2014
DOI: 10.1093/humrep/deu277
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Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles

Abstract: Not applicable.

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Cited by 222 publications
(150 citation statements)
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“…Preimplantation genetic screening is widely used to identify chromosomally normal (euploid) embryos and select them for intrauterine transfer in order to improve the clinical outcome of IVF. 1 Chromosomal mosaicism is a relatively common finding in IVF-derived human embryos. 2 Mosaic embryos, which are characterized by the presence of a mixture of diploid and aneuploid cell lines, are not usually transferred because they are deemed to be abnormal.…”
Section: Healthy Babies After Intrauterine Transfer Of Mosaic Aneuplomentioning
confidence: 99%
“…Preimplantation genetic screening is widely used to identify chromosomally normal (euploid) embryos and select them for intrauterine transfer in order to improve the clinical outcome of IVF. 1 Chromosomal mosaicism is a relatively common finding in IVF-derived human embryos. 2 Mosaic embryos, which are characterized by the presence of a mixture of diploid and aneuploid cell lines, are not usually transferred because they are deemed to be abnormal.…”
Section: Healthy Babies After Intrauterine Transfer Of Mosaic Aneuplomentioning
confidence: 99%
“…An analysis made using NGS was also performed for a couple carrying a Robertsonian translocation, and the whole process of diagnosing the translocation and aneuploidy of 24 chromosomes resulted in implantation of a healthy embryo and normal pregnancy development [17]. Similar findings were observed by Fiorentino et al [33], Tan et al [34] and Treff et al who successfully used next generation sequencing to identify monogenic diseases [35].…”
Section: Next Generation Sequencing (Ngs)mentioning
confidence: 85%
“…These are the MiSeq from Illumina and the Personal Genome Machine (PGM) from Thermo-Fisher Scientific [37,38,[51][52][53]. Following DNA amplification, approximately 50 ng of each DNA sample is enzymatically digested into millions of fragments and pooled for library preparation.…”
Section: Next Generation Sequencingmentioning
confidence: 99%