-
SPECTA RP-1759-AYA Sarcoma cohort
Study
EGAS00001005840
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
ALK_inhibitors_in_the_context_of_ALK_dependent_cancer_cell_lines
Study
EGAS00001000082
-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
BCR-ABL is enriched in S- and G2-cell cycle phases
Study
EGAS00001006769
-
TRACERx: TRAcking non-small cell lung Cancer Evolution through therapy (Rx). Pilot Study. Multi-region sequencing of early-stage NSCLCs.
Study
EGAS00001000809
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Study
EGAS00001000924
-
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
-
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Quantitative microbiome profiling disentangles inflammation- and bile duct obstruction-associated microbiota alterations across IBD/PSC diagnoses
Study
EGAS00001003600
-
Pangenomic classification of pituitary adenomas
Study
EGAS00001003642
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
-
English Longitudinal Study of Ageing Genome-wide genotyping using the Illumina HumanOmni2.5-8
Study
EGAS00001001036
-
Molecular dissection of germline chromothripsis in a developmental context
Study
EGAS00001001896
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer
Study
EGAS00001004228
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002322
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Study
EGAS00001000367
-
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Study
EGAS00001001245
-
Network-based systems pharmacology identifies heterogeneity in LCK and BCL2 signaling and differential vulnerability of T-cell acute lymphoblastic leukemia to targeted therapy
Study
EGAS00001004700
-
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Study
EGAS00001004754
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1
Study
EGAS00001001302
-
Exome sequencing data from two myelosarcomas
Study
EGAS00001002562
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Study
EGAS00001001487
-
Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Study
EGAS00001002248
-
BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
-
Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy
Study
EGAS00001003555
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors
Study
EGAS00001007550
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002255
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
Ongoing_mutagenesis_RNAseq
Study
EGAS00001002364
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Study
EGAS00001002496
-
Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy
Study
EGAS00001002515
-
MicroRNA expression in malignant and benign breast tissue – the Norwegian Women and Cancer study
Study
EGAS00001002671
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03
Study
EGAS00001002851
-
Whole genome characterisation of lung cancer organoids and tissue
Study
EGAS00001002899
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Study
EGAS00001002937
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Study
EGAS00001000680
-
Study the differences at the trascriptome level between iNKT and T cells
Study
EGAS00001003176
-
Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation
Study
EGAS00001000563
-
Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_
Study
EGAS00001000619
-
ICGC Oesophageal adenocarcinoma - normal samples
Study
EGAS00001000723
-
Deciphering Developmental Disorders (DDD)
Study
EGAS00001000775
-
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Study
EGAS00001000840
-
Whole Genome Sequencing to track subclonal heterogeneity in 18 samples from 3 Chronic Lymphocytic Leukemia patients subjected to repeated cycles of therapy.
Study
EGAS00001000885
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
High coverage target resequencing of coding and regulatory regions of 38 Parkinson disease genes associated either to the Mendelian or the sporadic forms of the disease
Study
EGAS00001000973
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Study
EGAS00001001084
-
Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci
Study
EGAS00001001085
-
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Papuan_Genotyping
Study
EGAS00001001587
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors.
Study
EGAS00001002335
-
Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Study
EGAS00001002567
-
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Study
EGAS00001000400
-
RNA-seq consisting of FASTQ paired-end reads from cancer samples
Study
EGAS00001003724
-
Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples
Study
EGAS00001003723
-
Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer
Study
EGAS00001000526
-
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands
Study
EGAS00001005048
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML
Study
EGAS00001003820
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Study
EGAS00001004886
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Study
EGAS00001005104
-
Profiling_molecular_heterogeneity_in_human_primary_microglia
Study
EGAS00001002494
-
Single cell RNAseq of PBMC from bladder cancer patients
Study
EGAS00001004008
-
The genomic and radiomic complexity of multifocal prostate cancer
Study
EGAS00001002767
-
VIKING Health Study - Shetland
Study
EGAS00001003872
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
Splicing patterns in SF3B1 mutated uveal melanoma generate shared immunogenic tumor-specific neo-epitopes
Study
EGAS00001005226
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840