-
MutWP5: CRUK Mutographs of Cancer: Breast: Reduction Mammoplasty (Exome)(Novaseq)
Dataset
EGAD00001010116
-
Mechanism and targeted therapy of Vemurafenib-Resistant Hairy-Cell Leukemia
Dataset
EGAD00001003923
-
Mechanism and targeted therapy of Vemurafenib-Resistant Hairy-Cell Leukemia
Dataset
EGAD00001003924
-
Adenoma development in familial adenomatous polyposis and MUTYH‐associated polyposis: somatic landscape and driver genes
Dataset
EGAD00001004332
-
Chordoma Sequencing Project RNAseq
Dataset
EGAD00001000653
-
Exome sequencing of Congenital Heart Disease families Leuven
Dataset
EGAD00001000796
-
463 newly diagnosed patients paired samples (Tumor/Normal)
Dataset
EGAD00001001358
-
Transcriptome and Exome from longitudinal samples of human glioblastoma
Dataset
EGAD00001001424
-
Lung Cell Atlas: Paediatric Spatial (2025-10-02)
Dataset
EGAD00001015723
-
Transcriptomics of human olfactory mucosa
Dataset
EGAD00001003213
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Dataset
EGAD00001004501
-
The British Autozygosity Populations BioResource (2019-08-14)
Dataset
EGAD00001005253
-
RNA sequencing of CD8 T cells from melanoma patients prior to and during checkpoint immunotherapy and untreated healthy controls
Dataset
EGAD00001005973
-
Raw microarray gene expression data from NPC samples_Cohort 1
Dataset
EGAD00001006273
-
Exploring the heterogeneity of sarcoma using single cell sequencing
Dataset
EGAD00001006786
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
Jackson Heart Study (JHS) Cohort
Study
phs000286
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
FIGHT-207: Anonymized Genomic Alterations and Clinical Responses
Study
phs003590
-
The NCAA-DoD Concussion Assessment, Research, and Education (CARE) Consortium
Study
phs002175
-
The National Institute of Neurological Disorders and Stroke (NINDS) Human Genetics Resource Center: DNA and Cell Line Repository (the NINDS Repository): Motor Neuron/Amyotrophic Lateral Sclerosis (ALS) Study
Study
phs000006
-
Identification of intronic sequences promoting natural skipping of ABCA4 exon 15 using long-read transcriptomics and midigene assays
Study
EGAS50000000071
-
High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation
Study
phs000187
-
Assessment of Health-related Quality of Life in Rare Kidney Stones
Study
phs001770
-
National Eye Institute (NEI) Age-Related Eye Disease Study 2 (AREDS2)
Study
phs002015
-
Population Architecture using Genomics and Epidemiology (PAGE): Multiethnic Cohort (MEC)
Study
phs000220
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Study
phs001263
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Study
phs000461
-
Transcriptomic Analysis of HIV-Infected Cells
Study
phs003095
-
Genome-wide Association Study of Myasthenia Gravis
Study
phs000726
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs000379
-
Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older
Study
phs000287
-
WGSPD Project 1: Whole Genome Sequencing for Schizophrenia and Bipolar Disorder
Study
phs002041
-
Adult Eosinophilic Esophagitis Registry Atlas
Study
phs003574
-
Human Dorsal Root Ganglion RNA Landscape Profiling for Neuropathic and Chronic Pain
Study
phs001158
-
OurHealth - Cardiovascular Disease in South Asians
Study
phs003821
-
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
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
-
Intra-tumor heterogeneity of localized lung adenocarcinomas defined by multi-region sequencing
Study
EGAS00001000930
-
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
-
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
-
Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer
Study
EGAS00001004935
-
Etiological Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndromes: A Natural History Study
Study
phs001481
-
Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Study
EGAS00001001694
-
Molecular Sub-grouping of CNS-PNET
Study
EGAS00000000116
-
SCANDARE MACARON
Study
EGAS50000000145
-
Evolutionary Trajectories of Small Cell Lung Cancer under Therapy
Study
EGAS50000000169
-
ARST17B2-Q Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs003192
-
Differential Gene Expression in Cryptorchid Testes
Study
phs001275
-
Genotyping NIGMS Chromosomal Aberration and Inherited Disorder Samples
Study
phs000269
-
Genetic analysis of patients with Inherited Retinal Dystrophies (IRDs) using next generation sequencing to identify the causative variants
Study
phs001619
