-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
-
Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
-
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Study
EGAS00001005647
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
PCGP Ph-like ALL
Study
EGAS00001000654
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
Mechanisms of active DNA demethylation in human monocytes
Study
EGAS00001004784
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Breast tissue methylation analysis
Study
EGAS00001005070
-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
WTCCC3_Anorexia_Nervosa
Study
EGAS00001000913
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Study
EGAS00001000924
-
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Study
EGAS00001001002
-
Genotype data of osteoarthritis cases from the UK collected by the arcOGEN Consortium (http://www.arcogen.org.uk/).
Study
EGAS00001001017
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Family-based GWAS for CRSwNP
Study
EGAS00001002665
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
-
HipSci Illumina 450K Methylation analysis - monogenic diabetes
Study
EGAS00001001275
-
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Study
EGAS00001001288
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
Papuan_Genotyping
Study
EGAS00001001587
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Genome_Diversity_in_Africa_Project__Benin
Study
EGAS00001001688
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
HipSci Methylation analysis for embryonic stem cell control lines
Study
EGAS00001001728
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Study
EGAS00001001844
-
HipSci HumanExome BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002005
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158