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Exome sequencing
Study
EGAS00001005761
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Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
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'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
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ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
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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
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Integrative analysis of small cell lung cancer
Study
EGAS00001000299
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Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
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Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
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Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
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Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
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Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
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Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
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Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome
Study
EGAS00001000442
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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
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Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
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Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
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Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
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Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing
Study
EGAS00001000850
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A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
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Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
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Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
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These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
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Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
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Genome of the Netherlands
Study
EGAS00001000644
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A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
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Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652
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Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
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Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
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Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
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Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
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Enhancer profiling to identify identifies epigenetic markers of endocrine resistance in metastatic castration resistant prostate cancer patients
Study
EGAS00001006161
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Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
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Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
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Systems biology of Colorectal Cancer
Study
EGAS00001000854
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Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
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Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
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Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
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BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
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BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
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Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
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BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
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Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
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Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
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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
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Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
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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
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MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
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Genome-wide prediction of human embryos
Study
EGAS00001001020
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Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
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Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
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Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
-
Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Study
EGAS00001001165
-
GWAS study on arsenic-exposed population
Study
EGAS00001001168
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Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
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Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
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Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
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Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
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Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
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Associations between APOE status and cognitive ability across the lifecourse
Study
EGAS00001001235
-
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
-
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
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001001316
-
JMML targeted sequencing (2013)
Study
EGAS00001001324
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
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Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
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Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
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GENETIC HISTORY OF ITALY
Study
EGAS00001001458
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GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
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T2D-GENES: Exome sequencing
Study
EGAS00001001460
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Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
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Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
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Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
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Genetic history of the Comorian populations.
Study
EGAS00001002565
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Genetic history of the Swahili population
Study
EGAS00001002569
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The multifaceted genomic history of Ashaninka from Amazonian Peru
Study
EGAS00001006958
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MeDALL epigenetics study
Study
EGAS00001002169
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Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
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This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
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TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
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Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
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Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
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Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
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Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
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Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Study
EGAS00001001542
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Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575