When it is complete in 2008 , earthscope ' s web of instruments will provide public data for geoscience , not unlike the way the human genome sequencing effort has for biology 在2008年完成之后，地球镜的仪器网络将会提供地质科学的公开数据，就如同人类基因组定序对生物学的贡献一般。
Evaluating these next - generation sequencing systems against one another and against the sanger method illustrates some of the factors that will influence their usefulness 当我们比较下一代定序系统之间的不同，以及它们与桑格法的差异时，会找到一些可能将会影响各种系统是否好用的因素。
This paper discusses the modem regression techniques used for ordinal data analysis and how to apply them into solving an important sampling problem in consumer confidence index survey 摘要本文讨论了对定序变量进行回归的技术，并探讨了如何用其解决消费者信心指数调查中抽样的重要问题。
Diagnostic uses might demand a reduction in error rates below the current hgp standard of 0 . 01 percent , because that still permits 600 , 000 errors per human genome 目前人类基因组计画的误差标准为0 . 01 % ，也就是人类基因组的序列中可能有60万个错误，相较之下，用于医疗诊断的定序误差必须更低。
But no special license is required to export dna synthesizers and sequencers and other automated machines that can make it much easier to engage in the genetic engineering of microorganisms 而dna合成仪与定序仪，以及其他的自动仪器，使微生物遗传工程学的研发工作更为容易，出口时却不需申请特别许可。
In sna , the meanings of , and the sequencing rules for , requests and responses used for managing the network , transferring data , and synchronizing the states of network components 在系统网络体系结构( sna )中,为了管理网络、传送数据以及为网络各组成部件的状态建立同步所使用的请求和响应的含义和定序的规则。
Using specially shot interviews with scientists and archive footage , the programme investigates the likely impact of the mapping of the human genome on future medicine and disease treatment 人类基因图谱定序完成，标志著科学踏足上另一个新里程。本节目探讨人类基因图谱对研制新药物及疾病治疗的贡献。原版英文发音。
Majumdar envisions nanofluidic transistors that could rapidly sort the slew of molecules in cells by their mass and charge , thereby helping to purify dna for sequencing or look for markers of disease 马强达希望，未来奈米流体电晶体可依照质量和电荷快速区分大量分子，进而协助筛选dna ，以便定序或寻找某种疾病的特徵。
If medicine is the primary driver of widespread sequencing , however , we will be largely resequencing the human genome looking for minute variations in individuals ' dna , and short read - lengths will not be such a problem 然而如果届时定序普及化的动机是医学上的需要，我们的工作主要是重新定序人类基因组，找寻个人dna中细微的差异，那麽读取长度短也就不是问题。
For example , two research groups , my own at harvard and one from 454 life sciences , recently published peer - reviewed descriptions of genome - scale sequencing projects that allow for a direct comparison 举例来说，我在哈佛大学的研究团队，和另一个来自454生命科学公司的团队，最近分别发表了基因组规模的定序计画说明，这些经过同侪审查的内容，提供了一个直接比较的机会。
