-
The Emirati T2T-level Pangenome: A complete Diploid Graph of 58 Genomes
Study
EGAS50000001232
-
Genetic mutation profiling of lymphomas arising in the uterine cervix and vagina
Study
JGAS000823
-
Genetic Legacy of Punan Hunter-Gatherer Groups in Indonesian Borneo
Study
EGAS00001004471
-
Transcriptome changes in circulating immune cells of critical COVID-19 patients predict a specific metabolic and epigenetic imprint
Study
EGAS50000000965
-
Circulating cell-free DNA methylation profiles as noninvasive multiple sclerosis biomarkers: A proof-of-concept study
Study
EGAS50000001277
-
Temptation Resistance Failures: Transdiagnostic Features and Influences
Study
phs004064
-
Kids First: The Genomic Architecture of Hirschsprung Disease (HSCR)
Study
phs003662
-
NHLBI TOPMed: African American Sarcoidosis Genetics Resource
Study
phs001207
-
CLL Genome
Study
EGAS00000000092
-
DNTR sequencing data of paediatric acute lymphoblastic leukemia
Study
EGAS50000001247
-
Childhood B-cell acute lymphoblastic leukemia genomic and transcriptomic data
Study
EGAS00001006863
-
Fluctuating DNA methylation tracks cancer evolution at clinical scale
Study
EGAS50000001192
-
MorphoITH: A Framework for Deconvolving Intra-Tumor Heterogeneity Using Tissue Morphology
Study
EGAS50000001064
-
WES-based association study of cefaclor-induced anaphylaxis
Study
EGAS50000001163
-
Heritable pulmonary arterial hypertension - new genetic findings and environmental triggers
Study
EGAS50000001275
-
Heritable pulmonary arterial hypertension - new genetic findings and environmental triggers
Dataset
EGAD50000001817
-
Exome Sequencing of familial and sporadic Meniere disease patients
Study
EGAS50000001178
-
Chicago Infant Mortality Study
Study
phs003790
-
Virginia PrIMeD Study
Study
phs003609
-
Identification of a Type 1 Diabetes-Associated T Cell Receptor Repertoire Signature from the Human Peripheral Blood
Study
phs003979
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study
Study
phs001048
-
HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium
Study
phs002267
-
Data access to Small RNA-Seq of MicroRNA's in Tear EV's of Ushers Syndrome patients
Dac
EGAC50000000711
-
MRCA and MRCE SNP genotypes
Study
EGAS00000000137
-
Canadian prostate cancer samples (CPC-GENE) for PanProstate study
Study
EGAS00001003037
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
Passive and active DNA methylation and the interplay with genetic variation in gene regulation
Study
EGAS00001000446
-
Whole genome sequencing data of pediatric hypodiploid acute lymphoblastic leukemia
Study
EGAS50000001305
-
ChIP-seq data in MSC_Pat and EWIma1 (FLI1 & H3K27ac)
Study
EGAS50000001172
-
RNA-seq data in hMPC, MSC_Pat and EWIma
Study
EGAS50000001173
-
De novo modeling of chromoplectic Ewing sarcoma tumors from patient-derived mesenchymal stem cells
Dataset
EGAD50000001673
-
DAC for Studies of "Genetics and Genomics of Cardiovascular Diseases" Group at MDC Berlin, Germany
Dac
EGAC50000000481
-
A prospective trial comparing adaptive long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia
Study
EGAS50000000573
-
Multiomic Landscape of Multiple Myeloma Precursor and Relapsed Disease
Study
phs003892
-
Exome Sequencing of Alcohol-Associated Hepatitis
Study
phs003659
-
Bone morphogenetic protein-9 controls pulmonary vascular growth and remodeling
Dataset
EGAD50000001496
-
Access to "BMP9 controls pulmonary vascular growth and remodeling"
Dac
EGAC50000000640
-
FLT3 is genetically essential for ITD-mutated leukemic stem cells but dispensable for human HSCs
Dataset
EGAD50000000636
-
Whole genome sequence: cardiomyopathy, 1 HCM patient
Study
JGAS000704
-
Whole genome sequence: cardiomyopathy, 1 myotonic dystrophy patient
Study
JGAS000706
-
Whole genome sequence: cardiomyopathy, 1 ARVC patient
Study
JGAS000705
-
Evidence for Enhancer Activity in Intron 1 of TNFRSF1A Using CRISPR/Cas9 in Human Induced Pluripotent Stem Cell-derived Macrophages
Study
EGAS50000000703
-
IDH-wildtype untreated human glioblastoma samples (GB-UK cohort), published in Noorani & Haughey et al 2025.
Study
EGAS00001008126
-
BAP1 study
Study
EGAS50000000235
-
Lessons learned from the exome sequencing of nine cases of infertility and the way forward
Study
EGAS50000001320
-
Exome Sequencing data from infertility cases.
