-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Bone_Cancer___Rare_Types_Whole_Genome
Study
EGAS00001000501
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Study
EGAS00001001002
-
MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Dilgom_Exome
Study
EGAS00001000086
-
Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
-
Exome and transcriptome sequencing of Desmoplastic Small Round Cell Sarcoma
Study
EGAS00001004575
-
Genomic study of an AT-AML
Study
EGAS00001004392
-
The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
-
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Study
EGAS00001001123
-
Congenital_anosmia_1
Study
EGAS00001001124
-
Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Study
EGAS00001003521
-
Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
-
Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
-
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
-
Immunogenomic landscape of hematological malignancies
Study
EGAS00001004444
-
Associations between APOE status and cognitive ability across the lifecourse
Study
EGAS00001001235
-
Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
-
Uterine leiomyoma: DNA methylation, chromatin activity and gene expression
Study
EGAS00001004499
-
UK10K NEURO UKSCZ
Study
EGAS00001000123
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Study
EGAS00001001184
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
HipSci HumanExome BeadChip analysis-Rare_BBS
Study
EGAS00001001272
-
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Study
EGAS00001001288
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
A reference map of potential determinants for the human serum metabolome
Study
EGAS00001004512
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Study
EGAS00001001844
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
UK10K_RARE_THYROID
Study
EGAS00001000131
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Phylogenetic evolution of metastatic melanoma.
Study
EGAS00001003582
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Genetic dysregulation of gene expression and splicing during a ten-year period of human aging in the PIVUS study
Study
EGAS00001003583