The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos

Reproductive BioMedicine Online

Volumn 31, Issue 1, 2015, Pages 62-70

  Fan, Junmei ^a   Wang, Li ^a   Wang, Hui ^a   Ma, Minyue ^a   Wang, Shufang ^a   Liu, Zhongyu ^a   Xu, Genming ^b   Zhang, Jianguang ^b   Cram, David S ^b   Yao, Yuanqing ^a  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b Berry Genomics   (China)

Author keywords

aneuploidy; chromosome disease; copy number variation (CNV); next generation sequencing (NGS); whole genome amplification (WGA)

Indexed keywords

GENOMIC DNA;

ANEUPLOIDY; ARTICLE; BLASTOCYST; CHROMOSOME; CHROMOSOME DELETION; CHROMOSOME DISORDER; CHROMOSOME STRUCTURE; CONTROLLED STUDY; COPY NUMBER VARIATION; DIAGNOSTIC TEST ACCURACY STUDY; EMBRYO; GENE AMPLIFICATION; HUMAN; HUMAN CELL; NEXT GENERATION SEQUENCING; SOTOS SYNDROME; VALIDATION STUDY; ANIMAL EMBRYO; CHROMOSOME DISORDERS; EVALUATION STUDY; HIGH THROUGHPUT SEQUENCING; HUMAN GENOME; PHYSIOLOGY; PRENATAL DIAGNOSIS; PROCEDURES; SENSITIVITY AND SPECIFICITY;

ANEUPLOIDY; CHROMOSOME DISORDERS; DNA COPY NUMBER VARIATIONS; EMBRYO, MAMMALIAN; GENOME, HUMAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PREIMPLANTATION DIAGNOSIS; SENSITIVITY AND SPECIFICITY;

EID: 84933501719     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/j.rbmo.2015.03.010     Document Type: Article

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