-
Endogenous CD4+ T Cells Recognize Neoantigens in Lung Cancer Patients, including KRAS and ERBB2 (Her2) Driver Mutations
Study
phs001805
-
Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival
Study
phs001982
-
A Dormant TIL Phenotype Defines Non-Small Cell Lung Carcinomas Sensitive to Immune Checkpoint Blockers
Study
phs001618
-
Mucosal Melanoma Targeted Exome Sequencing Study (UCSF)
Study
phs001594
-
Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT)
Study
phs001528
-
Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma
Study
phs001645
-
Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000516
-
MAITS in HCC
Study
phs003279
-
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): A Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study
Study
phs003066
-
Supraphysiologic MDM2 Expression Impacts P53-Independent Chromatin Networks and Therapeutic Responses in Sarcoma
Study
phs003272
-
Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL)
Study
phs002925
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
Genomic Studies for Understanding Etiology of Esophageal Adenocarcinoma (EsophagealAdenocarcinoma_Chinese)
Study
phs001696
-
Multiple Myeloma Genomic Study (MMGS)
Study
phs001323
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Genomic-Enabled Medicine for Recurrent Glioblastoma
Study
phs001460
-
National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda
Study
phs001705
-
Subtyping Sub-Saharan Esophageal Squamous Cell Carcinoma by Comprehensive Molecular Analysis
Study
phs001448
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1
Study
phs000563
-
Stand Up 2 Cancer (SU2C) Genomics-Enabled Medicine for Melanoma (GEMM) Trial
Study
phs001786
-
Genomic Characterization of Meningiomas
Study
phs000552
-
Defining T cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Study
phs001680
-
DNA and RNA Profiling Using Simultaneous Sequencing (Simul-seq)
Study
phs001214
-
Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology
Study
phs003084
-
Whole Genome Sequencing of Skull-Based Chordoma
Study
phs002301
-
Integrative Analysis of Tumor Biopsies on Sequential CTLA-4 and PD-1 Blockade Reveals Markers of Response and Resistance
Study
phs001425
-
RNA Sequencing of ECOG-E1308
Study
phs003320
-
Transcriptome and Epigenome of TIL Infusion for Cancer Immunotherapy
Study
phs002436
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma
Study
phs001433
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
The Genetic and Transcriptomic Evolution of Melanoma
Study
phs001550
-
Metagenomic Analysis to Identify Novel Infectious Agents in Systemic Anaplastic Large Cell Lymphoma
Study
phs002064
-
Case Study of Acquired Resistance to FGFR Inhibition in Cholangiocarcinoma using Targeted DNA and RNA Sequencing
Study
phs001924
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
RNASeq of Plasmacytoid Dendritic Cells in Head and Neck Squamous Cell Cancer Patients
Study
phs001824
-
NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Study
phs001941
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Study
phs001263
-
Development and Validation of Patient-Derived Xenografts from Fibrolamellar Carcinoma Human Tissue
Study
phs002435
-
National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma
Study
phs000144
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
PAK4 inhibition improves PD-1 blockade immunotherapy
Study
phs001919
-
Circulating Tumor DNA Sequencing Provides Comprehensive Mutation Profiling for Pediatric Central Nervous System Tumors
Study
phs003022
-
NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs001736
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625