-
Gene expression profiles of disseminated breast cancer cells
Study
EGAS00001004597
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005355
-
Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation.
Study
EGAS00001006364
-
Genomic and immune signatures predict clinical outcome in newly diagnosed multiple myeloma treated with immunotherapy regimens
Study
EGAS00001007404
-
Targeted gene panel sequencing of leiomyosarcoma
Study
EGAS50000000595
-
Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Study
EGAS00001008050
-
Targeted analysis of cell-free circulating tumor DNA is suitable for early relapse and actionable target detection in patients with neuroblastoma
Study
EGAS00001006027
-
Neurodegenerative_TGS
Study
EGAS00001002431
-
Exome_sequencing_of_EBV_driven_lymphoma
Study
EGAS00001001021
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
Genomic Analyses in Neoadjuvant Immunotherapy-Treated Head and Neck Cancers
Study
phs002864
-
Genomic Landscape of Human Skin at a Single-Cell Resolution
Study
phs001979
-
A comprehensive DNA methylation landscape of human and mouse cell lines derived from hematological malignancies
Study
EGAS50000000627
-
Somatic rearrangements causing oncogenic ectodomain deletions of FGFR1 in squamous cell lung cancer
Study
EGAS50000001368
-
Neoadjuvant immune checkpoint blockade in mismatch-repair proficient colon cancers
Study
EGAS50000000856
-
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Study
EGAS00001003893
-
Machine Learning Signal Enrichment for Ultrasensitive Plasma Tumor Burden Monitoring
Study
EGAS00001007451
-
Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring
Study
EGAS00001007545
-
Study of renal cancers and renal cancer metastases
Study
EGAS00001001176
-
Integrative genomic analyses of European intrahepatic cholangiocarcinoma: new ROS1 fusion gene and PBX1 as prognostic marker
Study
EGAS00001007525
-
Preoperative ipilimumab plus nivolumab in locoregionally advanced urothelial cancer (NABUCCO Cohorts 1 and 2)
Study
EGAS00001004521
-
Comprehensive Characterization of Early Relapse and End-Stage Relapsed Refractory Multiple Myeloma (HIPO K08K/H067/H021+nonHIPO)
Study
EGAS00001007469
-
Chordoma_Extension_Study
Study
EGAS00001000892
-
Chordoma_Extension__known_cancer_genes_
Study
EGAS00001000895
-
HNSCC Patients Treated with Immune Checkpoint Blockade
Study
EGAS50000001175
-
Neversmoker lung adenocarcinoma
Study
EGAS50000000232
-
Transcriptomic Profiles of Neoantigen-Reactive T Cells in Human Gastrointestinal Cancers
Study
phs002765
-
Prevalence and association of microsatellite instability and Lynch syndrome Pan-Cancer and development of a personalized cancer risk prediction tool for Lynch syndrome carriers in India
Study
EGAS50000001449
-
SCLC MeDIP
Study
EGAS50000000506
-
Gene expression analysis of clear cell renal cell carcinoma
Study
EGAS50000001324
-
2017_AML_WGS
Study
EGAS00001002388
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
AML_WES
Study
EGAS00001001559
-
2014_AML_WES_51 samples
Study
EGAS00001002819
-
Orphan_Tumour_Study_NB
Study
EGAS00001003445
-
2017_prospective_v2 Whole Exome Sequencing
Study
EGAS00001002628
-
Multiregion Whole Exome and Smart-Seq3 single cell RNA sequencing of Breast Tumors
Study
EGAS00001006851
-
Evaluation of capture and amplicon-based targeted sequencing methods on formalin-fixed tumours
Study
EGAS00001004965
-
Hi-C analysis of metastatic prostate tumors
Study
EGAS00001006604
-
Hi-C analysis of metastatic prostate tumors - Part 2
Study
EGAS00001006612
-
High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies
Study
EGAS00001004612
-
Mutation and Microsatellite Burden Predict Response to PD-1 Inhibition in Children with Germline DNA Replication Repair Deficiency: An Observational Registry Study
Study
EGAS00001005579
-
Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths
Study
EGAS00001007402
-
Breast_Heterogeneity_Validation
Study
EGAS00001001972
-
Cloning_of_the_breakpoint_of_a_novel_translocation_associated_with_T_acute_lymphoblastic_leukaemia
Study
EGAS00001000520
-
Exome sequencing of early and late passage Patient Derived Xenogratf Tumoroids with matched Patient Derived Xenogratfs and matched normal liver
Study
EGAS50000000185
-
Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000516
-
