Differential expression analysis for pathways.
Differential expression analysis for pathways.
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DOI:
10.1371/journal.pcbi.1002967
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发表时间:
2013
影响因子:
4.3
通讯作者:
Kolker E
中科院分区:
文献类型:
--
作者:
Haynes WA;Higdon R;Stanberry L;Collins D;Kolker E
Life science technologies generate a deluge of data that hold the keys to unlocking the secrets of important biological functions and disease mechanisms. We present DEAP, Differential Expression Analysis for Pathways, which capitalizes on information about biological pathways to identify important regulatory patterns from differential expression data. DEAP makes significant improvements over existing approaches by including information about pathway structure and discovering the most differentially expressed portion of the pathway. On simulated data, DEAP significantly outperformed traditional methods: with high differential expression, DEAP increased power by two orders of magnitude; with very low differential expression, DEAP doubled the power. DEAP performance was illustrated on two different gene and protein expression studies. DEAP discovered fourteen important pathways related to chronic obstructive pulmonary disease and interferon treatment that existing approaches omitted. On the interferon study, DEAP guided focus towards a four protein path within the 26 protein Notch signalling pathway. The data deluge represents a growing challenge for life sciences. Within this sea of data surely lie many secrets to understanding important biological and medical systems. To quantify important patterns in this data, we present DEAP (Differential Expression Analysis for Pathways). DEAP amalgamates information about biological pathway structure and differential expression to identify important patterns of regulation. On both simulated and biological data, we show that DEAP is able to identify key mechanisms while making significant improvements over existing methodologies. For example, on the interferon study, DEAP uniquely identified both the interferon gamma signalling pathway and the JAK STAT signalling pathway.
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影响因子:
12.3
作者:
Hung JH;Whitfield TW;Yang TH;Hu Z;Weng Z;DeLisi C
通讯作者:
DeLisi C
DOI:
10.2202/1544-6115.1418
发表时间:
2009-01-01
影响因子:
0.9
作者:
Dorum, Guro;Snipen, Lars;Saebo, Solve
通讯作者:
Saebo, Solve
影响因子:
7
作者:
Cha, Sangwon;Imielinski, Marcin B.;Karger, Barry L.
通讯作者:
Karger, Barry L.
影响因子:
9.6
作者:
Esther, Charles R., Jr.;Lazaar, Aili L.;Boucher, Richard C.
通讯作者:
Boucher, Richard C.
影响因子:
7.3
作者:
Gough, Nancy R;Yaffe, Michael B
通讯作者:
Yaffe, Michael B