NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study

phs001062.v4.p2.c1

phs001062.v5.p2

MLOF_HMB-PUB

NHLBI TOPMed: MyLifeOurFuture (MLOF) Research Repository of patients with hemophilia A (factor VIII deficiency) or hemophilia B (factor IX deficiency)

phs001515.v1.p1.c1

phs001515.v2.p2

MPP_HMB-NPU-MDS

NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP)

phs001544.v1.p1.c1

phs001544.v2.p1

PARTNERS_HMB

NHLBI TOPMed: Partners HealthCare Biobank

phs001024.v4.p1.c1

phs001024.v5.p1

pharmHU_HMB

NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)

phs001466.v1.p1.c1

phs001466.v2.p1

SAFHS_DS-DHD-IRB-PUB-MDS-RD

NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)

phs001215.v3.p2.c1

phs001215.v4.p2

SAPPHIRE_asthma_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)

phs001467.v1.p1.c1

phs001467.v2.p2

Sarcoidosis_DS-SAR-IRB

NHLBI TOPMed: African American Sarcoidosis Genetics Resource

phs001207.v2.p1.c1

phs001207.v3.p1

SAS_GRU-IRB-PUB-COL-NPU-GSO

NHLBI TOPMed: Genome-Wide Association Study of Adiposity in Samoans

phs000972.v4.p1.c1

phs000972.v5.p1

THRV_DS-CVD-IRB-COL-NPU-RD

NHLBI TOPMed: Rare Variants for Hypertension in Taiwan Chinese (THRV)

phs001387.v2.p1.c3

phs001387.v3.p1

WGHS_HMB

NHLBI TOPMed: Novel Risk Factors for the Development of Atrial Fibrillation in Women

phs001040.v4.p1.c1

phs001040.v5.p1

WHI_HMB-IRB

NHLBI TOPMed: Women's Health Initiative (WHI)

phs001237.v2.p1.c1

phs001237.v3.p1

WHI_HMB-IRB-NPU

NHLBI TOPMed: Women's Health Initiative (WHI)

phs001237.v2.p1.c2

phs001237.v3.p1

July 28th, 2023

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies. On July 28th 2023, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov before July 28th 2023 for assistance.

Studies to be updated:

STUDY / CONSENT NAME
FULL STUDY NAME
BDC Version
Updating to:

Amish_HMB-IRB-MDS

NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish

phs000956.v4.p1.c2

phs000956.v5.p1

AustralianFamilialAF_HMB-NPU-MDS

NHLBI TOPMed: Australian Familial Atrial Fibrillation Study

phs001435.v1.p1.c1

phs001435.v2.p1

CATHGEN_DS-CVD-IRB

NHLBI TOPMed - NHGRI CCDG: Early-onset Atrial Fibrillation in the CATHeterization GENetics (CATHGEN) Cohort

phs001600.v2.p2.c1

phs001600.v2.p2

ECLIPSE_DS-COPD-MDS-RD

NHLBI TOPMed: Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)

phs001472.v1.p1.c1

phs001472.v2.p1

GENOA_DS-ASC-RF-NPU

NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)

phs001345.v2.p1.c1

phs001345.v3.p1

GenSalt_DS-HCR-IRB

NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)

phs001217.v2.p1.c1

phs001217.v3.p1

GOLDN_DS-CVD-IRB

NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate

phs001359.v2.p1.c1

phs001359.v3.p1

miRhythm_GRU

NHLBI TOPMed: Defining the time-dependent genetic and transcriptomic responses to cardiac injury among patients with arrhythmias

phs001434.v1.p1.c1

phs001434.v2.p1

PARTNERS_HMB

NHLBI TOPMed: Partners HealthCare Biobank

phs001024.v4.p1.c1

phs001024.v5.p1

pharmHU_DS-SCD

NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)

phs001466.v1.p1.c3

phs001466.v2.p1

pharmHU_DS-SCD-RD

NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)

phs001466.v1.p1.c2

phs001466.v2.p1

pharmHU_HMB

NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)

phs001466.v1.p1.c1

phs001466.v2.p1

REDS-III_Brazil_SCD_GRU-IRB-PUB-NPU

NHLBI TOPMed: REDS-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)

phs001468.v2.p1.c1

phs001468.v3.p1

SAFHS_DS-DHD-IRB-PUB-MDS-RD

NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)

phs001215.v3.p2.c1

phs001215.v4.p2

SAPPHIRE_asthma_DS-ASTHMA-IRB-COL

NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)

phs001467.v1.p1.c1

phs001467.v2.p2

WGHS_HMB

NHLBI TOPMed: Novel Risk Factors for the Development of Atrial Fibrillation in Women

phs001040.v4.p1.c1

phs001040.v5.p1

June 30th, 2023

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies. On June 30th, 2023, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov before June 30th, 2023 for assistance.

