-
Warm_autopsy__mutational_signatures_and_clonal_units
Study
EGAS00001002216
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
Unraveling the genetic basis of a collagen migration defect in patients with a combined platelet dysfunction and reduced bone density
Dataset
EGAD00001000109
-
Mosaic_Colorectal_Metastasis
Study
EGAS00001000613
-
A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC
Study
phs001111
-
HIV-phyloTSI: Subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence data
Study
EGAS50000000895
-
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001004649
-
Mutations in SPINK2 induce azoospermia
Study
EGAS00001002450
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
Low Density Genotyping from the Fragile Families and Child Wellbeing Study
Study
phs002417
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
Clonal tracing with somatic epimutations reveals dynamics of blood aging
Study
EGAS00001008056
-
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
-
Melanoma_C32_ENU_resistance_to_Combination_Therapy
Study
EGAS00001001614
-
Melanoma_C32_ENU_Resistance_to_Single_Agent_Therapy
Study
EGAS00001001697
-
Immune signature of malignant melanoma in pregnancy
Study
EGAS50000000492
-
Angelman, Rett, Prader-Willi Syndromes Consortium (ARP) Angelman Syndrome Natural History Protocol
Study
phs000576
-
Mutations in GNAI2 Cause Developmental and Immune Dysregulation
Study
phs002817
-
Cas9-targeted-based long-read sequencing for genetic screening of RPE65 locus
Study
EGAS50000000596
-
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Study
JGAS000689
-
Rare Germline Variants in CDKN2A-Negative Children and Adolescents with Cutaneous Melanoma
Study
EGAS50000001311
-
Whole_Genome_Sequencing_of_JK_Family
Study
EGAS00001001323
-
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Study
EGAS00001000691
-
Genomic study of an AT-AML
Study
EGAS00001004392