-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001001565
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Investigating_the_genetics_of_immunity_against_Salmonella_in_humans
Study
EGAS00001001664
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
HipSci RNA sequencing for embryonic stem cell control lines
Study
EGAS00001001727
-
ENU_CCK_81_cetuximab_pilot_project
Study
EGAS00001001743
-
HipSci whole exome sequencing for embryonic stem cell control lines
Study
EGAS00001001726
-
HipSci genotyping microarray for embryonic stem cell control lines
Study
EGAS00001001730
-
ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
HipSci___RNAseq___Rare_BBS
Study
EGAS00001001318
-
HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713
-
HipSci expression microarray for embryonic stem cell control lines
Study
EGAS00001001729
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
WTCCC3_Anorexia_Nervosa
Study
EGAS00001000913
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
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
-
HipSci Illumina 450K Methylation analysis - monogenic diabetes
Study
EGAS00001001275
-
HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
-
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Study
EGAS00001001288
-
Papuan_Genotyping
Study
EGAS00001001587
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
HipSci Methylation analysis for embryonic stem cell control lines
Study
EGAS00001001728
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
HER2_positive_Breast_Cancer_
Study
EGAS00001000042
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
The patterns and dynamics of genomic instability in metastatic pancreatic cancer
Study
EGAS00000000064
-
Lethal malformation syndrome
Study
EGAS00001000061
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Study
EGAS00001000064
-
Congenital Heart Disease in UK Families
Study
EGAS00001000066
-
Triple_Negative_Breast_Cancer_Whole_Genomes
Study
EGAS00001000092
-
Triple_Negative_Breast_Cancer_sequencing
Study
EGAS00001000161
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
UK10K NEURO ASD TAMPERE
Study
EGAS00001000115
-
UK10K NEURO EDINBURGH
Study
EGAS00001000117
-
UK10K NEURO IMGSAC
Study
EGAS00001000120
-
UK10K_NEURO_MUIR
Study
EGAS00001000122
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
Balanced_Ependymoma
Study
EGAS00001000174
-
Paroxysmal_Neurological_Disorders_2
Study
EGAS00001000190
-
Breast_Cancer_Whole_Genome_Sequencing
Study
EGAS00001000210
-
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Study
EGAS00001000100
-
Genetic landscape of pediatric ependymoma
Study
EGAS00001000254
-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Study
EGAS00001000335
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
Whole Genome Methylation in CLL
Study
EGAS00001000272
-
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
-
UK10K NEURO UKSCZ
Study
EGAS00001000123
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
UK10K RARE CHD
Study
EGAS00001000125
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
UK10K_RARE_THYROID
Study
EGAS00001000131
-
A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation
Study
EGAS00001000145
-
Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing
Study
EGAS00001000329
-
Exome sequencing of patients with rare neurological disorders
Study
EGAS00001000159
-
Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Study
EGAS00001000166
-
Genetic landscape of pediatric Retinoblastoma
Study
EGAS00001000346
-
Balanced_Brain_Tumour_Whole_Genome_Sequencing
Study
EGAS00001000360
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Study
EGAS00001000367
-
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
-
Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
-
Paroxysmal_neurological_Disorders
Study
EGAS00001000386
-
Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes
Study
EGAS00001000228
-
RNAseq_Pulldown_
Study
EGAS00001000230
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000231
-
High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate
Study
EGAS00001000398
-
UK10K_OBESITY_GS
Study
EGAS00001000242
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Study
EGAS00001000449
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000551