-
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Study
EGAS00001002496
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Study
EGAS00001000680
-
Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation
Study
EGAS00001000563
-
Deciphering Developmental Disorders (DDD)
Study
EGAS00001000775
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Study
EGAS00001001084
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
Papuan_Genotyping
Study
EGAS00001001587
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
Profiling_molecular_heterogeneity_in_human_primary_microglia
Study
EGAS00001002494
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
Whole exome sequencing CYLD cutaneous syndrome
Study
EGAS00001003839
-
Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840
-
Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Study
EGAS00001003003
-
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Study
EGAS00001003184
-
An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy
Study
EGAS00001003234
-
RA-Map, A multi-omic survey of whole blood and subsets in early rheumatoid arthritis and vaccine study controls
Study
EGAS00001004424
-
Chromothripsis followed by circular recombination drives oncogene amplification in human cancer
Study
EGAS00001005424
-
Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue
Study
EGAS00001006124
-
Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Study
EGAS00001004663
-
Forty-Five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor
Study
EGAS00001003361
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
-
POPCOL: population-based colonoscopy.
Study
EGAS00001004869
-
Single-cell analysis reveals transcriptomic and epigenomic impacts on the maternal-fetal interface upon SARS-CoV-2 infection
Study
EGAS00001006263
-
Genomic landscape and molecularly-informed therapy in thymic carcinoma and other advanced thymic epithelial tumors (H021, HIPO)
Study
EGAS00001006408
-
DNA methylation-based classification of sinonasal tumors [Proteomics data]
Study
EGAS00001006712
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Study
EGAS00001006713
-
The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Study
EGAS00001007086
-
Digital tEchnology For Lung Cancer Treatment
Study
EGAS00001007219
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Study
EGAS00001007767
-
Colorectal Microenvironment Spatial Mapping
Study
EGAS00001008254
-
Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing
Dataset
EGAD00001006088
-
Tracking the evolution of esophageal squamous cell carcinoma under dynamic immune selection by multi-omics sequencing
Dataset
EGAD00001009482
-
Combined MEK and BCL-2/XL inhibition is effective in high-grade serous ovarian cancer patient-derived xenograft models and BIM levels are predictive of responsiveness
Dataset
EGAD00001005111
-
Cooperative activity of BRAF F595L and mutant HRAS in histiocytic sarcoma provides new insights into oncogenic BRAF signaling
Dataset
EGAD00001001384
-
Characterization and clinical relevance of the genomic alterations defining invasive lobular breast cancer
Dataset
EGAD00001001395
-
Longitudinal profiling of the immune response to Plasmodium vivax in naive hosts by RNA-sequencing
Dataset
EGAD00001006924
-
Molecular risk stratification in patients with T1 colorectal cancer_WES
Dataset
EGAD00001010890
-
Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high risk lineage ambiguous leukemia
Study
EGAS50000001255
-
Genome-wide cell-free DNA biological patterns in patients with cancer
Study
EGAS00001007400
-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
Impact of Respiratory Virus Infections and Bacterial Microbiome Shifts on Lymphocyte and Respiratory Function in Infants Born Prematurely or Full Term
Study
phs001347
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis (CLOVERS) (PETAL CLOVERS-BioLINCC)
Study
phs004080
-
Sickle Cell Disease Implementation Consortium Registry (SCDIC Registry-BioLINCC)
Study
phs004203
-
LLDeep DAG2+ scRNA-seq in PBMCs
Dataset
EGAD00010001315
-
sWGS data from 362 tumor with non muscle invasive bladder cancer and 30 blood samples (15 males and 15 females)
Dataset
EGAD50000000732
