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. 2008 Apr 15;36(10):3194–3201. doi: 10.1093/nar/gkm1156

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© 2008 The Author(s)

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 5. — The sequences for the influenza B strain (FluBHA) used to generate microarray probe sets are shown. Also presented are the conventional sequencing results from an influenza B Victoria lineage sample, the results obtained using the same sample for RPM v.1 microarray analysis, and the model prediction based on the conventional sequence. Region A represents a section sequence where SNPs are very far apart or close together. In this region, the model and microarray data are in good agreement. Region B sequences have SNPs with an intermediate frequency and the agreement between model and experiment is reduced. Region C is similar to B although the number of observed base calls observed is higher.