子序列 的英文怎麼說

中文拼音 [ziliè]
子序列 英文
subsequence
  • : 子Ⅰ名詞1 (兒子) son 2 (人的通稱) person 3 (古代特指有學問的男人) ancient title of respect f...
  • : Ⅰ動1 (排列) arrange; form a line; line up 2 (安排到某類事物之中) list; enter in a list Ⅱ名詞1...
  1. 2 the experimental principle and method of beam - foil spectroscopy are presented, and the application of the isoelectronic sequence in the analyses of spectra is described, cowan program for the theoretical calculations is introduced

    2介紹了束箔光譜學的實驗原理和方法,說明了等電子序列及其在譜線識別中的應用,介紹了用於理論計算的cowan程
  2. 4 the spectrum of highly ionized cu and ge was investigated by means of the beam - foil technique. by comparison with other experimental data we determined 42 energy levels of cu and 13 energy levels of ge. for the spectrum without experimental data for comparison, they are determined by isoelectronic sequence

    摘要4我們採用束箔光譜方法測量高離化態cu和ge束的光譜線,與文獻中的實驗數據相對照,確定了42條cu的譜線和13條ge的譜線,對于無實驗值可對照的譜線,利用理論值和實驗值進行等電子序列證明。
  3. To test the p7 promoter activity, a series of constructs were obtained by cloning the different dna fragments into the luciferase gene reporter vector pgl3 - b. when the constructs were transiently transfected into thp - 1 cells, luciferase activity assay showed that the core region of p7 promoter located at - - 165 bp

    第一部分的工作首先通過對人acat - 1基因p7啟動子序列進行5 '和3 ' -端的缺失的詳細分析,結果顯示最大報告基因轉錄表達活性位於- 612 - 165bp區段。
  4. 4 the pattern - based similar subsequence search method is presented

    提出了基於模式的子序列查詢方法。
  5. Longest increasing subsequence

    最長的遞增子序列
  6. The first is to prove the slln for a subsequence of sn / bn then reduce the problem for the whole sequence to that of the subsequence

    )的某個子序列服從強大數定律,再把這個結論推廣到整個上(如子序列方法) 。
  7. Then, the thesis proposed a novel pair - wise sequence global alignment method safss, which is based on the frequent subsequence

    然後提出一種基於頻繁子序列safss ( sequencealignmentbasedfrequentsub - sequences )的比對方法。
  8. Microcalorimetric study on deletion mutagenesis of the gene promoter sequences from the extremely halophilic archaea

    極端嗜鹽古生菌啟動子序列缺失突變的微量熱研究
  9. The c - phycocyanin ( cpc ) operon of blue - green alga ( or cyanobacteria ) arthrospira platensis fachb341 was cloned, sequenced and characterized by using chromoseme walking method. the sequence includes cpcb gene ( 519 bp ), cpca gene ( 489 bp ), cpch gene ( 357 bp ), and upstream sequence of cpcb ( 427 bp ) and upstream sequence of cpch genes ( 184 bp ), 111 bp of phycocyanin intergenetic spacer ( pc - igs ). upstream sequence of cpcb gene was ligated into promoter - probe vector pegfp - 1 and transformed into three systems : e. coli, synechocystis pcc 6803 and a. platensis fachb341 by supersonic and electrophoresis methods

    根據genbank中報道的節旋藻藻藍蛋白基因設計引物,首先克隆了鈍頂節旋藻( arthrospiraplatensisfachb341 )藻藍蛋白操縱中亞基基因、亞基基因部分及二者之間的間隔區( pc - igs )並進行測定,然後根據此測結果設計引物,通過染色體步移法克隆得到藻藍蛋白操縱長度為2086bp的基因片段,其中包括藻藍蛋白亞基基因( cpcb , 519bp ) ,亞基基因( cpca , 489bp ) ,連接蛋白h基因( cpch , 357bp ) ,亞基基因上游啟動子序列( 427bp )以及各基因之間的間隔區( pc - igs , 111bp ; cpch與cpca間隔區, 184bp ) 。
  10. Based on cdna sequences of ( 3 - carotene ketolase ( cr / ff ) and p - carotene hydroxylase ( c / - fz ), a 1. 6 kb crtw genomic sequence with six introns, and a 3kb crtz genomic sequence with five introns were clone, respectively. all the exon - intron junctions conform closely to gu - ag consensus splicing rule

