-
Epigenetic and transcriptional profile of memory B cells in Multiple sclerosis
Study
EGAS50000000872
-
Comprehensive biomarker analysis from phase II study of nivolumab in patients with thymic carcinoma
Study
JGAS000588
-
Expression profiling of Gorlin iPSCs in the osteoblast induction culture
Study
JGAS000218
-
Gene expression by RNAseq in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Study
EGAS00001003735
-
DNA methylation in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Study
EGAS00001003739
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort
Study
phs001782
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001108
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001060
-
Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Study
EGAS00001003412
-
shallow Whole-Genome sequencing of 14 TNBC tumor in the MATADOR trial - for in silico spike-in experiment
Dataset
EGAD50000001863
-
Multi-omics analyses of airway host-microbe interactions in chronic obstructive pulmonary disease identify potential therapeutic interventions
Study
EGAS00001006398
-
CASCADE metastatic melanoma study
Study
EGAS00001004950
-
Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes
Study
EGAS50000000536
-
Role of Microglia Somatic Mutations in Neurodegenerative Diseases
Study
phs002213
-
A single-chain derivative of the integrin β1-activating TS2/16 antibody potentiates organoid growth in Matrigel and Collagen hydrogels.
Study
EGAS50000001113
-
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
-
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Study
EGAS00001001018
-
Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Study
EGAS00001005909
-
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
-
Disease specific alterations in the olfactory mucosa of patients with Alzheimer’s disease
Study
EGAS00001006019
-
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Study
EGAS00001001515
-
Genetic Analysis of Tuberous Sclerosis Complex (TSC) Hypomelanotic Macules
Study
phs001236
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Study
EGAS00001004636
-
Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression
Study
EGAS00001006585
-
Assessment of Complex Chromosomal Changes in De-Identified Cell Lines
Study
phs004000
-
Natural variation of circulating RNAs in human serum
Study
EGAS00001002814
-
MDS 5q exomes
Study
EGAS50000000649
-
Primary_DIPG_expression_profiles
Study
EGAS00001007181
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda
Study
phs001705
-
Highly prevalent NF-kappa B signaling pathway-activating somatic mutations in intracranial aneurysms
Study
JGAS000591
-
Transcriptome analysis of iPSC-derived hepatocytes from Wilson's Disease patients and healthy controls
Study
JGAS000382
-
Whole Exome Sequencing of a Lung Adenocarcinoma Patient Across Three Time Points
Study
EGAS50000000812
-
Truncated FOS impairs osteogenic differentiation and induces prostaglandin and NFkB signalling in an in vitro cell-of-origin model for osteoid osteoma and osteoblastoma
Study
EGAS50000001291
-
Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
-
Mutations of whole genome sequencing in single cells in normal esophageal epithelium
Study
EGAS00001003281
-
Sequence analysis of colorectal serrated lesions
Study
JGAS000217
-
Butyrate producers as potential next-generation probiotics: safety assessment of the administration of Butyricicoccus pullicaecorum to healthy volunteers
Study
EGAS00001003276
-
Colorectal cancer study
Study
EGAS00001006489
-
Comprehensive analyses of genetic aberrations in gastroenterological tumors
Study
JGAS000269
-
Defective homologous recombination in HCC
Study
EGAS00001006599
-
Molecular Phenotype of Constitutional TET2 Haploinsufficiency in Humans
Study
EGAS00001003454
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
Pharmacogenomics of Mercaptopurine Intolerance in Children with Acute Lymphoblastic Leukemia (AALL03N1)
Study
phs002846
-
Investigation of BK Polyomavirus (BKPyV) and Molecular Signatures in UC specimens from Taiwan
Study
EGAS50000001063
-
Chromosome contacts in activated T cells identify autoimmune disease-candidate genes
Study
EGAS00001001961
-
Cerebrospinal Fluid Analysis of HIV-1 Viral Burden in HIV-1 Infected Subjects: Response to Antiretroviral Therapy
Study
phs001694
-
Construction of endoscopic biopsy banking for understanding the intestinal environment in colorectal diseases and exploratory studies using these banking systems.
Study
JGAS000655
-
Single cell sequencing data of PBMC and CSF from a cohort of Multiple Sclerosis patients and other neurological disease controls
Study
EGAS50000000739
-
Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231)
Study
EGAS00001006173
-
Exome & MiSeq sequencing of individuals with Huntington's disease
Study
EGAS00001006383
-
Serial TERT rearrangement breakpoint quantification in circulating tumor DNA enables minimal residual disease monitoring in patients with neuroblastoma
Study
EGAS00001007365
-
Amplicon sequencing of various tumors
Study
JGAS000366
-
Breast Cancer Follow Up Series
Study
EGAS00001000002
-
Analytical study of protein function and RNA expression involved in predicting treatment efficacy and adverse event development in lung cancer radiotherapy.
Study
JGAS000545
-
Spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma
Study
EGAS00001007981
-
Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
-
Targeted sequencing of breast cancer susceptibility genes for 1,995 Japanese breast cancer patients
Study
EGAS00001004630
-
3D-GSC_expression_profiles
Study
EGAS00001007182
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
Mesothelioma_Whole_Genomes
Study
EGAS00001000830
-
Germline sequencing
Study
EGAS00001006651
-
Lung Health Study (LHS-BioLINCC)
Study
phs004013
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2)
Study
phs001169
-
Volasertib preclinical activity in high-risk hepatoblastoma
Study
EGAS00001004827
-
Linguistic utterance counts for The admixture histories of Cabo Verde
Dataset
EGAD00001008978
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Atherosclerosis Risk in Communities (ARIC)
Study
phs000223
-
Methylation differences in trisomy 21 using monozygotic twins
Study
EGAS00001001051
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses
Study
phs001038
-
The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Study
EGAS00001000449
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
Study
EGAS50000000130
-
RTEL1 mutation as a modifier of Dyskeratosis Congenita in a family with a Telomerase RNA (hTR) template mutation and variant telomeric repeats
Study
EGAS50000001644
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
Combined Metabolic Activators Reduces Liver Fat in Nonalcoholic Fatty Liver Disease Patients
Study
EGAS00001005616
-
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Study
EGAS00001004455
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000073
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000107
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
Transcriptomic characterization of the histopathological growth patterns in breast cancer liver metastases
Study
EGAS50000000225
-
Paediatric Hepatic International Tumour Trial (JPLT2: PHITT)
Study
JGAS000236
-
54 metastatic colorectal cancer patients from Schleswig-Holstein in North Germany
Study
EGAS00001004108
-
ATAC-seq data in normal colon mucosa
Study
EGAS00001005281
-
Frequent mutation of the FOXA1 untranslated region in prostate cancer
Study
EGAS00001003113
-
RNA-Seq of GM adipose tissue samples
Dataset
EGAD00001010253
-
Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation
Study
EGAS00001007513
-
The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing
Study
EGAS00001006037
-
Whole exome sequencing in RVOT patients
Study
EGAS00001002319
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Study
phs000345
-
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer
Study
EGAS00001003830
-
Genomics of Circulating Tumor Cells
Study
phs000717