從你的基因解密 為生活 創造更美好的可能
 
 

NIFTY PLUS的好處與優勢

全球最大
全球最大華人基因資料庫比對
資深專科醫師
教授級資深遺傳諮詢專科醫師支持
案例最多
全球累積超過一百萬例成功經驗
業界唯一
業界唯一,雙胞胎臨床數據驗證
全球第一
全球第一 CFDA核准臨床檢測平台
在地服務
世界頂尖技術,基康在地服務
學會認證
美國病理學會(CAP)認證臨床實驗室

全球收案超過百萬例
最堅實的科學基礎 您最安心的選擇

BGI Dianostics實驗室發表 萬人規模NIFTY臨床驗證

  1. Noninvasive Prenatal Testing for Trisomy 21, 18 and 13 - Clinical Experience from 146,958 Pregnancies. Ultrasound Obstet Gynecol. 2015 May;45(5):530-8
  2. Clinical application of noninvasive prenatal testing for the detection of trisomies 21, 18, and 13: a hospital experience. Prenatal diagnosis 2014;34(11):1061-5 doi: 10.1002/pd.4428.
  3. Fetal aneuploidy screening by maternal plasma DNA sequencing: 'false positive' due to confined placental mosaicism. Prenat Diagn.2013 Feb;33(2):198-200.
  4. A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing. PLoS One.2013;8(1):e54236.
  5. Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors. Prenat Diagn.2012 Dec;32(13):1225-32.
  6. Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and ex chromosomal aneuploidies.BMC Med Genomics. 2012 Dec 1;5:57.
  7. Clinical utility of noninvasive fetal trisomy (NIFTY) test – early experience. J Matern Fetal Neonatal Med.2012 Oct;25(10):1856-9.
  8. Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing. J Matern Fetal Neonatal Med.2012 Aug;25(8):1370-4.
  9. Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing. PLoS One.2011;6(7):e21791.
  10. Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. BMJ.2011 Jan 11;342:c7401.

NIFTY雙胞胎臨床驗證

  1. Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies. Prenat Diagn. 2014 Apr;34(4):335-40.
  2. Non-invasive prenatal screening of fetal Down syndrome by maternal plasma DNA sequencing in twin pregnancies. J Matern Fetal Neonatal Med.2013 Mar;26(4):434-7.

NIFTY性染色體異常 臨床驗證

  1. Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies. Jiang et al. BMC Medical Genomics 2012, 5:57
  2. Non-invasive prenatal screening of fetal sex chromosomal abnormalities: perspective of pregnant women. The Journal of Maternal-Fetal and Neonatal Medicine, 2012; 25(12): 2616–2619
  3. Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X. Prenatal Diagnosis 2012, 32, 1114–1116.

NIFTY PLUS染色體片段缺失/重複 臨床驗證

  1. Genetic effects of a 13q31.1 microdeletion detected by noninvasive prenatal testing (NIPT). Int J Clin Exp Pathol. 2014 Sep 15;7(10):7003-11.
  2. A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing. Prenat Diagn.2013 Jun;33(6):584-90.