-
Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Study
EGAS00001004705
-
A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma
Study
EGAS00001004709
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
-
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Study
EGAS00001004719
-
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Study
EGAS00001003415
-
Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Study
EGAS00001004781
-
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
-
Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
-
Genomic_profiling_of_B_other_Adult_ALL_RNA
Study
EGAS00001003428
-
Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
-
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors
Study
EGAS00001003442
-
Analysis of error profiles in deep next-generation sequencing data
Study
EGAS00001003444
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
Exome sequencing of synchronous colorectal cancers
Study
EGAS00001003474
-
EXCEED Study
Study
EGAS00001003499
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Study
EGAS00001003528
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Study
EGAS00001003563
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
5- FU treated organoids
Study
EGAS00001003592
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
Human adipose tissue immune cells
Study
EGAS00001003725
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
-
Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method
Study
EGAS00001004408
-
Genetic control of naive T cell receptor gene usage in celiac disease
Study
EGAS50000001882
-
Personalized Medicine Based on Genomic Data
Study
JGAS000874
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Dataset
EGAD00001003246
-
Dataset of whole genome bisulfite data of 4 different monocyte samples
Dataset
EGAD00001003259
-
March 2017 data update (bam/fastq) (containing H3K27ac for CEMT_87, RNA-Seq for CEMT_141, CEMT_142, CEMT_145, CEMT_146, H3K27me3, H3K9me3, H3K4me3, H3K4me1, ChIP-Seq Input for CEMT_88, CEMT_90 and CEMT_91) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003272
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS)
Dataset
EGAD00001003130
-
December 2016 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003122
-
WGoxBS and SureSelect data of the POPS placenta samples
Dataset
EGAD00001003136
-
OT2_Solid_WXS_BL
Dataset
EGAD00001003385
-
OT2_Solid_WXS_T
Dataset
EGAD00001003386
-
Epigenetic profiles of neuroblastoma PDXs
Dataset
EGAD00001003394
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Dataset
EGAD00001003409
-
June 2017 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003414
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
The molecular landscape of colorectal cancer reveals genetic mutations - COCA-CN
Dataset
EGAD00001003304
-
Somatic Genetics of lesions from a POT1 patient (2017-04-27)
Dataset
EGAD00001003307
-
Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Dataset
EGAD00001003315