-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
Triple_Negative_Breast_Cancer_RNA_Sequencing
Study
EGAS00001000377
-
Paroxysmal_neurological_Disorders
Study
EGAS00001000386
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
BLUEPRINT Bisulfite-seq (CNAG)
Study
EGAS00001000418
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468