Shengpei Chen

发表

Performance Comparison between Rapid Sequencing Platforms for Ultra-Low Coverage Sequencing Strategy

J. Liu, Hancheng Zheng, Hui Jiang, 2014, PloS one.

PSCC: Sensitive and Reliable Population-Scale Copy Number Variation Detection Method Based on Low Coverage Sequencing

Xiuqing Zhang, Hui Jiang, R. Christensen, 2014, PloS one.

Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing

Xiuqing Zhang, Hui Jiang, T. Lau, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma

Ping Liu, Hui Jiang, Wen-ting Jiang, 2015, Genetics in Medicine.

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies

Hui Jiang, Yuan Wei, Yangyu Zhao, 2014, Prenatal diagnosis.

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

Yanyan Zhang, Xun Xu, Hui Jiang, 2014, Genetics in Medicine.

Noninvasive Fetal Trisomy ( NIFTY ) test : an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Xiuqing Zhang, 2013 .

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Hui Jiang, 2012, BMC Medical Genomics.

Noninvasive prenatal detection for Pathogenic CNVs

Hui Jiang, Wei Wang, Shengpei Chen, 2015 .

Noninvasive Prenatal Detection for Pathogenic CNVs: The Application in α-Thalassemia

N. Chen, Hui Jiang, Fang Chen, 2013, PloS one.

Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1

Xiuqing Zhang, Y. Liang, Hui Jiang, 2013, Biology of reproduction.

Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing

Jian Wang, Wei Wang, Hui Jiang, 2013, Genome Medicine.

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing

Ping Liu, Songgang Li, Xiuqing Zhang, 2013, Prenatal diagnosis.

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

Huanming Yang, L. Bolund, Xiuqing Zhang, 2014, GigaScience.

A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing

Xun Xu, Fang Chen, Ping Hu, 2013, PloS one.

Rapid detection of aneuploidies on a benchtop sequencing platform

Xiuqing Zhang, Hui Jiang, Wei Wang, 2013, Prenatal diagnosis.

Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma

Lin Li, Shibing Deng, Hongyue Dai, 2013, Genome research.

HIVID: an efficient method to detect HBV integration using low coverage sequencing.

Xun Xu, Guan Wang, Hui Jiang, 2013, Genomics.

Non-invasive fetal sex determination by maternal plasma sequencing and application in X-linked disorder counseling

Yanyan Zhang, Xiuqing Zhang, Hui Jiang, 2014, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Effective Noninvasive Zygosity Determination by Maternal Plasma Target Region Sequencing

Xun Xu, Hui Jiang, Yuan Wei, 2013, PloS one.

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

Xiuqing Zhang, Hui Jiang, Xun Xu, 2015, Clinical chemistry.

Prenatal Detection of Aneuploidy and Imbalanced Chromosomal Arrangements by Massively Parallel Sequencing

Hui Jiang, Fang Chen, Wei Wang, 2012, PloS one.

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.

Yanyan Zhang, Hui Jiang, Xun Xu, 2014, Gene.

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Xiuqing Zhang, 2012, BMC medical genomics.

The frequency modulated auditory evoked response (FMAER), a technical advance for study of childhood language disorders: cortical source localization and selected case studies

Wei-Mou Zheng, Songgang Li, J. Wang, 2013, BMC Neurology.