|Study ID||Alternative Stable ID||Type|
The aim of this study is to survey somatic mutations in human placentas.
Study Datasets 1 dataset.
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The human placenta harbours chromosomal aberrations that are absent from the fetus in one to two percent of pregnancies. This confined mosaicism suggests that embryonic genetic bottlenecks exist, which phylogenetically segregate placental tissue. Here, we studied the somatic genetic landscape of human placentas by whole genome sequencing of 86 placental biopsies and of 106 microdissections.
|HiSeq X Ten,Illumina NovaSeq 6000||278|
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