freepeople性欧美熟妇, 色戒完整版无删减158分钟hd, 无码精品国产vα在线观看DVD, 丰满少妇伦精品无码专区在线观看,艾栗栗与纹身男宾馆3p50分钟,国产AV片在线观看,黑人与美女高潮,18岁女RAPPERDISSSUBS,国产手机在机看影片

正文內(nèi)容

轉(zhuǎn)錄組學(xué)主要技術(shù)及其應(yīng)用研究(參考版)

2025-07-01 06:21本頁面
  

【正文】 31(19):567684.[15] Velculescu V E, Zhang L, Vogelstein B, et al. Serial analysis of gene expression [J]. Science, 1995, 270 (5235):484487.[16] Powell J. Enhanced concatemer cloning—a modification to the SAGE(serial analysis of gene expression)technique [J]. Nucleic Acids Res, 1998, 26: 34453446.[17] Hu M, Polyak K. Serial analysis of gene expression [J]. Nat Protoc, 2006, 1 (4): 17431760.[18] Brenner S, Johnson M, Bridgham J, et al. Gene expression analysis by massively parallel signature sequencing(MPSS) on microbead arrays [J]. Nat Biotechnol, 2000, 18 (6): 630634.[19] 陳杰. 大規(guī)模平行測序技術(shù)(MPSS)研究進(jìn)展 [J]. 生物化學(xué)與生物物理進(jìn)展, 2004, 31 (8): 761765.[20] Haas BJ, Zody MC. Advancing RNASeq analysis. Nat Biotechnol. 2010, 28(5): 421423.[21] Boguski M S, Tolstoshev C M, Bassett Jr D E. Gene discovery in dbEST [J]. Science, 1994, 265 (5181):19931994.[22] Aksoy I A, Wood T C, Weinshilboum R. Human liver estrogen sulfotransferase: identification by cDNA cloning and expression [J]. Biochem Biophys Res Commun, 1994, 200 (3): 16211629.[23] Velculescu V E, Zhang L, Vogelstein B, et al. Serial analysis of gene expression [J]. Science, 1995, 270 (5235):484487.[24] Powell J. Enhanced concatemer cloning—a modification to the SAGE(serial analysis of gene expression)technique [J]. Nucleic Acids Res, 1998, 26: 34453446.[25] Reinartz J, Bruyns E, Lin JZ, et al. Massively parallel signature sequencing (MPSS) as a tool for indepth quantitative gene expression profiling in all organisms [J]. Briefings in functional genomics amp。2003參考文獻(xiàn): [1] Lockhart DJ, Winzeler EA. Genomics, gene expression and DNA arrays. Nature, 2000, 405(6788): 827–836.[2] Velculescu VE, Zhang L, Zhou W, et al : Characterization of the yeast ,88(2):243一251.[3] Wang Z, Gerstein M, Snyder M. RNASeq: a revolutionary tool for transcriptomics [J]. Nat Rev Genet, 2009, 10(1): 5763.[4] Costa V, Angelini C, De Feis I, et al. Uncovering the plexity of transcriptomes with RNASeq [J]. J BiomedBiotechnol, 2010, 2010: 853916.[5] 祁潛, 劉永斌, 榮威樹. 轉(zhuǎn)錄組研究新技術(shù):KNA Se及其應(yīng)用[J]. 遺傳, 2011(10:1191 1202.[6] 李小白, 向林, 羅潔, (RNASeq)策略及其數(shù)據(jù)在分子標(biāo)記開發(fā)上的應(yīng)用[J]. 中國細(xì)胞生物學(xué)學(xué)報(bào). (5):720726.[7] [D]. 北京:北京交通大學(xué)計(jì)算機(jī)與信息技術(shù)學(xué)院,1998.[8] Ma J, Dunean D, Morrow DJ,, Fernandes, et al. Transcriptome profiling of maize anthers using genetic ablation to analyze Premeiotic and tapetal cell types. Plant J, 2007, 50:637一648.[9] Schena M, Shalon D, Heller R, et al. Parallel human genome analysis: microarraybased expression monitoring of 1000 Natl Acad Sci USA, 1996,93(20): 10614~10619.[10] Lipshutz D, Morris D, Chee M,et al. Using oligonucleotide probe arrays to access genetic diversity. BioTechniques, 1995, 19(3): 442~447[11] Lee M, Yang R, Hubbell E,et al. Accessing genetics information with highdensity DNA arrays. Science, 1996,274: 610~613[12] Ramsay G. DNA chips: stateofthe art. Nature Biotechnology,1998,16: 40~44.[13] Nelson N. Microarrays pave the way to 21stcenetury medicine. Journal of the National Cancer Institute, 1996,88(22): 1803~1805].[14] Tan PK,最后,標(biāo)準(zhǔn)的 RNASeq 技術(shù)不能提供序列轉(zhuǎn)錄的方向信息。其二是如何針對更復(fù)雜的轉(zhuǎn)錄組來識(shí)別和追蹤所有基因中罕見 RNA 亞型的表達(dá)變化
點(diǎn)擊復(fù)制文檔內(nèi)容
化學(xué)相關(guān)推薦
文庫吧 www.dybbs8.com
備案圖鄂ICP備17016276號(hào)-1