-
PELICAN45 RNAseq Dataset
Dataset
EGAD00001009997
-
multi-region sequencing of tumor samples from PDAC patients
Dataset
EGAD00001011109
-
Data for noninvasive lung cancer subtyping study
Dataset
EGAD00001015344
-
Exome sequencing data for 40 cases of alopecia areata and vitiligo
Study
EGAS00001003831
-
Kids First: Genomic Studies of Orofacial Cleft Birth Defects
Study
phs001168
-
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
-
Varieties of Impulsivity in Opiate and Stimulant Users
Study
phs001647
-
The Role of E2F4 in Controlling Resistance to Irinotecan (CPT-11) in Human Colon Cancer
Study
phs003560
-
Idiopathic Pulmonary Fibrosis Network (IPFNet) Sildenafil Trial of Exercise Performance in Idiopathic Pulmonary Fibrosis (IPFNet-STEP-IPF-BioLINCC)
Study
phs004085
-
Autism Post-Mortem Brain RNA-Sequencing: SRRM4 Splicing Study
Study
phs000872
-
Microbiome-Host Interactions in Oral Squamous Cell Carcinoma: a Metatranscriptomic Exploratory Study
Study
phs002678
-
Genome-Wide Association Study of the Taste and Hedonic Ratings of the Low-Calorie Sweetener Acesulfame Potassium
Study
phs004031
-
This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
-
eMERGE Network Study of the Genetic Determinants of Resistant Hypertension
Study
phs000297
-
Programmatic submission based on XML
Documentation
submission/metadata/submission/programmatic-submission-xml
-
Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response
Study
phs003149
-
Genetic Basis of Developmental Disabilities
Study
phs000337
-
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Study
phs000956
-
Safety and Efficacy of Intravenous Norepinephrine for Orthostatic Hypotension
Study
phs001769
-
Mechanisms of Risk for Sulfonamide Hypersensitivity
Study
phs001124
-
Identifying Novel Small RNA Biomarkers Unique to Patients with Gastric Cancer
Study
phs001767
-
Single-Cell Analysis of CD19-Specific CAR T Cell Treatment of Relapsed/Refractory CD19+ Acute Lymphoblastic Leukemia
Study
phs002966
-
Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR)
Study
phs000708
-
Epigenetics of Cocaine and Nicotine Addiction
Study
phs001377
-
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Study
phs000486
-
NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001345
-
Enhancing Open Data Sharing for Functional Genomics Experiments: Measures to Quantify Genomic Information Leakage and File Formats for Privacy Preservation
Study
phs003166
-
Genome Studies in Hereditary Spastic Paraplegia
Study
phs001080
-
NHLBI TOPMed: Coronary Artery Risk Development in Young Adults (CARDIA)
Study
phs001612
-
ChiLDReN/BA: Genetic Studies of Biliary Atresia in the Childhood Liver Disease Research Network
Study
phs003356
-
MUSIC: Long-TerM OUtcomes after the Multisystem Inflammatory Syndrome In Children
Study
phs002770
-
Rapid Early Action for Coronary Treatment (REACT-BioLINCC)
Study
phs003885
-
Asian Immune Diversity Atlas (AIDA) sQTL
Study
phs003848
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
Sequencing of 3D Organoids Derived From Colorectal Cancer Patients
Study
phs003965
-
Genomic Landscape of Multiple Myeloma and of its Precursor Conditions, and its Clinical Implications
Study
phs003846
-
Field Studies of Human Immunity to Amebiasis in Bangladesh
Study
phs001476
-
Involvement of the FGF8/FGF Receptor Signaling Pathway in the Maintenance and Progression of Fusion-Positive Rhabdomyosarcoma
Study
phs004009
-
Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
Study
JGAS000226
-
Cholesterol homeostasis and lipid raft dynamics at the basis of tumor-induced immune dysfunction in chronic lymphocytic leukemia
Study
EGAS50000000933
-
Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Study
EGAS00001003412
-
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Study
EGAS00001001288
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Study
EGAS00001004546
-
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
-
Analysis of error profiles in deep next-generation sequencing data
Study
EGAS00001003444
-
Exome sequencing from cfDNA blood samples. 159 samples at 2x101bp Illumina reads in Fastq format.
