-
A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation
Study
EGAS00001000145
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
Sex-biased patterns shaped the genetic history of Roma
Study
EGAS00001004207
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
Paroxysmal_Neurological_Disorders_2
Study
EGAS00001000190
-
Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Study
EGAS00001000455
-
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
-
GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Study
EGAS00001002937
-
Breast_Cancer_Somatic_Genetics_Study_
Study
EGAS00001000195
-
Triple_Negative_Breast_Cancer_Whole_Genomes
Study
EGAS00001000092
-
Integrated genetic and epigenetic analysis of myxofibrosarcoma
Study
EGAS00001002889
-
UK10K RARE CHD
Study
EGAS00001000125
-
ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
Triple_Negative_Breast_Cancer_sequencing
Study
EGAS00001000161
-
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Study
EGAS00001000213
-
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463
-
Molecular analysis of giant cell lesions
Study
EGAS00001002910
-
Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000231
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
Chromatin 3D interactions mediate genetic effects on gene expression
Study
EGAS00001003485
-
Genetic landscape of pediatric Rhabdomyosarcoma
Study
EGAS00001000256
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
Genetic landscape of pediatric Osteosarcoma
Study
EGAS00001000263
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
Characterization_of_individual_foci_of_multicentric_multifocal_breast_cancer_using_targeted_next_generation_sequencing
Study
EGAS00001000407
-
Targeted_sequencing_of_genes_recurrently_mutated_in_AML
Study
EGAS00001000408
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
Plasma pQTLs in INTERVAL cohort
Study
EGAS00001002555
-
Whole genome amplification and whole genome sequencing of human single cells
Study
EGAS00001003108
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
InsPIRE islets
Study
EGAS00001003997
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
HipSci Methylation analysis for embryonic stem cell control lines
Study
EGAS00001001728
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000551
-
Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia.
Study
EGAS00001003096
-
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002023
-
Heritable pulmonary arterial hypertension in a large Iberian family
Study
EGAS00001003123
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003136