Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

Thursday, October 29, 2015
A validation study on 47 embryonic trophectoderm samples demonstrates that shallow whole genome sequencing is a preferable alternative for array comparative genomic hybridization in detecting structural and numerical chromosomal rearrangements in preimplantation genetic diagnosis.

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Next generation sequencing The dawn of a new era for preimplantation genetic diagnostics

Wednesday, April 30, 2014
Reflections on "Development and validation of a next-generation sequencing–based protocol for 24-chromosome aneuploidy screening of embryos" by Fiorentino et al.

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