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   blast软件 的翻译结果: 查询用时:0.014秒
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blast软件
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  blast software
     is AF399873.Using blast software(NCBI),we found Fang-1is rat homologue of human AK001644.They share82%identical nucleotides,indicating the family proteins are very conserved.
     Blast软件(NCBI)分析显示Fang-1是人类基因AK001644在大鼠中的同源物,其编码区核苷酸同源性为82%,表明该家族蛋白具有保守性。
短句来源
     The sequencing result showed that the nucleotide acid sequences of RT-PCR products were the same as that of transgene analyzed by BLAST software.
     将RT-PCR产物测序后,用BLAST软件分析序列可知,该序列为细菌几丁质酶基因核苷酸序列而不是植物几丁质酶基因的核苷酸序列。
短句来源
     The analysis of BLAST software suggested thatσB gene had 88.1% identity compared to DRV 89026 France strain, amino acid sequence had 94.0% identity;
     核苷酸序列经BLAST软件分析表明:番鸭呼肠孤病毒MW9710株σB基因与番鸭呼肠孤病毒法国89026株同源性为88.1%;
短句来源
     With blast software we found Fang-1 has homolog (GenBank Accession NO. AK001644) in human, whose function keeps unclear.
     Blast软件分析后发现Fang—1在人类有同源基因,GenBank收录号为AK001644,但是该基因功能目前未知。
短句来源
     DNA sequencing determination results showed that the fragment length was 788bp. Sequence analysis with Blast software indicated that the deduced amino acid sequence was 64% of homology with the amino acid sequence of phytase gene phy(GenBank Accession:CAC48160) from Agrocybe pediades.
     DNA序列测定结果表明,该片段长度为788bp,采用Blast软件进行序列比对发现,该片段与平田头菇(Agrocybe pediades)的植酸酶基因phy(GenBankAccession:CAC48160)编码的氨基酸具有64%的序列同源性。
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  “blast软件”译为未确定词的双语例句
     It's HBV-DNA C region sequence had mutation on 2 sites (nt 2412 T/C; nt 2413 T/C)and 1 mutation P region (nt 741 A/G, also YMDD/YVDD) compared with HBV international Genbak reference sequence.
     对 1例 HBV- DNA在 10 7copies/ ml级标本进行 HBVDNA C区和 P区序列测定 ,用 BL AST软件与国际基因库对比 ,结果 ,C区 nt 2 4 12位 T→ C,nt 2 4 13位 T→ C,P区 nt 74 1位A→ G(YMDD→ YVDD)。
短句来源
     Conclusion:Oligonucleotide probes can be designed with BLAST program and Array Designer4.2 software,and become a foundation for depositing on gene chips as the basis of the microarray for Influenza Virus A detection.
     结论:利用BLAST软件和生物学软件Array Designer4.2设计流感病毒A诊断芯片的探针,可为后期打印成基因芯片,用于流感病毒A的检测打下基础。
短句来源
     Five rice back clones containing CHASE domains were obtained by Blast using Cre1a gene of Arabidopsis in NCBI,named OsCRL1a,OsCRL1b,OsCRL2,OsCRL3 and OsCRL4 respectively.
     将已知的拟南芥细胞分裂素受体Cre1a序列的保守区输入Blast软件,得到5个与拟南芥Cre1基因具有同源性的基因,即Os-CRL1a、OsCRL1b、OsCRL2、OsCRL3和OsCRL4。
短句来源
     Methods The genomic DNA of 22 WD patients was extracted and exons 5,8,12,13 were amplified by PCR. Screening for the mutations was done by direct sequencing and analysed by BLAST.
     方法提取22例WD患者外周血基因组DNA,聚合酶链反应(PCR)扩增ATP7B基因第5、8、12及13号外显子并进行DNA直接测序检测,应用在线BLAST软件分析。
短句来源
     The PCR products of vip3A,hblA,bceT and entS were purified and directly sequenced, and were compared with the known genes by BLAST on-line Software. Analysis results indicated that the sequence of vip3A ,hblA and bceT gene was 99% , 96%~98% and 97% homologous with the known genes of Bt or Bc, respectively.
     不含编码几丁质酶的基因 . 将vip3A、hblA、bceT和entS基因PCR产物回收纯化后直接测序 ,经在线的BLAST软件进行同源性分析 ,前两个基因片段与Bt已公布基因序列的相应片段同源性分别为 99%和 96 %~ 98% ,bceT基因片段与蜡质芽孢杆菌bceT相应片段同源性为 97% .
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  相似匹配句对
     Software & Tools
     软件
短句来源
     Software
     软件
短句来源
     GoBlast Is a Standalone Package That Integrates BLAST Search and GO Annotation
     整合BLAST搜索与GO注释的软件GoBlast
短句来源
     The bioinformatics analysis was performed with BioEdit,BLAST and EGAD.
     使用BioEdit、BLAST和EGAD等软件进行生物信息学分析。
短句来源
     Sub-Optimal Detection Algorithm of V-BLAST
     V-BLAST的次优译码
短句来源
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  blast software
Furthermore, these primers were compared with GenBank by using BLAST software and no similar sequences could be found.
      
