-
Transcriptome Sequencing of Pediatric Neuroblastoma
Study
phs000868
-
Subtyping Sub-Saharan Esophageal Squamous Cell Carcinoma by Comprehensive Molecular Analysis
Study
phs001448
-
Whole Genome Sequencing of Skull-Based Chordoma
Study
phs002301
-
High-Throughput RNA Isoform Sequencing using Programmable cDNA Concatenation
Study
phs003200
-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
Next Generation Mendelian Genetics: Muscle Hypertrophy
Study
phs000541
-
Transcriptional and Epigenetic Profiles of Male Breast Cancer at Single-Cell Resolution Nominate Salient Cancer Specific Enhancers
Study
phs003006
-
Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's or Parkinson's disease correlate with disease status and features of pathology
Study
phs000727
-
Genetic and Epigenetic Determinants of Pediatric Obesity-Associated Asthma
Study
phs001812
-
NCI CCSG CCDI Supplement Additional Genomic Submission
Study
phs002599
-
NSD2 E1099K Drives Relapse in Pediatric Acute Lymphoblastic Leukemia by Disrupting 3D Chromatin Organization
Study
phs003195
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Clear2Go - A Digital Identity Wallet for Health Status
Study
phs002628
-
Single Cell Analysis of Sporadic Human Basal Cell Carcinomas
Study
phs003103
-
Combined Targeting of CDK4/6 and HER2 Signaling in Orthotopic Patient-Derived Xenografts of HER2-Positive Breast Cancer Brain Metastases
Study
phs002482
-
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt AF Ablation Registry
Study
phs000997
-
Detection of Somatic Mutations In Vitro Aging Cells
Study
phs001867
-
Molecular Features of Hepatocellular Carcinoma Associated with 18F-Fluorocholine PET/CT Imaging Phenotype
Study
phs001784
-
Novel APC Promoter and Exon 1B Deletion and Allelic Silencing in Three Mutation-Negative Classic Familial Adenomatous Polyposis Families
Study
phs000904
-
Germline DNA Methylation Associated with Breast Cancer Predisposition
Study
phs001699
-
FinaleMe: Predicting DNA Methylation by the Fragmentation Patterns of Plasma Cell-Free DNA
Study
phs003287
-
EWS-WT1 Fusion Isoforms Establish Oncogenic Programs and Therapeutic Vulnerabilities in Desmoplastic Small Round Cell Tumors
Study
phs003682
-
ScRNA-seq of human kidney immune cells of patients with ANCA-associated glomerulonephritis, Lupus Nephritis against a healthy nephrectomy control
Dataset
EGAD50000000229
-
A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk
Dataset
EGAD50000000518
-
"BaTwa" populations from Zambia retain ancestry of past hunter-gatherer groups
Study
EGAS50000000378
-
Ancient genomes reveal insights into ritual life at Chichén Itzá
Study
EGAS50000000296
-
Proteomic predictors of individualized nutrient-specific insulin secretion in health and disease
Dataset
EGAD50000000519
-
Immune signature of malignant melanoma in pregnancy
Study
EGAS50000000492
-
Spatiotemporal single-cell roadmap of human skin wound healing
Study
EGAS50000000571
-
Gabriella Miller Kids First Pediatric Research Program in Bladder Exstrophy, Epispadias, Complex (BEEC)
Study
phs002173
-
Epigenomics of Prostate Cancer from Cell Free Plasma
Study
phs003482
-
Divergent WNT Signaling and Drug Sensitivity Profiles within Hepatoblastoma Tumors and Organoids
Study
EGAS50000000561
-
RNA-seq of longitudinal human blood and nose swab samples from a controlled human infection experiment with SARS-CoV-2 virus
Study
EGAS50000000667
-
High-resolution profile of neoantigen-specific TCR activation links moderate stimulation to increased resilience of engineered TCR-T cells
Study
EGAS50000000600
-
Oncogene activated human breast luminal progenitors contribute basally located myoepithelial cells
Study
EGAS50000000505
-
Addiction of Primary Cutaneous Gamma-Delta T-cell Lymphomas to JAK-STAT Signaling
Study
phs003837
-
Integrated Transcriptomic and Regulatory RNA Profiling Reflects Complex Pathophysiology and Uncovers a Conserved Gene Signature in End Stage Heart Failure RNA-Seq data
Study
EGAS50000000810
-
Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer
Study
EGAS50000000793
-
dbGaP Collection: Psychiatric Genomics Consortium (PGC) dbGaP Datasets
Study
phs001254
-
Comparison of transcriptomics profile of stem cell-derived beta cells from HUES8 and RC9
