Xuyang Yin

Shenzhen, 518083, China

Last Updated: 09/26/2026

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Found 8 publications

A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.

A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.

Journal: Journal of assisted reproduction and genetics

Published: May 31, 2020

Comprehensive preimplantation genetic testing by massively parallel sequencing.

Comprehensive preimplantation genetic testing by massively parallel sequencing.

Journal: Human reproduction (Oxford, England)

Published: November 25, 2019

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.

Journal: PloS one

Published: March 10, 2016

Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center.

Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center.

Journal: Prenatal diagnosis

Published: August 27, 2015

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

Journal: Clinical chemistry

Published: February 28, 2015

Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.

Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.

Journal: GigaScience

Published: January 25, 2014

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.

Journal: Biology of reproduction

Published: January 26, 2013

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing.

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing.

Journal: PloS one

Published: July 05, 2012

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Last Updated: 09/26/2026