分組序列 的英文怎麼說
中文拼音 [fēnzǔxùliè]
分組序列
英文
packet sequence-
The complete nucleotide sequence of the mitochondrial genome of f. limnocharis was detailedly compared with those of 5 other amphibians. the nucleotide sequences of 22 trna encoded by 6 amphibians mitochondrial genomes were combined and aligned to the homologous sequences of the 11 veterbrate taxa. using teleosts as outgroup, the phylogenetic analyses results show that mp, nj and ml trees all strongly support the monophyly of living amphibians with respect to other living tetrapods and favor a sister group relationship for caecilians and salamanders
我們在測定了澤蛙線粒體全基因組序列的基礎上，與已知其它的5種兩棲類進行詳細的比較分析，同時選擇了11種高等脊椎動物的線粒體全基因序列，以硬骨魚類做外群，用22個trna基因合併數據進行系統發生重建分析，結果表明mp 、 nj和ml樹都強力地支持現生兩棲類動物為單系群並且蠑螈類和蚓螈類為姐妹群關系（自引導值分別為92 、 99 、 100 ） 。In the present study, ghr that was similar to the conventional ghrs was termed as ghr1, and another type was termed as ghr2. meanwhile, using the same methods, zfghrl and zfghr2 were also isolated from zebra fish ( danio rerio ) est and htg genome sequences
同時，我們用相似的方法從斑馬魚的est序列和其高通量（ htg ）基因組序列分離出斑馬魚zfghr1和zfghr2 。Complete genome sequence of shigella flexneri 2a 301 strain and analysis of
痢疾桿菌全基因組序列及基因組島的分析Restriction enzymes and dna probes are used to determine the exact sequence, but it is possible to get a rough estimate by analyzing the frequency of recombination between the alleles of linked genes
雖然可以利用限制性內切酶和dna探針精確的分析出特定序列，但是在分析連鎖基因等位基因間的重組序列時，會出現不準確的估計。Saccharomyces cerevisiae ( s. cerevisiae ) is the one ot the first and well characterized eukaryotic organisms whose complete genome was sequenced. the next chanllenge is to elucidate its gene expression pattern and the functional mechanisms of the gene products
在所有的真核生物中，人們對釀酒酵母（ saccharomycescerevisiae ）分子遺傳學方面的認識最早，最先完成的真核生物基因組序列測定也是釀酒酵母的基因組序列。Three chloroplast transformation vectors including pds16s - cat, ptn1269 - bar and psp72 - n5 - bar - n3 were constructed, using ! 6s rrna or chln gene sequence as a homologous segment and cat or bar as a selective marker gene, respectively. foreign genes were introduced to the cells of d. salina by microprojectile bombardment method and a pilot chloroplast tran
3 .杜氏鹽藻葉綠體165出na基因的克隆和轉化載體的構建根據杜氏鹽藻的近緣藻類的葉綠體基因組序列資料，克隆了杜氏鹽藻葉綠體16srrna基因部分序列1100bp ，並利用克隆的16srrna鄭州大學2003年博士學位論文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序列，發現crtw和crtz分別包括6個和5個內含子序列，所有這11個內含子的剪切位點都符合gu - ag規律。We discuss the theory and technology of coding and cryptology in the study of information security and information reliability in the disseration. some valuable theoretic results are presented, most of these results are published on the important journey of china, parts of these results are used in some application system. in the design and analysis of error - correcting codes, we obtain the following results
本文探討了信息安全和信息可靠性研究中的編碼密碼理論與技術，在糾錯碼的設計與分析、序列密碼的設計與分析以及分組密碼的設計與分析等方面，得到了一些有價值的理論結果，大多數結果已在國內核心刊物上發表，有些結果已用於實際的應用系統。The biologic toxins produced by bacteria and virus have important effects to organic metabolism and reproduction. the study on bacterial toxin at molecular level, especially, on complete nucleotide sequence determination of pathogenic micro - organism has make it possible to comprehend pathogenic micro - organism pathogenesis and its rule. recently complete nucleotide sequences of near ten bacteria have been examined
細菌、病毒等所產生的生物性毒物對機體的代謝、繁殖機能有著重要的影響，目前對細菌毒素的研究比較透徹，已經上升到分子水平，特別是通過病原微生物全基因組序列的測定，使人們從更高層次上把握病原微生物的致病機理及其規律成為可能。The tuple supported accessing elements in the sequence using index notation, chopping out elements from the sequence using slices, and creating new tuples using a specific slice or by adding together different slices
Tuple通過以下方式支持訪問序列中的元素：使用索引符號，使用片段分離序列中的元素，以及使用特定的片段或將不同的片段添加在一起來創建新的元組。Basing on the analysis of above two algorithms, we propose a new algorithm, rp - all - pairs, which uses a method of randomized project to find ungapped local alignments in genomic sequence with up to a specified fraction of substitutions
在分析以上兩種方法的基礎上，本文提出了一種新的演算法： rp - all - pairs演算法。該演算法通過隨機投影發現基因組序列中含有特定部分的替換的無間隔局部對齊。Positive probe was made from the floral meristem materials cultured for 5 days and 10 days with hormones by rna reverse transcription and labelling with radioactive dctp ; two negative probes from uncultured explants and it cultured for 5 days and 10 days. then, we did calculating signal arrays, sequencing, sequence analysis and alignments on genebank etc. finally 229 different ests were got from the cdna library
