-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Multimodal single-cell and bulk glioma analyses
Study
EGAS00001005300
-
CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005408
-
Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
SudanMitoSeq: Sudanese mitochondrial sequencing
Study
EGAS00001005669
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
HipSci___Whole_Exome_sequencing___Congenital_hyperinsulinia
Study
EGAS00001001977
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Molecular_diagnosis_of_albinism
Study
EGAS00001002068
-
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort.
Study
EGAS00001002105
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
-
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Study
EGAS00001002578
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
DERMATLAS__Leiomyosarcoma_RNAseq
Study
EGAS00001007631
-
Analysis of the Elements Involved in the Enrichment of a Panel of Genomic Regions by Nanopore Sequencing Using Adaptive Sampling
Study
EGAS00001007375
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq)
Study
EGAS00001006016
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Study
EGAS00001000335
-
The_identification_of_genetic_vulnerabilities_in_head_and_neck_cancers_for_the_development_of_novel_therapies
Study
EGAS00001002204
-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
-
MeDALL epigenetics study
Study
EGAS00001002169
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
Human islet 3D chromatin maps provide insights into type 2 diabetes
Study
EGAS00001002917
-
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
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
-
The landscape of LAM disease
Study
EGAS00001003534
-
The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Study
EGAS00001002305
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Study
EGAS00001002344
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
-
Exome sequencing of HCV+ lymphoma
Study
EGAS00001006860
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Integrative genomic and transcriptomic analysis of adult leiomyosarcoma (HIPO-028, HIPO-018, HIPO-021)
Study
EGAS00001002437
-
HipSci___Whole_Exome_sequencing___Kabuki
Study
EGAS00001001981
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment
Study
EGAS00001002485
-
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Study
EGAS00001002506
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
-
PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
Whole exome sequencing of Parkinson's disease patients from the United Kingdom
Study
EGAS00001002156
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis
Study
EGAS00001007373
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Study
EGAS00001002657
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Study
EGAS00001002726
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Study
EGAS00001002758
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients
Study
EGAS00001002312
-
DNA methylation atlas of normal human cell types
Study
EGAS00001006791
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
GWAS data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004044