-
XClone for analyzing somatic copy number alterations
Study
EGAS00001007854
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
IMCISION RNAseq
Study
EGAS00001005454
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing
Study
EGAS00001006037
-
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
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
-
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
-
Single_cell_HSC_colony_WGS_many_years_post_allogeneic_bone_marrow_transplant
Study
EGAS00001003744
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
Facial Skin Biophysical Multi-Parameter and Microbiome-Based Korean Skin Cutoype (KSC) Determination
Study
EGAS00001007334
-
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
-
Neoadjuvant immune checkpoint blockade in high-risk resectable melanoma
Study
EGAS00001003178
-
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
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Study
EGAS00001003813
-
Genomic Landscape and Clonal Architecture in Pediatric Myeloid Neoplasms with Chromosome 7 Deletions
Study
EGAS00001008055
-
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
-
Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations
Study
EGAS00001005479
-
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
-
Spatio-temporal evolution of the primary glioblastoma genome
Study
EGAS00001001041
-
Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
ICGC PedBrain: Deep-sequencing of childhood brain tumors.
Study
EGAS00001000215
-
RNA-seq of Glioblastoma stem cells
Study
EGAS00001003070
-
Circulating cell-free DNA analysis in Small Cell Lung Cancer
Study
EGAS00001003110
-
Exome_sequencing_of_thyroid_disease_in_Val_Borbera
Study
EGAS00001000344
-
WGS of liver cancer in the Japanese population
Study
EGAS00001000678
-
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Study
EGAS00001000906
-
Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
-
FOXM1 is a biomarker of resistance to PI3Kα inhibition in ER+ breast cancer that is detectable using metabolic imaging (RNA-seq data)
Study
EGAS00001004452