Studies to be updated:

Study & Consent
Study Name
Current Version
Update To

ARIC_DS-CVD-IRB

NHLBI TOPMed - NHGRI CCDG: Atherosclerosis Risk in Communities (ARIC)

phs001211.v3.p2.c2

phs001211.v4.p3

ARIC_HMB-IRB

NHLBI TOPMed - NHGRI CCDG: Atherosclerosis Risk in Communities (ARIC)

phs001211.v3.p2.c1

phs001211.v4.p3

COPDGene_DS-CS-RD

NHLBI TOPMed: Genetic Epidemiology of COPD (COPDGene)

phs000951.v4.p4.c2

phs000951.v5.p5

COPDGene_HMB

NHLBI TOPMed: Genetic Epidemiology of COPD (COPDGene)

phs000951.v4.p4.c1

phs000951.v5.p5

CRA_DS-ASTHMA-IRB-MDS-RD

NHLBI TOPMed: The Genetic Epidemiology of Asthma in Costa Rica

phs000988.v4.p1.c1

phs000988.v5.p1

GALAII_DS-LD-IRB-COL

NHLBI TOPMed - NHGRI CCDG: Genes-Environments and Admixture in Latino Asthmatics (GALA II)

phs000920.v4.p2.c2

phs001189.v4.p1

HyperGEN_DS-CVD-IRB-RD

NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy

phs001293.v2.p1.c2

phs001293.v3.p1

HyperGEN_GRU-IRB

NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy

phs001293.v2.p1.c1

phs001293.v3.p1

Mayo_VTE_GRU

NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)

phs001402.v2.p1.c1

phs001402.v3.p1

MGH_AF_DS-AF-IRB-RD

NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study

phs001062.v4.p2.c2

phs001062.v5.p2

MGH_AF_HMB-IRB

NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study

phs001062.v4.p2.c1

phs001062.v5.p2

Sarcoidosis_DS-SAR-IRB

NHLBI TOPMed: African American Sarcoidosis Genetics Resource

phs001207.v2.p1.c1

phs001207.v3.p1

WHI_HMB-IRB

NHLBI TOPMed: Women's Health Initiative (WHI)

phs001237.v2.p1.c1

phs001237.v3.p1

WHI_HMB-IRB-NPU

NHLBI TOPMed: Women's Health Initiative (WHI)

phs001237.v2.p1.c2

phs001237.v3.p1

May 5th, 2023

The Database of Genotypes and Phenotypes (dbGaP) recently released a new version of one or more studies (listed below). On May 5th, 2023, the BDC ecosystem will begin updating these datasets, and the previous version will no longer be accessible. If you have approved access to a current version of a dataset listed below, and need to continue using the dataset, contact biodatacatalyst@nhlbi.nih.gov before May 5th, 2023 for assistance.

Studies to be updated:

STUDY / CONSENT NAME
FULL NAME
Current BDC Version
Will be updated to

CCAF_AF_GRU-IRB

NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study

phs001189.v3.p1.c1

phs001189.v4.p1

EOCOPD_DS-CS-RD

NHLBI TOPMed: Boston Early-Onset COPD Study

phs000946.v4.p1.c1

phs000946.v5.p1

CFS_DS-HLBS-IRB-NPU

NHLBI TOPMed: The Cleveland Family Study (CFS)

phs000954.v3.p2.c1

phs000954.v4.p2

JHS_HMB-IRB-NPU

NHLBI TOPMed: The Jackson Heart Study (JHS)

phs000964.v4.p1.c1

phs000964.v5.p1

JHS_DS-FDO-IRB-NPU

NHLBI TOPMed: The Jackson Heart Study (JHS)

phs000964.v4.p1.c2

phs000964.v5.p1

JHS_HMB-IRB

NHLBI TOPMed: The Jackson Heart Study (JHS)

phs000964.v4.p1.c3

phs000964.v5.p1

JHS_DS-FDO-IRB

NHLBI TOPMed: The Jackson Heart Study (JHS)

phs000964.v4.p1.c4

phs000964.v5.p1

FHS_HMB-IRB-MDS

NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study

phs000974.v4.p3.c1

phs000974.v5.p4

FHS_HMB-IRB-NPU-MDS

NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study

phs000974.v4.p3.c2

phs000974.v5.p4

HVH_HMB-IRB-MDS

NHLBI TOPMed: Heart and Vascular Health Study (HVH)

phs000993.v4.p2.c1

phs000993.v5.p2

HVH_DS-CVD-IRB-MDS

NHLBI TOPMed: Heart and Vascular Health Study (HVH)

phs000993.v4.p2.c2

phs000993.v5.p2

VAFAR_HMB-IRB

NHLBI TOPMed - NHGRI CCDG: The Vanderbilt AF Ablation Registry

phs000997.v4.p2.c1

phs000997.v5.p2

VU_AF_GRU-IRB

NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF)

phs001032.v5.p2.c1

phs001032.v6.p2

BAGS_GRU-IRB

NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados

phs001143.v3.p1.c1

phs001143.v4.p1

CHS_HMB-MDS

NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study

phs001368.v2.p2.c1

phs001368.v3.p2

CHS_HMB-NPU-MDS

NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study

phs001368.v2.p2.c2

phs001368.v3.p2

CHS_DS-CVD-NPU-MDS

NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study

phs001368.v2.p2.c4

phs001368.v3.p2

AACAC_HMB-IRB-COL-NPU

NHLBI TOPMed: Diabetes Heart Study (DHS) African American Coronary Artery Calcification (AA CAC)

phs001412.v2.p1.c1

phs001412.v3.p1

AACAC_DS-DHD-IRB-COL-NPU

NHLBI TOPMed: Diabetes Heart Study (DHS) African American Coronary Artery Calcification (AA CAC)

phs001412.v2.p1.c2

phs001412.v3.p1

Last updated