-
Regulatory Genomics of Human Embryonic Development
Study
phs001226
-
A Comprehensive Platform for Analyzing Longitudinal Multi-Omics Data
Study
phs003203
-
Single-cell RNA sequencing of human skin tumors (BCC, SCC and Melanoma)
Study
EGAS50000000365
-
Targeted Mutational Analysis of Intestinal T-cell Lymphomas, Using a Customized Targeted Amplicon Panel on the Ion Torrent PGM
Study
phs001126
-
Processing of tissue and cfDNA samples of CRC patients using Active-seq
Study
EGAS50000001226
-
Fragmentation signatures in cancer patients are similar to those in patients with vascular and autoimmune diseases
Study
EGAS00001008004
-
Full genome sequencing of a monozygotic twin discordant for schizophrenia
Study
EGAS00001000152
-
Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
-
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Study
EGAS00001003231
-
ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells-of-origin
Study
EGAS00001004913
-
Transcriptional and functional profiling defines human small intestinal macrophage subsets
Study
EGAS00001002093
-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
-
A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
-
Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer
Study
EGAS00001004486
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
-
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Study
EGAS00001003232
-
CCL22 chemokine mutations drive natural killer cell lymphoproliferative disease by biasing GPCR signaling
Study
EGAS00001006009
-
RNA-seq on patient-derived, stage II, CRC cell lines
Study
EGAS00001005948
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Immune variation leads to diverse outcomes in human malaria (2020-01-15)
Dataset
EGAD00001005790
-
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes
Study
EGAS00001007118
-
Kids First: Genetics of Pediatric Germ Cell Tumors
Study
phs002322
-
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
Study
EGAS00001000096
-
POU4F3 mutation screening in Japanese hearing loss patients.
Study
JGAS000093
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
ARID1A Mutations in Endometriosis-Associated Ovarian Carcinomas
Study
EGAS00000000075
-
Oral Microbiome in Esophageal Adenocarcinoma
Study
phs001527
-
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)
Study
phs001602
-
Differential Mutations in Matched Primary and Metastatic Colorectal Cancers
Study
phs001084
-
Metagenomic Deep Sequencing in Meningitis and Encephalitis
Study
phs001067
-
Chromothripsis orchestrates leukemic transformation in blast phase MPN through targetable amplification of DYRK1A
Study
EGAS00001007483
-
Establishment of an integrated database for clinical and genomic data in cancer
Study
JGAS000206
-
CUT&Tag sequencing of ZFHX4 and H3K27ac in midbrain dopaminergic neurons.
Study
EGAS50000001112
-
ScRNA-seq of PBMC and whole blood samples reveals a dysregulated myeloid cell compartment in severe COVID-19
Study
EGAS00001004571
-
MGMT genomic rearrangements contribute to chemotherapy resistance in gliomas
Dataset
EGAD00001006281
-
Convergent somatic evolution from early life in a germline ribosomopathy
Dataset
EGAD00001009061
-
Genetic analysis in lifestyle-related disease, arteriosclerotic disease, and aging-related diseases.
