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Method and apparatus for identifying, classifying, or quantifying protein sequences in a sample without sequencing

机译:无需测序即可鉴定,分类或定量样品中蛋白质序列的方法和装置

摘要

This invention provides methods by which biologically derived DNA sequences in a mixed sample or in an arrayed single sequence clone can be determined and classified without sequencing. The methods make use of information on the presence of carefully chosen target subsequences, typically of length from 4 to 8 base pairs, and preferably the length between target subsequences in a sample DNA sequence together with DNA sequence databases containing lists of sequences likely to be present in the sample to determine a sample sequence. The preferred method uses restriction endonucleases to recognize target subsequences and cut the sample sequence. Then carefully chosen recognition moieties are ligated to the cut fragments, the fragments amplified, and the experimental observation made. Polymerase chain reaction (PCR) is the preferred method of amplification. Another embodiment of the invention uses information on the presence or absence of carefully chosen target subsequences in a single sequence clone together with DNA sequence databases to determine the clone sequence. Computer implemented methods are provided to analyze the experimental results and to determine the sample sequences in question and to carefully choose target subsequences in order that experiments yield a maximum amount of information.
机译:本发明提供了方法,通过该方法可以确定混合样品或阵列的单序列克隆中的生物学来源的DNA序列,而无需测序即可分类。所述方法利用关于精心选择的靶子序列的存在的信息,所述靶子序列的长度通常为4至8个碱基对,并且优选地,样品DNA序列中靶子序列之间的长度以及包含可能存在的序列列表的DNA序列数据库。在样品中确定样品序列。优选的方法使用限制性核酸内切酶识别靶标亚序列并切割样品序列。然后,将精心选择的识别部分连接到切割的片段,扩增片段,并进行实验观察。聚合酶链反应(PCR)是首选的扩增方法。本发明的另一个实施方案使用有关在单个序列克隆中是否存在精心选择的靶子序列的信息以及DNA序列数据库来确定克隆序列。提供了计算机执行的方法来分析实验结果,确定所讨论的样品序列,并仔细选择目标子序列,以使实验产生最大的信息量。

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