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This is because that the structure of DNA sequences is difficult to be analyzed and recognized.

这是因为DNA序列的结构很难分析和识别。

Note that Unicode strings do not serve double duty as sequences of bytes.

注意,Unicode并不是提供了双重标准的字节序列。

In chapter five, let {Xt,i 1} be ρ-mixing sequences with identical distributions, which belong to domain of normal attraction with non-generational and stable distribution. With probability one, we have limsup a.s.

第五章,设{X_n,n≥1}是同分布ρ-混合序列,其分布属于特征指数为α(0<α<2)的非退化稳定分布的正则吸引场,证明了依概率1有

In chapter five, let {Xt,i 1} be ρ-mixing sequences with identical distributions, which belong to domain of normal attraction with non-generational and stable distribution. With probability one, we havelimsup a.s.

第五章,设{X_n,n≥1}是同分布ρ-混合序列,其分布属于特征指数为α(0<α<2)的非退化稳定分布的正则吸引场,证明了依概率1有

According to the gallus colony stimulating factor(colony-stimulating factor,CSF)cDNA sequences published by GenBank,a pairs of specific primer was designed,the local dorking was injected 100 μg/mL ConA,total RNA was extracted from feeding 24 hours lymphocyte from spleen,then dorking colony stimulating factorcDNA fragment was cloned by RT-PCR technology.

根据GenBank中报道的红原锦鸡集落刺激因子(Colony-stimulatingfactor,CSF)cDNA序列,利用Primer Premier5.0软件设计一对特异性引物,对本地肉鸡注射100μg/mL ConA试剂,饲养24 h后,取脾脏提取淋巴细胞总RNA,利用RT-PCR技术克隆集落刺激因子的cDNA片段。

According to the gallus colony stimulating factor (colony-stimulating factor, CSF) cDNA sequences published by GenBank, a pairs of specific primer was designed, the local dorking was injected 100 μg/mL ConA, total RNA was extracted from feeding 24 hours lymphocyte from spleen, then dorking colony stimulating factor cDNA fragment was cloned by RT-PCR technology.

根据GenBank中报道的红原锦鸡集落刺激因子(Colony-stimulatingfactor, CSF)cDNA序列,利用Primer Premier5.0软件设计一对特异性引物,对本地肉鸡注射100μg/mL ConA试剂,饲养24 h后,取脾脏提取淋巴细胞总RNA,利用RT-PCR技术克隆集落刺激因子的cDNA片段。

This text is mainly about the analysis of the palindromes of Y chromosome. We mainly used DOTTER program for detailed comparison of two sequences to obtain these results. The main contents are as follows:Chapter one mainly introduces the whole characteristics of human Y chromosome;Chapter two mainly describes the characteristics, functions and recombination modes of the palindromes in Y chromosome;Chapter three mainly analyses the symmetries of 8 palindromes of Y chromosome, we find a mechanism of symmetry breaking in P2 palindrome from a detailed analysis;initially introduces other 7 palindromes.

本文主要借助于DOTTER程序对Y染色体的回文序列进行分析,主要内容如下:第一章主要介绍人类Y染色体的整体特征;第二章主要描述Y染色体中回文序列的特征、功能及重组模式;第三章主要是对Y染色体8个回文序列的对称性分析,主要对P2回文进行了详细分析,提出了P2回文的对称性发生破缺的机理;对其他7个回文进行了初步分析。

This text is mainly about the analysis of the palindromes of Y chromosome. We mainly used DOTTER program for detailed comparison of two sequences to obtain these results. The main contents are as follows:Chapter one mainly introduces the whole characteristics of human Y chromosome;Chapter two mainly describes the characteristics, functions andrecombination modes of the palindromes in Y chromosome;Chapter three mainly analyses the symmetries of 8 palindromes of Y chromosome, we find a mechanism of symmetry breaking in P2 palindrome from a detailed analysis;initially introduces other 7 palindromes.

本文主要借助于DOTTER程序对Y染色体的回文序列进行分析,主要内容如下:第一章主要介绍人类Y染色体的整体特征;第二章主要描述Y染色体中回文序列的特征、功能及重组模式;第三章主要是对Y染色体8个回文序列的对称性分析,主要对P2回文进行了详细分析,提出了P2回文的对称性发生破缺的机理;对其他7个回文进行了初步分析。

Comparing the results of various sequences of double label should that the sequence of choice is PAP→ABC-HRP in double immunoperoxidase stain and PAP→ABC-AP and ABC-HRP→ ABC-AP in double immunoenzymatic stain.

通过比较酸洗脱法、氧化法、PBS直接漂洗法对胰岛细胞双重免疫组化染色的影响,发现三种对一染抗体的处理方法无显著的差异。

Therefore, the previous general view of the point that the centromere-related sequences have no key functions is doubtable according our results.

因此,对端粒相关序列没有重要功能的观点提出了质疑。

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