Targeted sequencing of embryonic variants Warm Autopsy

Study ID Alternative Stable ID Type
EGAS00001003952 Cancer Genomics

Study Description

Targeted sequencing of variants previously identified as embryonic from phylogenetic tree building of LCM WGS of PD28690.

Study Datasets 1 dataset.

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Dataset ID Description Technology Samples
During the course of a lifetime normal human cells accumulate mutations. Here, using multiple samples from the same individuals we compared the mutational landscape in 29 anatomical structures from soma and the germline. Two ubiquitous mutational signatures, SBS1 and SBS5/40, accounted for the majority of acquired mutations in most cell types but their absolute and relative contributions varied substantially. SBS18, potentially reflecting oxidative damage, and several additional signatures ... (Show More)
Illumina HiSeq 4000 85

Who archives the data?

There are no publications available