-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
Transcriptome Sequencing of Pediatric Neuroblastoma
Study
phs000868
-
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Study
phs000869
-
High-Risk Breast Cancer GWAS
Study
phs000929
-
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Study
phs000876
-
CAGE Profiling of ncRNAs in Hepatocellular Carcinoma Reveals a Strong Activation of Retroviral LTR Promoters in Virus-Induced Tumors
Study
phs000885
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
Mayo Clinic and Illumina Collaborative Early Stage Ovarian Cancer (ESOC) Study
Study
phs000897
-
Functionally-defined Therapeutic Targets in Diffuse Intrinsic Pontine Glioma (DIPG)
Study
phs000900
-
Molecular Basis of Neuroendocrine Prostate Cancer (Trento/Cornell/Broad 2015)
Study
phs000909
-
Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
Study
phs000913
-
Stand Up To Cancer East Coast Prostate Cancer Research Group
Study
phs000915
-
A Somatic Reference Standard for Cancer Genome Sequencing
Study
phs000932
-
Genomic Profiling of Melanoma
Study
phs000933
-
Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma
Study
phs000939
-
Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination
Study
phs000941
-
Genetic Analysis of Desmoplastic Melanoma
Study
phs000977
-
The Mutational Landscape of CTCL and Sezary Syndrome
Study
phs000994
-
Identification of Putative Neoantigens in Stage III Melanoma
Study
phs001005
-
Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Study
phs001006
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
GWAS in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture
Study
phs001025
-
Comprehensive Genomic Characterization of Acral Melanoma
Study
phs001036
-
Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses
Study
phs001038
-
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Study
phs001041
-
A Genome-Wide Association Study in Patients Experiencing Breast Events While Receiving Adjuvant Aromatase Inhibitors for Early Breast Cancer on NCIC CTG Trial MA.27
Study
phs001043
-
National Eye Institute (NEI) Exfoliation Genotyping Study
Study
phs001053
-
Genomic Characterization of Pediatric Low-Grade Gliomas
Study
phs001054
-
Transcriptional Profiling of PD-1+ and PD-1- Teff and Treg Cells in Glioblastoma and Health
Study
phs001079
-
Common deleterious germline variants shape the urothelial cancer genome
Study
phs001087
-
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Study
phs001091
-
Genomics of Hepatocellular Carcinoma
Study
phs001106
-
Melanoma and Cancer-Associated Fibroblast Short-Term Cultures Derived from Patient Metastases
Study
phs001115
-
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Study
phs001120
-
Integrated Genetic and Pharmacologic Interrogation of Rare Cancers
Study
phs001121
-
Somatic Mutational Analysis by Exome Sequencing Endometrial Carcinosarcomas
Study
phs001152
-
Somatic Mutational Analysis by Exome Sequencing Late-Stage Endometrioid Endometrial Carcinoma
Study
phs001153
-
Genomic Profiling of Sequentially Acquired Metastatic Sites from an "Exceptional Responder" Lung Adenocarcinoma Patient Reveals Extensive Genomic Heterogeneity and Novel Somatic Variants
Study
phs001159
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2)
Study
phs001169
-
CTSP: Clinical Trial Sequencing Project
Study
phs001175
-
Rare germline sequence variants, copy number variations, expression alterations, methylation variations and disease susceptibility in familial melanoma
Study
phs001177
-
TIGER-LC OncoVar Sequencing
Study
phs001199
-
NHLBI TOPMed: African American Sarcoidosis Genetics Resource
Study
phs001207
-
DNA and RNA Profiling Using Simultaneous Sequencing (Simul-seq)
Study
phs001214
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219
-
Gabriella Miller Kids First (GMKF) Pediatric Research Program in Susceptibility to Ewing Sarcoma Based on Germline Risk and Familial History of Cancer
Study
phs001228
-
Sequencing Lymphoma
Study
phs001229
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Phase 2)
Study
phs001239
-
Clonal Architectures and Driver Mutations in Metastatic Melanomas
Study
phs001241
-
Nasopharynx Cancer Whole Exome Sequencing
Study
phs001244