NIPT：NIPT ，無創(chuàng)產(chǎn)前篩查，是利用大規(guī)模平行測(cè)序等技術(shù)對(duì)母體外周血中的游離 DNA 進(jìn)行深度測(cè)序，獲取胎兒染色體信息的方法。傳統(tǒng)的產(chǎn)前篩查和診斷方法( 孕早期超聲檢查、孕中期血清學(xué)篩查、羊水細(xì)胞染色體核型分析) 均有一定的局限性，尤其穿刺法可能會(huì)傷害胎兒導(dǎo)致流產(chǎn)。隨著新一代測(cè)序技術(shù)研究的深入，無創(chuàng)性胎兒基因檢測(cè)得到了快速發(fā)展。
染色體非整倍體：染色體非整倍體是出生缺陷zui常見的遺傳性病 因，常見類型有 21-三體、18-三體、13-三體、X-三體等。患兒常表現(xiàn)為先天性非進(jìn)行性智力障礙，生長(zhǎng)發(fā)育遲緩和( 或)
合并畸形，目前尚無有效的治療方法。
使用Streck Cell-free DNA BCT采血管進(jìn)行無創(chuàng)產(chǎn)前篩查的文獻(xiàn)：
使用Streck Cell-free DNA BCT采血管采集保存運(yùn)輸孕婦外周血樣本。
使用PCR、高通量基因測(cè)序等檢測(cè)方法分析母體血漿中的胎兒游離DNA。
分析是否有常見胎兒遺傳?。喝w綜合征等。
參考文獻(xiàn)：
張媛媛,劉曉亮,初國銘,崔婉婷,何蓉,趙彥艷.無創(chuàng)性胎兒常見染色體非整倍體篩查與結(jié)果分析[J].山東醫(yī)藥,2017,57(20):1-4.
史曉琳,張志濤,劉彩霞.胎兒染色體非整倍體無創(chuàng)基因檢測(cè)在孕早期產(chǎn)前篩查的可行性臨床應(yīng)用研究[J].中國優(yōu)生與遺傳雜志,2014,22(03):44-47.
Cell-free DNA testing in the maternal blood in high-risk pregnancies after first trimester combined screening
Persico N., Boito S., Ischia B., Cordisco A., De Robertis V., Fabietti I., et al.
Prenatal Diagnosis, 2016.
關(guān)鍵詞：游離DNA 孕婦外周血 高風(fēng)險(xiǎn)妊娠
Application of risk score analysis to low?coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13
Tynan J.A., Kim S.K., Mazloom A.R., Zhao C., McLennan G., Tim R., et al.
Prenatal Diagnosis, 2015.
關(guān)鍵詞：全基因組測(cè)序 NIPT 三體綜合征21,18,13
Cell-free DNA analysis for noninvasive examination of trisomy
Norton M.E., Jacobsson B., Swamy G., Laurant L.C., Ranzini A.C., Brar H., et al.
The New England Journal of Medicine, 2015.
關(guān)鍵詞：游離DNA NIPT 三體
Cell-free DNA analysis in maternal plasma in cases of fetal abnormalities detected on ultrasound examination
Benachi A., Letourneau A., Kleinfinger P., Senat M.V.,
Gautier E., Favre R., et al. Obstetrics and Gynecology, 2015.
關(guān)鍵詞：游離DNA 超聲波
Clinical performance of non-invasive prenatal testing (NIPT) using targeted cell-free DNA analysis in maternal plasma with microarrays or next generation sequencing (NGS) is consistent across multiple controlled clinical studies
Stokowski R., Wang E., White K., Batey A., Jacobsson B., Brar H., et al.
Prenatal Diagnosis, 2015.
關(guān)鍵詞：NIPT 靶向游離DNA分析 孕婦外周血 微陣列 NGS 臨床研究
Fetal fraction of cell-free DNA in maternal plasma in the prediction of spontaneous preterm delivery
Quezada M.S., Francisco C., Dumitrascu-Biris D., Nicolaides K.H., Poon L.C.
Ultrasound in Obstetrics & Gynecology, 2015.
關(guān)鍵詞：母體血漿 游離DNA
Fetal sex and RHD genotyping with digital PCR demonstrates greater sensitivity than real-time PCR
Silence K.A., Roberts L.A., Hollands H.J., Thompson H.P., Kiernan M., Madgett T.E., et al.
Clinical Chemistry, 2015.
關(guān)鍵詞：PCR 基因表型 RHD
Noninvasive fetal genotyping of human plaet antigen-1a using targeted massively parallel sequencing
Wienzek-Lischka S., Krautwurst A., Frohner V., Hackstein H., Gattenlohner S., Brauninger A., et al.
Transfusion, 2015.
關(guān)鍵詞：NIPT 基因表型 血小板抗原 靶向測(cè)序
Performance of Momguard, a new non-invasive prenatal testing protocol developed in Korea
Lee M., Cho D., Won H., Hwang A., Jeong B., Kim J., et al. Obstetrics and Gynecology Science, 2015.
