-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
-
We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Study
EGAS00001002719
-
Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
-
An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors
Study
EGAS00001000057
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
-
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
-
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer
Study
EGAS00001002763
-
Insular Celtic population structure and genomic footprints of migration
Study
EGAS00001002769
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Study
EGAS00001000381
-
Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
-
Genome_Diversity_in_Africa_Project__Benin
Study
EGAS00001001688
-
The molecular landscape of colorectal cancer (5 cases)
Study
EGAS00001002374
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
Lethal malformation syndrome
Study
EGAS00001000061
-
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
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
HipSci genotyping microarray for embryonic stem cell control lines
Study
EGAS00001001730
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
The evolutionary landscape of colorectal tumorigenesis
Study
EGAS00001003066
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Whole_genome_sequencing_of_Italian_genetic_isolates__Friuli_Venezia_Giulia
Study
EGAS00001000252
-
Exome sequencing of advanced hepatocellular carcinoma
Study
EGAS00001003130
-
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
-
Recent genetic history of Denmark
Study
EGAS00001001868
-
Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing
Study
EGAS00001000329
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Balanced_Brain_Tumour_Whole_Genome_Sequencing
Study
EGAS00001000360
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
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
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
InsPIRE islets
Study
EGAS00001003997
-
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Study
EGAS00001000478
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Host genetic determinants of HIV infection
Study
EGAS00001005245
-
IBD_Whole_Genome_Sequencing
Study
EGAS00001002238
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Study
EGAS00001000980
-
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
Clinical and genetic analysis of a rare syndrome associated with neoteny
Study
EGAS00001002419
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Study
EGAS00001001165
-
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
-
Congenital Heart Disease in UK Families
Study
EGAS00001000066
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Study
EGAS00001000093
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
-
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463
-
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Study
EGAS00001002788
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
Family-based GWAS for CRSwNP
Study
EGAS00001002665
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678