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Detecting gene similarities using la...

Zhu, Qian.

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Detecting gene similarities using large-scale content-based search systems.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Detecting gene similarities using large-scale content-based search systems./
作者:	Zhu, Qian.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:	135 p.
附註:	Source: Dissertation Abstracts International, Volume: 78-04(E), Section: B.
Contained By:	Dissertation Abstracts International78-04B(E).
標題:	Computer science. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10167613
ISBN:	9781369219616

Detecting gene similarities using large-scale content-based search systems.
Zhu, Qian.

Detecting gene similarities using large-scale content-based search systems. - Ann Arbor : ProQuest Dissertations & Theses, 2016 - 135 p.

Source: Dissertation Abstracts International, Volume: 78-04(E), Section: B.

Thesis (Ph.D.)--Princeton University, 2016.

The accumulation of public gene expression datasets offers numerous opportunities for researchers to utilize these data to characterize gene functions, understand pathway actions, and formulate hypotheses about the molecular basis of human diseases. Yet, exploring this extremely large gene expression data collection has been challenging, due to a lack of effective tools in reusing existing datasets and exploring these datasets for targeted analyses. Particularly, a critical challenge is discovering robust gene signatures of biological processes and diseases, where this depends on the ability to detect similar genes that share gene expression patterns across a large set of conditions. This thesis discusses query-based systems that are intended for large-scale integration and exploration of gene similarities, and discusses their key biological applications.

ISBN: 9781369219616Subjects--Topical Terms:

523869
Computer science.

Detecting gene similarities using large-scale content-based search systems.
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500 $a Source: Dissertation Abstracts International, Volume: 78-04(E), Section: B.
500 $a Adviser: Olga G. Troyanskaya.
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520 $a The accumulation of public gene expression datasets offers numerous opportunities for researchers to utilize these data to characterize gene functions, understand pathway actions, and formulate hypotheses about the molecular basis of human diseases. Yet, exploring this extremely large gene expression data collection has been challenging, due to a lack of effective tools in reusing existing datasets and exploring these datasets for targeted analyses. Particularly, a critical challenge is discovering robust gene signatures of biological processes and diseases, where this depends on the ability to detect similar genes that share gene expression patterns across a large set of conditions. This thesis discusses query-based systems that are intended for large-scale integration and exploration of gene similarities, and discusses their key biological applications.
520 $a In the first part, I present SEEK, a search system and a novel algorithm for searching similar (or coexpressed) genes around a multigene query of interest. The search algorithm combines coexpressed genes using a sensitive dataset weighting algorithm for effective weighting of coexpression results. Notably, through the robust search of thousands of human datasets, the retrieval of functionally co-annotated genes always improves with the inclusion of more datasets, showing the promise of the large compendia. In the second part, I extend the work of SEEK to the expression compendia of 5 commonly studied model organisms. The new system ModSEEK enables accurate searches in a wider experimental variety, and has been extensively evaluated. In the third part, I propose a novel framework for integrating and comparing coexpression context across a pair of organisms. I leverage both comparative genomics orthology data and functional genomics coexpression data, in an unsupervised framework to identify pairs of genes in an orthologous group that are similarly highly coexpressed to an orthologous query in two organisms. I show that such functionally similar pairs of genes can be used to improve the performance of single-organism gene retrieval searches. In the final part, I demonstrate how coexpressed genes can be used to identify important transcription factors and dysregulated processes underlying breast cancer subtypes. This part highlights the promise of coexpressed genes in providing an understanding of cancer dysregulations.
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