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NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Study
phs001467
-
Genomics of Circulating Tumor Cells
Study
phs000717
-
Efficacy of Bitter Taste Blockers on Flavor Acceptance in a Human Population
Study
phs000839
-
Detecting and Subtyping Lung Cancer Through Analysis of Circulating Tumor DNA
Study
phs003570
-
Genetic Studies of Homologous Recombination Deficiency in Hispanic Gastric Cancer
Study
phs003251
-
Whole exome sequencing of bladder tumors
Study
EGAS50000001248
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
-
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Kidney_transplant_nephrectomy_scRNAseq
Study
EGAS00001003935
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
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RNAseq
Study
EGAS00001007165
-
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
Study
EGAS00001007542
-
TIGIT is the central player in T-cell suppression associated with CAR T-cell relapse in mantle cell lymphoma
Study
EGAS00001007113
-
Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes
Study
EGAS00001007157
-
Hematopoietic Cell Transplant for Sickle Cell Disease (HCT for SCD)
Study
phs002385
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing
Study
phs000778
-
Type 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008
Study
phs000180
-
Northwestern NUgene Project: Type 2 Diabetes
Study
phs000237
-
Ulcerative Colitis Human Microbiome Project (UCHMP)
Study
phs000262
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
Molecular defects in pseudohypoparathyroidism or related disorders
Study
phs000476
-
Atherosclerosis Risk in Communities (ARIC) Cohort
Study
phs000280
-
Temporal Lobe Epilepsy and Retrotransposons
Study
phs002067
-
Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor
Study
phs001507
-
NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)
Study
phs001662
-
Peking University BIOPIC Data Access Committee (PUBDAC).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 academic research institutions complying with the laws and bioethic regulation policies of China will be approved.
Dac
EGAC00001000551
-
Whole genome sequencing of Sinonasal hemangiopericytoma and patient derived cell line model
Study
EGAS50000000025
-
Gut 16S rRNA/FINRISK 2002
Study
EGAS50000000198
-
Brigham and Women's Hospital Multiple Sclerosis Genetic Collection
Study
phs000275
-
The Placenta Harbors a Unique Microbiome
Study
phs000735
-
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Study
phs001246
-
NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing
Study
phs001607
-
The molecular basis of inherited reproductive disorders
Study
phs000475
-
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Study
phs000491
-
Etiologic Studies of Macular Degeneration
Study
phs001896
-
Phase 2 Study of Pembrolizumab in Combination with Gemcitabine and Cisplatin as Neoadjuvant Therapy
Study
phs003452
-
E05-Bioenvironmental Psychiatry
Dac
EGAC50000000222
-
Moroccan Genome Project: Sequencing Data from 109 Whole Genomes of Moroccan Individuals
Study
EGAS50000000529
-
Transplant Outcomes in Aplastic Anemia (TOAA): GWAS and Whole Exome Sequence Data
Study
phs001710
-
ICARUS-BREAST01 Dataset
Dataset
EGAD50000000773
-
Transrenal DNA Analysis
Study
EGAS50000000766
-
Comprehensive genomic characterization of early stage bladder cancer - nanopore sequencing
Study
EGAS50000000510
-
Comprehensive genomic characterization of early stage bladder cancer - shallow whole genome sequencing data
Study
EGAS50000000513
-
Genotypic data of the individuals in HPP project
Dataset
EGAD00010002714
-
A Novel APP p.V742L variant in a patient with ischemic small vessel disease enhances FE65 signalling
Study
EGAS50000001283
-
ICARUS-BREAST01-ExomeSeq
Study
EGAS50000000542
-
Biobank Japan genotype and phenotype data
Study
JGAS000114
-
Transcriptome sequencing, DNA methylation analysis, and SNP array analysis of acute lymphoblastic leukemia in Down syndrome
Study
JGAS000147
-
Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
Study
JGAS000174
-
Phase II clinical trial of adult Philadelphia chromosome-negative precursor B-cell acute lymphocytic leukemia with combination chemotherapy
Study
JGAS000278
-
Multi-omics analysis of pediatric high-risk neuroblastoma
Study
JGAS000246
-
DAC for STimage project
Dac
EGAC50000000867
-
Long read whole genome sequencing data from brain postmortem tissue
Dataset
EGAD50000001349
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH
Study
EGAS00001002618
-
54 metastatic colorectal cancer patients from Schleswig-Holstein in North Germany
Study
EGAS00001004108
-
Yemen_and_Chad_Genotyping
Study
EGAS00001001231
-
Resistance_to_MAPK_inhibitor_induces_internal_duplication_in_BRAF
Study
EGAS00001001304
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
-
RNAseq_of_patients_with_Ewings_sarcoma
Study
EGAS00001000267
-
Ewings_Sarcoma_Rearrangement_Screen
Study
EGAS00001000362
-
Somatic_Variation_Angiosarcoma
Study
EGAS00001002610
-
Pre_clinical_evolution_of_haematological_malignancies
Study
EGAS00001002964
-
Exome_sequencing_of_patients_with_Ewings_sarcoma_
Study
EGAS00001000266
-
Isotype_resolved_sequencing_of_B_cell_receptor__in_health_and_disease
Study
EGAS00001002634
-
Mexican Biobank Project
Study
EGAS00001005797
-
RNA sequencing of multiple myeloma identifies genes dysregulated by structural variants.
Study
EGAS00001003411
-
PROJET DREPANOCYTOSE ET PALUDISME
Study
EGAS00001006008
-
Synthetic genotypes and phenotypes of 500.000 individuals
Study
EGAS00001006552
-
Whole-Transcriptomic Profiling of Sorted Human Renal Cell Carcinoma Immune Populations
Study
EGAS00001006593
-
WES on tumor DNA and germline DNA in pediatric cancer
Study
EGAS00001005429
-
Epigenetic, transcriptome and TF analysis of human NK cell and T cells
Dataset
EGAD00001008449
-
Activating AKT1 and PIK3CA mutations in metastatic castration-resistant prostate cancer
Dataset
EGAD00001006122
-
De novo mutations in cell-free foetal DNA (cffDNA)
Dataset
EGAD00001000596
-
Pheno-seq profiles of single clonal tumor spheroids derived from a patient with colorectal cancer
Dataset
EGAD00001004131
-
Spatiotemporal immune atlas of the first clinical-grade gene-edited pig-to-human kidney xenotransplant
Dataset
EGAD50000000359
-
The chemotherapeutic CX-5461 is extremely mutagenic and may increase cancer risk
Study
EGAS50000000023
-
Genomic Data Access Committee for Early and Late Onset Colorectal Cancer Study
Dac
EGAC50000000359
-
Testicular large B-cell lymphoma is genetically similar to PCNSL and distinct from nodal DLBCL
Study
EGAS50000000521
-
Dual inhibition of FLT3 and BCL-2 is effective in preclinical models of BCL11B-activated lineage ambiguous leukemia
Study
EGAS50000000978
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Dataset
EGAD00001001441
-
Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer
Study
EGAS00001004615
-
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Study
phs000596
-
GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts
Study
phs000389
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR)
Study
phs000708
-
Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome
Study
phs001779
-
ChiLDReN/BA: Genetic Studies of Biliary Atresia in the Childhood Liver Disease Research Network
Study
phs003356
-
Lung Cancer Genetic Study Among Asian Never Smokers
Study
phs002366
-
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
-
Molecular_diagnosis_of_albinism
Study
EGAS00001002068
-
Tracking the evolution of Therapy-Related Myeloid Neoplasms using chemotherapy signatures
Study
EGAS00001006903
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102