-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment
Study
EGAS00001004728
-
Phase Ib of olaparib and capivasertib
Study
EGAS00001004930
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations
Study
EGAS00001005479
-
Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses
Study
EGAS00001006660
-
ENOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003266
-
exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers
Study
JGAS000488
-
Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R)
Study
EGAS00001006538
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Health Professionals Follow-Up Study
Study
phs002460
-
Whole exome sequencing of tumors from the Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Dataset
EGAD00001010928
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases
Dataset
EGAD00001005197
-
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
-
Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Study
EGAS00001002626
-
Targeted_Sequencing_of_Human_Myeloid_Malignancies
Study
EGAS00001001289
-
Lymphocyte_LCM_WGS
Study
EGAS00001003384
-
Melanoma_post_mortem_analysis
Study
EGAS00001003531
-
_WGS__Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001004464
-
Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
-
A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
-
Targeted sequencing of genes recurrently mutated in AML - part2
Dataset
EGAD00001000747
-
TMD-AMKL targeted follow-up part 2
Dataset
EGAD00001000879