    本論文工作成功地克隆兩個關鍵酶基因的基因組,發現crtw和crtz分別包括6個和5個內含子序列,所有這11個內含的剪切位點都符合gu - ag規律。
  11. If the converged ritz value is unwanted then it must be removed from the subsequent of block lanczos factorizations. this is called purging

    如果所得到收斂的ritz值是不想要的,則把它從塊lanczos因分解的子序列中除去,即所謂清除。
  12. If the converged ritz values is wanted, it is necessary to keep it in the subsequent of block lanczos factorizations. this is called locking

    如果在迭代過程中所得到收斂的ritz值是想要的,則把它保存在塊lanczos因分解的子序列中,即所謂鎖定。
  13. Besides, vgb gene expression also increased the chitinase secretion. in order to make the vitreoscilla hemoglobin gene express in bacillus subtilis, an inducible promoter ( levansucrase ) was cloned from b. subtilis wb600 and ligated with a promoter - less vgb gene. the resulted gene is called sacvgb and was demonstrated to express in e, coli by sds - page and carbon monoxide binding assay

    由於vgb基因啟動不能在枯草桿菌中啟動表達,因此,根據已發表的果聚糖蔗糖酶基因( sacb )設計引物,從枯草桿菌wb600總dna中擴增出該基因的啟動片段,然後將其與vgb基因編碼區及終止子序列相連,成功地組建了sacvgb融合基因。
  14. Relativistic screening theory for ground configuration energies of b - like ions

    等電子序列基組態能量的相對論屏蔽理論計算
  15. According to the numbers of segmentations, dts has multi scale feature and can reflect different trend similarity of time series under various analyzing frequency. 2 ) an enhanced algorithm, based on dual threshold value, and the conception of sub - series linear are proposed. relative point average error is used to measure the linear degree of sub series, which produced by bottom _ up algorithm

    對應時間線性分段數目的不同,趨勢距離具有基於時間的多尺度分析特性,可以有效反應不同分析頻率下時間的相似程度; 2 )採用相對點平均殘差衡量bottom _ up演算法劃分的子序列線性度,提齣子序列線性度概念和一種雙誤差閥值改進演算法,大大提高了趨勢模型的準確性。
  16. Given a query sequence, the sub - sequences are looked up in the index to reduce the amount of time and searching involved

    給定一個被查詢,將根據索引來查詢子序列,從而減少查詢次數和時間。
  17. General method of similar sequence mining based on time series is to transform time series into discrete character series and cluster them into different sets, then compute the euclidean distance between querying series and these sets to measure their similarity

    摘要時間數據庫中相似子序列的搜索,常用滑動窗口、分形插值逼近等方法將時間分割成各子序列,線性擬合各分段子序列,計算查詢與各子序列的歐氏距離,滿足距離閾值條件的為相似子序列
  18. The phylogenetic tree of the potassium channel gene suggests that muntiacus crinifrons is original, and the basal split separates muntiacus and elaphodus. within the genus muntiacus, crinifrons is more closely related to muntjak, with reevesi as its sister species. in the other genus there is only one species elaphodus cephalophus

    根據鉀離通道蛋白基因的第4內含和第5外顯子序列構建的進化樹顯示:黑麂比較原始,首先與赤麂聚合,再與小麂聚合,最後與毛冠鹿屬的毛冠鹿聚合。
  19. A new e. coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1, bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed. 2, a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter. 3, another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19

    進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因,構建了大腸桿菌啟動探針載體phn1005 ,該載體上gfpmut3結構基因5 』端的bamhi位點可用來克隆具有啟動活性的dna片段並定量分析插入的啟動強度;其3 』端含rrnat1t2終止,可允許克隆強啟動;在bamhi上游同樣插入rrnat1t2終止以防止載體puc19上的啟動的轉錄通讀; gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止,可保證gfpmut3以正確的讀碼框翻譯。
  20. Objective to study the collapse of biomolecules, focusing on the effect of the composition of chain, temperature and stiffness on the chains self - assembly

    摘要目的研究生物分鏈的自組織坍塌過程;探討分子序列的組分、溫度和鏈的柔性對生物分自組織過程的影響。
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