-
Human Pancreatic Islet RNAseq - Lund
Study
EGAS00001004042
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
RNAseq_Pulldown_
Study
EGAS00001000230
-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682
-
Genetic_screening__of_GPI_anchor_protein_synthesis__
Study
EGAS00001001256
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Phenotyping data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004056
-
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Study
EGAS00001000478
-
Egypt_Genome_Project___low_coverage_whole_genome_sequencing
Study
EGAS00001000480
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Breast Cancer - Very young women
Study
EGAS00001001908
-
UK10K NEURO FSZ
Study
EGAS00001000118
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
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
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
UK10K_OBESITY_GS
Study
EGAS00001000242
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa
Study
EGAS00001001984
-
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000800
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
The Druze analysis group
Study
EGAS00001000963
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Metastatic_Breast_Cancer_Whole_Genome
Study
EGAS00001000902
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
-
CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
BLUEPRINT DNase accessibility (NCMLS)
Study
EGAS00001000351
-
High Altitude Pulmonary Hypertension
Study
EGAS00001003171
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
-
McGill Epigenomics Mapping Centre
Study
EGAS00001000995
-
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
-
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Systems biology of Colorectal Cancer
Study
EGAS00001000854
-
HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
-
HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers
Study
EGAS00001000867
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
-
Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Study
EGAS00001000924
-
The mission of the BIOS Consortium is to create a large-scale data infrastructure and to bring together BBMRI researchers focusing on integrative omics studies in Dutch Biobanks.
Study
EGAS00001001077
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
JMML targeted sequencing (2013)
Study
EGAS00001001324
-
GENETIC HISTORY OF ITALY
Study
EGAS00001001458
-
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001001565
-
Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
-
Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Study
EGAS00001000166
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Genetic sequencing of MODY patients.
Study
EGAS00001001699
-
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
-
BASIS_RNAseq
Study
EGAS00001000707
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713
-
Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252