-
Spatial atlas of human atherosclerosis highlights role of the microvasculature in disease
Study
EGAS50000000660
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
Human Brain Small Extracellular Vesicles Contain Selectively-Packaged, Full-Length mRNA
Study
EGAS50000000029
-
EATL-II STUDY
Study
EGAS00001001879
-
Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Study
EGAS00001000853
-
Transcriptome analysis in very preterm infants with chronic lung disease after birth
Study
EGAS00001002586
-
The chromatin accessibility signature of human immune aging stems from CD8+ T cells
Study
EGAS00001002605
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Study
EGAS00001003648
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
Genomic data from analysis of the human placenta, part of the Pregnancy Outcome Prediction study (POPs)
Study
EGAS00001002205
-
cfRRBS on cfDNA from pediatric cancer
Study
EGAS00001004194
-
HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Study
EGAS00001004723
-
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Study
EGAS00001003407
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Study
EGAS00001000716
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750
-
RNA_seq_of_Toxoplasma_gondii_response_in_human_macrophages
Study
EGAS00001001708
-
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
-
Resequencing_candidate_genes_for_male_spermatogenic_impairment
Study
EGAS00001002157
-
DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224
-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Molecular Subtype-specific Biomarkers Improves Colorectal Cancer Prognostication
Study
EGAS00001002376
-
Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors
Study
EGAS00001002528
-
Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Study
EGAS00001000213
-
Whole-exome sequencing reveals the origin and evolution of Hepato-Cholangiocarcinoma
Study
EGAS00001002783
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
Single_cell_analysis_T_cell_activation
Study
EGAS00001003479
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
DIME study: Safety, dose-response and efficacy of treatment with Anaerobutyricum soehgenii on glucose metabolism in human subjects with metabolic syndrome
Study
EGAS00001003498
-
Preeclampsia InterPregGen Consortium: Large-scale GWAS meta-analysis of maternal preclampsia cases and controls from Europe and Central Asia. Plus extension of earlier European fetal preeclampsia GWAS meta-analysis (see EGAS00001001048) by adding Central Asian fetal preeclampsia cases and controls. Datasets provided under this study are GWAS meta-analysis summary statistics and individual level GWAS genotype data. Related InterPregGen Consortium data are also provided under studies EGAS00001000416 and EGAS00001000417 (whole genome sequence data for 100 unrelated Uzbeks and 100 unrelated Kazakhs) and EGAS00001001048 (European fetal preeclampsia GWAS summary statistics and genotype data
Study
EGAS00001001266
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Study
EGAS00001003828
-
Single_cell_analysis_of_cytokine_induced_T_cell_states
Study
EGAS00001003215
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Fibroblast heterogeneity drives metastatic spread in breast cancer through distinct mechanisms
Study
EGAS00001003238
-
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
Study
EGAS00001004419
-
Detection of cell-free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
Study
EGAS00001003255
-
Molecular and functional profiling of plasmablastic lymphoma
Study
EGAS00001004659
-
Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer
Study
EGAS00001003487
-
Molecular diagnosis of albinism (2018-03-14)
Dataset
EGAD00001004039
-
single cell sequencing of resting and Influenza-stimulated mononcluear phagocytes of African and Europeans with varying degree of ex-vivo susceptibility to Influenza
Study
EGAS00001005000
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes
Study
EGAS00001007118
-
Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia
Study
EGAS00001007167
-
Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer'
Study
EGAS00001007773
-
Neuroblastoma heterogeneity
Study
EGAS00001007016
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325