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The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project
Study
phs001820
-
Targeted_sequencing_of_genes_recurrently_mutated_in_AML
Study
EGAS00001000408
-
Whole Genome Sequencing Analysis in a Family of Discordant Twins With Non-Syndromic Microtia and Hemifacial Microsomia: Identification of Novel Candidate Genes and Variants
Study
phs003216
-
Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms
Study
EGAS00001006174
-
Epigenome-wide methylation analysis of colorectal carcinoma, adenoma and normal tissue reveals novel biomarkers addressing unmet clinical needs
Study
EGAS00001007017
-
Acute Respiratory Distress Network (ARDSNet) Studies 01 and 03 Lower Versus Higher Tidal Volume, Ketoconazole Treatment and Lisofylline Treatment (ARMA/KARMA/LARMA) (ARDSNet-ARMA/KARMA/LARMA-BioLINCC)
Study
phs003734
-
Genetics of Human Inherited Retinal Diseases (GHIRD)
Study
phs001517
-
Prognostic and therapeutic significance of leukemia subtypes and minimal residual disease measurements in pediatric acute lymphoblastic leukemia treated with contemporary risk-directed trial: a cohort study
Study
EGAS00001004739
-
hereditary BrEAst Case CONtrol study (BEACCON)
Dataset
EGAD00001007025
-
Targeted sequencing of genes recurrently mutated in AML
Dataset
EGAD00001000606
-
Changes in Oral and Gut Microbiota and Incidence and Severity of Patient-Reported Symptoms in Pre- and Post-Kidney Transplant Patients
Study
phs002199
-
National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments
Study
phs000218
-
The Thrifty Microbiome: The Role of the Gut Microbiota in Obesity in the Amish
Study
phs000258
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Dental Caries: Whole Genome Association and Gene x Environment Studies
Study
phs000095
-
Drug development for pediatric cancers: the importance of patient' s genomic data re-use
Blog
drug-development-for-pediatric-cancers
-
Natural Killer Cell Therapies for Hematologic Malignancies
Study
phs002681
-
Identifying novel DNA damage response genes in radiosensitive individuals
Study
phs001911
-
DAC for Central African ancient demography processes NGS dataset
Dac
EGAC50000000447
-
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Study
phs001422
-
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Study
phs002225
-
Whole-genome sequencing of normal Singaporean volunteers
Study
EGAS00001004007
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
Study of Addiction: Genetics and Environment (SAGE)
Study
phs000092
-
Risk Assessment of Cerebrovascular Events (RACE) Study
Study
phs000456
-
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Study
phs000235
-
Upcycling and merging data to challenge the dogma and identify new therapeutic targets for Glioblastoma
Blog
upcycling-and-merging-data-to-challenge-glioblastoma
-
Genes and Blood Clotting Study (GABC)
Study
phs000304
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
Projects
Documentation
about/projects-and-funders/projects
-
Submitter Portal
Documentation
submission/metadata/submission/sequencing-phenotype/submitter-portal
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NIH RECOVER: A Multi-Site Observational Study of Post-Acute Sequelae of SARS-CoV-2 Infection in Adults
Study
phs003463
-
NIH RECOVER-Pediatric: Understanding the Long-Term Impact of COVID on Children and Families
Study
phs003461
-
Lung Tissue Research Consortium (LTRC-BioLINCC)
Study
phs003913
-
Framingham Cohort
Study
phs000007
-
Genetic Causes of Growth Disorders
Study
phs001617
-
Submission FAQ
Documentation
submission/metadata/submission/FAQ
-
Identifying Novel Small RNA Biomarkers Unique to Patients with Gastric Cancer
Study
phs001767
-
Providing access to COVID-19 data: one year later
Blog
providing-access-to-covid-19
-
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Study
phs000547
-
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Study
phs001616
-
The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
Study
phs001524
-
National Human Genome Research Institute (NHGRI) GENEVA Genome-Wide Association Study of Venous Thrombosis (GWAS of VTE)
Study
phs000289
-
Women's Health Initiative Clinical Trial and Observational Study - Imaging
Study
phs003824
-
Clonal dynamics of normal haematopoiesis across the human lifespan
Dataset
EGAD00001007851
-
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Study
phs001120
-
Identification of Genes Involved in Familial Coronary Artery Disease
