Multiple displacement amplification to create a long-lasting source of DNA for genetic studies - PubMed (original) (raw)
Review
Multiple displacement amplification to create a long-lasting source of DNA for genetic studies
Lovisa Lovmar et al. Hum Mutat. 2006 Jul.
Abstract
In many situations there may not be sufficient DNA collected from patient or population cohorts to meet the requirements of genome-wide analysis of SNPs, genomic copy number polymorphisms, or acquired copy number alternations. When the amount of available DNA for genotype analysis is limited, high performance whole-genome amplification (WGA) represents a new development in genetic analysis. It is especially useful for analysis of DNA extracted from stored histology slides, tissue samples, buccal swabs, or blood stains collected on filter paper. The multiple displacement amplification (MDA) method, which relies on isothermal amplification using the DNA polymerase of the bacteriophage phi29, is a recently developed technique for high performance WGA. This review addresses new trends in the technical performance of MDA and its applications to genetic analyses. The main challenge of WGA methods is to obtain balanced and faithful replication of all chromosomal regions without the loss of or preferential amplification of any genomic loci or allele. In multiple comparisons to other WGA methods, MDA appears to be most reliable for genotyping, with the most favorable call rates, best genomic coverage, and lowest amplification bias.
Copyright 2006 Wiley-Liss, Inc.
Similar articles
- Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplification.
Tzvetkov MV, Becker C, Kulle B, Nürnberg P, Brockmöller J, Wojnowski L. Tzvetkov MV, et al. Electrophoresis. 2005 Feb;26(3):710-5. doi: 10.1002/elps.200410121. Electrophoresis. 2005. PMID: 15690424 - Comparison of whole genome amplification methods for further quantitative analysis with microarray-based comparative genomic hybridization.
Lee YS, Tsai CN, Tsai CL, Chang SD, Hsueh DW, Liu CT, Ma CC, Lin SH, Wang TH, Wang HS. Lee YS, et al. Taiwan J Obstet Gynecol. 2008 Mar;47(1):32-41. doi: 10.1016/S1028-4559(08)60052-2. Taiwan J Obstet Gynecol. 2008. PMID: 18400580 - Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues.
Aviel-Ronen S, Qi Zhu C, Coe BP, Liu N, Watson SK, Lam WL, Tsao MS. Aviel-Ronen S, et al. BMC Genomics. 2006 Dec 12;7:312. doi: 10.1186/1471-2164-7-312. BMC Genomics. 2006. PMID: 17156491 Free PMC article. - Genomic DNA amplification by the multiple displacement amplification (MDA) method.
Lasken RS. Lasken RS. Biochem Soc Trans. 2009 Apr;37(Pt 2):450-3. doi: 10.1042/BST0370450. Biochem Soc Trans. 2009. PMID: 19290880 Review. - Whole genome amplification with Phi29 DNA polymerase to enable genetic or genomic analysis of samples of low DNA yield.
Silander K, Saarela J. Silander K, et al. Methods Mol Biol. 2008;439:1-18. doi: 10.1007/978-1-59745-188-8_1. Methods Mol Biol. 2008. PMID: 18370092 Review.
Cited by
- Droplet based whole genome amplification for sequencing minute amounts of purified Mycobacterium tuberculosis DNA.
Dippenaar A, Ismail N, Heupink TH, Grobbelaar M, Loubser J, Van Rie A, Warren RM. Dippenaar A, et al. Sci Rep. 2024 Apr 30;14(1):9931. doi: 10.1038/s41598-024-60545-1. Sci Rep. 2024. PMID: 38689002 Free PMC article. - Isothermal nucleic acid amplification and its uses in modern diagnostic technologies.
Srivastava P, Prasad D. Srivastava P, et al. 3 Biotech. 2023 Jun;13(6):200. doi: 10.1007/s13205-023-03628-6. Epub 2023 May 18. 3 Biotech. 2023. PMID: 37215369 Free PMC article. Review. - Benchmarking of Nanopore R10.4 and R9.4.1 flow cells in single-cell whole-genome amplification and whole-genome shotgun sequencing.
Ni Y, Liu X, Simeneh ZM, Yang M, Li R. Ni Y, et al. Comput Struct Biotechnol J. 2023 Mar 24;21:2352-2364. doi: 10.1016/j.csbj.2023.03.038. eCollection 2023. Comput Struct Biotechnol J. 2023. PMID: 37025654 Free PMC article. - Disjunction between canola distribution and the genetic structure of its recently described pest, the canola flower midge (Contarinia brassicola).
Campbell EO, Dupuis JR, Holowachuk J, Hladun S, Vankosky MA, Mori BA. Campbell EO, et al. Ecol Evol. 2020 Oct 26;10(23):13284-13296. doi: 10.1002/ece3.6927. eCollection 2020 Dec. Ecol Evol. 2020. PMID: 33304537 Free PMC article. - Disposable DNA Amplification Chips with Integrated Low-Cost Heaters.
Veltkamp HW, Akegawa Monteiro F, Sanders R, Wiegerink R, Lötters J. Veltkamp HW, et al. Micromachines (Basel). 2020 Feb 25;11(3):238. doi: 10.3390/mi11030238. Micromachines (Basel). 2020. PMID: 32106462 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous