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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW14_C
Dataset
EGAD00001001787
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RNA-sequencing data from vitamin C experiment
Dataset
EGAD00001010009
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CCMA-RNA
Dataset
EGAD00001010034
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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB62_M
Dataset
EGAD00001001780
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB52_C
Dataset
EGAD00001001763
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Germline variants in childhood melanoma
Dataset
EGAD00001010039
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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB58_C
Dataset
EGAD00001001772
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300BCG trained immunity scRNAseq
Dataset
EGAD00001010055
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Common clonal origin of chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia in a patient with a germline CHEK2 variant
Dataset
EGAD00001007644
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WXS files for paper titled 'Genomic Landscape of Pediatric Myelodysplastic Syndromes'
Dataset
EGAD00001003781
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BLUEPRINT release August 2016, RNA-Seq for monocyte - T=0days, on genome GRCh38
Dataset
EGAD00001002360
-
BLUEPRINT release August 2015, DNase-Hypersensitivity for inflammatory macrophage, on genome GRCh38
Dataset
EGAD00001001573
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Single cell epigenomic study of H3-K27M mutant diffuse midline glioma across age and location
Dataset
EGAD00001010170
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Whole Exome Sequencing
Dataset
EGAD00001004352
-
sWGS of matched patient and PDX ovarian tumour tissues
Dataset
EGAD00001008650
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Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884
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Bulk RNA-sequencing of AML blasts pre and post culture
Dataset
EGAD00001008773
-
Dataset for GIST-WHOLE_GENOME
Dataset
EGAD00001008876
-
BLUEPRINT release August 2015, RNA-Seq for plasma cell, on genome GRCh38
Dataset
EGAD00001001523
-
BLUEPRINT release August 2015, RNA-Seq for monocyte - None, on genome GRCh38
Dataset
EGAD00001001532
-
RNAseq FASTq files from 82 pre-treatment tumors from PURE01
Dataset
EGAD00001008003
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SPECTA: NGS Screening Program for Efficient Clinical Trial Access
Dataset
EGAD00001000894
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB33_F
Dataset
EGAD00001001731
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB51_F
Dataset
EGAD00001001761