-
Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Recursive splicing in long vertebrate genes
Study
EGAS00001001170
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
-
Sequencing_Acute_Myeloid_Leukaemia_
Study
EGAS00001000035
-
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
-
Gene fusion and transcriptomic landscapes of sarcomas
Study
EGAS00001002189
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Study
EGAS00001002217
-
Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Study
EGAS00001002239
-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
Pilot_experiment_on_functional_genomics_in_osteoarthritis
Study
EGAS00001001212
-
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
-
Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
-
DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
-
DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
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
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture
Study
EGAS00001002681
-
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
-
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
-
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
-
atrial appendage RNA-seq in non-, paroxysmal and persistent atrial fibrillation
Study
EGAS00001005295