• 分离病毒所作的基因序列分析表明,这些病毒从基因目前正在巴基斯坦流行的病毒相关。

    Genetic sequencing of the isolated viruses indicates they are genetically-related to viruses currently circulating in Pakistan.

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  • 令人惊奇通过genewise软件对蛋白质基因序列分析对比,低等动物海葵基因组成脊椎动物的非常相似,而昆虫蠕虫的大相径庭。

    The most surprising of these is that, genewise, the humble sea anemone looks a lot like a vertebrate, and not much like an insect or a worm.

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  • 水稻基因序列特征分析水稻基因组成结构规律具有重要意义。

    Featural analysis of rice gene is valuable for understanding the composition and structure features of the rice genome.

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  • 夏春;汪明朱凌云惠阳胡须干扰素基因分子克隆序列分析

    Sekellick MJ; Ferrandino'AF; Hopkins DA Chicken interferon gene: cloning, expression, and analysis.

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  • 方法白血病未知基因片段碱基序列网上多种公共生物信息资源进行比较,分析未知基因结构功能

    Methods Analysis of structure and function of the unknown genes in leukemia cells by compared its base sequence with multiple public bio information resource.

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  • 同源分析表明DNA水平上野桑蚕cyp305 B 1 V 1基因家蚕cyp305 B1基因同源性99%,推导氨基酸序列完全一致

    Homologous analysis showed that the DNA homology of CYP305B1V1 of silkworm and wild silkworm reaches 99%, which is consistent with deduced amino acid sequences.

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  • 研究结果表明这个长度热点突变区的核苷酸序列分析研究小麦山羊草叶绿体基因组之间遗传变异关系一个非常有效的途径

    The results indicate that the sequence analysis of the hotspot region is a very powerful tool to investigate genetic variations of chloroplast genome in Triticum and Aegilops.

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  • 目的分析散发甲状腺RET基因第11子碱基序列明确RET基因突变散发型甲状腺髓样关系

    Objective To explore the mutation of RET gene exon 11 in sporadic medullary thyroid carcinoma and to clarify the relationship between RET mutation and sporadic medullary thyroid carcinomas.

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  • 序列分析表明来自内生真菌BAPT基因片段序列红豆杉BAPT基因片段序列具有非常相似性(98.9%)。

    Sequence analysis showed high similarity (up to 98.9%) between fungal BAPT gene fragments and the counterparts from their yew hosts.

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  • 该文以DNA PCR扩增方法拟南基因DNA中克隆NPR1基因通过序列分析,所克隆NPR1 基因报道的基因序列完全一致。

    The NPR1 gene was amplified from Arabidopsis thaliana genome DNA by DNA-PCR method. The DNA sequenced analysis showed that the sequence of amplified NPR1 gene was the same as the published sequence.

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  • 方法采用基因克隆测序生物信息学技术分析HLA等位基因HLA已知基因序列差异

    Methods Molecular cloning, sequencing and bioinformatics techniques were used to identify the difference between the new HLA allele and other known alleles.

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  • 经d NA序列分析表明基因含有全部前导序列成熟蛋白编码部分从第一骨架引物所克隆的序列相符。

    DNA sequences analysis indicated that the cloned genes included the whole leader sequences and the mature Ig protein encoding regions.

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  • 这一结果提示水稻作为禾本科植物模式物种,类植物存在良好的基因共线性关系,水稻基因序列信息类植物基因研究分析具有重要参考价值

    The results suggested that rice, as model plant for Poaceae, should have significant genomic synteny with bamboos, and its genomic sequences are important resource for bamboo genome research.

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  • 结果序列分析结果表明小管ASBT基因序列小肠ASBT序列完全一致。

    RESULTS:The results revealed that the sequence of kidney ASBT cDNA gene was identical to that of human intestine ASBT gene.

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  • BLAST分析表明其中19EST序列已知功能基因序列同源性很高,分别植物的防卫反应、胁迫反应细胞解毒信号转导等

    BLAST analysis revealed that 19 ESTs had high homology with known genes in GenBank involved in defense response, stress reaction, disease defense detoxification and signal transduction.

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  • 水稻基因序列特征分析解水稻基因的组成结构规律具有重要意义。

    Most of the rice genome was anchored genetically by overgo hybridization, DNA gel blot .

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  • 因此选择对基因表达具有重要功能1其上游的调控区及下游外显子内含子交界序列通过直接测序法进行SNP筛查,进一步分析多态位点病窦的关联性

    Therefore the other aim of our study is to discover SNPs of HCN4 exon 1, including the regulatory sequence and exon-intron boundary of it, which plays an importable role of channel function.

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  • 通过互联网对测序获得核苷酸序列进行同源性分析预测新基因编码蛋白质结构功能。

    The positive clones were sequenced and the sequence data were analyzed using Nucleotide BLAST software of NCBI and Expert Protein Analysis System of Swiss Institute of Bioinformatics.

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  • 利用序列分析技术克隆抗逆相关基因,并通过原核表达体系基因技术进行功能验证。

    The function of gene has been identified using Prokaryotic expression system and Arabidopsis thaliana (A. thaliana) transformation systems. The study has got following results:1.

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  • 利用序列分析技术克隆抗逆相关基因,并通过原核表达体系基因技术进行功能验证。

    The function of gene has been identified using Prokaryotic expression system and Arabidopsis thaliana (A. thaliana) transformation systems. The study has got following results:1.

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