Dynamics of Genomic and Immune Responses During Primary Immunotherapy Resistance in Mismatch Repair Deficient Tumors
Study
phs002089
-
Genomic Characterization CS-MATCH-0007 Arm B
Study
phs002028
-
Genome-wide Association Study and Meta-Analysis of Ewing Sarcoma
Study
phs001549
-
Genomic Characterization CS-MATCH-0007 Arm Z1I
Study
phs002058
-
PDAC Prognosis Biomarkers in Genomic and Transcriptomic Molecular Data
Study
phs002347
-
Neuroblastoma Genome-Wide Association Study (NBL-GWAS)
Study
phs000124
-
Genomic Characterization CS-MATCH-0007 Arm Z1A
Study
phs001973
-
Whole Genome and Exon Capture Sequencing of Bladder Cancers
Study
phs000535
-
The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft
Study
phs000352
-
Genomic Characterization CS-MATCH-0007 Arm W
Study
phs001948
-
Genomic Characterization CS-MATCH-0007 Arm S2
Study
phs002178
-
Genomic Characterization CS-MATCH-0007 Arm R
Study
phs002029
-
Genomic Characterization CS-MATCH-0007 Arm S1
Study
phs002153
-
Genomic Characterization CS-MATCH-0007 Arm I
Study
phs002181
-
Genomic Characterization CS-MATCH-0007 Arm U
Study
phs002179
-
Genomic Characterization CS-MATCH-0007 Arm C1
Study
phs002177
-
Genomic Characterization CS-MATCH-0007 Arm P
Study
phs002152
-
Genomic Characterization CS-MATCH-0007 Arm Z1B
Study
phs002180
-
Genomic Alterations and Transcriptional Phenotypes in Circulating Tumor DNA and Matched Metastatic Tumor
Study
phs003689
-
Genomic Characterization CS-MATCH-0007 Arm Q
Study
phs001926
-
Establishment of xenogfafts and cultured cell lines from clinical samples
Study
JGAS000585
-
Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue
Study
EGAS00001006124
-
Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy
Study
EGAS00001002515
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Identification of neoantigen from MSI-CRC patient derived organoids and its application for targeting by autologous T cells
Study
EGAS00001006633
-
Colorectal Microenvironment Spatial Mapping
Study
EGAS00001008254
-
Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors
Study
EGAS00001007877
-
Clinical Sequencing Exploratory Research Consortium: Incorporation of Genomic Sequencing into Pediatric Cancer Care
Study
phs001683
-
Luminal breast epithelial cells from wildtype and BRCA mutation carriers harbor copy number alterations commonly associated with breast cancer
Study
EGAS00001007716
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
Combining a Universal Telomerase Based Cancer Vaccine with Ipilimumab in Patients with Metastatic Melanoma - Five-year Follow up of a Phase I/IIa Trial
Study
EGAS00001005253
-
Exploration of coding and non-coding variants in cancer using GenomePaint.
Study
EGAS00001004669
-
Integrated Genomic and Transcriptomic Analysis Reveals Unique Characteristics of Hepatic Metastases and Pro-metastatic Role of Complement C1q in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001004821
-
CEHM
Study
EGAS00001002366
-
Metabolic requirements of the metastasis-initiating tumour cell population using oral squamous cell carcinoma (OSCC) as a model system
Study
EGAS00001004765
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study
Study
phs001101
-
Genomic Characterization of Patient-Derived Xenograft Models to Improve Targeted Therapy for HER2+ Breast Cancer Brain Metastases Treatments
Study
phs001063
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
Combined Targeting of CDK4/6 and HER2 Signaling in Orthotopic Patient-Derived Xenografts of HER2-Positive Breast Cancer Brain Metastases
Study
phs002482
-
Tumor Infiltrating Lymphocytes (TIL) Recognize Unique Somatic Mutations and Mediate Objective Clinical Responses in Metastatic Breast Cancer
Study
phs002735
-
Singapore Gastric Cancer Consortium GeoMx DSP tissue microarray (SGCC TMA) cohort
Study
EGAS50000000640
-
ERBB2/HER2 alterations in ctDNA and metachronous tissues of patients with metastatic urothelial cancer - WGS
Study
EGAS50000001082
-
WES analysis of paired tumor and non-tumoral DNA of 4 patients with non-muscle-invasive bladder cancer
Study
EGAS50000001382
-
Clinical validity of post-surgery circulating tumor DNA (ctDNA) in stage III colon cancer patients treated with adjuvant chemotherapy: the PROVENC3 study
Study
EGAS50000000804
-
TMD_AMKL_targeted_follow_up
Study
EGAS00001000569
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565