Defining best practice for microarray analyses in nutrigenomic studies.

作者: Paola Garosi , Carlotta De Filippo , Marjan van Erk , Philippe Rocca-Serra , Susanna-Assunta Sansone

DOI: 10.1079/BJN20041385

关键词:

摘要: Microarrays represent a powerful tool for studies of diet-gene interactions. Their use is, however, associated with number technical challenges and potential pitfalls. The cost microarrays continues to drop but is still comparatively high. This, coupled the complex logistical issues performing nutritional microarray studies, often means that compromises have be made in type samples analysed. Additionally, variations between array platforms analytical procedures will almost inevitably lead differences transcriptional responses observed. Consequently, conflicting data may produced, important effects missed and/or false leads generated (e.g. apparent patterns differential gene regulation ultimately prove incorrect or not significant). This likely particularly true field nutrition, which we expect many dietary bioactive agents at nutritionally relevant concentrations elicit subtle changes transcription critically biological terms difficult detect reliably. Thus, great care should always taken designing executing studies. article seeks provide an overview both main practical theoretical considerations sources variation error. Wherever possible, recommendations are on what propose best approach. overall aims basic framework advice researchers who new promote discussion standardisation practice field. © Authors 2005.

参考文章(61)
Scott Taylor, Stephanie Smith, Brad Windle, Anthony Guiseppi‐Elie, Impact of surface chemistry and blocking strategies on DNA microarrays Nucleic Acids Research. ,vol. 31, ,(2003) , 10.1093/NAR/GNG086
B.M. Bolstad, R.A Irizarry, M. Astrand, T.P. Speed, A comparison of normalization methods for high density oligonucleotide array data based on variance and bias Bioinformatics. ,vol. 19, pp. 185- 193 ,(2003) , 10.1093/BIOINFORMATICS/19.2.185
Niels Tolstrup, Peter S Nielsen, Jens G Kolberg, Annett M Frankel, Henrik Vissing, Sakari Kauppinen, OligoDesign: optimal design of LNA (locked nucleic acid) oligonucleotide capture probes for gene expression profiling Nucleic Acids Research. ,vol. 31, pp. 3758- 3762 ,(2003) , 10.1093/NAR/GKG580
R. N. Van Gelder, M. E. von Zastrow, A. Yool, W. C. Dement, J. D. Barchas, J. H. Eberwine, Amplified RNA synthesized from limited quantities of heterogeneous cDNA. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 87, pp. 1663- 1667 ,(1990) , 10.1073/PNAS.87.5.1663
LR Baugh, AA Hill, EL Brown, Craig P Hunter, Quantitative analysis of mRNA amplification by in vitro transcription Nucleic Acids Research. ,vol. 29, ,(2001) , 10.1093/NAR/29.5.E29
Ahmed Ashour Ahmed, Maria Vias, N Gopalakrishna Iyer, Carlos Caldas, James D Brenton, None, Microarray segmentation methods significantly influence data precision Nucleic Acids Research. ,vol. 32, ,(2004) , 10.1093/NAR/GNH047
Ali Naderi, Ahmed A Ahmed, Nuno L Barbosa-Morais, Samuel Aparicio, James D Brenton, Carlos Caldas, None, Expression microarray reproducibility is improved by optimising purification steps in RNA amplification and labelling BMC Genomics. ,vol. 5, pp. 9- 9 ,(2004) , 10.1186/1471-2164-5-9
Paul K Tan, Thomas J Downey, Edward L Spitznagel Jr, Pin Xu, Dadin Fu, Dimiter S Dimitrov, Richard A Lempicki, Bruce M Raaka, Margaret C Cam, Evaluation of gene expression measurements from commercial microarray platforms Nucleic Acids Research. ,vol. 31, pp. 5676- 5684 ,(2003) , 10.1093/NAR/GKG763