-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
-
Copy number profiling of primary samples and cell lines of retinoblastoma
Study
EGAS00001001715
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
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
-
Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Study
EGAS00001001542
-
Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cells
Dataset
EGAD00001007029
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
-
The University of Hong Kong Colon Cancer GCV Study
Study
EGAS00001006707
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Study
EGAS00001008073
-
Whole exome and RNA sequencing of organoid samples derived from TRACERx patients
Study
EGAS00001008092
-
In this study, blood-brain barrier (BBB)-forming brain endothelial-like cells were generated from apolipoprotein E gene allele E4 (APOE4, high AD risk) and allele E3 (APOE3, lower AD risk) carrying patient-derived induced pluripotent stem cells (iPSCs). Cells were subsequently exposed to focused ultrasound and microbubbles (FUS+MB) to induce BBB opening and their transcriptome analysed. RNA sequencing (RNA-seq) results demonstrated minimal changes in the gene expression following FUS+MB suggesting safety of FUS+MB application in the clinical setting.
Study
EGAS00001005944
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
NEOPREDICT-Lung: Neoadjuvant Immunotherapy for Resectable NSCLC
Study
EGAS00001007753
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
H3Africa - Genomic and Environmental Risk Factors for Cardiometabolic Disease in Africans
Study
EGAS00001002482
-
Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
-
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
-
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021)
Study
EGAS00001002441
-
Polymorphisms in the mitochondrial genome are associated with bullous pemphigoid in Germans
Study
EGAS00001003932
-
Bulk-RNA Sequencing of high-grade pancreatic and non-pancreatic Neuroendocrine Neoplasms
Study
EGAS00001004861
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
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
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Study
EGAS00001004266
-
Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer.
Study
EGAS00001002609
-
Multiple Myeloma Total Therapy trial patient sequencing
Study
EGAS00001003223
-
Immune induction strategies to enhance the sensitivity to PD-1 blockade in metastatic triple negative breast cancer: the TONIC-trial
Study
EGAS00001003535
-
GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
-
Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Study
EGAS00001006419
-
Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Study
EGAS00001006420
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer
Study
EGAS00001004935
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Study
EGAS00001006595
-
ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Study
EGAS00001006883
-
One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
Molecular features of adenomas predicting metachronous colorectal cancer: a nested-case control study
Study
EGAS00001007039
-
Proteomic Analysis of Non-Muscle Invasive and Muscle Invasive Bladder Cancer Highlights Distinct Subgroups With Metabolic, Matrisomal, and Immune Hallmarks
Study
EGAS00001007290
-
A circulating biomarker for severity of facioscapulohumeral muscular dystrophy
Study
EGAS00001007350
-
Raw bulk TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008118
-
Single cell TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008161
-
RNAseq dataset for MALT1 in MCL
Dataset
EGAD00001009771
-
Dataset for Sarcoma RNA sequencing linked from study EGAS00001004813
Dataset
EGAD00001010276
-
Solve-RD_RND_cohort-1_DF1+2_V1
Dataset
EGAD00001009769
-
Molecular characterization of Barrett’s esophagus at single cell resolution
Study
EGAS00001005221
-
Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Study
EGAS00001007374
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Wellcome Trust Sanger Institute
Dac
EGAC00001000205
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
-
Neoadjuvant atezolizumab plus chemotherapy in gastric and gastroesophageal junction adenocarcinoma: the phase 2 PANDA trial
Study
EGAS50000000168
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Expanding the SPTBN1 Spectrum: A Case of Neurodevelopmental Disorder with GI and Musculoskeletal Involvement
Study
EGAS50000001213
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
Ancient Yakuts genomes and metagenomes
Dataset
EGAD50000001903
-
METABRIC
Study
EGAS00000000083
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Study
EGAS00001004666
-
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Study
EGAS00001005556
-
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
Scottish High Grade Serous Ovarian Cancer
Study
EGAS00001004410
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
APOBEC mutagenesis is a common process in normal human small intestine
Dataset
EGAD00001008764
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Study
EGAS00001005405
-
Characterization of Cell Free Plasma Methyl-DNA From Xenografted Tumors to Guide the Selection of Diagnostic Markers for Early-Stage Cancers
Study
EGAS00001006175
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
-
HCA_Thymus_Disease_DiGeorge_Transplant_RNA
Study
EGAS00001004025
-
High-resolution testing of ctDNA dynamics predicts survival in metastatic NSCLC
Study
EGAS00001006703
-
Influence of Genomic Landscape on Cancer Immunotherapy for Newly Diagnosed Ovarian Cancer: Biomarker Analyses from the IMagyn050 Randomized Clinical Trial
Study
EGAS00001006838
-
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - RNAseq
Study
EGAS00001006844
-
Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Study
EGAS00001003992
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing
Study
EGAS00001004832
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing
Study
EGAS00001004833
-
Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions(H021/INF)
Study
EGAS00001006939
-
ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA
Study
EGAS00001007077
-
The Haemgen RBC study
Study
EGAS00000000132
-
Warm_autopsy__mutational_signatures_and_clonal_units
Study
EGAS00001002216
-
SABE_1171_WGS_GVCF_IDX
Dataset
EGAD00001008203
-
CRCbiome: Gut metagenome of Norwegian screening participants using FIT sampling
Study
EGAS50000000170
-
Small RNA sequencing of endometrial cancer patients with samples collected prior to diagnosis and controls
Dataset
EGAD50000000391
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
-
Genome_Diversity_in_Africa_Project__Benin
Study
EGAS00001001688
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
-
Discrepancies in Tumour Mutation Burden (TMB) reporting from sequential Endobronchial ultrasound trans bronchial needle aspiration (EBUS TBNA) samples within single lymph node stations
Study
EGAS00001007484
-
Plasma MicroRNA Signatures of Aging
Study
EGAS00001008117
-
Multi-omics data of 1000 Inflammatory Bowel Disease patients
Study
EGAS00001002702
-
Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine
Study
EGAS00001007160
-
Dissociation of solid tumour tissues with cold active protease for single-cell RNA-seq minimizes conserved collagenase-associated stress responses
Study
EGAS00001003753
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
Clinical outcomes in ctDNA-positive urothelial carcinoma patients treated with adjuvant immunotherapy
Study
EGAS00001004997
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
Mutational dynamics of triple negative breast cancer over neoadjuvant chemotherapy treatment reveal frequent whole genome duplication events
Study
EGAS00001008261