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Whole genome sequencing of breast cancer and related clones
Dataset
EGAD00001010833
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Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients.
Study
EGAS00001005698
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Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
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Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
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Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
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Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
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DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
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Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
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Analysis of mechanisms of CD19- relapse following novel low affinity CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) in a Phase I clinical study in paediatric ALL: CARPALL
Study
EGAS00001003733
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Recursive splicing in long vertebrate genes
Study
EGAS00001001170
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
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HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
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APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
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MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
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Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
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Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
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Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma (H021)
Study
EGAS00001001845
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Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Study
EGAS00001003853
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Whole Genome Sequencing of Gingivo-buccal Cancer: ICGC-India Project_YR03
Study
EGAS00001001901
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Lineage-specific genome architecture links disease variants to target genes
Study
EGAS00001001911