首页> 外文会议>Pacific Symposium on Biocomputing '98 4-9 January 1998 Maui, Hawaii, USA >From Sequence to Struture To Literature: The Protocol Approach to Biolnformation
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From Sequence to Struture To Literature: The Protocol Approach to Biolnformation

机译:从序列到结构再到文学:生物信息学的协议方法

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Until the recent advent of high-throughput experimental data-acquisition in biology, the computational analyssi of the biological data was predominantly on an ad hoc basis-i.e. the application of a given piece of software on the biological data depended on the need of the moment. This "functional aprpoach" often resulted in piecemeal computational analysis with large amount of interventing "deadtime". The present high-throughput availability of experimental biological data requires a more streamlined and lintegrated "protocol approach". In this work, we illustrate such as user-friendly protocol using a common question frequently faced by a wet-lab bench-biologist-"Now that I have a DNA or protein sequence, what can I do with it using a computer?". As phrased, this question is steeped in the functional approach. In contrast, the protocol approch would re-phrase the same questions as "Now that I have a DNA or protein sequence. what can a computer do for me?". Our integrating tool can start with a sequence and build a substantial custom data-warehouse of computationally derived sequence information, structure information and relevant published literature, that is continually updated.
机译:直到最近在生物学中获得高通量实验数据的到来之前,生物学数据的计算分析主要是基于即席的。给定软件在生物学数据上的应用取决于当前的需要。这种“功能性的方法”通常会导致零碎的计算分析,并需要大量的“死时间”。目前实验生物学数据的高通量可用性需要更精简和整合的“协议方法”。在这项工作中,我们举例说明了一个用户友好的协议,该协议使用了一个湿实验室工作生物学家经常遇到的常见问题:“现在我已经有了一个DNA或蛋白质序列,我可以用计算机做什么呢?”。如所表述的那样,这个问题是功能性的方法。相比之下,协议方法将重新表述与“现在我具有DNA或蛋白质序列。计算机可以为我做什么?”相同的问题。我们的集成工具可以从序列开始,并建立一个庞大的自定义数据仓库,其中包含计算得出的序列信息,结构信息和相关的出版文献,并会不断对其进行更新。

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