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Single-cell somatic copy number variants in brain using different amplification methods and reference genomes
Dataset
EGAD50000000030
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RNAseq of medulloblastoma data (MB_COMICS cohort)
Study
EGAS50000000410
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NIHR BioResource Rare Diseases WGS project - Multiple Primary Malignant Tumours (MPMT) Rare Disease domain
Dataset
EGAD00001004521
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RNA-seq in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Dataset
EGAD50000000712
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Human primary and metastatic colorectal cancer (CRC) samples
Dataset
EGAD00001009712
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Human tumour and normal-matched WES
Dataset
EGAD00001006099
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RNA-seq
Dataset
EGAD00001011376
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Whole-genome sequencing
Dataset
EGAD00001011377
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Cell targeted amplification sequencing (cta-seq) of scRNA-seq sample
Dataset
EGAD50000001338
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Maternally-Inherited SPTBN1 Mutation
Dataset
EGAD50000001726