-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Study
EGAS00001001844
-
HipSci HumanExome BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002005
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
HipSci_RNASEQ_PID
Study
EGAS00001001990
-
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Study
EGAS00001002352
-
Hip OA Functional Genomics
Study
EGAS00001002483
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Study
EGAS00001002726
-
Himalayan_population_genetic_study
Study
EGAS00001002731
-
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS
Study
EGAS00001002747
-
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Study
EGAS00001002788
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___WG__Novaseq_
Study
EGAS00001003523
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Study
EGAS00001003528
-
5- FU treated organoids
Study
EGAS00001003592
-
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Study
EGAS00001003003
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
Exome sequencing of advanced hepatocellular carcinoma
Study
EGAS00001003130
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003137
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003139
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Multiple Sclerosis Replication Chip data (MS Chip)
Study
EGAS00001003216
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
Molecular phenotyping of MCA/ID patients to improve diagnosis
Study
EGAS00001003489
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia
Study
EGAS00001003627
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
Mapping_genetic_variants_underlying_gene_regulation_in_healthy_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003647
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003136
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Analysis of error profiles in deep next-generation sequencing data
Study
EGAS00001003444
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Study
EGAS00001000712
-
Autozygosity_pilot___QMUL
Study
EGAS00001000717
-
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
-
Genetics_and_Networks_of_Congenital_Heart_Defects
Study
EGAS00001000762
-
Integrative_genome_profiling_in_AML
Study
EGAS00001000858
-
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Study
EGAS00001000864
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
HipSci HumanExome BeadChip analysis-Healthy volunteers
Study
EGAS00001000866
-
HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers
Study
EGAS00001000867
-
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
-
Metastatic_Breast_Cancer_Whole_Genome
Study
EGAS00001000902
-
DKFZ-HIPO Project H021/NCT MASTER
Study
EGAS00001000948
-
BASIS_RNAseq
Study
EGAS00001000707
-
Barcelona_kids_with_melanoma
Study
EGAS00001000733
-
ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____
Study
EGAS00001000747
-
MYD88/TLR mutations in CLL
Study
EGAS00001000772
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Study
EGAS00001001123
-
Congenital_anosmia_1
Study
EGAS00001001124
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
HipSci___Whole_Exome_sequencing___Monogenic_Diabetes
Study
EGAS00001001140
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000800
-
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
-
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
-
Genetic_screening__of_GPI_anchor_protein_synthesis__
Study
EGAS00001001256
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
-
HipSci HumanExome BeadChip analysis-Rare_BBS
Study
EGAS00001001272
-
HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Study
EGAS00001001277
-
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946