Multiplexed genotyping with sequence-tagged molecular inversion probes (original) (raw)
- Article
- Published: 05 May 2003
- Johan Banér2,
- Maneesh Jain1 nAff3,
- Mats Nilsson2,
- Eugeni A Namsaraev1 nAff3,
- George A Karlin-Neumann1 nAff3,
- Hossein Fakhrai-Rad1 nAff3,
- Mostafa Ronaghi1,
- Thomas D Willis1 nAff3,
- Ulf Landegren2 &
- …
- Ronald W Davis1
Nature Biotechnology volume 21, pages 673–678 (2003)Cite this article
- 6324 Accesses
- 411 Citations
- 21 Altmetric
- Metrics details
Abstract
We report on the development of molecular inversion probe (MIP) genotyping, an efficient technology for large-scale single nucleotide polymorphism (SNP) analysis. This technique uses MIPs to produce inverted sequences, which undergo a unimolecular rearrangement and are then amplified by PCR using common primers and analyzed using universal sequence tag DNA microarrays, resulting in highly specific genotyping. With this technology, multiplex analysis of more than 1,000 probes in a single tube can be done using standard laboratory equipment. Genotypes are generated with a high call rate (95%) and high accuracy (>99%) as determined by independent sequencing.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
Similar content being viewed by others
References
- Patil, N. et al. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294, 1719–1723 (2001).
Article CAS Google Scholar - Syvanen, A.C. Accessing genetic variation: genotyping single nucleotide polymorphisms. Nat. Rev. Genet. 2, 930–942 (2001).
Article CAS Google Scholar - Nilsson, M. et al. Making ends meet in genetic analysis using padlock probes. Hum. Mutat. 19, 410–415 (2002).
Article CAS Google Scholar - Elnifro, E.M., Ashshi, A.M., Cooper, R.J. & Klapper, P.E. Multiplex PCR: optimization and application in diagnostic virology. Clin. Microbiol. Rev. 13, 559–570 (2000).
Article CAS Google Scholar - Lockhart, D.J. et al. Expression monitoring by hybridization to high-density oligonucleotide arrays. Nat. Biotechnol. 14, 1675–1680 (1996).
Article CAS Google Scholar - Schena, M., Shalon, D., Davis, R.W. & Brown, P.O. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science 270, 467–470 (1995).
Article CAS Google Scholar - Lyamichev, V. et al. Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes. Nat. Biotechnol. 17, 292–296 (1999).
Article CAS Google Scholar - Eis, P.S. et al. An invasive cleavage assay for direct quantitation of specific RNAs. Nat. Biotechnol. 19, 673–676 (2001).
Article CAS Google Scholar - Nilsson, M. et al. Padlock probes: circularizing oligonucleotides for localized DNA detection. Science 265, 2085–2088 (1994).
Article CAS Google Scholar - Lizardi, P.M. et al. Mutation detection and single-molecule counting using isothermal rolling-circle amplification. Nat. Genet. 19, 225–232 (1998).
Article CAS Google Scholar - Faruqi, A.F. et al. High-throughput genotyping of single nucleotide polymorphisms with rolling circle amplification. BMC Genomics 2, 4 (2001).
Article CAS Google Scholar - Antson, D.O., Isaksson, A., Landegren, U. & Nilsson, M. PCR-generated padlock probes detect single nucleotide variation in genomic DNA. Nucleic Acids Res. 28, E58 (2000).
Article CAS Google Scholar - Shoemaker, D.D., Lashkari, D.A., Morris, D., Mittmann, M. & Davis, R.W. Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar-coding strategy. Nat. Genet. 14, 450–456 (1996).
Article CAS Google Scholar - Zhang, D.Y., Brandwein, M., Hsuih, T.C. & Li, H. Amplification of target-specific, ligation-dependent circular probe. Gene 211, 277–285 (1998).
Article CAS Google Scholar - Abravaya, K., Carrino, J.J., Muldoon, S. & Lee, H.H. Detection of point mutations with a modified ligase chain reaction (Gap-LCR). Nucleic Acids Res. 23, 675–682 (1995).
