这种构建非同源对照模板的方法，简便易行，适应面广。
目的建立一个用于临床标本的体外非同源末端连接的检测体系。
Objective To develop an in vitro system for non-homologous end joining efficiency detected in clinical samples.
在宿主-寄生虫疾病中，像结核病，非同源蛋白质作为药物靶点是首选。
In host-parasite diseases like Tuberculosis, non-homologous proteins as drug target are first preference.
从筛选出的74个次级单拷贝中有效地鉴定出37个非同源的单拷贝片段。
A total of 37 non-homologous single-copy fragments were identified from 74 possible single-copies.
建立了玉米转基因成分中35s启动子非同源模板的竞争定量pcr检测系统。
The quantitative competitive polymerase chain reaction (QC-PCR) system of using 35s promoter heterologous template for the detection of genetically modified maize was developed in this study.
非同源染色体间带型各不相同，某些染色体具有易于识别，特征性较强的A型带标记。
All of the experimental materials had characteristics of a type banding patterns which could be recognized easily in some chromosome pairs.
大多数有效的药物靶点能够通过蛋白质相互作用网络分析，在大量非同源蛋白质间识别。
Most potent drug target can be identifying among large number of non-homologous protein through protein interaction network analysis.
对不同条件下的同源和非同源的SAR图像进行了大量的实验，给出了初步的匹配结果。
Numerous experiments were conducted for homologous and non-homologous SAR images under various conditions, and the preliminary matching conclusions were obtained.
英语语法中，同源宾语结构和与其形式雷同的非同源宾语结构的区分一直是一个有争议的问题。
The distinction between cognate object construction and non-cognate object construction has been a controversial topic in English grammar.
任何两个拥有相同抽象形的字符，只要不与来源准则和非同源准则的要求相抵触，即可以被统合为一。
Any two ideographs that possess the same abstract shape are then unified provided that their unification is not disallowed by either the Source Separation Rule or the Noncognate Rule.
结果获得了经非同源重组整合到酵母染色体上的能有效利用甲醇作为唯一碳源的PMD11和PMD16转化株。
Results the PMD11 and PMD16 transformants were obtained, capable of metabolizing methanol as sole carbon resource through non homologous integration into the yeast chromosome.
初步认为，次级联会产生的原因是非同源染色体之间的同祖关系。赖草染色体组J、N可能来自同一原始染色体组X。
The result showed that the secondary assocition originated from homoeology between J and N possibly originated from same genome X.
目前已鉴定的这一基因家族的多数成员均参与几种重要的DNA修复途径，包括碱基切除修复、同源重组修复和非同源末端重接。
Most members of the XRCC genes family participated in several DNA repair pathways, including base excision repair, homologous recombination repair and non-homologous end joining.
目前已鉴定的这一基因家族的多数成员均参与几种重要的DNA修复途径，包括碱基切除修复、同源重组修复和非同源末端重接。
Most members of the XRCC genes family participated in several DNA repair pathways, including base excision repair, homologous recombination repair and non-homologous end joining.
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