-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
ATAC-seq/ChIP part
Study
EGAS00001006520
-
GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
-
The Druze analysis group
Study
EGAS00001000963
-
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
-
Recent genetic history of Denmark
Study
EGAS00001001868
-
Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia
Study
EGAS00001001876
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
McGill Epigenomics Mapping Centre
Study
EGAS00001000995
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
-
Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
Study
EGAS00001003875
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Study
EGAS00001001165
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Study
EGAS00001003981
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
GWAS data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004044
-
RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes
Study
EGAS00001004071
-
HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
-
HipSci___Whole_Exome_sequencing___Ataxia
Study
EGAS00001001978
-
HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002008
-
HipSci HumanExome BeadChip analysis - Alport Syndrome
Study
EGAS00001002009
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Study
EGAS00001000100
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
-
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002013
-
Hypothalamic transcriptome in Prader-Willi syndrome
Study
EGAS00001002901
-
HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002015
-
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Study
EGAS00001000367
-
HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002025
-
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Study
EGAS00001001245
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247