-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Dilgom_Exome
Study
EGAS00001000086
-
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Study
EGAS00001000093
-
Exome sequencing
Study
EGAS00001005761
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
-
Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
-
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome
Study
EGAS00001000442
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
-
Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing
Study
EGAS00001000850
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Genome of the Netherlands
Study
EGAS00001000644
-
A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
-
Systems biology of Colorectal Cancer
Study
EGAS00001000854
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
-
Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Study
EGAS00001000980
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004