Information Retrieval for Large-scale Genomic Analysis
Information Retrieval for Large-scale Genomic Analysis
批准号:
6359286
负责人:
RIMLI SENGUPTA
金额:
$13.59万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-01 至 2002-08-31
中文摘要
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英文摘要
DESCRIPTION: (provided by applicant) This project supports the continuation of
the PI1's interdisciplinary training started in September 1999 with a Sloan/DOE
fellowship in Computational Molecular Biology. The PI1's immediate career
objective is to complete a transition into computational molecular biology by
forging an independent research trajectory within this exciting field.
University of Washington is a uniquely suitable place for making such a
transition: it has several strong biology programs as well as a strong computer
science department, with considerable synergy among them through active
collaborations, joint courses, and seminars. The PI its a computer scientist by
training, and based on initial investigations is convinced that her expertise
in designing efficient algorithms can be gainfully employed to address
challenging computational problems arising from the emergent need for global
analysis of massive biological datasets, for example, the human genome. Her
long term interest in this field, however, is fueled largely by the tantalizing
vision of contributing to real biological knowledge. To realize this vision,
she plans to acquire expertise in experimental techniques that will allow her
to test biological hypotheses arising from computational analyses, through an
extensive regimen of hands-on, lab-intensive coursework. The specific research
problem the FLPI proposes to explore is to apply information retrieval
techniques (which have been widely applied with great success in developing
search engines for the world-wide web) for large-scale analysis of genomic
sequence and gene expression data. She plans to build computational models of
the untranslated promoter regions upstream of coexpressed eukaryotic genes, by
identifying composite regulatory motifs that determine the genes' specific
expression pattern. -Such composite motifs may be composed of the binding sites
of several regulatory factors that coordinately control expression. These
models are then to be used to classify promoter regions of unannotated genes,
thereby providing a hypothesis for their function. This research has the
potential to lead to novel computational methods for classification of
eukaryotic promoter regions in particular, and for functional genomics in
general. The intensive training afforded through the planned training
activities and the proposed research will enable the PI1 to successfully
complete the transition into being an independent investigator in computational
molecular biology.
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