-
TallFlow: Lineage tracing of immunophenotypic sub populations in T-cell Acute lymphoblastic leukemia by (sc-)WGS
Study
EGAS00001007446
-
Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Study
EGAS00001005539
-
scRNAseq
Study
EGAS50000000344
-
Characterization of T cell tumor infiltration in brain metastases through the analysis of the cerebrospinal fluid
Study
EGAS00001004751
-
Small molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma (RNAseq dataset)
Study
EGAS00001004748
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001005827
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001006088
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001006122
-
Single cell characterization of arrested B-lymphoid differentiation and leukemic cell states in ETV6-RUNX1-positive pediatric leukemia
Study
EGAS00001004374
-
RNA sequencing of subchondral bone from patients that underwent a joint replacement surgery due to osteoarthritis.
Study
EGAS00001004476
-
Colorectal cancer cells possess an equipotent capacity to enter a developmental pausing-like state to survive chemotherapy
Study
EGAS00001004773
-
Whole Exome Sequencing of Schizophrenia cases and controls performed at the Broad Institute on a cohort from Bristol, UK
Study
EGAS00001006274
-
Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer
Study
EGAS00001004615
-
Mutations in ALK signaling pathways conferring resistance to ALK inhibitor treatment lead to collateral vulnerabilities in neuroblastoma cells
Study
EGAS00001005791
-
Human skeletal muscle CD90+ fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients
Study
EGAS00001005599
-
Single-cell RNA sequencing of a PBMC sample collected from a male with 45,X/48,XYYY karyotype
Study
EGAS00001005697
-
Longitudinal monitoring of disease burden and response using ctDNA from dried blood spots in xenograft models
Study
EGAS00001006134
-
Molecular determinants of outcomes in relapsed mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial
Study
EGAS00001006342
-
Complex patterns of genomic heterogeneity identified in 42 tumor samples and ctDNA of a pulmonary atypical carcinoid patient
Study
EGAS00001006530
-
Therapeutic vulnerabilities in CCA from different etiologies identified using integrative multi-omics enhancer activity profiling
Study
EGAS00001007309
-
Targeted exome DNA sequencing analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67
Study
EGAS00001007303
-
Patient-derived organoids identify tailored therapeutic options and determinants of plasticity in sarcomatoid urothelial bladder cancer
Study
EGAS00001007430
-
omnix_himalaya
Dataset
EGAD00010001470
-
omnix_tibet
Dataset
EGAD00010001473
-
The study of response to EGFR Blockade in Colorectal Cancer
Dataset
EGAD00001001628
-
The study of response to EGFR Blockade in Colorectal Cancer
Dataset
EGAD00001001674
-
T-ALL transcriptome sequence study
Dataset
EGAD00001000849
-
Imputation-Based Meta-Analysis of Severe Malaria in Three African Populations
Study
EGAS00001000807
-
MPN_Genomes_validation_and_interim_samples
Study
EGAS00001000766
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_2
Study
EGAS00001002372
-
Metastatic_Prostate_Follow_Up_2
Study
EGAS00001000756
-
ICR MOPOPGEN UK exome control series
Study
EGAS00001001667
-
Metastatic_Prostate_Follow_Up
Study
EGAS00001000730
-
Plasma DNA profile in DNASE1L3 deficiency
Study
EGAS00001004342
-
Engineered_cartilage__deriving_design_principles_from_human_developmental_pathways
Study
EGAS00001006224
-
An approach for evaluating the effects of dietary fiber polysaccharides on the human gut microbiome and plasma proteome
Study
EGAS00001005330
-
scRNA mCRC PDO
Study
EGAS00001006214
-
Engineered_cartilage__deriving_design_principles_from_human_developmental_pathways
Study
EGAS00001006443
-
Summary statistics for cervical cancer GWAS
Dataset
EGAD00001004361
-
WGS data for NRF2 study
Dataset
EGAD00001002244
-
CPC-GENE Prostate Cancer Heterogeneity Study
Dataset
EGAD00001002885
-
AML-MRD
Dataset
EGAD00001005270
-
Summary statistics
Dataset
EGAD00001009775
-
National Institute on Aging (NIA) Long Life Family Study (LLFS)
Study
phs000397
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study
Study
phs001844
-
DAC for the study molecular biomarkers associated with the diagnosis and severity of genetic and diseases from PAIDI-BIO354 GENYO-UGR)
Dac
EGAC00001003090
-
DAC for study involving the spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma at Imperial College London.