-
Polygenic Risk Score for the Prediction of Breast Cancer Is Related to Lesser Terminal Duct Lobular Unit Involution of the Breast
Study
phs002062
-
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
Study
phs000858
-
Genomic Factors Involved in Chromosome Rearrangements
Study
phs000845
-
Anorexia Nervosa Genetics Initiative (ANGI)
Study
phs001541
-
Massachusetts General Hospital (MGH) Atrial Fibrillation Study
Study
phs001001
-
Genomic Correlates of Response and Resistance to Immune Checkpoint Blockade in Solid Tumors
Study
phs001565
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Covidseeker and COVID-19 Citizen Science: Leveraging Citizen Science and Real-Time Geospatial Temporal Mobile Data for Digital Contact Tracing and SARS-CoV-2 Hotspotting
Study
phs002519
-
International Collaboration of Incident HIV and HCV in Injecting Cohorts (InC3)
Study
phs002310
-
Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing
Study
phs000816
-
Dynamics of Genomic and Immune Responses During Primary Immunotherapy Resistance in Mismatch Repair Deficient Tumors
Study
phs002089
-
Pancreatic Cancer Case Control Association Study
Study
phs000648
-
Host Response to Respiratory Infections
Study
phs002442
-
RNAseq Transcriptomic Analyses of European Ancestry Samples in MGS Dataset
Study
phs001932
-
Emory University African American Vaginal, Oral, and Gut Microbiome in Pregnancy Cohort Study
Study
phs001865
-
Somatic L1 Retrotransposition in Colorectal Tumors
Study
phs000536
-
Natural History of and Genetic Modifiers in Spinocerebellar Ataxias
Study
phs001332
-
MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2
Study
phs001965
-
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
Study
phs001846
-
Childhood Cancer Data Initiative (CCDI): OncoKids - NGS Panel for Pediatric Malignancies
Study
phs002518
-
African American Breast Cancer GWAS
Study
phs000851
-
OncoArray: Oral and Pharynx Cancer
Study
phs001202
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: Cleveland Clinic Cohort
Study
phs001871
-
Modeling Malignant Progression in Glioma
Study
phs002607
-
Women's Interagency HIV Study (WIHS)
Study
phs001503
-
Molecular Basis of Neuroendocrine Prostate Cancer (Trento/Cornell/Broad 2015)
Study
phs000909
-
NIDDK International IBD Genetics Consortium Repository Global Screening Array
Study
phs002336
-
Yale Center for Mendelian Genomics (YCMG)
Study
phs000744
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: eMERGE - Northwestern Cohort
Study
phs001913
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
The Surveillance Monitoring for ART Toxicities (SMARTT) and the Women and Infants Transmission Study (WITS)
Study
phs002061
-
Sexual dimorphism in human immune system aging
Study
phs001934
-
Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA)
Study
phs001123
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): REasons for Geographic and Racial Differences in Stroke (REGARDS)
Study
phs002919
-
Infant Immune Responses to Early Life Vaccinations
Study
phs002926
-
Pediatric Preclinical Testing Consortium (PPTC)
Study
phs001437
-
Transfer Learning Associates CAFs with EMT and Inflammation in Tumor Cells in Human Tumors and Organoid Co-Culture in Pancreatic Ductal Adenocarcinoma
Study
phs003563
-
Beta-Blocker Evaluation in Survival Trial (BEST-BioLINCC)
Study
phs003730
-
Single-cell RNA sequencing of 16 NPM1 mutated AML patients
Study
EGAS50000000332
-
Immune Determinants of Resistance to PD-1 Blockade in Renal Cell Carcinoma
Study
phs003618
-
Platinum Pedigree Consortium Long-Read Sequencing
Study
phs003793
-
Longitudinal Study of Vaginal Flora
Study
phs002367
-
Immediate Postoperative Minimal Residual Disease Detection with MAESTRO Predicts Recurrence and Survival in Head and Neck Cancer Patients Treated with Surgery
Study
phs003981
-
Identification and characterization of tertiary lymphoid structures in brain metastases
Study
EGAS50000000563
-
Human papillomavirus integration induces oncogenic host gene fusions in oropharyngeal cancers
Study
EGAS50000000892
-
SUDC Registry and Research Collaborative
Study
phs003383
-
Disease-Linked Regulatory DNA Variants and Homeostatic Transcription Factors in Epidermis
Study
phs003977
-
Childhood Cancer Data Initiative (CCDI): Molecular Characterization Initiative
Study
phs002790
-
Whole genome sequencing data from tumor and normal samples
Dataset
EGAD50000001909
-
LifeChange Data Access Committee
Dac
EGAC50000000713