-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
Whole exome and transcriptome sequencing of biliary tract cancer
Study
EGAS00001000950
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
HipSci RNA sequencing for embryonic stem cell control lines
Study
EGAS00001001727
-
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Study
EGAS00001002164
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
HipSci Illumina 450K Methylation analysis - monogenic diabetes
Study
EGAS00001001275
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183
-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
MeDALL epigenetics study
Study
EGAS00001002169
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population
Study
EGAS00001002226
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
-
Genome of the Netherlands
Study
EGAS00001000644
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Suppressors and activators of JAK-STAT signaling at diagnosis and relapse of acute lymphoblastic leukemia in Down Syndrome
Study
EGAS00001002410
-
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Study
EGAS00001000691
-
Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
-
IBD_Whole_Genome_Sequencing
Study
EGAS00001002238
-
Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
-
Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
GENETIC HISTORY OF ITALY
Study
EGAS00001001458
-
Osteosarcoma_Whole_Genome
Study
EGAS00001000147
-
HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001001565
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
Whole genome and RNA sequencing of paediatric glioblastoma in the ICGC PedBrain project
Study
EGAS00001001139
-
The molecular landscape of colorectal cancer (5 cases)
Study
EGAS00001002374