-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
Adeno-associated virus in the liver: natural history and consequences in tumor development
Study
EGAS00001003310
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
Phase Ib of olaparib and capivasertib
Study
EGAS00001004930
-
Assessment of the Toll-like receptor 3 response in hepatocytes
Study
EGAS00001005147
-
IMCISION RNAseq
Study
EGAS00001005454
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Size-tagged preferred ends in maternal plasma DNAshed light on the production mechanism and showutility in noninvasive prenatal testing
Study
EGAS00001002831
-
Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA
Study
EGAS00001003160
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
-
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Study
EGAS00001000961
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Single cell transcriptomics of human adrenal gland reveal chromosomal alterations in adrenocortical cells
Study
EGAS00001007488
-
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Study
EGAS00001000554
-
Whole exome sequencing in RVOT patients
Study
EGAS00001002319
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
-
Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq.
Study
EGAS00001000793