| [1] Navin N,Kendall J,Troge J,et al.Tumour evolution inferred by single-cell sequencing[J].Nature,2011，472（7341）：90-94.[2] Lu S,Zong C,Fan W,et al.Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing[J]. Science,2012，338（6114）：1627-1630.[3] Hou Y,Fan W,Yan L,et al.Genome analyses of single human oocytes[J].Cell,2013， 155（7）：1492-1506.[4] Yin X,Tan K,Vajta G,et al.Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts[J].Biol Reprod,2013，88（3）：69.[5] Tan Y,Yin X,Zhang S,et al.Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing[J].Gigascience,2014，3（1）：30.[6] Treff NR,Fedick A,Tao X,et al.Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease[J].Fertil Steril,2013，99（5）：1377-1384.[7] Xu Y,Chen S,Yin X，et al.Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a beta-thalassemia family[J].Clin Chem,2015，61（4）：617-626.[8] Fiorentino F,Bono S,Biricik A,et al.Application of next-genera tion sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles[J].Hum Reprod,2014，29（12）：2802-2813.[9] Lukaszuk K,Pukszta S,Wells D,et al.Routine use of next-generation sequencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in vitro fertilization cycles[J].Fertil Steril,2015,103（4）：1031-1036.[10] Wang L,Wang X,Zhang J,et al.Detection of chromosomal aneuploidy in human pre-implantation embryos by next generation sequencing[J].Biol Reprod,2014,90（5）:95.[11] Huang J,Yan L,Fan W,et al.Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos[J].Fertil Steril,2014,102（6）：1685-1691.（2015-12-28 收稿） |
