Treffer: The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models.

Title:
The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models.
Authors:
Shi, L., Campbell, G., Jones, W.D., Campagne, F., Wen, Z., Walker, S.J., Su, Z., Chu, T.M., Goodsaid, F.M., Pusztai, L., Shaughnessy, J.D., Oberthuer, A., Thomas, R.S., Paules, R.S., Fielden, M., Barlogie, B., Chen, W., Du, P., Fischer, M., Furlanello, C., Gallas, B.D., Ge, X., Megherbi, D.B., Symmans, W.F., Wang, M.D., Zhang, J., Bitter, H., Brors, B., Bushel, P.R., Bylesjo, M., Chen, M., Cheng, J., Chou, J., Davison, T.S., Delorenzi, M., Deng, Y., Devanarayan, V., Dix, D.J., Dopazo, J., Dorff, K.C., Elloumi, F., Fan, J., Fan, S., Fan, X., Fang, H., Gonzaludo, N., Hess, K.R., Hong, H., Huan, J., Irizarry, R.A., Judson, R., Juraeva, D., Lababidi, S., Lambert, C.G., Li, L., Li, Y., Li, Z., Lin, S.M., Liu, G., Lobenhofer, E.K., Luo, J., Luo, W., McCall, M.N., Nikolsky, Y., Pennello, G.A., Perkins, R.G., Philip, R., Popovici, V., Price, N.D., Qian, F., Scherer, A., Shi, T., Shi, W., Sung, J., Thierry-Mieg, D., Thierry-Mieg, J., Thodima, V., Trygg, J., Vishnuvajjala, L., Wang, S.J., Wu, J., Wu, Y., Xie, Q., Yousef, W.A., Zhang, L., Zhang, X., Zhong, S., Zhou, Y., Zhu, S., Arasappan, D., Bao, W., Lucas, A.B., Berthold, F., Brennan, R.J., Buness, A., Catalano, J.G., Chang, C., Chen, R., Cheng, Y., Cui, J., Czika, W., Demichelis, F., Deng, X., Dosymbekov, D., Eils, R., Feng, Y., Fostel, J., Fulmer-Smentek, S., Fuscoe, J.C., Gatto, L., Ge, W., Goldstein, D.R., Guo, L., Halbert, D.N., Han, J., Harris, S.C., Hatzis, C., Herman, D., Huang, J., Jensen, R.V., Jiang, R., Johnson, C.D., Jurman, G., Kahlert, Y., Khuder, S.A., Kohl, M., Li, J., Li, M., Li, Q.Z., Li, S., Liu, J., Liu, Y., Liu, Z., Meng, L., Madera, M., Martinez-Murillo, F., Medina, I., Meehan, J., Miclaus, K., Moffitt, R.A., Montaner, D., Mukherjee, P., Mulligan, G.J., Neville, P., Nikolskaya, T., Ning, B., Page, G.P., Parker, J., Parry, R.M., Peng, X., Peterson, R.L., Phan, J.H., Quanz, B., Ren, Y., Riccadonna, S., Roter, A.H., Samuelson, F.W., Schumacher, M.M., Shambaugh, J.D., Shi, Q., Shippy, R., Si, S., Smalter, A., Sotiriou, C., Soukup, M., Staedtler, F., Steiner, G., Stokes, T.H., Sun, Q., Tan, P.Y., Tang, R., Tezak, Z., Thorn, B., Tsyganova, M., Turpaz, Y., Vega, S.C., Visintainer, R., von Frese, J., Wang, C., Wang, E., Wang, J., Wang, W., Westermann, F., Willey, J.C., Woods, M., Wu, S., Xiao, N., Xu, J., Xu, L., Yang, L., Zeng, X., Zhang, M., Zhao, C., Puri, R.K., Scherf, U., Tong, W., Wolfinger, R.D.
Contributors:
MAQC Consortium
Publication Year:
2025
Collection:
Université de Lausanne (UNIL): Serval - Serveur académique lausannois
Document Type:
Fachzeitschrift article in journal/newspaper
Language:
English
Relation:
Nature Biotechnology; 1546-1696[electronic], 1087-0156[linking]; https://iris.unil.ch/handle/iris/72677; serval:BIB_48AD782C95FB; 000280757500023
DOI:
10.1038/nbt.1665
Accession Number:
edsbas.6F8F6E69
Database:
BASE

Weitere Informationen

Gene expression data from microarrays are being applied to predict preclinical and clinical endpoints, but the reliability of these predictions has not been established. In the MAQC-II project, 36 independent teams analyzed six microarray data sets to generate predictive models for classifying a sample with respect to one of 13 endpoints indicative of lung or liver toxicity in rodents, or of breast cancer, multiple myeloma or neuroblastoma in humans. In total, >30,000 models were built using many combinations of analytical methods. The teams generated predictive models without knowing the biological meaning of some of the endpoints and, to mimic clinical reality, tested the models on data that had not been used for training. We found that model performance depended largely on the endpoint and team proficiency and that different approaches generated models of similar performance. The conclusions and recommendations from MAQC-II should be useful for regulatory agencies, study committees and independent investigators that evaluate methods for global gene expression analysis.