Abstract
We developed a general method, microarray-based genomic selection (MGS), capable of selecting and enriching targeted sequences from complex eukaryotic genomes without the repeat blocking steps necessary for bacterial artificial chromosome (BAC)-based genomic selection. We demonstrate that large human genomic regions, on the order of hundreds of kilobases, can be enriched and resequenced with resequencing arrays. MGS, when combined with a next-generation resequencing technology, can enable large-scale resequencing in single-investigator laboratories.
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Acknowledgements
Funding for this work was provided by the US National Institutes of Health (NIH) National Institute of Mental Health RO1 MH076439-03 (MEZ) and by the Gift Fund, NIH.
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T.J.A. and C.M. are employees of NimbleGen Systems, Inc.
Supplementary information
Supplementary Text and Figures
Supplementary Figures 1–2, Supplementary Methods, Supplementary Table 1 (PDF 1776 kb)
Supplementary Data 1
Oligonucleotide Capture Probes for 50kb FMR1 Genomic Region (DOC 25359 kb)
Supplementary Data 2
Oligonucleotide Capture Probes for 304kb FMR1/FMR2 Genomic Region (DOC 28891 kb)
Supplementary Data 3
DNA Sequence Data for 50kb Region (ZIP 65 kb)
Supplementary Data 4
DNA Sequence Data for 304kb Region (ZIP 1893 kb)
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Okou, D., Steinberg, K., Middle, C. et al. Microarray-based genomic selection for high-throughput resequencing. Nat Methods 4, 907–909 (2007). https://doi.org/10.1038/nmeth1109
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DOI: https://doi.org/10.1038/nmeth1109
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