-
Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
-
Spatial Transcriptomics on prostate cancer heterogeneity
Study
EGAS00001003001
-
RNA-seq profiling of NKX6.1 reporter iPSC lines for isolation and analysis of functionally relevant neuronal and pancreas populations
Study
EGAS00001002802
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Study
EGAS00001003363
-
Feasibility and safety of a multi-cancer blood test for screening and intervention
Study
EGAS00001004372
-
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
-
Multi-layered population structure in Island Southeast Asians
Study
EGAS00001001738
-
A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Study
EGAS00001001805
-
The Acquisition of Molecular Drivers in Pediatric Therapy-Related Myeloid Neoplasms
Study
EGAS00001004850
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Molecular profiling of metastatic uveal melanoma
Study
EGAS00001004296
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
Integrative molecular analysis of pediatric Anaplastic large cell lymphoma reveals subtypes with distinct immune suppression signatures.
Study
EGAS00001004189
-
Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
-
Massively parallel single-cell B-cell receptor sequencing enables rapid discovery of diverse antigen-reactive antibodies
Study
EGAS00001003663
-
Mutational signatures of environmental carcinogens in human tissue organoids
Dataset
EGAD00001015616
-
Mutational signatures of environmental carcinogens in human tissue organoids – WGS Bulk Normals
Dataset
EGAD00001015630
-
HGSC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003268
-
Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Exome Sequencing
Study
EGAS00001006529
-
Mutational Mechanisms in Multiply Relapsed Pediatric Acute Lymphoblastic Leukemia
Study
EGAS00001007900
-
Single-cell chromatin accessibility landscape identifies tissue repair program in human regulatory T cells
Study
EGAS00001004900
-
Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Whole Transcriptome Sequencing
Study
EGAS00001006528
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
Phylogenetic reconstruction of adult blood cancer reveals early origins and lifelong evolution - TGS
Dataset
EGAD00001007715
-
Hydroxyurea to Prevent Organ Damage in Children with Sickle Cell Anemia (BABY HUG) Phase III Clinical Trial and Follow-Up Observational Studies I and II
Study
phs002415
-
Study on the Genetics of Alcoholism (COGA): African American Family GWAS
Study
phs000976
-
Walter and Eliza Hall - Aix-Marseille Université
Dac
EGAC50000000655
-
BLUEPRINT Bisulfite-seq and Whole Genome Sequencing of mantle cell lymphoma
Study
EGAS00001001638
-
The Melbourne Urological Research Alliance (MURAL) Collection of Patient-Derived Models of Prostate Cancer
Study
phs003369
-
Genomic Analysis of Head and Neck Cancers
Study
phs001623
-
Genomic Profiling of Sequentially Acquired Metastatic Sites from an "Exceptional Responder" Lung Adenocarcinoma Patient Reveals Extensive Genomic Heterogeneity and Novel Somatic Variants
Study
phs001159
-
Genetics of Glucose Regulation in Gestation and Growth (Gen3G) Cohort - Placenta Transcriptomics RNA Sequencing
Study
phs003151
-
Comprehensive Genomic Data Deposition for Pancreatic Cancer Precision Medicine Studies: Clinical Trials NCT02451982 and NCT02648282
Study
phs003600
-
Loss of SDHB promotes dysregulated iron homeostasis, oxidative stress and sensitivity to ascorbate
Study
EGAS00001005279
-
Aberrant Oligoclonal Hematopoiesis in Remission AML and Relapse from Rare Cells Genomically Resembling Leukemic Blasts
Study
phs001408
-
Transcriptome profiling of patient derived neural stem cells highlights the importance of CTNND2 and WNT signaling in early neuralization
Study
EGAS50000000323
-
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
Study
EGAS00001000933
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
-
Using human induced pluripotent stem cells (iPSC) and iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia.
Study
EGAS00001002895
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
-
Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma
Study
EGAS00001003251
-
Somatic mutation and selection at epidemiological scale - Sanger_NanoSeq_RandD
Dataset
EGAD00001015624
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
Structural Expression of BMMF in tissues of colorectal, lung and pancreatic cancer patients
Study
EGAS00001006744
-
RNA sequencing of CCO- and CCO+ human hepatocytes
Study
EGAS00001006984