| 1. | The targeting sequence should take
瞄准定位大约需要 |
| 2. | The paper pays great attention to how to improve the precision of alignment between query sequence and target sequence
本文的研究重点是如何提高查询序列和目标序列的排列精度。 |
| 3. | The length of the slice may be different from the length of the assigned sequence , thus changing the length of the target sequence , if the object allows it
片断的长度可能和被赋序列的长度不同，那就改变目标序列的长度，如果该对象允许的话。 |
| 4. | This process is composed of such sections as recognition of target template , alignment between query sequence and target sequence , modeling , evaluation of structure rationality
这个过程包括以下几个部分:目标模板的识别、查询序列和目标序列的排列、构建模型和模型的结构合理性评估。 |
| 5. | Dna sequence analysis indicated that tn5gusa5 is prone to insert into low gc content regions ; guanine is a preferential base at the first place and cytosine at the last site of target sequence
在质粒上tn5gusa5也倾向于插入低gc含量区；碱基g和c分别在靶序列的首位和末尾出现的几率高。 |
| 6. | According to the above , this paper mainly does research on three aspects : using profile - profile method in the process of getting alignment between target sequence and model sequence , data smooth we use in
最后,我们还参与了casp7的蛋白质结构预测的评比,对获得的未知序列通过profile - profile方法生成的五个蛋白质结构进行结构合理性评估。 |
| 7. | 3 . the mechanism of dna integration mediated by homologous recombination in chloroplast transformation was tentatively explored . we isolated two chloroplast dna fragments from brassica napus and used them as targeting sequence to integr
成功地通过h次转化获得整合并表达多基因的转基因烟草，缩短了研究周期，对相关转基因植物的研究有一定参考价值。 |
| 8. | Pcr amplification of hla - dqa1 use the extracted genome dna as template , amplify the target sequence . examine the products by page . the bands is clear and the length is 538bp as it shows , which matches the design
结果1 . hla一dqai基因片段的pcr扩增以提取的全基因组dna为模板，行pcr扩增，产物用聚丙烯酞胺凝胶电泳检测，可见条带清晰，产物长度538bp ，与设计相符。 |
| 9. | Pcr amplification of the target sequence design a pair of primers ac - coding to the conservative region of hla - dqa1 exon 2 , and lable the sence strand by fitc . make the fiuorescenced strand the advantage strand by assym - metric pcr . 3
样本靶序列的pcr扩增在hla - dqa1第二外显子保守区域设计一对引物，并在正义链引物5 ’作fitc标记，以荧光标记单链为优势链，行不对称扩增。 |