Dac
EGAC00001003515
-
DAC for datasets from study 'Single-nucleus multi-omic sequencing of the human motor cortex in ALS/ALS-FTD'
Dac
EGAC50000000856
-
FRIGE IHG Data Access Committee reviews the aim and methodology of the proposed study for which access to anonymised data is requested.
Dac
EGAC00001003629
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005346
-
Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Study
EGAS00001008050
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Germany
Study
EGAS00001005858
-
A cycling, progenitor-like cell population at the root of atypical teratoid rhabdoid tumor subtype differentiation trajectories
Study
EGAS00001008123
-
RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines
Study
EGAS00001007618
-
Gene expression profiles of disseminated breast cancer cells
Study
EGAS00001004597
-
Precise reconstruction of the tumor microenvironment using bulk RNA-seq and a unique machine learning-based algorithm trained on artificial transcriptomes
Study
EGAS00001006272
-
resistance to FGFR inhibitor from RNA sequencing
Study
EGAS50000000306
-
Targeted gene panel sequencing of leiomyosarcoma
Study
EGAS50000000595
-
Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome
Study
EGAS00001004593
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Study
EGAS00001004975
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005355
-
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Study
EGAS00001005368
-
Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA
Study
EGAS00001005740
-
Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation.
Study
EGAS00001006364
-
transcriptome analysis of NK cells sorted from PBMCs at baseline and after addition of a T cell dependent bispecific antibody (TDB)
Study
EGAS00001006914
-
The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling
Study
EGAS00001006960
-
Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases
Study
EGAS00001007575
-
This is a test to check the WEBIN functionality
Study
EGAS00001008448
-
EXCEED Study HRC imputation
Dataset
EGAD00010001685
-
NSAID-LIV
Dataset
EGAD00010001422
-
HGP-U-1
Dataset
EGAD00010001472
-
LICA-CN project - 116 liver cancer cases
Study
EGAS00001002300
-
Whole_exome_sequencing_of_inflammatory_bowel_disease_cases
Study
EGAS00001000530
-
Complete Genomics dataset for study EGAS00001002275.
Dataset
EGAD00001003187
-
Datasets 929/938
Dataset
EGAD00001004457
-
ChIP-Seq of TFEB in LT-HSC
Study
EGAS00001005462
-
Integrative Molecular Classification of Meningiomas
Study
EGAS00001004982
-
Cell-free DNA cleavages analysis (human)
Study
EGAS00001006701
-
National Institute on Aging (NIA) Late-Onset Alzheimer's Disease Genetics Initiative: The Multiplex Family Study
Study
phs000160
-
Phenotypic and Genotypic Study of Keratoconus
Study
phs003168
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
The National Myelodysplastic Syndromes (MDS) Study
Study
phs002714
-
Framingham Cohort
Study
phs000007
-
Data access committee for study - The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program "CASCADE".
Dac
EGAC00001000574
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cambridge, UK
Study
EGAS00001005854
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Dublin, Ireland.
Study
EGAS00001005844
-
Whole Exome Sequencing of Bipolar cases and controls performed at the Broad Institute on a cohort from Cardiff, UK (Craddock)
Study
EGAS00001005845
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from London, UK
Study
EGAS00001005851
-
Nordic Samples on build 36
Study
EGAS00000000030
-
Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.
Study
EGAS00001004084
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Umea, Sweden.
Study
EGAS00001005842
-
H3K27ac ChIP-seq of lung neuroendocrine tumors
Study
EGAS50000000057
-
Transcriptome Sequencing Data of High Grade Serous Ovarian Cancer
Study
EGAS00001004714
-
Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease
Study
EGAS00001005348
-
Targeted analysis of cell-free circulating tumor DNA is suitable for early relapse and actionable target detection in patients with neuroblastoma
Study
EGAS00001006027
-
A single cell view on host immune transcriptional response to in vivo BCG-induced trained immunity
Study
EGAS00001006990
-
Analysis of circulating miRNAs for the identification of new prognostic and predictive markers in gastro-entero-pancreatic neuroendocrine tumour (GEP-NET)
Study
EGAS00001007227
-
GWAS data of the AlpeDPD study
Dataset
EGAD00010002684
-
EGA_PBC_phased
Dataset
EGAD00010001533