-
Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Study
EGAS00001004781
-
Lung Adenocarcinoma Promotion by Air Pollutants
Study
EGAS00001006951
-
Segmental_cherry_angioma_case
Study
EGAS00001008212
-
Whole_Exome_sequencing_in_a_large_IBD_pedigree
Study
EGAS00001000240
-
The MD Anderson Colorectal Cancer Case Control Study
Study
phs002691
-
Susceptibility to Respiratory Infections Due to Autosomal Recessive IFIH1 Mutations
Study
phs001235
-
Integrated Genetic and Pharmacologic Interrogation of Rare Cancers
Study
phs001121
-
Complement C1s deficiency in a male Caucasian patient with systemic lupus erythematosus: A case report
Study
EGAS50000000707
-
Germline WES of serrated polyposis syndrome
Study
EGAS50000000765
-
NHLBI TOPMed - NHGRI CCDG: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Study
phs001395
-
RNA004 DRS METTL5 variant
Study
EGAS50000001321
-
Genotype data from Nagahama cohort project
Study
JGAS000012
-
Whole genome sequencing of AML with FUS-ERG
Study
JGAS000587
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
-
Molecular characterization of hepatocellular carcinoma in patients with non-alcoholic steatohepatitis
Study
EGAS00001005222
-
Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma
Study
EGAS00001006133
-
Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
Studies of Left Ventricular Dysfunction (SOLVD-BioLINCC)
Study
phs003668
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Dataset
EGAD00001006171
-
Single-Cell DNA Methylation Profiling via scTAMseq
Dataset
EGAD00001015498
-
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Study
phs000927
-
Discovery of Colorectal Cancer Susceptibility Genes in High-Risk Families
Study
phs001787
-
Genetic Causes of Congenital Anosmia
Study
phs003328
-
Northwestern NUgene Project: Type 2 Diabetes
Study
phs000237
-
Acute Respiratory Distress Syndrome Clinical Network: Fluid and Catheter Treatment Trial (ARDSNet FACTT-BioLINCC)
Study
phs004165
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
EGAD00010000624
Dataset
EGAD00010000624
-
EGAD00010000626
Dataset
EGAD00010000626
-
Rare germline variants in patients with personal and family history of colorectal cancer
Dataset
EGAD50000000861
-
EDi019-A / SAMEA4774918 WGS data
Dataset
EGAD50000001029
-
RCi009-A / SAMEA4339688 WGS data
Dataset
EGAD50000001030
-
EDi018-A / SAMEA4771918 WGS data
Dataset
EGAD50000001027
-
EDi016-A / SAMEA4562366 WGS data
Dataset
EGAD50000001032
-
EDi017-A / SAMEA4768918 WGS data
Dataset
EGAD50000001033
-
EDi010-A / SAMEA4459354 WGS data
Dataset
EGAD50000001038
-
EDi012-A / SAMEA4459361 WGS data
Dataset
EGAD50000001046
-
EDi015-A / SAMEA4459373 WGS data
Dataset
EGAD50000001047
-
EDi011-A / SAMEA4459357 WGS data
Dataset
EGAD50000001050
-
BIONi010-A / SAMEA3105765 WGS data
Dataset
EGAD50000001054
-
EDi013-A / SAMEA4459365 WGS data
Dataset
EGAD50000001057
-
RBi001-A / SAMEA3368212 WGS data
Dataset
EGAD50000001058
-
RCi006-A / SAMEA3962402 WGS data
Dataset
EGAD50000001059
-
RCi004-A / SAMEA3106011 WGS data
Dataset
EGAD50000001069
-
RCi005-A / SAMEA3961534 WGS data
Dataset
EGAD50000001071
-
UOXFi007-A / SAMEA103988274 WGS data
Dataset
EGAD50000001079
-
WTSIi009-A / SAMEA2593858 WGS data
Dataset
EGAD50000001085
-
UKKi019-A / SAMEA17624668 WGS data
Dataset
EGAD50000001094
-
Genomic Rearrangements in Pediatric Cancer
Study
EGAS00001005312
-
Wistar PDX Development and Trial Center
Study
phs002432
-
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Study
phs000486
-
Discovery and validation of an ancillary genomic test of malignancy for primary melanocytic tumors
Study
EGAS50000000887
-
Puerto Rico Heart Health Program (PRHHP-BioLINCC)
Study
phs003930
-
RNA seq on 19 samples of Radiation-Induced Meningiomas
Study
EGAS00001002318
-
18 Whole Exome Sequencing for Radiation Induced-Meningiomas
Study
EGAS00001002317
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
Study
EGAS00001002840
-
Single Cell Targeted Sequence Capture
Dataset
EGAD00001001450
-
Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation.
Study
EGAS00001005887
-
Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target
Study
EGAS00001008039
-
The Natural History of Mucolipidosis Type IV
Study
phs001329
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
Gynecology and Lubricant Effects (GALE) Study
Study
phs002211
-
Drug Development against Tumor Microtube Networks in Glioblastoma
Study
EGAS50000000477
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
-
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Study
EGAS00001000572
-
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Study
EGAS00001002344
-
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Study
EGAS00001001515
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005215
-
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Integrative Multi-Omics and Drug Sensitivity Profiling Reveals Potential Predictive Biomarkers in Pediatric Solid Tumors from the INFORM Registry
Study
EGAS00001008249
-
A Study of the Genetic Causes of Complex Pediatric Disorders
Study
phs000490
-
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Study
phs003315
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Study
EGAS00001006260
-
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Study
phs002462
-
Discovering the Genetic Basis of Cleft Palate: CIDR
Study
phs002220
-
CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq)
Study
phs002337
-
ARRA - NHLBI Lung Cohorts Sequencing Project: Genetic modifiers of
Study
phs000254
-
The Cardiopulmonary Effects of Particulate Exposure
Study
phs000968
-
Study of Tumor Recurrence Related to the Expression of the PAX3-FOXO1 Oncogenic Transcription Factor in Fusion-Positive Rhabdomyosarcoma
Study
phs002344
-
Investigating Genetics in Suspected Congenital Syndromes
Study
phs003453
-
Synthetic - FEGA Sweden Heilsa synthetic dataset December 2023
Study
EGAS50000000086
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Reference exome data for Australian Aboriginal populations to support health-based research
Study
EGAS00001003745
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Study
EGAS00001006576
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021)
Study
EGAS00001006629
-
A Phase II Clinical Trial of the PARP Inhibitor Talazoparib in BRCA1 and BRCA2 Wild-Type Patients
Study
phs002803
-
Transcriptome sequencing across a prostate cancer cohort identifies PCAT-1, an unannotated lincRNA implicated in disease progression
Study
phs000443
-
A Translational, Pharmacodynamic and Pharmacokinetic Phase IB Clinical Study of Everolimus in Resectable Non-Small Cell Lung Cancer
Study
phs000829
-
Kbtbd13 knock-down restores muscle function in a human-based mouse model of nemaline myopathy type 6
Study
EGAS50000001678
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224
-
Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma
Study
EGAS00001002588