Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data

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Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data. / Yang, Lei; Rau, Martin Holm; Yang, Liang; Høiby, Niels; Molin, Søren; Jelsbak, Lars.

In: B M C Microbiology, Vol. 11, 01.01.2011, p. 184.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Yang, L, Rau, MH, Yang, L, Høiby, N, Molin, S & Jelsbak, L 2011, 'Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data', B M C Microbiology, vol. 11, pp. 184. https://doi.org/10.1186/1471-2180-11-184, https://doi.org/10.1186/1471-2180-11-184

APA

Yang, L., Rau, M. H., Yang, L., Høiby, N., Molin, S., & Jelsbak, L. (2011). Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data. B M C Microbiology, 11, 184. https://doi.org/10.1186/1471-2180-11-184, https://doi.org/10.1186/1471-2180-11-184

Vancouver

Yang L, Rau MH, Yang L, Høiby N, Molin S, Jelsbak L. Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data. B M C Microbiology. 2011 Jan 1;11:184. https://doi.org/10.1186/1471-2180-11-184, https://doi.org/10.1186/1471-2180-11-184

Author

Yang, Lei ; Rau, Martin Holm ; Yang, Liang ; Høiby, Niels ; Molin, Søren ; Jelsbak, Lars. / Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data. In: B M C Microbiology. 2011 ; Vol. 11. pp. 184.

Bibtex

@article{1ac7b1dcfb6b4883b7d108913da31ae0,
title = "Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data",
abstract = "BackgroundBacteria employ a variety of adaptation strategies during the course of chronic infections. Understanding bacterial adaptation can facilitate the identification of novel drug targets for better treatment of infectious diseases. Transcriptome profiling is a comprehensive and high-throughput approach for characterization of bacterial clinical isolates from infections. However, exploitation of the complex, noisy and high-dimensional transcriptomic dataset is difficult and often hindered by low statistical power. ResultsIn this study, we have applied two kinds of unsupervised analysis methods, principle component analysis (PCA) and independent component analysis (ICA), to extract and characterize the most informative features from transcriptomic dataset generated from cystic fibrosis (CF) Pseudomonas aeruginosa isolates. ICA was shown to be able to efficiently extract biological meaningful features from the transcriptomic dataset and improve clustering patterns of CF isolates. Decomposition of the transcriptomic dataset by ICA also facilitates gene identification and gene ontology enrichment. ConclusionsOur results show that P. aeruginosa employs multiple patient-specific adaption strategies during the early stage infections while certain essential adaptations are evolved in parallel during the chronic infections. ",
author = "Lei Yang and Rau, {Martin Holm} and Liang Yang and Niels H{\o}iby and S{\o}ren Molin and Lars Jelsbak",
year = "2011",
month = jan,
day = "1",
doi = "10.1186/1471-2180-11-184",
language = "English",
volume = "11",
pages = "184",
journal = "BMC Microbiology",
issn = "1471-2180",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data

AU - Yang, Lei

AU - Rau, Martin Holm

AU - Yang, Liang

AU - Høiby, Niels

AU - Molin, Søren

AU - Jelsbak, Lars

PY - 2011/1/1

Y1 - 2011/1/1

N2 - BackgroundBacteria employ a variety of adaptation strategies during the course of chronic infections. Understanding bacterial adaptation can facilitate the identification of novel drug targets for better treatment of infectious diseases. Transcriptome profiling is a comprehensive and high-throughput approach for characterization of bacterial clinical isolates from infections. However, exploitation of the complex, noisy and high-dimensional transcriptomic dataset is difficult and often hindered by low statistical power. ResultsIn this study, we have applied two kinds of unsupervised analysis methods, principle component analysis (PCA) and independent component analysis (ICA), to extract and characterize the most informative features from transcriptomic dataset generated from cystic fibrosis (CF) Pseudomonas aeruginosa isolates. ICA was shown to be able to efficiently extract biological meaningful features from the transcriptomic dataset and improve clustering patterns of CF isolates. Decomposition of the transcriptomic dataset by ICA also facilitates gene identification and gene ontology enrichment. ConclusionsOur results show that P. aeruginosa employs multiple patient-specific adaption strategies during the early stage infections while certain essential adaptations are evolved in parallel during the chronic infections.

AB - BackgroundBacteria employ a variety of adaptation strategies during the course of chronic infections. Understanding bacterial adaptation can facilitate the identification of novel drug targets for better treatment of infectious diseases. Transcriptome profiling is a comprehensive and high-throughput approach for characterization of bacterial clinical isolates from infections. However, exploitation of the complex, noisy and high-dimensional transcriptomic dataset is difficult and often hindered by low statistical power. ResultsIn this study, we have applied two kinds of unsupervised analysis methods, principle component analysis (PCA) and independent component analysis (ICA), to extract and characterize the most informative features from transcriptomic dataset generated from cystic fibrosis (CF) Pseudomonas aeruginosa isolates. ICA was shown to be able to efficiently extract biological meaningful features from the transcriptomic dataset and improve clustering patterns of CF isolates. Decomposition of the transcriptomic dataset by ICA also facilitates gene identification and gene ontology enrichment. ConclusionsOur results show that P. aeruginosa employs multiple patient-specific adaption strategies during the early stage infections while certain essential adaptations are evolved in parallel during the chronic infections.

U2 - 10.1186/1471-2180-11-184

DO - 10.1186/1471-2180-11-184

M3 - Journal article

C2 - 21851621

VL - 11

SP - 184

JO - BMC Microbiology

JF - BMC Microbiology

SN - 1471-2180

ER -

ID: 40217024