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  Algorithms for differential splicing detection using exon arrays: a comparative assessment

Zimmermann, K., Jentsch, M., Rasche, A., Hummel, M., & Leser, U. (2015). Algorithms for differential splicing detection using exon arrays: a comparative assessment. BMC Genomics, 2015:. doi:10.1186/s12864-015-1322-x.

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資料種別: 学術論文

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Zimmermann.pdf (出版社版), 703KB
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https://hdl.handle.net/11858/00-001M-0000-002A-5544-1
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Zimmermann.pdf
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© 2015 Zimmermann et al.; licensee BioMed Central

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 作成者:
Zimmermann, Karin1, 著者
Jentsch, Marcel2, 著者
Rasche, Axel3, 著者           
Hummel, Michael4, 著者
Leser, Ulf1, 著者
所属:
1Department of Computer Science,Knowledge Management in Bioinformatics, Humboldt Universität zu Berlin, Rudower Chaussee 25, 12489 Berlin, Germany, ou_persistent22              
2Department of Mathematics and Computer Science, Freie Universität Berlin, Berlin, Germany, ou_persistent22              
3Bioinformatics (Ralf Herwig), Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_2385701              
4Institut fuer Pathologie CBF, Charite - Universitätsmedizin Berlin, Hindenburgdamm 30, 12200 Berlin, Germany, ou_persistent22              

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キーワード: Alternative splicing, Differential splicing, Exon arrays, Method comparison, Parameter influence
 要旨: Background: The analysis of differential splicing (DS) is crucial for understanding physiological processes in cells and organs. In particular, aberrant transcripts are known to be involved in various diseases including cancer. A widely used technique for studying DS are exon arrays. Over the last decade a variety of algorithms for the detection of DS events from exon arrays has been developed. However, no comprehensive, comparative evaluation including sensitivity to the most important data features has been conducted so far. To this end, we created multiple data sets based on simulated data to assess strengths and weaknesses of seven published methods as well as a newly developed method, KLAS. Additionally, we evaluated all methods on two cancer data sets that comprised RT-PCR validated results. Results: Our studies indicated ARH as the most robust methods when integrating the results over all scenarios and data sets. Nevertheless, special cases or requirements favor other methods. While FIRMA was highly sensitive according to experimental data, SplicingCompass, MIDAS and ANOSVA showed high specificity throughout the scenarios. On experimental data ARH, FIRMA, MIDAS, and KLAS performed best. Conclusions: Each method shows different characteristics regarding sensitivity, specificity, interference to certain data settings and robustness over multiple data sets. While some methods can be considered as generally good choices over all data sets and scenarios, other methods show heterogeneous prediction quality on the different data sets. The adequate method has to be chosen carefully and with a defined study aim in mind.

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言語: eng - English
 日付: 2015-02-042015-02-27
 出版の状態: オンラインで出版済み
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 識別子(DOI, ISBNなど): DOI: 10.1186/s12864-015-1322-x
 学位: -

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出版物 1

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出版物名: BMC Genomics
種別: 学術雑誌
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出版社, 出版地: BioMed Central
ページ: - 巻号: 2015 通巻号: 16:136 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1471-2164
CoNE: https://pure.mpg.de/cone/journals/resource/111000136905010