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Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Dataset
EGAD00001001691
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The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006643
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The evolving mutational landscape of normal human esophagus
Dataset
EGAD00001004158
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A compendium of mutational signatures due to environmental exposures
Dataset
EGAD00001004583
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Next Generation Sequencing in an IBD Pedigree Whole Genome Data
Dataset
EGAD00001000399
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The landscape of somatic mutation in normal colorectal epithelial cells
Dataset
EGAD00001004193
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WGBS data of solid liver tumor DNA, and WGBS data of cell-free DNA derived from human blood, for CancerDetector study
Dataset
EGAD00001004317
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Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
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Targeted Sequencing of 173 genes
Dataset
EGAD00001002115
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Massive parallel RNA sequencing of highly purified mesenchymal cells derived from bone marrow specimens of 45 low-risk myelodysplastic syndrome cases
Dataset
EGAD00001002658
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Comparison of transcriptional response of induced pluripotent stem (iPS) cell-derived and monocyte-derived macrophages to bacterial lipopolysaccharide stimulation
Dataset
EGAD00001001106
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The evolving mutational landscape of normal human esophagus
Dataset
EGAD00001004159
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Reconstruction of human phylogenetic trees using single-cell genome sequencing
Study
EGAS00001004824
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RNA sequencing of CD8 T cells from melanoma patients prior to and during checkpoint immunotherapy and untreated healthy controls
Study
EGAS00001004081
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Characterization of MCSP+ melanoma DCC and MelDCC lines
Study
EGAS00001006702
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Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Study
EGAS00001006962
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cfDNAme allows early prediction of PE
Study
EGAS00001007071
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iNeuron_RNAseq
Study
EGAS00001004238
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PEACE melanoma 14
Study
EGAS00001007081
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Single-cell and bulk RNA-sequencing of nivolumab-treated glioblastoma
Study
EGAS00001007110
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Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Study
EGAS00001007146
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Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
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This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Study
EGAS00001007818
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Cold Ischemia Study
Study
EGAS00001008233