-
UK10K_RARE_SIR
Study
EGAS00001000130
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-009
Study
EGAS00001004290
-
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Study
EGAS00001000273
-
Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
-
UK10K RARE CHD
Study
EGAS00001000125
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR02
Study
EGAS00001001028
-
P647_Targeted_resequencing_project
Study
EGAS00001000305
-
Mutational Patterns in Metastatic Cutaneous Squamous Cell Carcinoma
Study
EGAS00001003370
-
Exome sequencing of a novel cervical cancer cell line
Study
EGAS00001003343
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Study
EGAS00001003443
-
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Study
EGAS00001004327
-
Molecular determinants of response to PD-L1 blockade across tumor types
Study
EGAS00001004343
-
Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins
Study
EGAS00001001240
-
Clonal selection and double hit events involving tumor suppressor genes underlie relapse from total therapy
Study
EGAS00001001810
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Study
EGAS00001001515
-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
Ethiopia_Genome_Project__low_coverage_
Study
EGAS00001000238
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
The Prediction and Prevention of Preeclampsia
Study
EGAS00001001898
-
The_Genomic_Advances_in_Sepsis__GAinS__RNA_seq
Study
EGAS00001003772
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Study
EGAS00001003780
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Study
EGAS00001002406
-
Genome-wide DNA Methylation is Predictive of Outcome in Juvenile Myelomonocytic Leukemia
Study
EGAS00001002700
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Study
EGAS00001005053
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-010
Study
EGAS00001004291
-
This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
-
A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling
Study
EGAS00001004018
-
Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
-
Hypoxia acts as an environmental cue for the human TRM differentiation program
Study
EGAS00001005286
-
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
-
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Study
EGAS00001005098
-
Variation and transmission of the human gut microbiota across generations - shotgun data
Study
EGAS00001005649
-
Variation and transmission of the human gut microbiota across generations - 16S data
Study
EGAS00001005651
-
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
Study
EGAS00001005878
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005215
-
Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067)
Study
EGAS00001004363
-
tFL with a PMBL GE signature
Study
EGAS00001005870
-
The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels
Study
EGAS00001003239
-
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Study
EGAS00001004455
-
Whole Exome Sequencing PPGL
Study
EGAS00001006043
-
Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19
Study
EGAS00001005529
-
Stereotyped B-cell responses are linked to IgG constant region polymorphisms in multiple sclerosis
Study
EGAS00001005745
-
Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors
Study
EGAS00001004694
-
RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3
Study
EGAS00001004798
-
Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
-
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Androgen receptor blockade promotes response to BRAF/MEK-targeted therapy
Study
EGAS00001006196
-
WXS and RNA-seq for 22 patients treated with radiation + immunotherapy
Study
EGAS00001006212
-
Sex chromosome aneuploidies give rise to changes in the circular RNA profile
Study
EGAS00001006404
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
Whole genome sequencing delineates regulatory, structural, and cryptic splice variants in early onset cardiomyopathy
Study
EGAS00001004929
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Significant and pervasive effects of RNA degradation on Nanopore direct RNA sequencing
Study
EGAS00001006542
-
Host pathogen interaction long read transcriptome
Study
EGAS00001006779
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC-- CA209-025
Study
EGAS00001004292
-
T cell responses of ALS patients
Study
EGAS00001006675
-
Longitudinal evaluation of serum microRNAs as biomarkers for neuroblastoma burden and therapeutic p53 reactivation
Study
EGAS00001006678
-
Hexanucleotide repeat expansions in C9orf72 alter microglial responses and prevent a coordinated glial reaction in ALS
Study
EGAS00001006711
-
T cell landscape definition by multi-omics identifies galectin-9 as novel immunotherapy target in chronic lymphocytic leukemia (CLL)
Study
EGAS00001006864
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection
Study
EGAS00001006909
-
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis using bronchial specimens
Study
EGAS00001007089
-
Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
-
Human liver NPCs single cell project
Study
EGAS00001007194
-
Transcriptomics identifies blunted immunomodulatory effects of vitamin D in people with multiple sclerosis
Study
EGAS00001007254
-
Targeting TRIP13 in Wilms Tumor with Nuclear Export Inhibitors
Study
EGAS00001007389
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types
Study
EGAS00001007412
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq)
Study
EGAS00001007428
-
Integrated genomic analysis for HCC
Study
EGAS00001007957
-
Detection of cancers three years prior to diagnosis using plasma cell-free DNA
Study
EGAS00001008068
-
Integrative Multi-Omics and Drug Sensitivity Profiling Reveals Potential Predictive Biomarkers in Pediatric Solid Tumors from the INFORM Registry
Study
EGAS00001008249
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes
Dataset
EGAD00001006231
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
Convergent somatic mutations in effectors of insulin signalling in chronic liver disease
Dataset
EGAD00001006255
-
PSCP_bisulphite analysis in hESCs (2018-08-13)
Dataset
EGAD00001004295
-
FASTQ files of total RNA-Seq data from the POPS PET (pre-eclamptic) samples
Dataset
EGAD00001003508
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Dataset
EGAD00001007862
-
Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Dataset
EGAD00001008616
-
Mutational landscape of normal epithelial cells in Lynch Syndrome patients
Dataset
EGAD00001008092
-
RNA-seq analysis of transcriptome variation with human ESC subclones
Dataset
EGAD00001004266
-
Dataset for soft_tissue_tumor-RNA
Dataset
EGAD00001008859
-
Neutrophils and emergency granulopoiesis drive immune suppression and an extreme response endotype during sepsis
Dataset
EGAD00001010927
-
EPICC: Evolutionary Predictions in Colorectal Cancer
Dataset
EGAD00001008140
-
FASTQ files of total RNA-Seq data from the POPS SGA (Small for Gestational Age) samples
Dataset
EGAD00001003507
-
Genetic drivers of epigenetic and transcriptional variation of human immune responses to infection (RNA-seq, ATAC-seq and ChIPmentation)
Dataset
EGAD00001008422