-
HipSci___Whole_Exome_sequencing___Ataxia
Study
EGAS00001001978
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
HipSci_RNASEQ_PID
Study
EGAS00001001990
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002030
-
Molecular_diagnosis_of_albinism
Study
EGAS00001002068
-
The Asian Diversity Project: genotyping of 37 Asian populations and ethnic groups
Study
EGAS00001002100
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing
Study
EGAS00001000329
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Study
EGAS00001002164
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
MeDALL epigenetics study
Study
EGAS00001002169
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
IBD_Whole_Genome_Sequencing
Study
EGAS00001002238
-
Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Study
EGAS00001002248
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
-
Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
H3Africa - Genomic and Environmental Risk Factors for Cardiometabolic Disease in Africans
Study
EGAS00001002482
-
Next_gen_seq_of_eye_cancers
Study
EGAS00001002309
-
Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients
Study
EGAS00001002312
-
Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Study
EGAS00001002352
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
Clinical and genetic analysis of a rare syndrome associated with neoteny
Study
EGAS00001002419
-
CEHM
Study
EGAS00001002366
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
A biobank of patient-derived pediatric brain tumor models
Study
EGAS00001002536
-
PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Congenital Heart Disease in UK Families
Study
EGAS00001000066
-
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
-
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
-
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
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
-
UK10K NEURO ASD TAMPERE
Study
EGAS00001000115
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Study
EGAS00001002726
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
UK10K NEURO EDINBURGH
Study
EGAS00001000117
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
UK10K NEURO FSZ
Study
EGAS00001000118
-
Himalayan_population_genetic_study
Study
EGAS00001002731
-
X chromosomal genetic variants are associated with childhood obesity
Study
EGAS00001002738
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Study
EGAS00001000064
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Study
EGAS00001002746
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
-
Insular Celtic population structure and genomic footprints of migration
Study
EGAS00001002769
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
UK10K NEURO IMGSAC
Study
EGAS00001000120
-
UK10K_NEURO_MUIR
Study
EGAS00001000122
-
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Study
EGAS00001000864
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
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
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
20_Matched_Pair_Breast_Cancer_Genomes
Study
EGAS00001000170