-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002698
-
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Study
phs002462
-
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Study
phs000539
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Health Information National Trends Survey-SEER (HINTS-SEER)
Study
phs004065
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001060
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001108
-
Comprehensive spatial landscape and plasticity of immunosuppressive fibroblasts in breast cancer
Study
EGAS50000000220
-
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Study
EGAS00001002239
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
GOSH_Childhood_Leukemia_Behjati_WellcomeCore_RNA
Study
EGAS00001007616
-
Profiling the genomic landscape and evolutionary history of polyploid giant cancer cells in undifferentiated pleomorphic sarcomas
Dataset
EGAD50000002084
-
Complete DNA/RNA sequencing dataset for Australian ICGC ovarian cancer sequencing project 2014-07-07
Dataset
EGAD00001000877
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002696
-
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Study
phs000559
-
A Study of the Genetic Causes of Complex Pediatric Disorders
Study
phs000490
-
Next Generation Mendelian Genetics: Neonatal Diabetes
Study
phs000542
-
Genomic Data Archive From the Network for Pancreatic Organ Donors With Diabetes
Study
phs002861
-
MATISSE WES and bulk RNA-sequencing data
Study
EGAS50000001003
-
TDP43 proteinopathy leads to divergent cryptic splicing in the cortex and spinal cord
Study
EGAS50000000575
-
Global Anaplastic Thyroid Cancer Initiative
Study
EGAS00001002234
-
Integrative_genome_profiling_in_AML
Study
EGAS00001000858
-
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome
Study
EGAS00001007079
-
RNA sequencing from patient-derived intestinal organoids
Dataset
EGAD50000000492
-
Whole exome and targeted DNA sequencing data for formalin-fixed paraffin embedded tissue from de novo small cell prostatic carcinoma cases
Dataset
EGAD00001004139
-
ICGC PCAWG Dataset: MALY-DE_PCAWG_WGS_BWA
Dataset
EGAD00001002123
-
ICGC PCAWG Dataset: EOPC-DE_PCAWG_WGS_BWA
Dataset
EGAD00001002124
-
ICGC PCAWG Dataset: PBCA-DE_PCAWG_WGS_BWA
Dataset
EGAD00001002127
-
Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Vaccination Social Network Diffusion for Diverse Criminal Legal Involved Communities
Study
phs003234
-
Platinum Genomes
Study
phs001224
-
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Study
phs001588
-
Whole genome sequencing of core-binding factor leukemia
Study
phs000414
-
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
-
Count Me In (CMI): The Metastatic Prostate Cancer (MPC) Project (CMI-MPCproject)
Study
phs001939
-
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Study
phs000770
-
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Study
phs002033
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
Use of new methodologies to achieve a thorough molecular characterization in pediatric acute leukemia
Study
EGAS50000000701
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Study
EGAS00001000572
-
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
Study
EGAS00001000096
-
DAC Admixture histories of São Tomé e Príncipe
Dac
EGAC50000000437
-
A practical guide for mutational signature analysis in hematological malignancies
Dataset
EGAD00001005028