-
HipSci___Whole_Exome_sequencing___Monogenic_Diabetes
Study
EGAS00001001140
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
-
The landscape of LAM disease
Study
EGAS00001003534
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
-
Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy
Study
EGAS00001003555
-
Genetic sequencing of MODY patients.
Study
EGAS00001001699
-
The Asian Diversity Project: genotyping of 37 Asian populations and ethnic groups
Study
EGAS00001002100
-
RNA-seq as a tool for evaluating human embryo competence
Study
EGAS00001003667
-
Infant Glioma Molecular Subtype
Study
EGAS00001003714
-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
HipSci whole exome sequencing for embryonic stem cell control lines
Study
EGAS00001001726
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
HipSci expression microarray for embryonic stem cell control lines
Study
EGAS00001001729
-
Epigenetic and metabolomic data from type 2 diabetes adolescents
Study
EGAS00001003816
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Study
EGAS00001003813
-
Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
-
ENU_CCK_81_cetuximab_pilot_project
Study
EGAS00001001743
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Study
EGAS00001001277
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
Determination of the molecular nature of the Vel blood group by exome sequencing
Study
EGAS00001000069
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Mapping_gene_environment_interactions_in_macrophages
Study
EGAS00001002268
-
Low_depth_whole_genome_sequencing_across_multiple_isolated_populations
Study
EGAS00001001597
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Study
EGAS00001000381
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease
Study
EGAS00001002275
-
HipSci genotyping microarray for embryonic stem cell control lines
Study
EGAS00001001730
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
Balanced_Brain_Tumour_Whole_Genome_Sequencing
Study
EGAS00001000360
-
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
-
HG Transcriptome sequencing in the INTERVAL cohort
Study
EGAS00001003346
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Study
EGAS00001000100
-
UK10K NEURO FSZ
Study
EGAS00001000118
-
Balanced_Ependymoma
Study
EGAS00001000174
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
UK10K_OBESITY_GS
Study
EGAS00001000242
-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299