-
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
-
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
-
SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples
Study
EGAS00001005039
-
An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons
Study
EGAS00001006289
-
H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
-
Gut microbiota of the Pinggu cohort
Dataset
EGAD00001007064
-
Tumor transcriptome profiling from the OAK and POPLAR randomized clinical trials of atezolizumab in 2L NSCLC
Dataset
EGAD00001007703
-
WTSI CGP Data access committee
Dac
EGAC00001000000
-
NPC genome-wide human SNP array data
Dataset
EGAD00010002296
-
Efficacy of two different FGFR-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation
Study
EGAS50000000015
-
snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis
Study
EGAS00001007635
-
Single-cell profiling reveals mechanisms of response to anti-PD-L1 versus anti-PD-L1 combined with anti-CTLA4 in head and neck squamous cell carcinoma
Study
EGAS50000000037
-
Single cell RNAseq of stenotic, inflamed and non-inflamed transmural lesions from patients with Crohn's disease
Dataset
EGAD50000000559
-
Dataset developed for use with EOSC4Cancer of synthetic colorectal cancer tumor/normal pairs.
Dataset
EGAD50000000564
-
Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositis
Study
EGAS50000000310
-
Reconstructing oral cavity tumor evolution through brush biopsy
Study
EGAS50000000602
-
IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assay
Study
EGAS50000000624
-
Full characterization of structural variation
Study
EGAS50000000520
-
Identifying New Genetic Subtypes in Follicular Lymphoma
Study
EGAS50000000435
-
Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Study
EGAS50000000484
-
A neoadjuvant, phase II trial demonstrates efficacy and tolerability of Talimogene laherparepvec in cutaneous basal cell carcinoma (NeoBCC trial)
Study
EGAS50000000252
-
snRNA: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000786
-
bulk ATACseq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000787
-
scATAC: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000788
-
bulk RNA-seq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000789
-
Human inflammatory cardiomyopathies following SARS-CoV2 infection and COVID-19 vaccination
Study
EGAS50000000769
-
3D tissue engineered human skeletal muscle modelling Facioscapulohumeral Muscular Dystrophy
Study
EGAS50000000502
-
Use of new methodologies to achieve a thorough molecular characterization in pediatric acute leukemia
Study
EGAS50000000701
-
APOBEC3 mutagenesis drives therapy resistance in breast cancer
Study
EGAS50000000875
-
Hematopoietic Tet2 inactivation enhances the response to checkpoint blockade immunotherapy
Study
EGAS50000001191
-
Drug Development against Tumor Microtube Networks in Glioblastoma
Study
EGAS50000000477
-
Recurrent intra-tumour heterogeneity is a hallmark of metastatic prostate cancer
Study
EGAS50000001312
-
Bruno et al.: Interferon gamma rebalances immunopathological signatures in Chronic Granulomatous Disease through metabolic rewiring
Study
EGAS00001005463
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
Emergence of oncofetal plasticity is ubiquitous in early colorectal cancers
Study
EGAS50000001532
-
Assessing gene expression profiling from FFPE Patient Samples: A Comparison of Two Library Preparation Approaches and Recommendations
Study
EGAS50000001066
-
Myeloid cell networks govern re-establishment of original immune landscapes in recurrent ovarian cancer
Study
EGAS50000001069
-
LySeqST: A targeted sequencing assay for robust genomic classification of diffuse large B-cell lymphoma
Study
EGAS50000001601
-
Genentech Colon Cancer Screen
Study
EGAS00001000288
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Single cell sequencing of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis
Study
EGAS00001002845
-
Finding the way towards the eradication of therapy-related myeloid neoplasms
Blog
eradication-of-therapy-related-myeloid-neoplasms
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Molecular characteristics in Burkitt lymphoma over age groups
Study
EGAS00001005270
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
The Genomic Landscape of Childhood and Adolescent Melanoma
Study
EGAS00001000901
-
The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied.
Study
EGAS00001003848
-
Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors
Study
EGAS00001004878
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Patient-derived pediatric brain tumor organoids faithfully recapitulate primary tumors
Study
EGAS00001008305
-
Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Study
EGAS00001005268
-
Tumor-derived exosomes modulate PD-L1 expression in monocytes
Study
EGAS00001002377
-
Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19
Study
EGAS00001005735
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Ethiopia_Genome_Project__high_coverage_
Study
EGAS00001000237
-
Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Study
EGAS00001007108
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation
Study
EGAS00001007263
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
Single_Cell_Sequencing_of_Sperm__scSperm_
Study
EGAS00001000935
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Study
EGAS00001003963
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183
-
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Study
EGAS00001002211
-
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Study
EGAS00001000572
-
Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease
Study
EGAS00001001303
-
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
-
High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube
Study
EGAS00001002589
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
-
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Study
EGAS00001002344
-
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Study
EGAS00001001386
-
Ewing and Ewing-like-sarcoma tumoroid biobank reveals distinct drug sensitivities: translocation makes the difference
Study
EGAS00001007941
-
Pooled scRNA-seq of iPSC-derived neural stem cells from ADHD and control individuals
Study
EGAS00001008169
-
Mapping_gene_environment_interactions_in_macrophages
Study
EGAS00001002268
-
Genomic profiling of Acute Lymphoblastic Leukemia in Ataxia Telangiectasia patients reveals tight link between ATM mutations and chromothripsis
Study
EGAS00001002270
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
Direct Detection of Early-stage Cancers Using Circulating Tumor DNA
Study
EGAS00001002577
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data
Study
EGAS00001002728
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126