Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”

Ryan Allison; Martin Kimberly A.

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Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”

机译：评论“低胎儿分数下的非侵袭产前筛选：比较全基因组测序和单核苷酸多态性方法”

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《Prenatal Diagnosis》 |2017年第7期|共2页
作者
Ryan Allison; Martin Kimberly A.;
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Natera StatisticsSan Carlos CA USA;

NateraSan Carlos CA USA;

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正文语种 eng
中图分类妇科学;
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1. Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” [J] . Ryan Allison, Martin Kimberly A. Prenatal Diagnosis . 2017,第7期

机译：评论“低胎儿分数下的非侵袭产前筛选：比较全基因组测序和单核苷酸多态性方法”
2. Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods [J] . Artieri Carlo G., Haverty Carrie, Evans Eric A., Prenatal Diagnosis . 2017,第5期

机译：低胎儿馏分的非侵入性产前筛选：比较全基因组测序和单核苷酸多态性方法
3. Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” [J] . Muzzey Dale, Haverty Carrie, Evans Eric A., Prenatal Diagnosis . 2017,第7期

机译：对“低胎儿馏分的非侵入性产前筛选的反应：全基因组测序和单核苷酸多态性方法的比较”
4. Comparing multiple testing correction methods between two softwares for single nucleotide polymorphisms association analyses: Using OPRD1 and diastolic blood pressure in methadone maintenance patients as an example [C] . Chang Yao-Sheng, Tsou Hsiao-Huei, Wang Sheng-Chang, IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology . 2013

机译：比较两个软件之间针对单核苷酸多态性关联分析的多种测试校正方法：以美沙酮维持患者的OPRD1和舒张压为例
5. Identification of gene-specific single nucleotide polymorphisms within the canine genome and their use to determine nucleotide diversity and inbreeding coefficients within the canine genome. [D] . Brouillette, James A. 2010

机译：犬基因组中基因特异性单核苷酸多态性的鉴定及其在确定犬基因组中核苷酸多样性和近交系数中的用途。
6. Comment on Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods [O] . Allison Ryan, Kimberly A. Martin -1

机译：关于低胎儿无创产前筛查：比较全基因组测序和单核苷酸多态性方法的评论
7. Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods” [O] . Dale Muzzey, Carrie Haverty, Eric A. Evans, 2017

机译：对“低胎儿分数的非侵入产前筛选的反应：比较全基因组测序和单核苷酸多态性方法”

Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”

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