-
IDH-wildtype untreated human glioblastoma samples (GB-UK cohort), published in Noorani & Haughey et al 2025.
Study
EGAS00001008126
-
Prevention and Early Treatment of Acute Lung Injury Network - Reevaluation of Systemic Early Neuromuscular Blockade (PETAL ROSE-BioLINCC)
Study
phs003878
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) Network - Functional, Imaging, and Respiratory Evaluation in CORAL (PETAL FIRE CORAL-BioLINCC)
Study
phs004130
-
International Verapamil SR/Trandolapril [INVEST] Genes Study
Study
phs002319
-
Intra-tumor heterogeneity and clonal evolution of papillary renal cell carcinoma
Study
phs001573
-
Genetic Markers of Lipids in Indians: A Validation Study of Most Relevant Findings of Genome-Wide Association Studies
Study
phs003469
-
Tumor Evolution Analysis Uncovered Immune-Escape Related Mutations in Relapsed Diffuse Large B-Cell Lymphoma
Study
EGAS50000000032
-
TARGET Trial Study Cohort
Study
phs003720
-
PCR-free shallow whole genome sequencing for chromosomal copy number detection from plasma of cancer patients is an efficient alternative to the conventional PCR-based approach
Study
EGAS00001004692
-
Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Study
EGAS00001007099
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Study
EGAS00001004160
-
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
-
Neoantigen responses to Immunotherapy in Prostate Cancer
Study
EGAS00001004050
-
Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Study
EGAS00001001437
-
Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
-
RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia
Study
EGAS00001006460
-
PD-L1 blockade in combination with carboplatin as immune induction in metastatic lobular breast cancer: the GELATO-trial
Study
EGAS00001006902
-
EGAD00010000211
Dataset
EGAD00010000211
-
A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Dataset
EGAD50000001712
-
MutWP4: CRUK Grand Challenge Mutographs of Cancer: Gastric Organoids (2019-08-07)
Dataset
EGAD00001005234
-
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Study
phs000956
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome
Study
phs001779
-
Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression
Study
phs000713
-
Puerto Rico Heart Health Program (PRHHP-BioLINCC)
Study
phs003930
-
Clonal Lineage Tracing of Primary Human Cortical Progenitors, Cell Type Profiles in the Brain Vasculature and Genotyping Data for 22q11DS and Control iPS Lines
Study
phs002624
-
Immunohistochemical and molecular pathological search in gastrointestinal tumors
Study
JGAS000538
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Study
EGAS00001000318
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
Characterization of a human iPSC-derived endocrine pancreas model
Study
EGAS00001001803
-
Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms
Study
EGAS00001004383
-
Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort
Study
EGAS00001002499
-
Functional Mapping of AKT Signaling and Biomarkers of Response From the FAIRLANE Trial of Neoadjuvant Ipatasertib Plus Paclitaxel for Triple-Negative Breast Cancer
Study
EGAS00001005892
-
Single_cell_measurements_to_characterise_B_cell_repopulation_in_SLE_after_rituximab_therapy__a_pilot_study
Study
EGAS00001006798
-
cfDNA dataset from the urine supernatant of ovarian cancer patients and healthy controls
Study
EGAS00001007238
-
Multi-region sequencing of RCC with VTT and metastasis using WES and RNAseq
Dataset
EGAD00001008441
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Dataset
EGAD00001007872
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Pomalidomide for the Treatment of Bleeding in HHT (PATH-HHT)
Study
phs003948
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015471
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA)
Study
phs000236
-
WES Elucidation of Pathogenetic Mechanisms for Immune System Disorders and NIAID Pilot of Genetic Incidental Finding Management
Study
phs001561
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: PEGASUS-TIMI 54
Study
phs002243
-
A Phase 2 Study of Tipifarnib in Large Granular Lymphocyte (LGL) Leukemia
Study
phs000594
-
Center for Education and Drug Abuse Research (CEDAR)
Study
phs001649
-
Regulatory Changes in Glioblastoma Brain Tumors and Xenografts Wave 1
Study
phs001646
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: ENGAGE Atrial Fibrillation-TIMI 48
Study
phs002774
-
ImmunAID
Study
EGAS50000001393
-
POU4F3 mutation screening in Japanese hearing loss patients.
