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There was also not any haploid metaphases (n=16 or 19) was detected in hybrids. However, about 1-2% metaphases observed in this study was allopolyploid. GISH proved that they was made up of haploid genomes of M. nobilis (n=16) and triploid genomes of C. farreri (n=57). GISH was also employed to detect different chromosome components and identify donor chromatin in hybrids between C. farreri♀×A.

但我们检测到了约1-2%异源多倍体的分裂相,GISH分析后发现这些分裂相是由单倍的华贵栉孔扇贝的染色体和多倍的栉孔扇贝染色体组成,比如论文中图示了一个异源四倍体的分裂相,它是由单倍的华贵栉孔扇贝的染色体(n=16)和三倍的栉孔扇贝染色体(3n=57)组成。

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。

The analysis of genetic diversity between different chromosomes showed that the polymorphic loci distribution of Chr.6,Chr.9 and Chr.11 was evener and the polymorphism information content was also more than others chromosomes.

不同染色体间的遗传多样性分析结果表明,Chr.6、Chr.9、Chr.11三条染色体的多态性位点分布较均匀且多态性信息含量也较多,整体遗传多样性丰富程度高于其他染色体。

They are often morphologically distinct from A chromosomes, being smallerand more highly heterochromatic in most cases. B chromosomes do not pair with Achromosomes, and they are inherited in a non-Mendelian way, exhibiting meiotic andmitotic instability and nondisjunction. However, B chromosome DNA is quiteidentical to the corresponding sequence on the A chromosome complement. So far afew B chromosome specific DNA sequence have been identified. Specific DNAsequences on B chromosome have been the attractive research area on Bchromosomes.

现已在千余种植物和近三百种动物中被发现。B染色体与物种中正常染色体不同:独立于整倍体基因组之外,减数分裂时不与A染色体发生联会和配对,细胞分裂后期不分离,非孟德尔遗传,富含异染色质,不含对宿主主要性状有影响的基因等。B染色体DNA的分子组成既与A染色体极为相似,具有A染色体DNA分子组成的一般特征:富含重复序列和转座成分,染色体三大功能组件DNA高度同源;又与之相区别,含有B染色体特异的DNA序列,这些DNA序列可以为探讨B染色体的起源和进化提供有价值的信息。

Polysomy, which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell.

多染色体包括三染色体都是一条或多条染色体代替了正常细胞中的两条染色体形成的。

Embedding the gradient direction search and new kinds of evaluation functions into the Genetic Algorithm, a special hybrid Genetic Algorithm with mutation along the weighted gradient direction to solve non-linear programming problems is developed. Then in Chapt 4, a type of nonlinear programming problems with fuzzy objective and fuzzy resources constraints is discussed, in which the objective is ill-defined and the resources possess two different types of fuzzy resources, i. e., tolerance and imprecision. By way of description and formulation of fuzzy objective and fuzzy resources, the problem with fuzzy objective and two different types of fuzzy resources is modelled into a fuzzy nonlinear programming model FO/RNLP and interpreted as three equivalent alternative crisp model to reflect the variety of the environment and the subjective and preference of the decision maker .

本文首先针对遗传算法在求解非线性规划问题中存在的问题,首次提出非可行点/染色体的主导准可行方向,准可行方向,及非可行点属于可行域的可行度等新概念,借助于模糊思想,提出了描述和度量非可行染色体的新方法;通过嵌入非可行染色体的信息于评价函数中,提出了三种新的评价非可行染色体的评价函数;把传统的启发式方法-梯度方向搜索和新的评价函数嵌入到遗传算法中,提出了一种沿加权梯度方向变异的新型混合式遗传算法;第四章针对生产实际中非清晰定义的模糊目标和两种类型的模糊资源,建立了一类连续型模糊目标/资源约束非线性规划问题的模型FO/RNLP。

In this study, genetic analyses were conducted to determine the genetic basis in an elite resistant inbred line Siyi with complete resistance to maize dwarf mosaic. A new genetic model, two dominant complementary genes conditioning the resistance, were found by Mendelian genetic analysis based on parents, F1, F2 and backcrosses in three successive years' field trails. The two genes were further mapped near the centromere of chromosome 3 and 6, respectively by tightly linked microsatellite markers using 242 plants from F2 generation. The resistance gene on chromosome 3 is 1.0 cM apart from the flanking markers phi053 and umc1527, respectively. Whereas the linkage distance between two flanking markers bnlg1600 and phi075 and resistance gene on chromosome 6 was 1.0 and 4.0 cM, respectively. Genotypic analysis of the plants from testcross and F3 populations supported the new genetic manners.

课题组通过连续三年的抗病鉴定,在国内种质资源中筛选出一份综合农艺性状优良、配合力较高的自交系四一,三年的表型遗传研究和两年的分子标记工作,发现四一中的玉米矮花叶病抗性是由两对显性互补基因控制的,进而利用F2作图群体,把发现的两个基因定位在第三和第六染色体的着丝点附近,并获得了双侧紧密连锁的分子标记连锁图谱,其中第三染色体上的分子标记UMC1527和phi053从抗病基因双侧逼近1 cM,而第六染色体上的分子标记phi075、bnlg1600从抗病基因双侧分别逼近4 cM和1 cM;利用B2群体、F2:3家系、BC3F1群体和带有第三、第六染色体抗病基因以及两个抗病基因的近等基因系,进一步证实了四一中成株期抗性是由两个显性互补基因控制的。

The configuration of metaphase chromosome; three kinds of functional elements about chromosome DNA; karyotype and chromosome bandings; giant chromosome.

三 中期染色体的形态结构;染色体DNA的三种功能元件;核型与染色体显带;巨大染色体。

Monosomy and srisomy are the conditions in which one or three homologs occur respectively, instead of the normal two.

单染色体以及三染色体都是正常的染色体缺失或增加一条染色体造成的。

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