-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study
Study
phs000100
-
NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry
Study
phs001545
-
Transcriptomic analysis of B-cell acute lymphoblastic leukaemia (B-ALL) patients treated on the ALL09 clinical trial
Study
EGAS50000001109
-
Recording physiological history of cells with chemical labeling.
Study
EGAS50000000056
-
Identification of germline variants in Medullary thyroid carcinoma (MTC) by whole- exome sequencing
Study
EGAS50000000061
-
RNA sequencing data from glioblastoma primary cell lines treated with indisulam
Study
EGAS50000000680
-
ECM-free patient-derived organoids preserve diverse prostate cancer lineages and uncover in vitro-enriched cell types
Study
EGAS50000000807
-
MATISSE bulk RNA-sequencing data
Dataset
EGAD50000001470
-
EGA synthetic data
Documentation
synthetic-data
-
Size-tagged preferred ends in maternal plasma DNAshed light on the production mechanism and showutility in noninvasive prenatal testing
Study
EGAS00001002831
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Study
EGAS00001000961
-
MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition
Study
EGAS00001002115
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
Adeno-associated virus in the liver: natural history and consequences in tumor development
Study
EGAS00001003310
-
WGS of liver cancer in the Japanese population
Study
EGAS00001000678
-
Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
Molecular sub-classification of hormone receptor-positive breast cancer
Study
EGAS00001004594
-
Single-cell RNA sequencing of 22 Hodgkin lymphoma tumors and 5 reactive lymph nodes
Study
EGAS00001004085
-
Patient-derived organoids as a novel tool to study cervical cancer
Study
EGAS00001004439
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Sperm_PacBio_CCS_sequencing
Study
EGAS00001004958
-
RP-1843 Arcagen - Gastrointestinal rare cancers (GI)
Study
EGAS00001006299
-
Single cell whole genome sequencing of high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001006347
-
ATAC-Seq of inflamed and non-inflamed biopsies
Study
EGAS00001007344
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step toward Biomarker Development
Study
phs001281
-
CPTAC: Microscaled Proteogenomic Methods for Precision Oncology
Study
phs001907
-
BPH Tissues for Cell Culture and Analysis - Spatial Transcriptomics Identifies Candidate Stromal Drivers of Benign Prostatic Hyperplasia
Study
phs003477
-
Comprehensive Genomic Data Deposition for Pancreatic Cancer Precision Medicine Studies: Clinical Trials NCT02451982 and NCT02648282
Study
phs003600
-
ABO: a 3D stroma-supported culture platform enabling full human B lymphopoiesis for disease modeling and gene therapy development
Study
EGAS50000001693
-
Human Dicer is required for cell-intrinsic immunity to self-dsRNA
Study
EGAS50000001409
-
How to encrypt files with Crypt4gh
Documentation
submission/data/file-preparation/crypt4gh
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
-
WES of adult intellectual disabilities with co-morbid psychiatric disorders (2019-08-07)
Dataset
EGAD00001005236
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Autism - Simons Simplex Collection (SSC)
Study
phs001676
-
Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival
Study
phs001982
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Study
phs002044
-
NCI Cancer Model Development for the Human Cancer Model Initiative (HCMI)
Study
phs001486
-
Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Study
EGAS00001001437
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
Combination of ribociclib and gemcitabine for the treatment of medulloblastoma
Study
EGAS00001006001
-
HudsonAlpha Institute for Biotechnology Clinical Sequencing Exploratory Research (CSER): Genomic Diagnosis in Children with Developmental Delay
Study
phs001089
-
NSIGHT North Carolina Newborn Exome Sequencing for Universal Screening (NC NEXUS)
Study
phs002095
-
Profiling Genome-Wide Circulating ncRNAs for the Early Detection of Lung Cancer
Study
phs004166
-
Characterization of Cell Free Plasma Methyl-DNA From Xenografted Tumors to Guide the Selection of Diagnostic Markers for Early-Stage Cancers
Study
EGAS00001006175
-
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Study
phs001317