關(guān)鍵詞：NIPT
Placental mosaicism for trisomy 13: a challenge in providing the cell-free fetal DNA testing
Liu X.Y., Zhang H.G., Wang R.X., Chen S., Yu X.W., Liu R.Z. Journal of Assisted Reproduction and Genetics, 2014.
關(guān)鍵詞：三體綜合征 游離DNA
Screening for trisomies 21, 18 and 13 by cell-free DNA analysis of maternal blood at 10-11 weeks’ gestation and the combined test at 11-13 weeks
Quezada M.S., Gil M.M., Francisco C., Orosz G., Nicolaides K.H. Ultrasound in Obstetrics & Gynecology, 2015.
關(guān)鍵詞：三體綜合征 游離DNA 孕婦外周血
The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform
Jeon J.Y., Zhou Y., Li Y., Guo Q., Chen J., Quan S., et al. PLoS One, 2014.
關(guān)鍵詞：NIPT 半導(dǎo)體測(cè)序法
Cell-free DNA analysis for trisomy risk assessment in first-trimester twin pregnancies
Gil, M.D., Quezada M.S., Bregant B., Syngelaki A., Nicolaides K.H. Fetal Diagnosis and Therapy, 2014.
關(guān)鍵詞：游離DNA 三體 雙胞胎 風(fēng)險(xiǎn)篩查
Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe
Stumm M., Entezami M., Haug K., Blank C., Wustemann M., Schulze B., et al.
Prenatal Diagnosis, 2014.
關(guān)鍵詞：NIPT 平行測(cè)序
UK NHS pilot study on cell-free DNA testing in screening for fetal trisomies: factors affecting uptake
Gil M.M., Giunta G., Macalli A., Poon L.C., Nicolaides K.H. Ultrasound in Obstetrics & Gynecology, 2014.
關(guān)鍵詞：游離DNA 胎兒三體篩查
Akonni TruTip and Qiagen methods for extraction of fetal circulating DNA-evaluation by real-time and digital PCR
Holmberg R.C., Gindlesperger A., Stokes T., Lopez D., Hyman L., Freed M., et al.
PLoS One, 2013.
關(guān)鍵詞：循環(huán)DNA PCR
Microarray-based cell-free DNA analysis improves noninvasive prenatal testing
Juneau K., Bogard P.E., Huang S., Mohensi M., Wang E.T., Ryvkin P., et al.
Fetal Diagnosis and Therapy, 2014.
關(guān)鍵詞：微陣列 游離DNA NIPT
Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
Fairbrother G., Johnson S., Musci T.J., Song K. Prenatal Diagnosis, 2013.
關(guān)鍵詞：NIPT 游離DNA 三體綜合征
Non-invasive prenatal chromosomal aneuploidy testing – clinical experience: 100,000
clinical samples
McCullough R.M., Almasri E.A., Guan X., Geis J.A., Hicks S.C., Mazloom A.M., et al.
PLoS One, 2014.
關(guān)鍵詞：NIPT 染色體非整倍體檢測(cè) 臨床
Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fractions
Hooks J., Wolfberg A.J., Wang E.T., Struble C.A., Zahn J., Juneau K., et al.
Prenatal Diagnosis, 2014.
關(guān)鍵詞：NIPT 風(fēng)險(xiǎn)評(píng)估 胎兒性染色體非整倍體
Performance of screening for aneuploidies by cell-free DNA analysis of maternal blood in twin pregnancies
Bevilacqua E., Gil M.M, Nicolaides K.H., Ordonez E., Cirigliano V., Dierickx H., et al.
Ultrasound in Obstetrics & Gynecology, 2014.
關(guān)鍵詞： 游離DNA 孕婦外周血 雙胞胎 產(chǎn)前篩查
European non-invasive trisomy evaluation (EU?NITE) study: a multicenter prospective CoHort study for noninvasive fetal trisomy 21 testing
Verweij E.J., Jacobsson B., van Scheltema P.A., de Boer M.A., Hoffer M.J.V., Hollemon D., et al.
Prenatal Diagnosis, 2013.
關(guān)鍵詞：NIPT 三體綜合征21
Gestational age and maternal weight effects on fetal cfDNA in maternal plasma
Wang E., Batey A., Struble C., Musci T., Song K., Oliphant A. Prenatal Diagnosis, 2013.
關(guān)鍵詞：cfDNA
High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma
Jensen T.J., Zwiefelhofer T., Tim R.C., Dzakula Z., Kim S.K., Mazloom A.R., et al.
PLoS One, 2013.
關(guān)鍵詞：高通量測(cè)序 胎兒染色體非整倍體 母體血漿
Implementation of maternal blood cell-free DNA testing in early screening for aneuploidies
Gil M.M., Quezada M.S., Bregant B., Ferraro M.,
Nicolaides K.H.
Ultrasound Obstetrics & Gynecology, 2013.