Study
JGAS000093
-
Gene expression signatures associated with chronic endometritis revealed by RNA sequencing
Study
JGAS000621
-
Molecular analysis of diffuse cerebellar gliomas
Study
JGAS000106
-
Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas
Study
JGAS000022
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Deep single-cell RNA sequencing data for 11138 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive CRC patients. The DATA ACCESS AGREEMENT is provided at https://github.com/zhangyybio/single-T-cell-data-access. Applicants can request access to the data by directly downloading it or by sending an email to cancerpku@pku.edu.cn. The process that is used to approve an application includes verifying the institution, participants and research purposes of the application. In general this process will take about two weeks. In principal, any scientific research program complying with the laws and bioethic regulation policies of China will be approved.
Study
EGAS00001002791
-
ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Study
EGAS00001006883
-
European Genome-phenome Archive 15th Anniversary Celebration
Blog
15-anniversary
-
HGSC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003268
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004414
-
Single Cell Analysis of Human Airways in Healthy and Asthma volunteers
Dataset
EGAD00001005064
-
Risk Assessment of Cerebrovascular Events (RACE) Study
Study
phs000456
-
NHLBI TOPMed: MESA and MESA Family AA-CAC
Study
phs001416
-
Prematurity and Respiratory Outcomes Program (PROP) Core Database Protocol (PROP-BioLINCC)
Study
phs004117
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001442
-
Identification of Somatic Changes in Tumors from Fanconi Anemia Patients
Study
phs002652
-
Bacterial Vaginosis, Cervical Immune Cells and HIV Susceptibility
Study
phs002329
-
Effectiveness and Safety of Intermittent Antimicrobial Therapy for the Treatment of New Onset Pseudomonas Aeruginosa Airway Infection in Young Patients With Cystic Fibrosis (EPIC-BioLINCC)
Study
phs004067
-
Expanding the SPTBN1 Spectrum: A Case of Neurodevelopmental Disorder with GI and Musculoskeletal Involvement
Study
EGAS50000001213
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Study
EGAS00001005405
-
scRNAseq data of CAP
Dataset
EGAD50000000321
-
Phylogenetic reconstruction of adult blood cancer reveals early origins and lifelong evolution - WGS
Dataset
EGAD00001007714
-
Phylogenetic reconstruction of adult blood cancer reveals early origins and lifelong evolution - TGS
Dataset
EGAD00001007715
-
RaScALL: Rapid (Ra) screening (Sc) of RNA-seq data for prognostically significant genomic alterations in acute lymphoblastic leukaemia (ALL)
Dataset
EGAD00001009087
-
Distribution of ctDNA levels in plasma of early-stage non-small cell lung cancer patients measured using personalised ctDNA analysis
Dataset
EGAD00001006230
-
Whole exome and Transcriptome sequencing of treatment-naïve esophageal adenocarcinoma biopsies and matched peripheral blood mononuclear cells
Dataset
EGAD00001010876
-
A Study to Assess the Cardiovascular, Cognitive, and Subjective Effects of Atomoxetine in Combination with Intravenous Methamphetamine
Study
phs001195
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
Genomics of Opioid Pharmacogenomics and Acute/Chronic Postsurgical Pain after Major Surgery in Children
Study
phs002105
-
Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome
Study
phs001292
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors
Study
phs002236
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines
Study
phs001581
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Cardiology Biobanking for Biomarker Discovery
Study
phs002726
-
Transcriptomic Profile of Whole Blood Cells from Elderly Subjects fed Probiotic Bacteria Lactobacillus rhamnosus GG ATCC 53103 (LGG) in a Phase I Open Label Study
Study
phs000928
-
National Institute of Arthritis and Musculoskeletal and Skin Diseases and Istanbul Faculty of Medicine Genome-wide Association Study of Behçet's Disease (Turkish)
Study
phs000272
-
Immune-Related Adverse Events after Immune Checkpoint Blockade-Based Therapy are Associated with Improved Survival in Advanced Sarcoma
Study
phs003284
-
CRCbiome: Gut metagenome of Norwegian screening participants using FIT sampling
Study
EGAS50000000170
-
Lung Health Study (LHS-BioLINCC)
Study
phs004013
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
-
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Study
phs000559
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population
Study
phs002985