Comprehensive chromosomal and mitochondrial copy number profiling in human IVF embryos

Validation of a next-generation sequencing–based protocol for 24-chromosome aneuploidy screening of blastocysts

Noninvasive chromosome screening of human embryos by genome sequencing of embryo culture medium for in vitro fertilization

Chromosomal analysis of blastocysts from balanced chromosomal rearrangement carriers

Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid

A New Next-generation Sequencing-based Assay for Concurrent Preimplantation Genetic Diagnosis of Charcot-Marie-Tooth Disease Type 1A and Aneuploidy Screening

Uniform and accurate single-cell sequencing based on emulsion whole-genome amplification

Single Cell Whole-Genome Amplification and Sequencing Methodology and Applications

Single Cell Transcriptome Amplification with MALBAC

Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by nextgeneration sequencing with linkage analyses