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Methods for cluster analysis and val...
~
Kosorukoff, Alexander Lvovich.
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Methods for cluster analysis and validation in microarray gene expression data.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Methods for cluster analysis and validation in microarray gene expression data./
作者:
Kosorukoff, Alexander Lvovich.
面頁冊數:
103 p.
附註:
Source: Dissertation Abstracts International, Volume: 67-07, Section: B, page: 3903.
Contained By:
Dissertation Abstracts International67-07B.
標題:
Biology, Bioinformatics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3223632
ISBN:
9780542774423
Methods for cluster analysis and validation in microarray gene expression data.
Kosorukoff, Alexander Lvovich.
Methods for cluster analysis and validation in microarray gene expression data.
- 103 p.
Source: Dissertation Abstracts International, Volume: 67-07, Section: B, page: 3903.
Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2006.
Motivation. Unsupervised learning or clustering is frequently used to explore gene expression profiles for insight into both regulation and function. However, the quality of clustering results is often difficult to assess and each algorithm has tunable parameters with often no obvious way to choose appropriate values. Most algorithms also require the number of clusters to be predetermined yet this value is rarely known and, thus, is arrived at by subjective criteria. Here we present a method to systematically address these challenges using statistical evaluation.
ISBN: 9780542774423Subjects--Topical Terms:
1018415
Biology, Bioinformatics.
Methods for cluster analysis and validation in microarray gene expression data.
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Source: Dissertation Abstracts International, Volume: 67-07, Section: B, page: 3903.
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Adviser: Sylvian Ray.
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Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2006.
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Motivation. Unsupervised learning or clustering is frequently used to explore gene expression profiles for insight into both regulation and function. However, the quality of clustering results is often difficult to assess and each algorithm has tunable parameters with often no obvious way to choose appropriate values. Most algorithms also require the number of clusters to be predetermined yet this value is rarely known and, thus, is arrived at by subjective criteria. Here we present a method to systematically address these challenges using statistical evaluation.
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Method. The method presented compares the quality of clustering results in order to choose the most appropriate algorithm, distance metric and number of clusters for gene network discovery using objective criteria. In brief, two quality assessment metrics are used: the Consensus Share (CS) and the Feature Configuration Statistic (FCS). CS is the percentage of genes (not gene pairs) that are identically clustered in several clusterings and FCS is a measure of randomness of the observed configuration of transcription factor binding sites among clustered genes.
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Results. We evaluate this method using both artificial and yeast microarray data. By choosing parameters settings that minimize FCS values and maximize CS values we show major advantages over other clustering methods in particular for identifying combinatorially regulated groups of genes. The results produced provide remarkable enrichment for cis-regulatory elements in clusters of genes known to be regulated by such elements and evidence of extensive combinatorial regulation. Moreover, the method can be generalized when prior information about cis-regulatory sites is absent or it is desirable to calculate FCS values based on functional categorization.
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