-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption
Study
phs001491
-
RNA-Sequencing of B-Lymphoblastic Leukemia with Glucocorticoids and PI3K Delta Inhibition
Study
phs003085
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Systems genetics in human endothelial cells identifies non-coding variants modifying enhancers, expression, and complex disease traits
Study
phs002057
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
Enrichment of Lung Microbiome with Supraglottic Taxa which is Associated with Increased Pulmonary Inflammation
Study
phs000633
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
A super-enhancer associated with CD47 links pro-inflammatory signaling to CD47 upregulation in breast cancer
Study
phs001264
-
Indexing Genes Impacted by Copy Number Variation in Developmental Disorders
Study
phs001154
-
Genomic Profiling of Peripheral T-cell Lymphoma
Study
phs001962
-
Genomic Analysis of Pediatric Low Grade Gliomas
Study
phs000614
-
A New Pipeline to Predict and Confirm Tumor Neoantigens Predicts Better Response to Checkpoint Blockade
Study
phs002269
-
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Study
phs000299
-
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Study
phs002653
-
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Study
phs001041
-
University of Texas PDX Development and Trial Center Grant
Study
phs001980
-
Extent and Significance of Bacterial DNA Integrations in the Human Cancer Genome
Study
phs001936
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells
Study
phs001205
-
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Study
phs000942
-
Targeted Linked-Read DNA-seq Analysis of Castration-Resistant Prostate Cancers
Study
phs003343
-
Center for Sub-Cellular Genomics
Study
phs002120
-
Molecular Characterization of Hemimegalencephaly
Study
phs002156