Nevertheless, no conclusive homology with CaCV either was established using the Blast software.
      
The BLAST software package even provides a clustering program, called blastclust.
      
Then, the sequences were introduced into the BLAST software to search for homologous sequences in the database.
      
We have fed the sequence data on the Internet and analyzed them using nucleotide blast software of NCBI.
      
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We designed a experiment to obtain porcine GRF cDNA. Total RNA and mRNA were extracted from porcine hypotheiemus. Primers were designed according to publised porcine GRF cDNA sequence. RT-PCR was carried out to the standard method. PCRproduct was cloned to T-vector. Positive clone was selected and sequenced. The result showed that the cloned cDNA was not GRF gene. We anylyzed the sequence in Internet by Blast, finding no similar.

用根据GRF设计的引物,以猪的下丘脑总RNA和mRNA为模板、进行RT—PCR扩增.将扩增产物纯化并克隆到T载体(pGEM3—Zf),自动测序仪测定其序列.发现所克隆的基因并非GRF基因.应用BLAST软件对其在INTERNET作了分析,未能确定为何种基因.

The orchid

运用现代分子技术对分离于韩国果园中的共生真菌进行了鉴定,经显微观察及PCR-RAPD分析可将收集菌株分为不同组群。不同植物、不同真菌的共生反应类型不同,所有采集的真菌分离株均能刺激果树根的生长,有时甚至能刺激兰属温带果树茎干的生长。5种真菌的18srDNA序列经BLAST软件分析,证明它们分属于3个组,其中有2个种:葡萄丝粒菌及内生丝核菌可以确定,基于18srDNA树状分枝图与植物反应类型的不同相一致,但与PCR-RAPD多态性分析结果不同,韩国当地春兰分离株与严重的土传病害丝核菌及镰刀菌不同,这种不同可通过不同引物的PCR-RAPD技术进行鉴别。

Objective \ To investigated molecular events associated with the dysfunction of

目的为了研究自发性高血压大鼠(SHR)胸腺功能异常的分子机制,我们用cDNA代表性差异分析cDNArepresen-tationaldiferenceanalysis(RDA)技术比较了SHR与其正常血压对照(WKY)大鼠二者胸腺基因表达的差异。方法用cDNA代表性差异分析技术比较了SHR和WKY大鼠胸腺基因表达的差异。差异表达的cDNA接入T—载体进一步进行差异筛选。挑选阳性克隆进行测序并用BLAST软件进行同源性分析。最后用Northern杂交分析验证差异筛选的结果。结果挑选了4个差异筛选的阳性克隆进行测序,序列同源性分析表明它们均与胰岛素-I基因序列高度一致。Northern杂交结果证实了胰岛素-I基因在SHR胸腺中表达降低。结论运用cDNA代表性差异分析技术,结合差异筛选方法,本文观察到SHR胸腺中胰岛素-I基因表达降低,提示局部微环境中的胰岛素缺乏在SHR胸腺细胞的发育异常中可能起一定的作用。

 
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