用在含有外源激素的培養基上培養5天（花分生組織開始形成）和10天（花分生組織已基本形成）的風信子外植體為材料，構建起cdna文庫。利用cdnamicroarrray技術，經過雜交篩選和est分析序列分析，最終從cdna文庫中獲得了229個不同的外源激素誘導響應的基因序列。Then, 5. 5kb thrombiotin gene was amplified with the same technique from the genome of a baby ' s blood, which included the begining part of intronl to the teminator. in addition, 6. 0kb and 1. 8kb homlogous arms were also amplified from a cow with high yield. the 6. 0kb homologous arm contains the promotor, extron 1, extron2, extron3 and intron 1, intron2 and part of the intron3 fragment, while the 1. 8kb homologous right arms contains exon13, exon14 and part of intron 13, the whole intron14 and part intron 14 of asl - casein gene of bovine
通過長片段pcr從高產奶牛的基因組中獲得了打靶所需的長、短同源臂序列，長度分別為6 . 0kb和1 . 8kb ，位於s1 -酪蛋白基因的5上游區到第三內含子和十二到十四內含子；從綿羊全血基因組克隆得到了綿羊的-酪蛋白基因啟動子區到第二內含子區4 . 1kb的5調控序列；利用同對引物克隆得到了水牛的同基因序列；從廣西當地一嬰兒臍血基因組中通過獲得了人血小板生成素基因，位於第1內含子到終止子後部分的序列，長達5 . 5kb 。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子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子自組織過程的影響。In order to form a chloroplast transformation system of d. salina, we have conducted some studies including its sensitivity to antibiotics, the activity of promoter, cloning of the chloroplast genes and construction of transformation vectors, so far a pilot transformation system of the d. salina chloroplast has been completed. methods : the sensitivity of d. salina to seven antibiotics or herbicide used commonly in gene engineering was studied and the biological activity of atpa promoter from c. reinhardtii chloroplast was tested by using enhanced green fluorescent protein ( egfp ) as a reporter. primers were designed in the conservative encoding regions according to the chloroplast genomes from four algae which have close genetic relationship with d. salina, and the sequences of 16s rrna, chll and chln of d. salina chloroplast were cloned and sequenced, respectively
方法:根據杜氏鹽藻的近緣藻類的葉綠體基因組序列資料，在基因編碼區的高度保守區域設計引物，克隆了杜氏鹽藻葉綠體165識na基因、咖l基因和ch n基因，並分別以165識na基因和chln基因序列為同源片段，以cat和bar基因為篩選標記基因構建了三套杜氏鹽藻葉綠體轉化載體: 2鄭州大學2003年博士學位論文杜氏鹽藻（ d ~ iiellasalina ）葉綠體轉化研究pds165一eaf 、 ptn1269一bar和psp72一5一bar一3 ，用基因槍法轉化杜氏鹽藻，初步建立起杜氏鹽藻葉綠體轉化體系。The hemaglutinin ( ha ) of aiv plays the key role in determing the pathogenicity, cell receptor binding property and host range of the virus. the homology of the ha sequences reported and registered in genbank of different strains of h _ ( 5 ). h _ ( 9 ) subtype was respectively analyzed and compared with each other. the conservative domin of ha seqence of h _ ( 5 ), h _ ( 9 ) subtype was selected for pcr amplification. two sets of specific primers were designed
本研究根據genbank中查出的禽流感病毒h _ 5亞型，禽流感病毒h _ 9亞型的ha片段基因組序列，利用dnasis軟體分別對aiv的h _ 5 、 h _ 9亞型ha基因區域進行同源性比較，設計篩選出兩對聯合pcr反應的特異性引物，其中一對是h _ 9亞型通用引物，擴增出ha片段695bp ，另一對引物為h _ 5亞型的通用引物，擴增出的ha區域部分目的片段約為448bp 。Using the monoclonal antibody to rev and the anti - sera against the rev env gp90 - gst fusion protein. the molecular cloned virus was detected by ifa. we also amplified the gp90 from the cells infected with the molecular cloned virus by polymerase chain reaction. all these results indicated the recombinant plasmid containing the total rev genome cdna is infectious
對snv株前病毒全基因組cdna克隆進行酶切，將酶切產物分別克隆進puc18中，分別將各個亞克隆進行測序，按照酶切位點和已知的部分序列以及rev物理圖譜將測得的序列進行拼接，完成了rev全基因組序列。The heart of versa is the traversal expression which matches patterns in the model s graph
迄今為止，問題跟蹤器的示例是由一組xml文件組成的，這些文件是rdf模型各部分的序列化。According to the published nucleotide sequences of genome of classical swine fever virus ( csfv ) strains shimen, hclv and paderborn, 11 pairs of specific primers were designed and synthesized, eleven fragments had been successfully amplified from csfv gxwz02 strain by rt - pcr. these amplified fragments were cloned into pgem - t or pmd18 - t and sequenced
根據已發表的豬瘟病毒（ classicalswinefevervirus ， csfv ） shimen株、 hclv株和paderborn株的全基因組序列，設計併合成11對引物，應用rt - pcr技術，成功地分11個片段擴增了csfv廣西流行毒株gxwz02的全基因組，並將這11個基因片段克隆到pgem - t和pmd18 - t載體上，測定其核苷酸序列。A new method for the splicing - site recognition of rice dna sequences was designed. based on the gt - ag intron organization principal, support vector machines ( svm ) was used to predict the splicing sites. through machine learning, a model was built on some test data set of true and pseudo splicing sites
根據真核生物內含子在剪切位點前後存在保守堿基的特徵，用支持向量機技術構建分類器模型，有效地在基因組序列中識別剪接位點， 3位點識別的準確度87 . 96 ，在5位點識別的準確度達85 . 41 。分享友人