-
Raw bulk TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008118
-
PacBio Rare Disease Study
Study
EGAS00001008170
-
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
-
Genome_Diversity_in_Africa_Project__Benin
Study
EGAS00001001688
-
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
-
Whole_genome_sequencing_of_Italian_genetic_isolates__Friuli_Venezia_Giulia
Study
EGAS00001000252
-
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
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients
Study
EGAS00001002312
-
Next_gen_seq_of_eye_cancers
Study
EGAS00001002309
-
The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Study
EGAS00001002305
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Genome-to-genome analysis highlights the impact of the human innate and adaptive immune systems on the hepatitis C virus
Study
EGAS00001002324
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
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
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
CEHM
Study
EGAS00001002366
-
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
-
The molecular landscape of colorectal cancer (5 cases)
Study
EGAS00001002374
-
Clinical and genetic analysis of a rare syndrome associated with neoteny
Study
EGAS00001002419
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
Genomic landscape of oral cancers (Complete Genomics WGS)
Study
EGAS00001002393
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
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
-
Cell fate mapping of human glioblastoma reveals an invariant stem cell hierarchy pre- and post-treatment
Study
EGAS00001002424
-
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Integrative genomic and transcriptomic analysis of adult leiomyosarcoma (HIPO-028, HIPO-018, HIPO-021)
Study
EGAS00001002437
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
H3Africa - Genomic and Environmental Risk Factors for Cardiometabolic Disease in Africans
Study
EGAS00001002482
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Congenital Heart Disease in UK Families
Study
EGAS00001000066
-
Hip OA Functional Genomics
Study
EGAS00001002483
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment
Study
EGAS00001002485
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Study
EGAS00001002506
-
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
-
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
-
A biobank of patient-derived pediatric brain tumor models
Study
EGAS00001002536
-
Genomic landscape of human diversity across Madagascar
Study
EGAS00001002549
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
-
Genomic diversity of the African-descent Makranis of Pakistan
Study
EGAS00001002558
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
Genetic history of the Swahili population
Study
EGAS00001002569
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
UK10K NEURO ASD TAMPERE
Study
EGAS00001000115
-
The_genetics_of_thinness_compared_to_obesity
Study
EGAS00001002624
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
UK10K NEURO EDINBURGH
Study
EGAS00001000117
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002643
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
Family-based GWAS for CRSwNP
Study
EGAS00001002665
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Study
EGAS00001002657
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Study
EGAS00001000064
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
The Human Phenotype Project (HPP) is a large-scale deep-phenotype prospective longitudinal and ethnically diverse cohort
Study
EGAS00001008040
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
-
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