關(guān)鍵詞：cfDNA 染色體非整倍體 早期篩查
Influence of temperature during transportation on cell-free DNA analysis
Hidestrand M., Stokowski R., Song K., Oliphant A., Deavers J., Goetsch M., et al.
Fetal Diagnosis and Therapy, 2012.
關(guān)鍵詞：溫度影響 cfDNA運(yùn)送
Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples
Futch T., Spinosa J., Bhatt S., de Feo E., Rava R.P., Sehnert A.J. Prenatal Diagnosis, 2013.
關(guān)鍵詞：NIPT（無創(chuàng)產(chǎn)前篩查） 胎兒染色體非整倍體
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
Wang Y., Chen Y., Tian F., Zhang J., Song Z., Wu Y., et al. Clinical Chemistry, 2013.
關(guān)鍵詞：性染色體非整倍體 無創(chuàng)產(chǎn)前檢測(cè) 母體染色體嵌合
Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing
Wong D., Moturi S., Angkachatchai V., Mueller R., DeSantis G., van den Boom D., et al.
Clinical Biochemistry, 2013.
關(guān)鍵詞：血液采集 運(yùn)輸 保存 cfDNA 產(chǎn)前檢測(cè)
SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy
Samango-Sprouse C., Banjevic M., Ryan A., Sigurjonsson S., Zimmermann B., Hill M., et al.
Prenatal Diagnosis, 2013.
關(guān)鍵詞：SNP 無創(chuàng)產(chǎn)前檢測(cè) 性染色體非整倍體
Non-invasive chromosomal evaluation (NICE) study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
Norton M.E., Brar H., Weiss J., Karimi A., Laurent L.C., Caughey A.B., et al.
American Journal of Obstetrics & Gynecology, 2012.
關(guān)鍵詞：無創(chuàng)染色體檢查 三體綜合征21 18
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18
Sparks A.B., Struble C.A., Wang E.T., Song K., Oliphant A. American Journal of Obstetrics & Gynecology, 2012.
關(guān)鍵詞：無創(chuàng)產(chǎn)前檢測(cè) 游離DNA三體綜合征 21,18
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy
Sparks A.B., Wang E.T., Struble C.A., Barrett W., Stokowski R., McBride C., et al.
Prenatal Diagnosis, 2012.
關(guān)鍵詞：cfDNA 胎兒三體綜合征
The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy
Brar H., Wang E., Struble C., Musci T.J., Norton M.E.
The Journal of Maternal-Fetal and Neonatal Medicine, 2012.
關(guān)鍵詞：cfDNA 孕婦外周血 胎兒三體綜合征
Trisomy 13 detection in the first trimeters of pregnancy using a chromosome-selective cell?free DNA analysis method
Ashoor G., Syngelaki A., Wang E., Struble C., Oliphant A., Song K., et al.
Ultrasound in Obstetrics & Gynecology, 2013.
關(guān)鍵詞：三體綜合征13 cfDNA
DNA sequencing of maternal plasma to detect Down Syndrome: an international clinical validation study
Palomaki G.E., Kloza E.M., Lambert-Messerlian G.M., Haddow J.E., Neveux L.M., Ehrich M., et al.
Genetics in Medicine, 2011.
關(guān)鍵詞：DNA測(cè)序 孕婦外周血 唐氏綜合征 臨床
Validation of targeted sequencing of single?nucleotide polymorphisms for non?invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X and Y
Nicolaides K., Syngelaki A., Gil M., Atanasova V., Markova D. Prenatal Diagnosis, 2013.
關(guān)鍵詞：
Implementing prenatal diagnosis based on cell?free fetal DNA: accurate identification of factors affecting fetal DNA yield
Barrett A.N., Zimmermann B.G., Wang D., Holloway A., Chitty L.S. Clinical Chemistry, 2011.
關(guān)鍵詞：產(chǎn)前診斷 胎兒游離DNA
Streck Cell-Free DNA BCT® 血漿游離DNA采血管
產(chǎn)品英文名稱：Streck Cell-Free DNA BCT® BLOOD COLLECTION TUBE
產(chǎn)品中文名稱：Streck BCT® 血漿游離DNA采血管
Streck 血漿游離DNA采血管是一種直接提取的全血收集管，用于收集、運(yùn)輸和儲(chǔ)存血液樣本。Streck 血漿游離DNA采血管內(nèi)含防腐劑，它能穩(wěn)定有核血細(xì)胞，防止細(xì)胞基因組DNA的釋放，保護(hù)血漿游離循環(huán)DNA和循環(huán)腫瘤細(xì)胞（CTC）。
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品牌 | 貨號(hào) | 產(chǎn)品描述 | 包裝 |
Streck | 218962 | Cell-Free DNA BCT® BLOOD COLLECTION TUBE Cell-Free DNA BCT®血漿游離DNA采血管 | 100管/盒 |
Streck | 230253 | Cell-Free DNA BCT® BLOOD COLLECTION TUBE Cell-Free DNA BCT®血漿游離DNA采血管（混合塑料） | 100管/盒 |
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