Validation of next-generation sequencing for comprehensive chromosome screening of embryos

Reproductive BioMedicine Online

Volumn 31, Issue 6, 2015, Pages 760-769

  Kung, Allen ^a   Munné, Santiago ^a   Bankowski, Brandon ^b   Coates, Alison ^b   Wells, Dagan ^c  

^a Reprogenetics LLC   (United States)

^b Oregon Reproductive Medicine   (United States)

^c UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

aneuploidy; comprehensive chromosome screening; embryo; next generation screening; preimplantation genetic diagnosis

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; BLASTOCYST; BLASTOMA; CELL SCREENING; CHROMOSOME; COMPARATIVE GENOMIC HYBRIDIZATION; EMBRYO; FEMALE; GENE AMPLIFICATION; HUMAN; INTERMETHOD COMPARISON; NEXT GENERATION SEQUENCING; SENSITIVITY AND SPECIFICITY; VALIDATION STUDY; CELL LINE; CYTOLOGY; DIAGNOSTIC ERROR; GENETIC SCREENING; HIGH THROUGHPUT SEQUENCING; HUMAN CHROMOSOME; MAMMALIAN EMBRYO; METABOLISM; PREGNANCY; PREIMPLANTATION GENETIC DIAGNOSIS; PROCEDURES; STANDARDS; STATISTICS AND NUMERICAL DATA;

ADULT; ANEUPLOIDY; CELL LINE; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC ERRORS; EMBRYO, MAMMALIAN; FEMALE; GENETIC TESTING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PREGNANCY; PREIMPLANTATION DIAGNOSIS; SENSITIVITY AND SPECIFICITY;

EID: 84951299176     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/j.rbmo.2015.09.002     Document Type: Article

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