-
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
-
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
-
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