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Comparative study of single-nucleotide polymorphism array and next generation sequencing based strategies on triploid identification in preimplantation genetic diagnosis and screen

Triploidy occurred about 2-3% in human pregnancies and contributed to approximately 15% of chromosomally caused human early miscarriage. It is essential for preimplantation genetic diagnosis and screen to distinct triploidy sensitively. Here, we performed comparative investigations between MALBAC-NG...

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Dettagli Bibliografici
Pubblicato in:Oncotarget
Autori principali: Xu, Jiawei, Niu, Wenbin, Peng, Zhaofeng, Bao, Xiao, Zhang, Meixiang, Wang, Linlin, Du, Linqing, Zhang, Nan, Sun, Yingpu
Natura: Artigo
Lingua:Inglês
Pubblicazione: Impact Journals LLC 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5348434/
https://ncbi.nlm.nih.gov/pubmed/27833086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.13247
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