他们用已知细菌基因的蓝图重建整个基因序列，把由自动基因测序器以化学方式制造的基因粘在一起。
They took the blueprint of a known bacterial genome and rebuilt the entire sequence, stitching together genes chemically manufactured by an automated DNA synthesizer.
因为基因的植入有可能导致危险的基因突变。除此之外，研究人员还必须想办法让植入的基因在细胞分化时自动分解。
Because adding new genes may cause unsafe mutations, the researchers must also figure out how to make the new genes delete themselves during cellular division.
自动化dna分析在诸如染色体作图，基因组测序以及DNA、RNA与蛋白质互作这类领域的应用潜力巨大。
Automated DNA synthesis has been essential in such fields as chromosome mapping, genomic sequencing and the study of interactions between DNA, RNA and proteins.
这就是MAGE——多元自动化基因工程的缩写。
This is MAGE, a somewhat contrived acronym for multiplex automated genome engineering.
在基因表达程序设计(GEP)基础上，从自动程序设计方法学的观点出发，对程序重用的程序表示方法进行了研究。
Based on the gene expression programming (GEP) proposed by Feriera, from the viewpoint of methodology of automatic programming, this paper investigates the representation of program for program reuse.
自动的基因识别和颜色编码增加了摘要的可读性，并显著地加速了文献研究。
The automatic gene recognition and color coding increases the readability of abstracts and significantly speeds up literature research.
针对HPV病毒的检测难题，设计一种将荧光偏振技术用于病原微生物检测和基因分析的荧光偏振自动检测系统。
Considering the difficulties of HPV detection, an automatic detection system is designed with fluorescence polarization technology, which is used in pathogenic germs detections and gene analyses.
图像预处理、图像网格半自动划分或自动划分是基因芯片数据处理前的重要步骤。
Image preprocessing, half-automatic gridding or automatic gridding (image segmentation) are important tasks before data analysis.
本文通过分析基因芯片的图象特征，提出了基于变形模板技术的基因芯片杂交样点自动识别方法。
In this paper, based on the recognized microarray image features, an automatic spot identification method using the deformable template technique is proposed.
该技术速度快，易于自动化，特别适合大量单碱基突变基因的筛查。
This method is characteristic of high speed, easy automation, and is especially suitable for high throughput screening.
候选网自动搜寻器用所有的基因去计算被扰的反应径或网的显著性，以消除因忽微阵实验中的非显著差表现基因而遗失任何重要资讯的情形。
AutoSCAN USES all genes to compute the significance of perturbed pathways or network to eliminate the loss of any important information about insignificant genes in microarray.
SNP位点是目前基因多态性研究的主要内容，包括检测分型和功能活性研究两个层次，已经建立了高度自动化和高通量的SNP检测分型技术。
Single Nucleotide polymorphism (SNP) site is the main content of genetic polymorphism study, which includes detection of gene type and research on function and activity.
将该种模型运用于公开的白血病基因表达数据集进行实验，实验表明该方法能自动获取基因表达数据的聚类数，并得到较高的分类准确率。
We applied the model to analyze the expression data set of leukaemia. The experimental result proved that this model can get cluster Numbers automatically and a high accuracy of classification.
而DNA自动机已经可以根据一定的逻辑在体外调控基因的表达，为基因功能的研究提供了一种新的方法。
Moreover, DNA automaton could also be used to regulate gene expression in vitro logically. This provided a novel method for gene function analysis.
这种关系可自动为缺乏特征的基因组产生功能预测。
This relation automatically yields a number of functional predictions for poorly characterized genomes.
DNA微阵列技术以其高通量、自动化、平行化、快速化的优势，成为后基因组时代在转录组水平进行肿瘤基因表达谱分析的最强有力工具。
With the advantages of high throughput, automation and speed, DNA microarray is becoming the most powerful tool in cancer research in the post-genome age.
DNA微阵列技术以其高通量、自动化、平行化、快速化的优势，成为后基因组时代在转录组水平进行肿瘤基因表达谱分析的最强有力工具。
With the advantages of high throughput, automation and speed, DNA microarray is becoming the most powerful tool in cancer research in the post-genome age.
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