-
High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation
Study
phs000187
-
Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy
Study
phs002826
-
Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level
Study
phs002756
-
ARST17B2-Q Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs003192
-
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Study
phs001526
-
CTSP: Clinical Trial Sequencing Project
Study
phs001175
-
Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile
Study
phs000748
-
TREM2+ Cells in Human Basal Cell Carcinomas
Study
phs003242
-
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Study
phs000559
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Phase 2)
Study
phs001239
-
Characterization of a Metastatic Cervical Cancer Patient and HPV18 Integration Using Next Generation Sequencing
Study
phs000628
-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
Genomic Analysis of Low Grade B-Cell Lymphoma
Study
phs002552
-
Genomic Features of Lung Adenocarcinoma from Individuals with <= 10 Pack-Year Smoking History
Study
phs002556
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Avelumab or M7824 for People with Recurrent Respiratory Papillomatosis
Study
phs002373
-
Genomic and Transcriptomic Landscape of Fibrolamellar Hepatocellular Carcinoma
Study
phs000709
-
Oral Microbiome in Esophageal Adenocarcinoma
Study
phs001527
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
Primary Cytotoxic T Cell Lymphomas Harbor Recurrent Targetable Alterations in the JAK-STAT Pathway
Study
phs002499
-
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Study
phs002462
-
Effects of tobacco smoking on the tumor immune microenvironment in head and neck squamous cell carcinoma
Study
phs001994
-
Whole Transcriptome Sequencing of Resectable Stage III/IV Melanoma Evaluated After Starting Hu14.18-IL2 Predicts Outcome
Study
phs001947
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs000351
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
University of North Carolina at Chapel Hill (UNC) Hepatocellular Carcinoma Study by Exome Sequencing (HCCSES)
Study
phs000627
-
Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas
Study
phs000739
-
Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
Study
phs000913
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Study
phs000580
-
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Study
phs001120
-
Genomic and Transcriptomic Profiling of Patients with Malignant Pleural and Peritoneal Mesothelioma: The NCI Cohort
Study
phs002207
-
Primary Prostate Tumor Tissue DNA Methylation Profiles
Study
phs001921
-
Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo
Study
phs002334
-
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Study
phs001819
-
Landscape of Intratumoral NK Cell and ILC in Head and Neck Squamous Cell Carcinoma
Study
phs002002
-
A Somatic Reference Standard for Cancer Genome Sequencing
Study
phs000932
-
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Study
phs001658
-
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step toward Biomarker Development
Study
phs001281
-
Exome Sequencing Analysis of Cutaneous Squamous Cell Carcinoma
Study
phs000785
-
Molecular Subtyping Reveals Immune Alterations Associated with Progression of Bronchial Premalignant Lesions
Study
phs003185
-
Ultrasensitive Profiling of UV Mutations in Facial Tumors in TSC
Study
phs002914
-
Genomic Evolution of Low- and High-Grade Glioma
Study
phs002034
-
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Study
phs001091
-
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Study
phs001331
-
Whole Exome Sequencing for Colorectal Cancer
Study
phs000410
-
Sequencing of Cervical Cancer
Study
phs000723
-
Combined Tumor and Immune Signals From Genomes or Transcriptomes Predict Outcomes of Checkpoint Inhibition in Melanoma
Study
phs002683
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219