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ABSTRACT: Purpose
Fetal cells in maternal blood are a pure source of fetal genomic DNA for noninvasive prenatal testing (NIPT), if successfully isolated. We assessed whether single-cell genome and transcriptome sequencing (G&T-seq) can be applied to efficiently isolate fetal nucleated red blood cells (fNRBCs) suitable for genetic testing.Methods
Using umbilical cord blood as a model, we isolated 165 single NRBC candidates from four samples and 12 single lymphocytes as controls from one sample. G&T-seq was used to estimate the maturation stage of each NRBC candidate from the transcriptome data, and genomic integrity was assessed using shallow whole-genome sequencing (WGS) data.Results
Multi-dimensional scaling (MDS) of the transcriptome data revealed that five NRBC candidates
SUBMITTER: Ito N
PROVIDER: S-EPMC12401139 | biostudies-literature | 2025 Jan-Dec
REPOSITORIES: biostudies-literature