重叠基因表达，借鉴生物基因片段重叠表达，引入重叠基因概念，节约了表达空间；
Overlapped gene expression. It borrows the idea of overlap gene expression from biological study, introduces overlapped gene expression, and saves space for gene expression.
如果是这样，那就表明另外的的基因重叠，是没什么影响的，也就是说遗传的影响也很小，收养的儿童，和他们的兄弟姐妹会很相似吗？
If so, then it would show that that extra overlap in genes doesn't really matter and so, it would suggest a low role of heredity Are adopted children highly similar to? Their brothers and sisters?
这种方法首先将一个基因组切割成细微片段，小到足够测序仪器对其进行处理，然后使用电脑，通过对比重叠部分将这些碎片再缝合起来。
This first shreds a genome into pieces small enough for sequencing machines to handle, then stitches the sequenced pieces back together by matching the overlaps using a computer.
同时，一张尼安德特人基因排列次序草图也没有提供任何证据证明他们与我们的基因库有所重叠。
Meanwhile, a first-draft sequence of the Neanderthal genome offers no sign that they contributed to our gene pool.
通过抑制特定基因，他们有系统地造成“形成多个口头波兰人(”户主“)…变形主体轴…和重叠的触角。”
By suppressing certain genes, they systematically caused "formation of multiple oral poles (" heads")... deformation of the main body axis... and duplication of tentacles."
再经重叠pcr技术将这两段DNA连接在一起，构成完整的ZP3基因的编码区。
Then with overlapping PCR technology to link this two DNA together to form a complete ZP 3 gene encoding.
基因（常为种内同源基因）间功能有重叠的现象。
Redundancy --- The situation in which genes (often paralogous) have overlapping functions.
方法：采用重叠区扩增基因拼接法。
结论：重叠延伸pcr是一种获得重构基因的简捷方法。
Conclusion Splicing overlap extension by PCR is a convenient method to obtain recombinant gene.
方法用PCR方法扩增il_3信号肽序列和人内皮抑素基因，然后采用重叠延伸pcr拼接的方法将两者拼接和扩增。
METHODS IL_3 signal sequence and human endostatin gene were amplified with PCR and spliced with overlap extension PCR.
链霉菌基因组中常见连续两个基因重叠的现象（如ATGA），这为基因的同框敲除或取代研究带来很大困扰。
The gene overlapping(ATGA) is widespread in streptomycetes, making it difficult to perform in-frame deletion or replacement for functional analysis of target genes.
“多种物质成瘾在某一染色体上定位的峰值的比较，部分证实了基因易损性对不同物质有重叠。”李说。
"The comparison of peaks for addictions to multiple substances on certain chromosomal locations confirms that genetic vulnerability to different substances overlaps, in part," li says.
它的不育性是受两对具有相同作用的重叠性基因控制。
The "No. 117A" is controled by two pairs overlapping recessive genes in all ready alike functions.
事实上，“多半现在人类基因的总计现在告诉我们，我们在基因上都是相似的，并且还有相当巨大程度的重叠。”
In fact, "most of what's coming out of modern human genetics now tells us... we are all genetically similar, and there is a tremendous degree of overlap."
建立一种用于克隆全长基因的、限制性内切酶介导的重叠延伸法 。
The overlap extension mediated by restriction endonuclease to obtain the full length gene was established.
人类基因组计划是将人类的基因组DNA序列分为大小为150-200碱基片段，装载到定位重叠的细菌克隆中，力求每个克隆序列的准确率大于99.9%。
For Human Genome Project planning digested human gene DNA sequence into many 150-200bp fragments, and reconstructed into the germ clone and to be sure the accuracy is over 99.9%.
在回顾性复习这些病例的基础上，作者发现伴 ZC3H7B-BCOR 基因融合的ESS构成了高级别 ESS一种新的亚型，并且该亚型与黏液样型平滑肌肉瘤在形态学上有显著的重叠。
On the basis of the review of these cases, we find that ESS with ZC3H7B-BCOR fusion constitutes a novel type of high-grade ESS and shares significant morphologic overlap with myxoid leiomyosarcoma.
这个候选基因能够同时影响这三种能力，这个结果表明在语言、言语和阅读能力之间存在一条共同通路，从而导致这三种能力的增强或缺陷存在交错重叠（相互影响）。
The finding that a candidate gene could influence all three abilities suggests a common pathway that could contribute to overlapping strengths or deficiencies across speech, language and reading.
基因组浏览器是允许用户在一个参考序列(例如一个染色体或片段重叠群)环境内，可视化dna、蛋白质或其他序列特征的软件。
A genome browser is software that allows users to visualize DNA, protein, or other sequence features within the context of a reference sequence, such as a chromosome or contig.
采用基因本体论对这两个网络重叠区域进行基因分类后发现，这些编码的蛋白质主要集中在对刺激物的应答途径之中。
The overlap regions between them were classified by gene ontology and indicated that most proteins encoded by genes fall into the response pathway on stimulus.
由于这种病毒的基因组高度压缩导致P35S和编码多功能蛋白P6的VI基因存在着重叠。
The genetic organization of the densely packed genome of this virus results in sequence overlap between P35S and viral gene VI, encoding the multifunctional P6 protein.
由于这种病毒的基因组高度压缩导致P35S和编码多功能蛋白P6的VI基因存在着重叠。
The genetic organization of the densely packed genome of this virus results in sequence overlap between P35S and viral gene VI, encoding the multifunctional P6 protein.
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