-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
Analysis of mechanisms of CD19- relapse following novel low affinity CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) in a Phase I clinical study in paediatric ALL: CARPALL
Study
EGAS00001003733
-
Epigenetic and metabolomic data from type 2 diabetes adolescents
Study
EGAS00001003816
-
Pilot_experiment_on_functional_genomics_in_osteoarthritis
Study
EGAS00001001212
-
reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T-Cells
Study
EGAS00001001568
-
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
-
FetalQuant-SD: Accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA
Study
EGAS00001001611
-
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
Study
EGAS00001000933
-
Field_effect_of_healthy_and_diseased_livers
Study
EGAS00001002382
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
-
Genomic landscape of human diversity across Madagascar
Study
EGAS00001002549
-
Genetic history of the Swahili population
Study
EGAS00001002569
-
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
-
The_genetics_of_thinness_compared_to_obesity
Study
EGAS00001002624
-
Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture
Study
EGAS00001002681
-
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Study
EGAS00001002746
-
Whole exome sequencing of longitudinal samples from a melanoma patient receiving MEK plus CDK4/6 inhibitor therapy.
Study
EGAS00001002846
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
-
Using human induced pluripotent stem cells (iPSC) and iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia.
Study
EGAS00001002895
-
The whole blood of female volunteers and sperm from the male volunteer were used to extract genomic DNA to do whole genome sequencing. Distinguished SNPs between parental genomes were retained to analyze parental allele-specific DNA methylation and chromatin accessibility in scCOOL-seq data.
Study
EGAS00001002987
-
Pheno-Seq, linking 3D phenotypes of clonal tumor spheroids to gene expression
Study
EGAS00001002999
-
Somatic mutations reveal lineage relationships and age-related mutagenesis in human hematopoiesis
Study
EGAS00001003068
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors
Study
EGAS00001000708
-
RNA Editing in breast cancer
Study
EGAS00001000495
-
Analysis of translatome, truncating mutations, lncRNA, circRNA and microproteins of 80 human DCM cases and controls
Study
EGAS00001003263
-
ALPI deficiency causes refractory Inflammation Bowel Disease
Study
EGAS00001003350
-
Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level
Study
EGAS00001004335
-
Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade
Study
EGAS00001004353
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Genome-wide prediction of human embryos
Study
EGAS00001001020
-
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Study
EGAS00001001112
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Study
EGAS00001001199
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Epigenetic dynamics of monocyte to macrophage differentiation
Study
EGAS00001001595
-
Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer
Study
EGAS00001004572
-
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19
Study
EGAS00001004772
-
The genetic structure of Norway
Study
EGAS00001004826
-
atrial appendage RNA-seq in non-, paroxysmal and persistent atrial fibrillation
Study
EGAS00001005295
-
Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer
Study
EGAS00001001839
-
HCA_Placental_Infection_Atlas
Study
EGAS00001004722
-
Reference exome data for Australian Aboriginal populations to support health-based research
Study
EGAS00001003745
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854