STATISTICAL ANALYSIS OF LONG DNA SEQUENCES
长 DNA 序列的统计分析
基本信息
- 批准号:5211842
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Rapid accumulation of genomic sequences has increased the demand for
methods to decipher the genetic information gathered in data banks such as
GenBank. While many methods for a thorough micro-analysis of small
sequences have been developed in the past, there is still a shortage of
powerful procedures for macro-analyses of large DNA sequences. Combining
statistical analysis and modern computer power makes it feasible to search
with high speed for diagnostic patterns within long sequences and to
evaluate similarities and differences between them in order to recover much
of the biochemical information hidden in these organic molecules.
The objectives of the proposed study are to develop novel methods of
computerized statistical analysis and simultaneously apply them to analyze
available large genomic sequences, as the genomes of the medically
important herpesvirus family.
The methods aim at the identification of biologically active sites (e.g.
origins replication, and nucleosome positioning signals). The anticipated
approach is based on an automated scanning of long DNA letter sequences and
to find similarities or differences between sequences, e.g., by using
dinucleotide distance measures. Probabilistic criteria (as r-scan and
spectral envelopes) will be applied to all detected sites of possible
biological interest to sort out the most likely candidates among them.
This project seeks close collaboration between experimental and theoretical
scientists, namely virologists and mathematicians. The interdisciplinary
approach ensures that the theoretical work is linked to current biomedical
problems and that newly developed methods are immediately applied.
基因组序列的快速积累增加了对
破译数据库中收集的遗传信息的方法,例如
GenBank. 虽然有许多方法可以对微小物质进行彻底的微观分析
过去已开发出序列,但仍存在短缺
用于大型 DNA 序列宏观分析的强大程序。 组合
统计分析和现代计算机能力使搜索变得可行
具有高速诊断模式的长序列和
评估它们之间的异同,以便恢复更多
隐藏在这些有机分子中的生化信息。
拟议研究的目标是开发新方法
计算机统计分析并同时应用它们进行分析
可用的大型基因组序列,如医学上的基因组
重要的疱疹病毒家族。
这些方法旨在鉴定生物活性位点(例如
复制起点和核小体定位信号)。 预计的
方法基于长 DNA 字母序列的自动扫描
寻找序列之间的相似性或差异,例如,通过使用
二核苷酸距离测量。 概率标准(如 r 扫描和
光谱包络)将应用于所有可能检测到的位置
生物学上的兴趣是从其中挑选出最有可能的候选人。
该项目寻求实验和理论之间的密切合作
科学家,即病毒学家和数学家。 The interdisciplinary
方法确保理论工作与当前的生物医学联系起来
问题并立即应用新开发的方法。
项目成果
期刊论文数量(0)
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会议论文数量(0)
专利数量(0)
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