본문 바로가기
KERD
논문KCI 등재

An Attempt for Combining Microarray Data Sets by Adjusting Gene Expressions

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류의학일반

초록

Purpose: The diverse experimental environments in microarray technology, such as the different platforms or different RNA sources, can cause biases in the analysis of multiple microarrays. These systematic effects present a substantial obstacle for the analysis of microarray data, and the resulting information may be inconsistent and unreliable. Therefore, we introduced a simple integration method for combining microaray data sets that are derived from different experimental conditions, and we expected that more reliable information can be detected from the combined data set rather than from the separated data sets. Materials and Methods: This method is based on the distributions of the gene expression ratios among the different microarray data sets and it transforms, gene by gene, the gene expression ratios into the form of the reference data set. The efficiency of the proposed integration method was evaluated using two microarray data sets, which were derived from different RNA sources, and a newly defined measure, the mixture score. Results: The proposed integration method intermixed the two data sets that were obtained from different RNA sources, which in turn reduced the experimental bias between the two data sets, and the mixture score increased by 24.2%. A data set combined by the proposed method preserved the inter-group relationship of the separated data sets. Conclusion: The proposed method worked well in adjusting systematic biases, including the source effect. The ability to use an effectively integrated microarray data set yields more reliable results due to the larger sample size and this also decreases the chance of false negatives. (Cancer Res Treat. 2007;39:74-81)

Abstract

Purpose: The diverse experimental environments in microarray technology, such as the different platforms or different RNA sources, can cause biases in the analysis of multiple microarrays. These systematic effects present a substantial obstacle for the analysis of microarray data, and the resulting information may be inconsistent and unreliable. Therefore, we introduced a simple integration method for combining microaray data sets that are derived from different experimental conditions, and we expected that more reliable information can be detected from the combined data set rather than from the separated data sets. Materials and Methods: This method is based on the distributions of the gene expression ratios among the different microarray data sets and it transforms, gene by gene, the gene expression ratios into the form of the reference data set. The efficiency of the proposed integration method was evaluated using two microarray data sets, which were derived from different RNA sources, and a newly defined measure, the mixture score. Results: The proposed integration method intermixed the two data sets that were obtained from different RNA sources, which in turn reduced the experimental bias between the two data sets, and the mixture score increased by 24.2%. A data set combined by the proposed method preserved the inter-group relationship of the separated data sets. Conclusion: The proposed method worked well in adjusting systematic biases, including the source effect. The ability to use an effectively integrated microarray data set yields more reliable results due to the larger sample size and this also decreases the chance of false negatives. (Cancer Res Treat. 2007;39:74-81)

참고문헌 (18)

  1. Breitling R, "Loss of compartmentalization causes misregulation of lysine biosynthesis in peroxisome-deficient yeast cells", 1, pp.978~986 (2002)
  2. Lee PD, "Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies", 12, pp.292~297 (2002)
  3. Rhodes DR, "Meta-analysis of microarrays: interstudy validation of gene expression profiles reveals pathway dysregulation in prostate cancer", 62, pp.4427~4433 (2002)
  4. Choi JK, "Combining multiple microarray studies and modeling interstudy variation", 19(1), pp.184~190 (2003)
  5. Detours V, "Integration and cross-validation of high-throughput gene expression data: Comparing heterogeneous data sets", 546, pp.98~102 (2003)
  6. Ramaswamy S, "A molecular signature of metastasis in primary solid tumors", 33, pp.49~54 (2003)
  7. Xin W, "Dysregulation of the annexin family protein family is associated with prostate cancer progression", 162, pp.255~261 (2003)
  8. Sorlie T, "Repeated observation of breast tumor subtypes in independent gene expression data sets", 100, pp.8418~8423 (2004)
  9. Choi JK, "Integrative analysis of multiple gene expression profiles applied to liver cancer study", 565, pp.93~100 (2004)
  10. Kuo WP, "Analysis of matched mRNA measurements from two different microarray technologies", 18, pp.405~412 (2002)
  11. Alter O, "Singular value decomposition for genome-wide expression data processing and modelling", 97, pp.10101~10106 (2000)
  12. Nielsen TO, "Molecular characterisation of soft tissue tumours: a gene expression study", 359, pp.1301~1307 (2002)
  13. Benito M, "Adjustment of systematic microarray data biases", 20, pp.105~114 (2004)
  14. Jiang H, "Joint analysis of two microarray gene-expression data sets to select lung adenocarcinoma marker genes", 5, pp.81~ (2004)
  15. Park T, "Combining multiple microarrays in the presence of controlling variables", 2, pp.1682~1689 (2006)
  16. Kim TM, "Determination of genes related to gastrointestinal tract origin cancer cells using a cDNA microarray", 11, pp.79~86 (2005)
  17. Feldman AL, "Advantages of mRNA amplification for microarray analysis", 33, pp.906~914 (2002)
  18. Schneider J, "Systematic analysis of T7 RNA polymerase based in vitro linear RNA amplification for use in microarray experiments", 5, pp.29~ (2004)

관련 논문AI추천

이 간행물의 다른 논문 (7건)