Dataset
EGAD50000001881
-
McGill Reproductive Genetics Data Access Committee
Dac
EGAC50000000775
-
Nanopore sequencing of FSHD, BAMS and healthy control fibroblast cell lines
Study
EGAS50000001065
-
DNA Replication Speed controls Epigenome Integrity and T Cell Fate
Study
EGAS50000001273
-
Ultra-long whole-genome and Cas9-targeted nanopore sequencing of fibroblasts: FSHD, BAMS, healthy controls
Dataset
EGAD50000001551
-
Walter and Eliza Hall - Aix-Marseille Université
Dac
EGAC50000000655
-
genetic analysis of carcinogenesis in GAPPS
Study
JGAS000843
-
The Genetic Analysis of multiple sclerosis
Study
EGAS00000000101
-
The brain neurovascular epigenome and its association with dementia
Study
EGAS50000001160
-
Huch Lab, Max Planck Institute of Molecular Cell Biology and Genetics
Dac
EGAC50000000112
-
APC-related multiple salivary gland lesions
Study
EGAS50000001159
-
Pipeline Olympics: Continuous benchmarking of computational workflows for DNA methylation sequencing data
Study
EGAS50000000541
-
LifeChange Data Access Committee
Dac
EGAC50000000713
-
Recurrent intra-tumour heterogeneity is a hallmark of metastatic prostate cancer
Study
EGAS50000001312
-
UMCG Immunogenetics DAC
Dac
EGAC50000000785
-
ATACseq in blood-derived monocytes from CGD patients
Study
EGAS00001005915
-
Methylation sequencing of CSF-derived cell free DNA
Study
EGAS50000001365
-
Development of Novel Chondrosarcoma Organoid Models for Drug Discovery
Study
JGAS000834
-
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
Study
EGAS50000000906
-
Processing of tissue and cfDNA samples of CRC patients using Active-seq
Study
EGAS50000001226
-
Dynamic human admixture histories over the past ~1,300 years at the northern Himalayan frontier
Study
EGAS50000001342
-
Whole-exome variant calling of individuals from the study of familial pulmonary fibrosis in the Canary Islands
Study
EGAS50000000782
-
Epigenetic analysis of clear cell renal cell carcinoma using ChIP-seq
Dataset
EGAD50000001886
-
Insights into BRCA1 and TP53 associated breast cancer development from integrated whole genome analysis of mouse model mammary tumors
Study
EGAS50000001402
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.
Dac
EGAC50000000169
-
Idiopathic Scoliosis (SNP-array & WES study)
Study
EGAS00001008152
-
scATAC-seq and combined scRNA-seq of the human first trimester neurodevelopment
Study
EGAS00001007472
-
Spatial Dynamics of the Developing Human Heart
Study
EGAS50000001122
-
Genetic differences between primary colorectal cancer and its paired synchronous and metachronous metastases
Study
EGAS50000000996
-
A distinct monocyte cellular state links systemic immune dysregulation to pulmonary impairment in long COVID
Study
EGAS50000001215
-
Spatial Dynamics of the Developing Heart (single-cell)
Study
EGAS50000001029
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Study
EGAS50000000283
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Dataset
EGAD50000000410
-
NICOLA Epigenetic Data Wave 1 - Beta values
Dataset
EGAD50000001965
-
Nala TAS-LRS PGx Study
Study
EGAS50000001116
-
Spatial multiomic analyses reveal carcinogenic pathways in end-stage renal disease
Study
JGAS000855
-
NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)
Study
phs001215
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
ATAC-seq: Acquired non-permissive bone marrow microenvironment impairs hematopoietic stem cell proliferation and maintenance and B-cell development post-HSCT
Study
EGAS50000001438
-
Axes of Biological Variation in Diffuse Large B-Cell Lymphoma
Study
EGAS50000001227
-
Genetics of gene expression in primary human immune cells
Study
EGAS00000000109
-
Genome-wide methylation profiling by high-throughput sequencing of tissue (resident) versus blood circulating memory T lymphocyte populations
Study
EGAS50000000085
-
Methylation clocks - individual colon, small intestine and endometrial crypts
Study
EGAS00001005514
-
Integrated genetic analysis of primary CNS lymphoma
Study
EGAS00001007222
-
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
-
Khoe-San Genome Project
Study
EGAS50000001408
-
Khoe-San genome Project (KSGP)
Dac
EGAC50000000798
-
Methylome study on human spermatogenic cells
Study
EGAS00001007449
-
An allele-resolved nanopore-guided tour of the human placental methylome
Study
EGAS50000001301
-
OurHealth - Cardiovascular Disease in South Asians
Study
phs003821
-
A Case Controlled Etiologic Study of Sarcoidosis (ACCESS-BioLINCC)
Study
phs004276
-
Development of Novel Histiocytic Sarcoma Organoid Model for Drug Discovery
Study
JGAS000807
-
Development of Novel Synovial Sarcoma Organoids Models for Drug Discovery
Study
JGAS000806
-
Complex genotype-phenotype relationships shape the response to treatment of Down Syndrome Childhood Acute Lymphoblastic Leukaemia
Study
EGAS50000001287
-
The cellular state space of AML unveils novel NPM1 subtypes with distinct clinical outcomes and immune evasion properties
Study
EGAS50000001084