Article CAS Google Scholar - Banér, J., Nilsson, M., Mendel-Hartvig, M. & Landegren, U. Signal amplification of padlock probes by rolling circle replication. Nucleic Acids Res. 26, 5073–5078 (1998).
Article Google Scholar - Gharavi, A.G. et al. IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. Nat. Genet. 26, 354–357 (2000).
Article CAS Google Scholar - Fakhrai-Rad, H., Pourmand, N. & Ronaghi, M. Pyrosequencing: an accurate detection platform for single nucleotide polymorphisms. Hum. Mutat. 19, 479–485 (2002).
Article CAS Google Scholar - Ronaghi, M. Pyrosequencing sheds light on DNA sequencing Genome Res. 11, 3–11 (2001).
Article CAS Google Scholar - Fan, J.B. et al. Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. Genome Res. 10, 853–860 (2000).
Article CAS Google Scholar - Landegren, U., Kaiser, R., Sanders, J. & Hood, L. A ligase-mediated gene detection technique. Science 241, 1077–1080 (1988).
Article CAS Google Scholar
Acknowledgements
We thank K. Tran, T. Brundage, J. Patterson, E. Prakash and C. Bruckner for technical assistance and T. Jones and P. Oefner for helpful discussions. This work was supported by NIH HG00205. The work in Uppsala was supported by the Beijer and Wallenberg Foundations, the Research Councils of Sweden for natural science and for medicine, the Swedish Cancer Fund and Polysaccharide Research AB (Uppsala).
Author information
Author notes
- Paul Hardenbol, Maneesh Jain, Eugeni A Namsaraev, George A Karlin-Neumann, Hossein Fakhrai-Rad & Thomas D Willis
Present address: ParAllele BioScience, 384 Oyster Point Blvd Suite 8, S., San Francisco, California, 94080, USA
Authors and Affiliations
- Stanford Genome Technology Center, Stanford University, 855 California Avenue, Palo Alto, 94304, California, USA
Paul Hardenbol, Maneesh Jain, Eugeni A Namsaraev, George A Karlin-Neumann, Hossein Fakhrai-Rad, Mostafa Ronaghi, Thomas D Willis & Ronald W Davis - Department of Genetics and Pathology, The Beijer Laboratory, Rudbeck Laboratory, Uppsala, Se-751 85, Sweden
Johan Banér, Mats Nilsson & Ulf Landegren
Authors
- Paul Hardenbol
You can also search for this author inPubMed Google Scholar - Johan Banér
You can also search for this author inPubMed Google Scholar - Maneesh Jain
You can also search for this author inPubMed Google Scholar - Mats Nilsson
You can also search for this author inPubMed Google Scholar - Eugeni A Namsaraev
You can also search for this author inPubMed Google Scholar - George A Karlin-Neumann
You can also search for this author inPubMed Google Scholar - Hossein Fakhrai-Rad
You can also search for this author inPubMed Google Scholar - Mostafa Ronaghi
You can also search for this author inPubMed Google Scholar - Thomas D Willis
You can also search for this author inPubMed Google Scholar - Ulf Landegren
You can also search for this author inPubMed Google Scholar - Ronald W Davis
You can also search for this author inPubMed Google Scholar
Corresponding author
Correspondence toMostafa Ronaghi.
Ethics declarations
Competing interests
P.H., M.J., E.A.N., G.A.K.-N., H. F.-R. and T.D.W. are currently employed by ParAllele Bioscience (South San Francisco, California), a company that is commercializing the Molecular Inversion Probe Assay. M.R., U.L. and R.W.D. are shareholders of ParAllele Bioscience. J.B. and M.N. have no association with the company.
Rights and permissions
About this article
Cite this article
Hardenbol, P., Banér, J., Jain, M. et al. Multiplexed genotyping with sequence-tagged molecular inversion probes.Nat Biotechnol 21, 673–678 (2003). https://doi.org/10.1038/nbt821
- Received: 18 October 2002
- Accepted: 21 February 2003
- Published: 05 May 2003
- Issue Date: 01 June 2003
- DOI: https://doi.org/10.1038/nbt821