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Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
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Solid_WXS_MET-XEN
Dataset
EGAD00001002106
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Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (ChIP-Seq for CD14-positive, CD16-negative classical monocyte, on genome GRCh37)
Dataset
EGAD00001002672
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Genetics and Networks of Congenital Heart Defects
Dataset
EGAD00001002251
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A comprehensive characterisation and analysis of human breast cancers through whole-genome sequencing
Dataset
EGAD00001002740
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Somatic mutations and single cell transcriptomes reveal the root of malignant rhabdoid tumours
Dataset
EGAD00001006296
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MutWP1: CRUK Grand Challenge Mutographs of Cancer: Kidney (1)
Dataset
EGAD00001006427
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Development, maturation and maintenance of human prostate inferred from somatic mutations
Dataset
EGAD00001006591
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Combinatorial CRISPR screen identifies fitness effects of paralogues FAM50A and FAM50B
Dataset
EGAD00001006649
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Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Dataset
EGAD00001006151
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Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
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Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Dataset
EGAD00001006287
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IBD Whole Genome Sequencing (2019-04-01)
Dataset
EGAD00001004880
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An Integrated Approach to Patient Stratification and Therapy Selection in Acute Myeloid Leukemia
Dataset
EGAD00001006701
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Fetal origins of malignant germ cell tumours
Dataset
EGAD00001007037
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Exome Sequencing to Identify Causes of Leukaemia Predisposing Congenital Neutropenias (2019-08-19)
Dataset
EGAD00001005264
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Phylogenetic reconstruction of adult blood cancer reveals early origins and lifelong evolution - WGS
Dataset
EGAD00001007714
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Epigenetic, transcriptome and TF analysis of human NK cell and T cells
Dataset
EGAD00001008449
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Phylogenetic reconstruction of adult blood cancer reveals early origins and lifelong evolution - TGS
Dataset
EGAD00001007715
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Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Dataset
EGAD00001007736
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Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Dataset
EGAD00001005466
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Single Cell RNAseq at various stages of HiPSCs differentiating toward definitive endoderm and endoderm derived lineages
Dataset
EGAD00001005741
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Somatic mutation and clonal evolution in premalignant lung disease - WGS (2020-01-15)
Dataset
EGAD00001005786
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Peripheral blood RNA-sequencing in 4,732 participants of the INTERVAL cohort
Dataset
EGAD00001008015
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RNA sequencing of Human Organoid Lines
Dataset
EGAD00001007971