Study
JGAS000016
-
Presence of fungal infection in brains of patients with Parkinsons disease (PD)
Study
EGAS00001003644
-
germline variants in children with hematological cancer
Study
EGAS00001006907
-
CAF-S3 subset in human breast and ovarian cancers
Study
EGAS00001003344
-
SNP array study in Autism Spectrum Disorder patients
Study
EGAS00001005606
-
Genomic Profiling of Peripheral T-cell Lymphoma
Study
phs001962
-
Genomic landscapes of endometrioid and mucinous ovarian cancers and morphologically similar tumor types
Study
EGAS50000000523
-
Relapse CHL study
Study
EGAS00001008222
-
Targeted sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas
Study
EGAS00001005680
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Human Lung Tissue eQTL Study
Study
phs001745
-
Transcriptomic profiling of circulating regulatory T cells from follicular lymphoma patients before and after Lenalidomide treatment
Study
EGAS50000001048
-
Ribosome profiling shows variable sensitivity to detect open reading frames for conventional and different types of cryptic T cell antigens
Study
EGAS50000000322
-
IMCISION RNAseq
Study
EGAS00001005454
-
Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures
Study
EGAS00001004503
-
The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia
Study
phs002297
-
Development of a fully human glioblastoma-in-brain-spheroid model for accelerated translational research
Study
EGAS50000000757
-
Recursive splicing in long vertebrate genes
Study
EGAS00001001170
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Study
EGAS00001001199
-
Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer
Study
EGAS00001004572
-
Mutations in SPINK2 induce azoospermia
Study
EGAS00001002450
-
Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosissusceptibility
Study
EGAS00001005911
-
Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma
Study
EGAS00001003251
-
Upper cortical layer-driven network impairment in schizophrenia
Study
EGAS00001006495
-
Structural Expression of BMMF in tissues of colorectal, lung and pancreatic cancer patients
Study
EGAS00001006744
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Dataset
EGAD00001000817
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
Genetics of Prostate Cancer in Africa
Study
phs002718
-
Circulating tumor DNA dynamics reveal KRAS G12C mutation heterogeneity and response to treatment with the KRAS G12C inhibitor divarasib in solid tumors
Study
EGAS50000000315
-
Circulating Tumor DNA Analysis in ERBB2-Amplified Colorectal Cancer: Biomarker Analysis of the MyPathway Trial
Study
EGAS50000000916
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Study
EGAS00001004160
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
MalariaGEN case-control study in the Gambia
Study
EGAS00000000026
-
SCLC ctDNA sequencing
Study
EGAS00001003984
-
SCC ctDNA sequencing
Study
EGAS00001003987
-
The mutational landscape and its longitudinal dynamics in relapsed and refractory Hodgkin lymphoma
Study
EGAS50000000149
-
Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart
Study
phs002725
-
Single Cell Omics Resolves Transcriptional Alterations in Sjogren's Syndrome
Study
phs002446
-
GWA Study of Oral Cavity, Pharynx and Larynx Cancers in European, and North and South American Populations - CIDR
Study
phs002503
-
RNA-Seq analysis of cocaine use disorder in Brodmann Area 9
Study
EGAS50000000150
-
Detection of causative structural variants using long read whole genome sequencing in patients with non-syndromic autism spectrum disorder
Study
EGAS50000000842
-
Bevacizumab plus erlotinib in advanced solid cancers with Krebs cycle gene mutations: A multicenter phase II study
Study
EGAS50000001243
-
Next Generation Mendelian Genetics: Familial Hemophagocytic Lymphohistiocytosis
Study
phs000537
-
Genomics of Relapsed Small Cell Lung Cancer Progression
Study
phs001049
-
Exploring the Genomic Dark Matter of Neurodevelopmental Disorders
Study
phs002937
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Severe Asthma Research Program (SARP)
Study
phs002913
-
Radiation-Related Genomic Profile of Papillary Thyroid Cancer after the Chernobyl Accident
Study
phs001134
-
Genetic Analysis of Epidermal Inclusion Cysts
Study
phs003776
-
Whole genome sequencing data of pediatric hypodiploid acute lymphoblastic leukemia
Study
EGAS50000001305
-
Transcriptome analysis of a novel human iPSC-derived 3D cortical tissue model – 2D versus 3D co-culture comparison
Study
EGAS50000001392
-
Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions
Study
EGAS00001003148
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001004147
-
Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002438
-
RNA-seq of uncultured CD112high and CD112low long-term(LT) human hematopoietic stem cells (HSC) and cultured and lentiviral transduced (CTRL, INKA1-OE) LT- and short-term HSC from umbilical cord blood
Study
EGAS00001004768
-
Residual ANTXR1+ myofibroblasts after chemotherapy inhibit anti-tumor immunity via YAP1 signaling pathway
Study
EGAS50000000136
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219