-
WTCCC case-control study for Coronary Artery Disease - Combined Controls
Study
EGAS00000000004
-
WTCCC case-control study for Type 1 Diabetes - Combined Controls
Study
EGAS00000000015
-
WTCCC case-control study for Coronary Artery Disease, Hypertension, T2D - combined cases
Study
EGAS00000000005
-
WTCCC case-control study for Type 2 Diabetes - Combined Controls
Study
EGAS00000000017
-
Intrapatient tumor heterogeneity and clonal evolution in metastatic salivary gland cancer: an autopsy study
Study
EGAS50000001420
-
Genome-wide study of resistance to severe malaria in eleven worldwide populations
Study
EGAS00001001311
-
FASTQ files of the Exome-Seq data for the study "Genomic landscape of lung adenocarcinoma in East Asians"
Dataset
EGAD00001004422
-
Amplicon sequencing libraries from the study "Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study".
Dataset
EGAD00001002896
-
EBNA2 ChIP-Re-ChIP in primary B-cells infected with EBV virus
Study
EGAS00001007626
-
A genome-wide association study for nasopharyngeal carcinoma in Hong Kong population
Study
EGAS00001006102
-
Epigenome-wide association study of asthma remission in whole blood and nasal epithelium
Study
EGAS00001004766
-
Genetic analysis of short stature using whole exome sequencing
Study
EGAS50000000578
-
Multiple Myeloma GWAS Meta-analysis
Study
EGAS50000000292
-
Discordant_Monozygotic_Twins_ALS (Epigenetics)
Study
EGAS00001008053
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
Somatic_mutations_in_twin_breast_cancers
Study
EGAS00001002379
-
NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study
Study
phs000974
-
Acral melanoma study whole exomes
Dataset
EGAD00001000061
-
Whole genome sequencing dataset of 200 trio families from the CHILD cohort study.
Study
EGAS00001006725
-
Genomics and Epigenomics of the Elderly Response to Pneumococcal Vaccines
Study
phs002361
-
Imaging: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Study
phs003963
-
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
Type 1 Diabetes Genetics Consortium (T1DGC): Case-only RNA-Seq Study
Study
phs001426
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study
Study
phs001398
-
Multi-Ethnic Study of Atherosclerosis (Electrocardiogram Tracing Repository)
Study
phs003703
-
Single Cell RNA Sequencing of Human Hematopoiesis
Study
phs002750
-
Changes in CRISPR/Cas9 Outcomes depending on the usage of Pifithrin-alpha
Study
EGAS50000000656
-
Clonal hematopoiesis in metastatic urothelial and renal cell carcinoma
Study
EGAS50000000870
-
Genomic sequencing data for PNG15 and PNG16
Study
EGAS50000001105
-
CFTR Gene Variant Detection in Moroccan Individuals via Nanopore Long-Read Sequencing
Study
EGAS50000001423
-
NGS-based targeted exome sequencing of osteosarcoma
Study
JGAS000282
-
Next-generation sequencing-based comprehensive genetic analysis of undiagnosed disease
Study
JGAS000522
-
Single_Cell_Targeted_Sequence_Capture
Study
EGAS00001000435
-
SFHS_pedigrees
Study
EGAS00001000078
-
WTCCC2 Bacteraemia Susceptibility (BS) samples
Study
EGAS00001001756
-
Fungal infection in neural tissue from Amyotrophic Lateral Sclerosis
Study
EGAS00001002473
-
BS-seq in plasma of CRC patients
Study
EGAS00001003117
-
DNA-seq from plasma of 14 liver transplantation patients
Study
EGAS00001003116
-
SCLC ctDNA sequencing
Study
EGAS00001003984
-
Whole genome and exome sequencing data of invasive micropapillary carcinoma of breast
Study
EGAS00001005902
-
SCC ctDNA sequencing
Study
EGAS00001003987
-
The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
Study
EGAS00001006796
-
Whole-Exome Sequencing Study of Diabetic Nephropathy
Study
phs003429
-
Analysis of chromosomal background of cancerous mutations using a long-read sequencer
Study
JGAS000349
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
CAR_T_cell_Study
Study
EGAS00001004718
-
Targeted sequencing of paired tumour/blood of 78 Ta stage bladder cancer patients
Study
EGAS00001005766
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Amplified EPOR/JAK2 genes define a unique subtype of acute erythroid leukemia
Study
EGAS00001005810
-
Oncogenic cooperation between the TCF7-SPI1 fusion and NRAS(G12D) requires β-catenin activity to drive T-cell acute lymphoblastic leukemia.
Study
EGAS00001005097