-
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
-
Molecular Evolution of Cancer
Study
phs001255
-
Loss of IFN-gamma Signaling in Tumor Cells Associates with Primary Resistance to Anti-CTLA-4 Therapy
Study
phs001257
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Study
phs001263
-
Oncoarray Consortium - Lung Cancer Studies
Study
phs001273
-
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Study
phs001271
-
Exome Sequencing of Chordoma Cases
Study
phs001280
-
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step toward Biomarker Development
Study
phs001281
-
CPTAC Proteogenomic Study
Study
phs001287
-
CIDR: NCI Genome Wide Predictors of Survival in Colorectal Cancer
Study
phs001290
-
National Eye Institute (NEI) Primary Open-Angle African American Glaucoma Genetics (POAAGG) Study
Study
phs001312
-
Multiple Myeloma Genomic Study (MMGS)
Study
phs001323
-
Glioma International Case Control Study (GICC)
Study
phs001319
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Study
phs001331
-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Gut Microbiome and Types of Colorectal Polyps
Study
phs001381
-
Single-cell RNA-Seq of human lymphoma reveals malignant B cell diversity and patterns of T cell immune checkpoint co-expression
Study
phs001378
-
University of Texas at Austin (UTA) Histone Modification and Gene Expression Profiling in 9 Primary Glioblastoma Multiforme, 2 Anaplastic Astrocytomas and Two Meningiomas
Study
phs001389
-
OncoArray: Prostate Cancer
Study
phs001391
-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
Whole exome sequencing and methylation profiling of uveal melanoma
Study
phs001421
-
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Study
phs001422
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
Genomic Analysis of Pre-Treatment and Autopsy Glioblastoma Specimens
Study
phs001424