-
Single cell whole genome sequencing of luminal breast epithelial cells from wildtype and BRCA mutation carriers
Dataset
EGAD50000000883
-
Data Access Committee of CiRA Foundation
Dac
EGAC50000000128
-
scRNA-seq dataset, RCC
Dataset
EGAD50000000566
-
iNHL WXS Data Commitee
Dac
EGAC50000000488
-
Data access policy
Dac
EGAC50000000504
-
SUM-seq data for spontaneous differentiation of iPSCs upon perturbation of GATA2, NR4A2 or SOX17
Dataset
EGAD50000001205
-
The Emirati T2T-level Pangenome: A complete Diploid Graph of 58 Genomes
Dataset
EGAD50000001756
-
Circulating Biomarker Laboratory within the Division of Cancer of Imperial College London
Dac
EGAC50000000768
-
A single-cell atlas of the early COPD lung - Nanopore long-read
Dataset
EGAD50000001002
-
Transcriptomics for IMMU-SCCHN1 cohort
Dataset
EGAD50000002206
-
Bleomycin Induced Pneumonitis WGS dataset
Dataset
EGAD50000002221
-
Single Cell RNASeq for ARMS tumors
Dataset
EGAD50000002241
-
Single cell RNA-sequencing of tissues from NSCLC patients treated with chemoimmunotherapy
Dataset
EGAD00001009778
-
Peruvian Genome Project
Dataset
EGAD00001007082
-
Whole Genome Sequences of 18th century African descended individuals from Charleston, South Carolina.
Dataset
EGAD00001009643
-
Whole-genome plasma DNA sequencing in CRC patients under anti-EGFR therapy
Dataset
EGAD00001000748
-
COMPARE study: participants typed during UK Biobank version 2 array development phase
Dataset
EGAD00001005023
-
The British Autozygosity Populations BioResource (2018-06-06)
Dataset
EGAD00001004150
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Dataset
EGAD00001003783
-
Adeno-associated virus in the liver: natural history and consequences in tumor development
Dataset
EGAD00001004484
-
IG-MYC ALL - DNA and RNA sequencing
Dataset
EGAD00001008705
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002697
-
Subset of EGAS00001005112 (The INFORM Precision Medicine Study for High-Risk Pediatric Malignancies, 17 exomes) which is used in EGAS00001005243 (Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B)
Dataset
EGAD00001007864
-
Whole-exome sequencing of 20 samples of actinic keratosis (10s) and cutaneous squamous cell carcinoma (10s)
Dataset
EGAD00001003765
-
Whole genome sequence of third generation family member (SFHS)
Dataset
EGAD00001001454
-
Chordoma Sequencing Project Whole Genome
Dataset
EGAD00001000721
-
Identification of drug resistance genes in cancer cell lines by insertional mutagenesis
Dataset
EGAD00001002207
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs) from plasma DNA of BC, CRC and NSCLC patients
Dataset
EGAD00001006301
-
Chracterising cellur pathways underlying CD3/CD28 activation of human CD4+ cells
Dataset
EGAD00001006611
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - WGS
Dataset
EGAD00001011645
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
-
Renal habitat WXS
Dataset
EGAD00001010125
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - RNA
Dataset
EGAD00001011646
-
University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders)
Study
phs000436
-
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307
-
Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE)
Study
phs003619
-
Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Global Alliance to Prevent Prematurity and Stillbirth (GAPPS)
Study
phs003620
-
Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Ischemia (BEST CLI-BioLINCC)
Study
phs003844
-
The circulating cell-free DNA landscape in sepsis is dominated by impaired liver clearance
Study
EGAS50000001033
-
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Study
EGAS00001002272
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Study
phs000547
-
Genetic Causes of Growth Disorders
Study
phs001617
-
Summary Statistics GWAS SSNS
Dataset
EGAD00010002316
-
Mitochondrial DNA mosaicism in human somatic cells
Dataset
EGAD50000000373
-
PRADO trial - Personalized response-directed surgery and adjuvant therapy after neoadjuvant ipilimumab plus nivolumab in stage III melanoma
Dataset
EGAD50000000393
-
Raw scRNA-seq data from B-lineage cells in the blood of celiac disease patients
Dataset
EGAD50000000340