Study
EGAS50000000905
-
INfluenza Vaccine to Effectively Stop Cardio Thoracic Events and Decompensated Heart Failure (INVESTED)
Study
phs004011
-
Changes in AXL and/or MITF melanoma subpopulations in patients receiving immunotherapy
Study
EGAS50000001080
-
Single cell transcriptomics of human kidney organoid endothelium reveals vessel growth processes and arterial maturation upon transplantation
Study
EGAS50000001068
-
ERBB2/HER2 alterations in ctDNA and metachronous tissues of patients with metastatic urothelial cancer - WGS
Study
EGAS50000001082
-
ERBB2/HER2 alterations in ctDNA and metachronous tissues of patients with metastatic urothelial cancer - Targeted
Study
EGAS50000001081
-
Systematic Analysis of Transcription Program Regulation by Transcription Factor EB (TFEB)
Study
phs002099
-
ATACseq - Notch Signaling Maintains a Progenitor-Like Subclass of Hepatocellular Carcinoma
Study
EGAS50000000516
-
ABHD11 inhibition drives sterol metabolism to modulate T cell effector function and alleviate autoimmunity
Study
EGAS50000001297
-
High Sensitivity ctDNA Analysis Using a Novel Panel and NOIR-SS Technology for Monitoring Advanced Urothelial Carcinoma
Study
JGAS000836
-
A non-canonical lymphoblast in refractory childhood T-cell leukaemia
Study
EGAS50000000767
-
Development of Novel Synovial Sarcoma Organoids Models for Drug Discovery
Study
JGAS000806
-
WES analysis of paired tumor and non-tumoral DNA of 4 patients with non-muscle-invasive bladder cancer
Study
EGAS50000001382
-
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Study
JGAS000141
-
CAGE analysis for endometrial carcinoma
Study
JGAS000124
-
Expression quantitative trait loci analysis using human immune cells in a Japanese population
Study
JGAS000085
-
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Study
JGAS000103
-
Whole exome sequencing of uterine adenomyosis
Study
JGAS000169
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
JGAS000600
-
RNA expression profiling of neuromuscular diseases and viral diseases
Study
JGAS000064
-
Japanese Reference Genome JG1
Study
JGAS000259
-
Germline pathogenic variant and gastric cancer risk
Study
JGAS000592
-
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Study
JGAS000485
-
Adult B-precursor acute lymphoblastic leukemia RoCK and ROI single-cell transcriptome
Study
EGAS50000001366
-
Whole genome sequencing data of paediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001079
-
B cell activation
Study
EGAS50000001468
-
Drug Perturbation of Primary Lymphoma Patient Samples and RNA Sequencing
Study
EGAS50000001500
-
PD-associated regulatory variants in human dopaminergic neurons reveals modulators of SCARB2 and BAG3 expression
Dataset
EGAD50000002258
-
Discordant_Monozygotic_Twins_ALS(Transcriptomics)
Study
EGAS50000000909
-
Spatial predictors of response to immunotherapy in microsatellite stable metastatic colorectal cancer
Dataset
EGAD50000002244
-
Primary breast tumor heterogeneity through therapy
Study
EGAS00001003168
-
RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder
Study
EGAS00001001840
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA
Study
EGAS00001003634
-
WXS of 147 lung cancer patients treated with immunotherapy
Study
EGAS00001003781
-
Canadian Prostate Cancer Genome Network
Study
EGAS00001000900
-
RNA_sequencing
Study
EGAS00001000310
-
Molecular profiling of EBV associated diffuse large B-cell lymphoma
Study
EGAS00001006400
-
Breast Cancer - Very young women
Study
EGAS00001001908
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis
Study
EGAS00001001035
-
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
-
Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Study
EGAS00001004534
-
Leucocyte eQTLs in autoimmune disease and health
Study
EGAS00001001251
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
TMD_AMKL_targeted_follow_up
Study
EGAS00001000569
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium
Study
EGAS00001001180
-
TMD_AMKL_targeted_follow_up_part_2
Study
EGAS00001000732
-
Transcriptomics_of_human_olfactory_mucosa
Study
EGAS00001001486
-
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Study
EGAS00001000085
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Study
EGAS00001002709