-
Lung Tissue Research Consortium (LTRC-BioLINCC)
Study
phs003913
-
NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A)
Study
phs001661
-
Genetic Markers of Caries Risk in Diverse Underserved Children: CIDR
Study
phs003280
-
Precision High Intensity Training Through Epigenetics (PHITE)
Study
phs003873
-
Targeting EGFR in NF1 Mutant Melanoma
Study
phs003906
-
Health Effects of Arsenic Longitudinal Study
Study
phs003839
-
Pomalidomide for the Treatment of Bleeding in HHT (PATH-HHT)
Study
phs003948
-
Lipid Research Clinics - Prevalence Study (LRC-PS-BioLINCC)
Study
phs003995
-
Genomics of Substance Use Disorders in Latin American Populations
Study
phs003558
-
Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia
Study
phs001110
-
3D tissue engineered human skeletal muscle modelling Facioscapulohumeral Muscular Dystrophy
Study
EGAS50000000502
-
SPECIAL (scATACseq): Dissecting the melanoma ecosystem one cell at the time during immunotherapy
Study
EGAS50000001014
-
X chromosome dosage and the genetic impact across human tissues
Study
EGAS00001006996
-
Functional Variant rs9344 at 11q13.3 Regulates CCND1 Expression in Multiple Myeloma with t(11;14)
Study
phs003997
-
Single-Cell Mitochondrial Mutation Lineage Tracing of Non-Dysplastic and Dysplastic Barrett's Esophagus
Study
phs003949
-
Field Studies of Human Immunity to Amebiasis in Bangladesh
Study
phs001476
-
Germline Genomic Analyses of Breast Cancer in Latinas
Study
phs003144
-
NHLBI TOPMed: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS)
Study
phs001927
-
Nanopore sequencing of blood, saliva, buccal mucosa samples of patients with inherited retinal disorders
Study
EGAS50000000440
-
Admixture histories of São Tomé e Príncipe.
Dataset
EGAD50000001348
-
DUX4 activates novel intergenic transcripts and isoforms in a tissue-specific context
Study
EGAS50000000503
-
SARS-CoV-2 induced alterations of the upper airway DNA methylome exert long-term impacts on ciliary genes involved in ciliary function
Study
EGAS50000000273
-
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci.
Study
EGAS50000000370
-
Use of new methodologies to achieve a thorough molecular characterization in pediatric acute leukemia
Study
EGAS50000000701
-
TRIGR collaboration between University of Helsinkin and Children's Mercy Research Institute
Dac
EGAC50000000543
-
Integrated targeted deep sequencing reveals unique tissue-of-origin and donor cell-free DNA signatures in transplant recipients
Study
EGAS50000000987
-
Genetic differences between primary colorectal cancer and its paired synchronous and metachronous metastases
Dataset
EGAD50000001460
-
Leukemia Relapse via Genetic Immune Escape after Allogeneic Hematopoietic Cell Transplantation
Study
phs003235
-
10x Multiome from Human Fetal Heart
Study
phs003778
-
Capturing the Genetic Diversity of the Himba Population
Study
phs001995
-
Epi4K: Gene Discovery in 4,000 Epilepsy Genomes
Study
phs000653
-
Decoding Human Endogenous Retrovirus Expression in Liver Metastatic Colorectal Cancers: Implications for Diagnosis and Prognosis
Study
EGAS50000000307
-
Genetic Modifiers of Duchenne Muscular Dystrophy
Study
phs003680
-
Somatic Mutations and Their Etiological Determinants for Breast Cancer in African American Women (B-CAUSE Study)
Study
phs003962
-
Kids First: Genetics of Pediatric Germ Cell Tumors
Study
phs002322
-
Study on the Genetics of Alcoholism (COGA): Smoke Screen and Exome Sequencing
Study
phs001208
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
APOBEC3 mutagenesis drives therapy resistance in breast cancer
Study
EGAS50000000875
-
BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes
Study
EGAS00001002070
-
Human four week embryo head as reference for generating an enhancer compendium for neuronal and neural crest development using neural tube organoids.
Study
EGAS50000001031
-
Whole Exome Sequencing Data of prDLBCL
Dataset
EGAD50000000591
-
DNAmet
Study
EGAS50000001051
-
miRNA seq
Study
EGAS50000001050
-
Diagnostic Genomic Analysis is Prognostic in AYA ALL Patients Treated on a MRD-Stratified Paediatric Protocol
Study
EGAS50000000752
-
Whole Exome Sequencing Data of indolent primary renal B-Cell lymphomas
Study
EGAS50000000774
-
Genetic and Hormonal Contributions to Gene Expression in Immune Cells
Study
phs003860
-
Childhood Cancer Data Initiative (CCDI): NCI-COG Pediatric MATCH Precision Medicine Clinical Trial
Study
phs002883
-
dbGaP Collection: NIH Autism -omics Studies
Study
phs000764
-
Genetic Analysis of Tuberous Sclerosis Complex (TSC) Hypomelanotic Macules
Study
phs001236
-
dbGaP Collection: Open Translational Science in Schizophrenia (OPTICS)
Study
phs000887