-
Mapping_genetic_variants_underlying_gene_regulation_in_inflammed_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003770
-
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982
-
HipSci___Whole_Exome_sequencing___PID
Study
EGAS00001001983
-
HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002006
-
HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002010
-
HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002011
-
HipSci HumanExome BeadChip analysis - Battens disease
Study
EGAS00001002016
-
HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome
Study
EGAS00001002024
-
HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002026
-
HipSci HumanHT 12 Expression BeadChip analysis - Macular Dystrophy
Study
EGAS00001002029
-
HipSci HumanHT 12 Expression BeadChip analysis - Battens disease
Study
EGAS00001002031
-
Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Study
EGAS00001004019
-
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
-
Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Study
EGAS00001002730
-
INSIGHT: VHL Case Report
Study
EGAS00001005895
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
Exome sequencing of Fibromyalgia patients
Study
EGAS00001003826
-
Leeds Melanoma Cohort (LMC) gene expression study
Study
EGAS00001002922
-
Whole-exome sequencing of intravascular large B-Cell lymphoma
Study
EGAS00001003970
-
Oesophageal_Adenocarcinoma_Organoids_Iso_Seq
Study
EGAS00001004051
-
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
-
Role of cohesin/CTCF in human monocyte differentiation
Study
EGAS00001005508
-
Transcriptional changes in GBM through therapy
Study
EGAS00001003790
-
Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001002165
-
Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia
Study
EGAS00001005605