Study
EGAS00001006656
-
Integrated genomic analyses reveal molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma
Study
EGAS00001005503
-
Dac for "MediMer: A versatile do-it-yourself peptide-receptive MHC class I multimer platform for tumor neoantigen-specific T cell detection"
Dac
EGAC50000000064
-
Netherlands Cancer Institute (NKI-AVL) general DAC
Dac
EGAC50000000055
-
Genome Wide Association Studies in Alopecia Areata
Study
phs000586
-
Antibody Repertoires in CVID
Study
phs000934
-
Treatment of genetic screening of hypertriglyceridemia type I, III, and V - HTG Amsterdam
Study
phs000511
-
Human PI3Kγ Deficiency with Immunodeficiency and Tissue Immunopathology
Study
phs001848
-
McQuillin_Global_London_SCZ_Bipolar_WES
Dac
EGAC50000000311
-
Stanford Acute Myeloid Leukemia Single-Cell DNA Sequencing
Study
phs003853
-
Exploring Genomic Mutations in Gastric Cancer among Japanese Populations
Study
JGAS000754
-
Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas
Study
JGAS000284
-
Whole-genome-sequencing, Whole-exome-sequencing and RNA-sequencing in Sporadic ALS
Study
JGAS000393
-
WGS analysis of a glioma initiating cell line
Study
JGAS000096
-
Elucidation of molecular mechanism of NAFLD-HCC
Study
JGAS000523
-
Targeted sequencing of cell free DNA samples from oligometastatic colorectal cancer patients
Study
JGAS000196
-
Target sequencing of refractory adult Ph-negative B-ALL 1 patient
Study
JGAS000483
-
Metabolome analysis of persons with type 2 diabetes with or without diabetic complications
Study
JGAS000572
-
Whole exome sequencing, RNA sequencing and single-cell RNA sequencing of 4 melanoma patients
Study
JGAS000285
-
Elucidation of male-specific genetic regulation through multi-layered omics analysis
Study
JGAS000862
-
Flexible and rapid validation of structural variants using adaptive sampling
Dac
EGAC50000000748
-
Whole exome and RNA sequencing of patient-derived and COPA-engineered human intestinal organoids
Study
JGAS000881
-
PRPH2-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish Cohort
Study
EGAS50000000847
-
Genentech Small Cell Lung Cancer (SCLC) Screen
Study
EGAS00001000334
-
DNA sequencing of sgRNAs enriched from the CRISPR-Cas9 screened HCC organoids
Study
EGAS50000001130
-
Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
Study
EGAS00001000566
-
Pediatric B-cell precursor acute lymphoblastic leukemia Micro-C sequencing
Study
EGAS50000000764
-
Non-coding RNAs in breast cancer
Study
EGAS00001003353
-
Angiosarcoma_follow_up_study
Study
EGAS00001000405
-
Unraveling the Physiological Impact of ANGPTL8 Loss-of-Function Variants in Humans
Study
EGAS50000001482
-
Bioinformatics analysis of chimerism in monochorionic dizygotic twins
Study
EGAS00001005997
-
Analysis_of_somatic_mutations_in_normal_blood__AML_and_MDS_samples
Study
EGAS00001000525
-
Single-cell RNAseq of hematological toxicity following CAR-T cells injection
Study
EGAS50000000776
-
Tumor cells metabolically resist immune-checkpoint therapy by macrophage efferocytosis-mediated fatty acid recycling
Study
EGAS50000001416
-
Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens
Study
EGAS00001000297
-
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
Study
EGAS00001001598
-
MPN_mutation_order_followup
Study
EGAS00001000663
-
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility
Study
EGAS50000000397
-
Progressive multifocal leukoencephalopathy (PML)
Study
EGAS50000000139
-
MNM - Temporal variability in Quantitative Microbiome Profiles
Study
EGAS00001005686
-
EBV_AID_project
Study
EGAS00001000955
-
Osteosarcoma_Whole_Genome
Study
EGAS00001000147
-
The landscape of LAM disease
Study
EGAS00001003534
-
ctDNA detectability and representativeness in seven body liquids from female patients with metastatic breast cancer - lpWGS
Study
EGAS50000001302
-
ctDNA detectability and representativeness in seven body liquids from female patients with metastatic breast cancer - WES
Study
EGAS50000001303
-
cfRRBS data plasma healthy donors
Study
EGAS50000000376
-
Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2
Study
EGAS00001000402
-
The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS50000000203
-
INVADE cohort
Study
EGAS50000000219
-
Co-infection of fungi and bacteria in brain tissue of Alzheimer’s patients.
Study
EGAS00001002766
-
The integrated genomic and immune landscapes of lethal metastatic breast cancer.
Study
EGAS00001002703
-
Transcriptional Reference Map of Human Natural Killler Cells
Study
EGAS50000000014
-
Prognostic_factors_in_prostate_cancer__deep_sequencing_pilot_project_TAPG
Study
EGAS00001000879