-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
Himalayan_population_genetic_study
Study
EGAS00001002731
-
X chromosomal genetic variants are associated with childhood obesity
Study
EGAS00001002738
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Study
EGAS00001002746
-
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS
Study
EGAS00001002747
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes
Study
EGAS00001000228
-
A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation
Study
EGAS00001000145
-
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Study
EGAS00001002758
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer
Study
EGAS00001002763
-
20_Matched_Pair_Breast_Cancer_Genomes
Study
EGAS00001000170
-
Insular Celtic population structure and genomic footprints of migration
Study
EGAS00001002769
-
Sex-biased patterns shaped the genetic history of Roma
Study
EGAS00001004207
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
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
-
Paroxysmal_Neurological_Disorders_2
Study
EGAS00001000190
-
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
-
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
-
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Study
EGAS00001002903
-
ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Study
EGAS00001002937
-
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
-
Triple_Negative_Breast_Cancer_sequencing
Study
EGAS00001000161
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Study
EGAS00001000213
-
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
-
Molecular analysis of giant cell lesions
Study
EGAS00001002910
-
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
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
Genetic landscape of pediatric Rhabdomyosarcoma
Study
EGAS00001000256
-
Genetic landscape of pediatric Osteosarcoma
Study
EGAS00001000263
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
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