4.8 Article

A modular analysis framework for blood genomics studies: Application to systemic lupus erythematosus

期刊

IMMUNITY
卷 29, 期 1, 页码 150-164

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2008.05.012

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资金

  1. NCI NIH HHS [P01 CA084512-05A29004, P01 CA084512-05A2, R01 CA078846-05, R01 CA078846-09, R01 CA078846-08, P01 CA084512-079002, P01 CA084512, P01 CA084512-079004, P01 CA084512-040003, R01 CA078846-06, R01 CA078846-07, P01 CA084512-01A10003, P01 CA084512-030003, P01 CA084512-069004, R01 CA078846-02, P01 CA084512-069002, P01 CA084512-05A20005, P01 CA084512-06, R01 CA078846-04, R01 CA078846, P01 CA084512-070005, P01 CA084512-060005, P01 CA084512-07, P01 CA084512-020003, R01 CA078846-10, R01 CA078846-01A1, R01 CA078846-03, P01 CA084512-05A29002] Funding Source: Medline
  2. NIAID NIH HHS [U19 AI057234-06, R01 AI068842-03, U19 AI057234-05, R01 AI068842-01, U19 AI057234-010004, U19 AI057234-05S1, U19 AI057234-03, U19 AI057234-010005, R01 AI068842-04, U19 AI057234, U19 AI057234-02, U19 AI057234-05S10013, R01 AI068842, U19 AI057234-01, U19 AI057234-05S19003, U19 AI057234-04, R01 AI068842-02, U19 AI057234-010006, U19 AI057234-05S10012] Funding Source: Medline
  3. NIAMS NIH HHS [P50 AR054083-029001, P50 AR054083-01, P50 AR055503-020004, P50 AR055503, R01 AR050770-05A1, P50 AR054083-030001, R01 AR050770-03, P50 AR054083-019001, P50 AR054083-020001, P50 AR054083, R01 AR050770, R01 AR050770-02, R01 AR050770-04, P50 AR054083-010001, R01 AR050770-06, P50 AR054083-03, P50 AR055503-010004, R01 AR050770-01, P50 AR054083-02] Funding Source: Medline
  4. PHS HHS [U19 AIO57234-02, R01 I068842] Funding Source: Medline

向作者/读者索取更多资源

The analysis of patient blood transcriptional profiles offers a means to investigate the immunological mechanisms relevant to human diseases on a genome-wide scale. In addition, such studies provide a basis for the discovery of clinically relevant biomarker signatures. We designed a strategy for microarray analysis that is based on the identification of transcriptional modules formed by genes coordinately expressed in multiple disease data sets. Mapping changes in gene expression at the module level generated disease-specific transcriptional fingerprints that provide a stable framework for the visualization and functional interpretation of microarray data. These transcriptional modules were used as a basis for the selection of biomarkers and the development of a multivariate transcriptional indicator of disease progression in patients with systemic lupus erythematosus. Thus, this work describes the implementation and application of a methodology designed to support systems-scale analysis of the human immune system in translational research settings.

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