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     The result shows: this model can estimate the gene's relative effect under some hypothetical conditions, and thus presents a method and theoretical basis for translating gene code into quantitative trait.
     结果表明,在拟定的条件下,此模型可以对基因座位的相对作用加以估计,从而为从基因密码到数量性状的翻译提供了一定的方法与理论依据.
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     From Gene Genetic Code to Genomics and Bioinformatics
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The error performance is optimized by transforming the non-unitary space-time code into unitary space-time code.
      
This report is a summary of the continuing efforts of several teams at the Naval Surface Warfare Center, Dahlgren Divsion (NSWCDD) to evaluate technologies and to define and refine a process to reengineer Navy legacy CMS-2 code into Ada.
      
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The first ATG rule for recognizing the start codon of gene coding sequences is given. Using the known genes in yeast genome to examine the first ATG rule, its accuracy is 99.9%.For ATG started genes of E.coli and B.subtilis genome, its accuracy is 92.9% and 81.0% respectively. The lengths between LTer and the start codon (denoted as D value) of genes are analyzed. The average length for yeast genes is 17 bases for E.coli and B.subtilis ATG started genes,and the D value is 36 bases and 33 bases respectively.But...

The first ATG rule for recognizing the start codon of gene coding sequences is given. Using the known genes in yeast genome to examine the first ATG rule, its accuracy is 99.9%.For ATG started genes of E.coli and B.subtilis genome, its accuracy is 92.9% and 81.0% respectively. The lengths between LTer and the start codon (denoted as D value) of genes are analyzed. The average length for yeast genes is 17 bases for E.coli and B.subtilis ATG started genes,and the D value is 36 bases and 33 bases respectively.But for nonATG started genes of E.coli and B.subtilis, the D value is 39 bases and 32 bases respectively. The differences of coding sequences and promotor sequences between eukaryote and prokaryote are explained.We suggest that the sequences between LTer and start codon are probably the main structure of promoter sequence of mRNA.

提出了一个识别基因起始密码子的第一ATG规则.用酵母基因组中的已知基因检验,正确率为99.9%;用大肠杆菌基因组中已知以ATG起始的基因进行检验,正确率为92.9%;用枯草杆菌基因组中已知以ATG起始的基因的进行检验,正确率为81.0%.统计了L-Ter(上游最后一个终止密码)到起始密码子之间的距离(记为D值),酵母的平均长度是17个碱基;在大肠杆菌和枯草杆菌中,以ATG起始的基因的D值分别是36和33个碱基;以非ATG起始的基因的D值分别是39和32个碱基.解释了真核和原核生物D值差别的原因;发现大肠杆菌和枯草杆菌中,以ATG起始的基因和以非ATG起始的基因序列的构造差异.认为L-Ter到起始密码子之间的序列可能是mRNA先导序列的主要结构.

A dominant molecular marker regression model is established, and molecular marker materials expressed in the form of orthogonal table are studied. The result shows: this model can estimate the gene's relative effect under some hypothetical conditions, and thus presents a method and theoretical basis for translating gene code into quantitative trait.

建立了显性分子标记回归模型,并对以正交表形式表现的分子标记资料进行了研究.结果表明,在拟定的条件下,此模型可以对基因座位的相对作用加以估计,从而为从基因密码到数量性状的翻译提供了一定的方法与理论依据.

 
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