-
Melanoma_post_mortem_analysis
Study
EGAS00001003531
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
NHLBI GO-ESP: Family Studies (Hematological Cancers)
Study
phs000632
-
DNA Methylation in Prostate Tumor and Paired Benign Tissue for African and European Ancestry Men
Study
phs003516
-
Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
-
Intra-tumor heterogeneity of localized lung adenocarcinomas defined by multi-region sequencing
Study
EGAS00001000930
-
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
-
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
-
Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk
Study
phs002566
-
The Haplotype-Resolved Genome and Epigenome of the Aneuploid HeLa Cancer Cell Line
Study
phs000642
-
Immune heterogeneity in small cell lung cancer and vulnerability to immune checkpoint blockade
Study
EGAS50000000138
-
Resistance to anti-EGFR therapy in colorectal cancer
Study
EGAS00001000582
-
Characterization_of_genomic_landscape_of_Peripheral_T_cell_Lymphomas__not_otherwise_specified__PTCL_NOS_
Study
EGAS00001002057
-
Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study
Study
EGAS00001007363
-
Dynamics of sequence and structural cell-free DNA landscapes in small-cell lung cancer
Study
EGAS00001006831
-
Massachusetts General Hospital (MGH)/Broad Hurthle cell carcinoma whole exome sequencing study
Study
phs001580
-
Identification of 22 Novel Loci Associated with Susceptibility to Testicular Germ Cell Tumors
Study
phs001349
-
Genomic Predictors of Response to Immune Checkpoint Therapy
Study
phs001493
-
MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2
Study
phs001965
-
The Ultrasound Study of Tamoxifen
Study
phs003183
-
National Institutes of Health H3Africa African Collaborative Center for Microbiome and Genomics Research (ACCME)
Study
phs001945
-
NHLBI TOPMed: Genetic Study of Atherosclerosis Risk (GeneSTAR)
Study
phs001218
-
Functionally-defined Therapeutic Targets in Diffuse Intrinsic Pontine Glioma (DIPG)
Study
phs000900
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP)
Study
phs001544
-
Evolutionary Analysis of Chronic Lymphocytic Leukemia Cells During Relapse After Allogeneic Hematopoietic Stem Cell Transplant
Study
phs001998
-
Genetic Analysis of Skin Cells
Study
phs003282
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
RNA sequencing of surgically removed lung adenocarcinoma afterwards treated with immune checkpoint inhibitors
Study
JGAS000675
-
The Formation and Propagation of Human Robertsonian Chromosomes
Study
phs003920
-
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Study
EGAS00001001084
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Study
EGAS00001007172
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
Oncogenic chimeric transcription factors drive tumor-specific transcription, processing, and translation of silent genomic regions
Study
EGAS00001006293
-
single-stranded DNA study
Study
EGAS00001005093
-
Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors
Study
EGAS00001007550
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
Immunoreactive_p53_areas_in_human_skin_2
Study
EGAS00001004463
-
Clonal Evolution of PPM1D Mutations in the Spectrum of Myeloid Disorders
Study
EGAS50000000840
-
PD1-targeted delivery of an IL-2 variant induces a multifaceted anti-tumoral T cell response in human lung cancer
Study
EGAS50000000396
-
Chordoma_Targeted_Sequencing_Study
Study
EGAS00001000280
-
Osteosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000278
-
Meningioma_Targeted_Sequencing_Study
Study
EGAS00001000282
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Study
EGAS00001005981
-
Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Study
EGAS00001006793
-
Bone marrow single cell genomics from blood cancer samples
Study
EGAS00001007332
-
Clinical Sequencing Exploratory Research (CSER): Clinical sequencing in cancer: Clinical, ethical, and technological studies
Study
phs000999
-
Single Cell RNA-Seq Reveals Malignant and Stromal Programs Associated with Metastasis in Head and Neck Cancer
Study
phs001474
-
Collagen XVII Promotes Pancreatic Cancer Through Regulation of PIK3R5
Study
phs003641
-
Ultra-sensitive tumor-informed ctDNA monitoring of treatment response in advanced esophagogastric cancer patients
Study
EGAS50000001224
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Study
EGAS00001006879
-
ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer
Study
phs001221
-
INTEGRATIVE MOLECULAR ANALYSIS OF SKIN TUMORS FROM CYLD CUTANEOUS SYNDROME PATIENTS
Study
EGAS50000000247
-
Childhood Cancer Data Initiative (CCDI): Clonal Evolution During Metastatic Spread in High-Risk Neuroblastoma
Study
phs003111
-
National Cancer Institute (NCI) Waldenstrom Macroglobulinemia Genome-wide Association Study
Study
phs001284
-
Subclonal variation in patients with pediatric T-lymphoblastic leukemia (T-ALL)
Study
EGAS50000000794
-
Clonal hematopoiesis in rheumatoid arthritis
Study
EGAS50000000890
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Multiple_Myeloma_Diagnosis_to_Relapse_study_samples
Study
EGAS00001001299
-
Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants
Study
EGAS00001006532
-
WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Study
EGAS00001002416
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Study
EGAS00001002933
-
Lymphoctye_colony_WGS
Study
EGAS00001002948
-
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
-
Single_cell_resolution_of_human_CNV_body_map
Study
EGAS00001003162
-
Exceptional Responders Initiative
Study
phs001145
-
Identification of Somatic Changes in Tumors from Fanconi Anemia Patients
Study
phs002652
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
Neoadjuvant atezolizumab plus chemotherapy in gastric and gastroesophageal junction adenocarcinoma: the phase 2 PANDA trial
Study
EGAS50000000168
-
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Study
EGAS00001005556
-
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - RNAseq
Study
EGAS00001006844
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000160
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000162
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000158
-
Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
-
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Study
phs001526
-
GeneScreen, a Population Based, Targeted Genomic Screening Study
Study
phs001817
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma
Study
phs000734
-
Metastatic Colorectal Adenocarcinoma Tumor Purity Assessment from Whole Exome Sequencing Data
Study
phs003059
-
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Study
phs003317
-
Genomic Profiling of Melanoma
Study
phs000933
-
Structure of the Mucosal and Stool Microbiome in Lynch Syndrome
Study
phs002343
-
Ipilimumab and Decitabine in Treating Patients With Relapsed or Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia
Study
phs003015
-
MP2PRT: Genomic and Molecular Characterization of Biomarkers Associated with Tumor Angiogenesis, DNA Repair, and Immunologic Tolerance using Samples from the NRG Oncology Phase 3 Randomized Trial, GOG-0240 (NCT00803062)
Study
phs002293