Study
phs000514
-
Exome Sequencing Reveals Frequent Inactivating Mutations in BAP1, ARID1A, and PBRM1 in Intrahepatic Cholangiocarcinomas
Study
EGAS00001001108
-
Characterization of Sex Differences in Human Placentas
Study
phs002240
-
Establishment of xenogfafts and cultured cell lines from clinical samples
Study
JGAS000585
-
RNA-Seq studies of Gene Expression in Cells and Networks in FI and ACC in Autism
Study
phs000609
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse)
Study
EGAS00001004696
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human)
Study
EGAS00001004897
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Study
EGAS00001006926
-
Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis
Study
phs001902
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Study
EGAS00001006372
-
Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal
Study
phs003003
-
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Study
EGAS50000000298
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
An instructive role for IL7RA in the development of human B-cell precursor leukemia
Study
EGAS00001005347
-
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Study
EGAS00001003213
-
Efficacy of CDK4/6i in preclinical models of malignant pleural mesothelioma
Study
EGAS00001005352
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Mediators of Atherosclerosis in South Asians Living in America Study (MASALA)
Study
phs002980
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Study
phs001819
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Study
phs002653
-
Cell-free DNA fragmentation patterns and personalized sequencing reveal circulating tumor DNA in urine and plasma of glioma patients
Study
EGAS00001004355
-
Total RNAseq in the sporadic ALS and healthy control motor cortex
Study
EGAS00001004286
-
Increased mutation accumulation during fetal development in Down syndrome
Study
EGAS00001003982
-
H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
-
Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases in the Czech Republic
Study
EGAS50000000442
-
Genetic analysis in monozygotic twins discordant for bipolar disorder
Study
JGAS000014
-
THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Study
EGAS00001002201
-
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Study
EGAS00001005019
-
Ultrasensitive Profiling of UV Mutations in Facial Tumors in TSC
Study
phs002914
-
Combination of CDK4/6 with BET-bromodomain and PI3K/mTOR inhibitors in medulloblastoma in vitro and in vivo
Study
EGAS00001006286
-
Whole-genome variant calling of individuals from the study of allergic diseases in the Canary Islands
Study
EGAS50000000299
-
Inter and intra - tumor heterogeneity in Colorectal Cancer
Study
EGAS00001002150
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
Bulk and single-cell RNA-sequencing data from five lines of human iPSC-derived (hiPSC-derived) astrocytes (3 in-house and 2 commercial lines), both alone and in co-culture with neurons, to define the molecular response of astrocytes to misfolded alpha-synuclein
Study
EGAS50000000751
-
A Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B is Associated with Leukocytosis, Lymphadenopathy, Splenomegaly, Necrotizing Granulomas, Hyper-IgM and Thrombocytopenia
Study
phs001479
-
A Genome-Wide Association Study for Post-bronchodilator Lung Function in Children with Asthma
Study
phs001216
-
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study
Study
EGAS00001002527
-
Application of short-RNA-seq in post-mortem human hippocampi from the Calgary Brain Bank (CBB) to assess transcriptome-wide deregulation in processing of SINE Alu RNAs in Alzheimer’s disease
Study
EGAS00001004973
-
Fgl2 Regulates FcγRIIB+ CD8+ T Cell Responses during Infection
Study
phs003870
-
The genomic landscape of relapsed infant and childhood KMT2A-rearranged acute leukemia
Study
EGAS00001008197
-
Genetic Study of Northern Kenya Pastoral Populations
Study
phs002654
-
Evaluation of whole genome sequencing utility in identifying driver alterations in cancer genome
Study
JGAS000715
-
Atherosclerosis Risk in Communities (ARIC) Cohort
Study
phs000280
-
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
Using RNA-sequencing to characterize the resistance to lirafugratinib
Study
EGAS50000001370
-
Whole genome sequencing delineates regulatory, structural, and cryptic splice variants in early onset cardiomyopathy
Study
EGAS00001004929